1. Medicine

Bisphosphonate drugs have actions in the lung and inhibit the mevalonate pathway in alveolar macrophages

  1. Marcia A Munoz
  2. Emma K Fletcher
  3. Oliver P Skinner
  4. Julie Jurczyluk
  5. Esther Kristianto
  6. Mark P Hodson
  7. Shuting Sun
  8. Frank H Ebetino
  9. David R Croucher
  10. Philip M Hansbro
  11. Jacqueline R Center
  12. Michael J Rogers  Is a corresponding author
  1. Garvan Institute of Medical Research and St Vincent’s Clinical School, UNSW Sydney, Australia
  2. Victor Chang Cardiac Research Institute Innovation Centre, Australia
  3. School of Pharmacy, University of Queensland, Australia
  4. BioVinc, United States
  5. University of Southern California, United States
  6. Centre for Inflammation, Centenary Institute and University of Technology Sydney, Australia
https://doi.org/10.7554/eLife.72430
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Cite this article
  1. Marcia A Munoz
  2. Emma K Fletcher
  3. Oliver P Skinner
  4. Julie Jurczyluk
  5. Esther Kristianto
  6. Mark P Hodson
  7. Shuting Sun
  8. Frank H Ebetino
  9. David R Croucher
  10. Philip M Hansbro
  11. Jacqueline R Center
  12. Michael J Rogers
(2021)
Bisphosphonate drugs have actions in the lung and inhibit the mevalonate pathway in alveolar macrophages
eLife 10:e72430.
https://doi.org/10.7554/eLife.72430
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Abstract

Bisphosphonates drugs target the skeleton and are used globally for the treatment of common bone disorders. Nitrogen-containing bisphosphonates act by inhibiting the mevalonate pathway in bone-resorbing osteoclasts but, surprisingly, also appear to reduce the risk of death from pneumonia. We overturn the long-held belief that these drugs act only in the skeleton and show that a fluorescently labelled bisphosphonate is internalised by alveolar macrophages and large peritoneal macrophages in vivo. Furthermore, a single dose of a nitrogen-containing bisphosphonate (zoledronic acid) in mice was sufficient to inhibit the mevalonate pathway in tissue-resident macrophages, causing the build-up of a mevalonate metabolite and preventing protein prenylation. Importantly, one dose of bisphosphonate enhanced the immune response to bacterial endotoxin in the lung and increased the level of cytokines and chemokines in bronchoalveolar fluid. These studies suggest that bisphosphonates, as well as preventing bone loss, may boost immune responses to infection in the lung and provide a mechanistic basis to fully examine the potential of bisphosphonates to help combat respiratory infections that cause pneumonia.

Editor's evaluation

Your paper is a careful analysis to understand the effects of bisphosphonates, long thought to act only on osteoclasts to block bone resorption, on the lung. You show that drugs in this class act on pulmonary macrophages and block protein prenylation. This leads to an enhanced response to bacterial endotoxin and immune response to bacterial endotoxin with increased levels of cytokines and chemokines in bronchoalveolar fluid – a series of events that may explain reduced rates of pneumonia seen in patients treated with these drugs. This clinical observation has long defied our understanding.

https://doi.org/10.7554/eLife.72430.sa0

Introduction

Nitrogen-containing bisphosphonates (N-BPs) are a class of bone-seeking drugs used worldwide as the frontline treatment for disorders of excessive bone resorption such as post-menopausal osteoporosis and cancer-associated bone disease (Russell, 2011). By virtue of their avidity for calcium ions, N-BPs bind rapidly to the skeleton, where they are internalised by bone-degrading osteoclasts (Russell et al., 2008; Rogers et al., 2020). Intracellularly, N-BPs disable osteoclast function by inhibiting the enzyme farnesyl diphosphate (FPP) synthase in the mevalonate pathway (van Beek et al., 1999; Dunford et al., 2001), thereby preventing the post-translational prenylation of small GTPase proteins necessary for osteoclast function (Luckman et al., 1998; Fisher et al., 1999).

There is increasing evidence that N-BP drugs, such as zoledronic acid (ZOL), have benefits beyond preventing bone loss (Center et al., 2020), and, unexpectedly, N-BP therapy has recently been linked to reduced risk of mortality from pneumonia (Colón-Emeric et al., 2010; Sing et al., 2020). In a randomised, controlled trial of >2000 hip fracture patients, ZOL therapy reduced the risk of death by 28% compared to placebo infusion (Lyles et al., 2007). Retrospective analysis also suggested that ZOL-treated patients were less likely to die from pneumonia than placebo-treated subjects (Colón-Emeric et al., 2010). Recently, a ‘real-world’ population-based, observational study of hip fracture patients aged 50 years or above also showed a significant reduction in risk of pneumonia and pneumonia mortality in hip fracture patients that had received N-BP therapy compared to no treatment or other osteoporosis medications (Sing et al., 2020). Similar findings were reported in the post hoc analysis of a randomised controlled trial of ZOL in women over the age of 65 years (Reid et al., 2021). Pneumonia is the most frequent cause of admission to ICU, and a study of long-term patients in respiratory ICU revealed a significant reduction in mortality in people treated with the N-BP pamidronate compared to those without treatment (Schulman et al., 2016). Furthermore, in a retrospective cohort study of ICU subjects, we showed a 59% reduction in mortality in patients treated with bisphosphonate prior to hospitalisation (Lee et al., 2016). However, the mechanisms underlying the surprising beneficial effects of these drugs on pneumonia and in ICU patients are unknown.

Globally, respiratory diseases constitute the most common cause of death, and thus, therapies that boost the immune response to common lung infections are urgently needed. Bacterial infections such as Streptococcus pneumoniae, Haemophilus influenzae, Chlamydia pneumoniae, and Staphylococcus aureus are the main cause of community-acquired pneumonia. Importantly, these pathogens also underlie severe complications of viral respiratory disease that can significantly increase morbidity and mortality. For example, influenza-related mortality is often associated with pneumonia caused by co- or secondary bacterial infection (Morris et al., 2017). In this study, we debunk the long-held view that N-BP drugs act only in the skeleton in healthy mice and show that even a single dose of N-BP in mice is sufficient to affect tissue-resident macrophages, including lung alveolar macrophages (AMΦ), boosting their response to bacterial endotoxin.

Results and discussion

Systemically administered N-BP is internalised by tissue-resident macrophages outside the skeleton

We previously reported that cultured macrophages and tumour-associated macrophages in vivo, like osteoclasts, have the ability to internalise N-BP by endocytosis (Thompson et al., 2006; Junankar et al., 2015). Given the important role of AMΦ in lung homeostasis and the initial immune response to respiratory infection (Byrne et al., 2015; Crane et al., 2018), we focused on whether these cells are capable of internalising a systemically administered, fluorescently labelled analogue of ZOL (AF647-ZOL). Like most other fluorescently labelled N-BPs (Roelofs et al., 2010), AF647-ZOL did not inhibit protein prenylation compared to the parent N-BP (ZOL) when tested in cultures of bone marrow-derived macrophages (BMDM; Figure 1a), but can be used to track drug uptake by cells in vivo (Junankar et al., 2015). Animals were injected with a single intravenous (i.v.) dose of AF647-ZOL, and cells collected by bronchoalveolar lavage (BAL) were analysed by flow cytometry. In the absence of immune challenge in mice, approximately 90% of cells in BAL were AMΦ (Figure 1—figure supplement 1). Importantly, >98% of AMΦ (TCRβ-B220-CD11blo/-CD11chiF4/80+) in BAL samples were clearly labelled with AF647-ZOL 4 hr after i.v. administration (Figure 1b–d).

Figure 1 with 1 supplement see all
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Bisphosphonate is internalised by alveolar and peritoneal macrophages in vivo.

(a) An in vitro prenylation assay detects unprenylated Rab GTPases (uRabs) in bone marrow-derived macrophages after culture for 24 hr with 1, 5, or 10 μM zoledronic acid (ZOL) compared to 1, 5, or 10 μM AF647-ZOL. (b) FACS plots showing the percentage of labelled single cells in bronchoalveolar lavage (BAL) samples after one intravenous (i.v.) dose of AF647-ZOL compared to saline-treated mice. (c) AF647-ZOL-positive cells were predominantly alveolar macrophages (AMΦ), that is, B220-TCRb-, CD11c+F4/80+ singlets. (d) Histograms show AF647-ZOL mean fluorescence intensity (MFI) of AMΦ in BAL samples from n = 3 control mice (white) and n = 3 AF647-ZOL-treated mice (grey). (e) FACS plot illustrating the percentages of small peritoneal macrophages/SPMΦ (B220-TCRb- singlets, CD11bintF4/80int) and large peritoneal macrophages/LPMΦ (B220-TCRb- singlets, CD11bhiF4/80hi) in peritoneal lavage. (f) Percentage of labelled peritoneal cells 4 hr after one i.v. injection of saline (left) or AF647-ZOL (right). (g) The labelled cell population (AF647-ZOL+, 82.4%) in (f) consists predominantly of CD11bhiF4/80hi LPMΦ. (h) Histograms show the MFI of LPMΦ from saline- (white) and AF647-ZOL-treated (grey) mice. (i) MFI (AF647 MFI) values from SPMΦ and LPMΦ isolated from saline- or AF647-ZOL-treated animals. Bars represent mean ± SD (n = 3 mice per group in (h, i); each symbol represents the measurement from an individual mouse). FACS plots in (b, c, e–g) are representative of three mice per group.

Figure 1—source data 1

In vitro prenylation assay of BMDM following treatment with ZOL or AF647-ZOL.

https://cdn.elifesciences.org/articles/72430/elife-72430-fig1-data1-v1.zip
Figure 1—source data 2

In vitro prenylation assay of BMDM following treatment with ZOL or AF647-ZOL, showing cropped regions of the blot (uRabs and loading control).

https://cdn.elifesciences.org/articles/72430/elife-72430-fig1-data2-v1.zip

As a comparison with AMΦ, we also examined N-BP uptake in peritoneal macrophages (PMΦ). Under baseline conditions, 80% of cells obtained by peritoneal lavage (PL) consisted of PMΦ (B220- TCRb- Siglec-F- Ly6G- CD11b+ F4/80+), most of which were CD11bhiF4/80hi large PMΦ, with a less abundant population of CD11b+F4/80int small PMΦ (Ghosn et al., 2010; Cassado Ados et al., 2015; Figure 1e, Figure 1—figure supplement 1). Similar to BAL cells, approximately 80% of peritoneal cells incorporated AF647-ZOL after a single i.v. dose (Figure 1f), the majority of which (99%) were CD11bhiF4/80hi large PMΦ (Figure 1g and h). In contrast, the CD11b+F4/80int small PMΦ incorporated negligible amounts of fluorescently labelled ZOL (Figure 1i). The reason why uptake of N-BP occurred selectively in large PMΦ rather than in small PMΦ remains to be determined, although these subsets differ in their origin, phenotype, and function (Cassado Ados et al., 2015).

In addition to the well-described uptake of N-BP by osteoclasts in bone (Rogers et al., 2020; Coxon et al., 2008), these findings clearly demonstrate that N-BP can also be efficiently internalised in vivo by tissue-resident macrophages outside the skeleton, including AMΦ in the lung and LPMΦ in the peritoneal cavity.

A single i.v. dose of N-BP is sufficient to inhibit the mevalonate pathway in alveolar and peritoneal macrophages

Despite the rapid bone-targeting property of N-BPs, it has been shown in rodents that small amounts of ZOL can accumulate in soft tissues (Green and Rogers, 2002); however, the concentrations that can be achieved are unknown. To determine whether tissue-resident macrophages can incorporate sufficient N-BP in vivo to have a pharmacologic effect, we analysed two biochemical outcomes that, together, are reliable features of intracellular N-BP action in cells (Rogers et al., 2020): (i) the cytoplasmic build-up of the upstream metabolite isopentenyl diphosphate (IPP) and its isomer dimethylallyl diphosphate (DMAPP) (Räikkönen et al., 2009); and (ii) reduced production of the isoprenoid lipid geranylgeranyl diphosphate (GGPP), with the consequent accumulation of unprenylated small GTPase proteins including those of the Rab and Rho superfamilies (Luckman et al., 1998; Figure 2a). To address whether the potent N-BP ZOL has pharmacological effects on AMΦ and PMΦ, we used liquid chromatography tandem mass spectrometry (LC-MS/MS) to examine the accumulation of IPP/DMAPP and a sensitive biochemical in vitro assay to detect changes in the level of unprenylated Rab proteins (Ali et al., 2015; Rogers et al., 2020).

Figure 2
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Systemically administered bisphosphonate has pharmacological activity on the mevalonate pathway in alveolar and peritoneal macrophages in vivo.

(a) Flux though the mevalonate pathway (black arrows) enables prenylation of Rab GTPases by utilising geranylgeranyl diphosphate (GGPP) (step 1); inhibition of farnesyl diphosphate (FPP) synthase by nitrogen-containing bisphosphonate (N-BP) (step 2) causes upstream build-up of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (step 3) and prevents downstream Rab prenylation by reducing GGPP synthesis (red arrows, step 4). (b) Detection of IPP/DMAPP (arrowhead) by liquid chromatography tandem mass spectrometry (LC-MS/MS) in cells from bronchoalveolar lavage (BAL) (left) and peritoneal lavage (PL) (right) samples 48 hr after intravenous (i.v.) zoledronic acid (ZOL) or saline treatment. Coloured peaks in the chromatogram depict the relative abundance of IPP/DMAPP. (c) Detection of unprenylated Rab GTPases (uRabs) in cells from BAL (left) and PL (right) samples 48 hr after i.v. ZOL or saline treatment. Data are representative of three separate experiments.

Figure 2—source data 1

Original blots of the in vitro prenylation assay of BAL cells and PL cells, following treatment of mice with a single i.v. dose of ZOL.

https://cdn.elifesciences.org/articles/72430/elife-72430-fig2-data1-v1.zip
Figure 2—source data 2

Original blots of the in vitro prenylation assay of BAL cells and PL cells following treatment of mice with a single i.v. dose of ZOL, showing cropped regions of the blots (uRabs and loading control) and molecular mass markers.

https://cdn.elifesciences.org/articles/72430/elife-72430-fig2-data2-v1.zip

LC-MS/MS analysis showed that IPP/DMAPP was undetectable in extracts of BAL or PL cells from saline-treated mice, but there was a clear increase in the level of IPP/DMAPP in BAL and PL cells collected 48 hr after a single i.v. injection of ZOL (Figure 2b). Importantly, ZOL treatment also resulted in a marked accumulation of unprenylated Rab proteins in BAL and PL cell samples (Figure 2c). It is unlikely that such an effect of N-BP on protein prenylation in macrophages in vivo could have been detected using the relatively insensitive western blot approach previously employed to study bone-resorbing osteoclasts, which engulf large amounts of N-BP (Frith et al., 2001; Rogers et al., 2020). However, the development of a much more sensitive in vitro prenylation assay (Ali et al., 2015) now allows the detection of subtle effects on protein prenylation in cells outside the skeleton that may internalise much smaller quantities of N-BP.

Together with the evidence for uptake of N-BP by AMΦ and large PMΦ and (Figure 1), these findings demonstrate unequivocally that systemic administration of N-BP has pharmacological activity outside the skeleton in healthy mice. We show that a single dose of ZOL is sufficient to inhibit the mevalonate pathway in tissue-resident macrophages (AMΦ and PMΦ), causing a build-up of IPP/DMAPP metabolites and an accumulation of unprenylated small GTPase proteins – characteristic hallmarks of N-BP action (Rogers et al., 2020). Although still to be confirmed in humans, our findings overturn the long-standing textbook paradigm that N-BP drugs, which have been in clinical use for several decades (Russell, 2011), act only in the skeleton. Our findings also shed new light on the commonest side effect of N-BP therapy, a transient acute phase response. This was previously thought to be caused by the accumulation of IPP in circulating monocytes, which then activates Vγ9Vδ2-T cells to produce TNFα and IFNγ (Roelofs et al., 2009). Our findings suggest that tissue-resident macrophages, such as AMΦ and large PMΦ, are in fact a more likely source of the IPP responsible for the activation of Vγ9Vδ2-T cells.

Treatment with N-BP in vivo enhances the production of cytokines and chemokines in response to immune challenge

We recently reported that loss of protein prenylation in cultured monocytes promotes the formation of the NLRP3 inflammasome, resulting in increased caspase-1-mediated processing of pro-IL-1β following bacterial endotoxin (lipopolysaccharide [LPS]) stimulation (Skinner et al., 2019). Therefore, we next examined whether N-BP-mediated inhibition of protein prenylation in tissue-resident macrophages alters the response to LPS in vivo, particularly in the lung. Mice were challenged intranasally (i.n.) or intraperitoneally (i.p.) with LPS 48 hr after i.v. administration of ZOL or saline (Figure 3a). ZOL treatment alone did not alter the percentage, total number or viability of AMΦ recovered in BAL samples (Figure 3—figure supplement 1), nor had any effect on the levels of cytokines/chemokines in BAL fluid (Figure 3b). However, i.n. LPS administration in ZOL-treated mice resulted in a significant increase (2.5- to 5.0-fold) in the production of proinflammatory cytokines IL-1β, IL-6, TNFα, G-CSF, GM-CSF and chemokines CXCL1, CCL2, CCL3, CCL4, and CCL5 in BAL fluid compared to control mice (Figure 3b). This increase in cytokine and chemokine release was not associated with changes in the percentage or total number of AMΦ, or in the number or viability of cells in BAL fluid (Figure 3—figure supplement 1).

Figure 3 with 1 supplement see all
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Zoledronic acid (ZOL) treatment enhances the production of inflammatory cytokines in response to endotoxin challenge in vivo.

(a) Schedule of intravenous (i.v.) ZOL administration 48 hr prior to intranasal (i.n.) or intraperitoneal (i.p.) lipopolysaccharide (LPS) treatment and subsequent collection of bronchoalveolar lavage (BAL) or peritoneal lavage (PL) fluid, respectively. (b) Multiplex analysis of cytokines and chemokines in BAL fluid from saline- or ZOL-treated mice after i.n. LPS challenge, and (c) in peritoneal fluid, and serum after i.p. LPS challenge. In (b), bars represent mean ± SD, n = 8–9 mice per group with LPS, or n = 3–5 mice per group with ZOL/saline alone; ***p<0.001, ****p<0.0001, ANOVA with Tukey’s post hoc test. In (c), bars represent mean ± SD, n = 5 mice per group; *p<0.05, unpaired t-test with Welch’s correction; each symbol represents the measurement from an individual mouse. (d) Western blot detection of mature, extracellular IL-β in conditioned medium from PL cells, isolated from a ZOL- or saline-treated mouse, then stimulated ex vivo with LPS or LPS+ nigericin. Relative levels of IL-β were calculated by densitometry and are shown below each lane. The blot shown is representative of three independent experiments.

Figure 3—source data 1

Western blot of conditioned media using anti-IL-1β shows a single 17 kDa band of cleaved IL-1β.

https://cdn.elifesciences.org/articles/72430/elife-72430-fig3-data1-v1.zip

I.p. LPS challenge of ZOL-treated mice also resulted in a significant elevation in IL-1β in peritoneal fluid, and CCL2 and CCL5 in serum, compared to controls (Figure 3c). Furthermore, peritoneal cells from ZOL-treated mice produced almost three times more IL-1β upon ex vivo stimulation with LPS and nigericin (a well-described NLRP3 activator) (Figure 3d) than cells from control mice. IL-1β is primarily produced by monocytes/macrophages (Kany et al., 2019), the predominant cell type in PL (Figure 1—figure supplement 1). Thus, our results strongly suggest that macrophages are the most likely source of IL-1β in PL fluid. Importantly, treating the mice with ZOL did not cause IL-1β release from peritoneal cells stimulated ex vivo with LPS in the absence of nigericin (Figure 3d), and this is in accord with our previous finding that inhibition of the mevalonate pathway alone does not trigger NLRP3 inflammasome assembly but enhances its activation (Skinner et al., 2019).

The observations described here begin to provide a plausible mechanistic explanation for the decreased risk of pneumonia mortality associated with N-BP treatment (Colón-Emeric et al., 2010; Sing et al., 2020; Reid et al., 2021). AMΦ are one of the first lines of defence against common respiratory tract infections (Byrne et al., 2015), and inhibition of the mevalonate pathway in these cells may help boost the initial response to bacterial as well as viral lung infections by a variety of routes (Figure 4). First, uptake of N-BP into cells causes the accumulation of IPP/DMAPP (Figure 2b), which activates human Vγ9Vδ2-T cells (Thompson and Rogers, 2004). Vγ9Vδ2-T cells are non-conventional T cells with potent antibacterial and antiviral activity that recognise phosphoantigens, including IPP, derived from the mevalonate or DOXP pathways in bacterial pathogens (Tanaka et al., 1995; Jomaa et al., 1999). There is considerable interest in the use of N-BP-expanded γ,δ-T cells as an immunotherapy for cancer (Clézardin and Massaia, 2010; Tanaka, 2020) as well as viral diseases (Juno and Kent, 2020). Indeed, N-BP-expanded Vγ9Vδ2-T cells reduce disease severity and mortality from influenza A virus (IAV) infection in humanised mice (Tu et al., 2011; Zheng et al., 2015). Second, the genome of some pathogens such as IAV encodes proteins with a prenylation motif, which require the host cells' mevalonate pathway to enable prenylation and allow pathogen propagation (Marakasova et al., 2017). Agents that block the mevalonate pathway (such as statins) or that inhibit prenylation (such as lonafarnib, currently in clinical trials for hepatitis delta virus infection), have well-described antiviral or antimicrobial effects (Parihar et al., 2019; Einav and Glenn, 2003). Intriguingly, simvastatin was shown to improve outcomes in hospitalised older adults with community-acquired pneumonia (Sapey et al., 2019). Third, inhibition of FPP synthase by N-BP in AMΦ mimics the decreased flux through the mevalonate pathway in macrophages in response to endogenous IFN signalling, which serves to limit viral uptake and replication by several mechanisms including the synthesis of 25-hydroxycholesterol (Robertson and Ghazal, 2016; Cyster et al., 2014). Fourth, lack of protein prenylation (Figure 2c) enhances NLRP3 inflammasome activation and promotes the release of IL-1β (Skinner et al., 2019). IL-1β is a central mediator of the innate immune response that orchestrates the production of a cascade of cytokines and chemokines (Garlanda et al., 2013). Our observation that systemic ZOL treatment significantly enhanced the release of IL-1β and several other cytokines and chemokines in lung, peritoneum, and serum after LPS challenge (Figure 3) is consistent with increased inflammasome activation. Our findings are also consistent with previous reports suggesting that ZOL treatment causes polarisation of tumour-associated macrophages towards an M1-like, pro-inflammatory phenotype by inhibiting the mevalonate pathway (Coscia et al., 2010; Comito et al., 2017). Further studies are necessary to determine exactly how ZOL alters the phenotype of AMΦ. Importantly however, despite the ability of ZOL to enhance cytokine and chemokine production, to our knowledge there is no evidence that N-BP therapy exacerbates lung inflammation in pneumonia patients and, on the contrary, N-BP treatment appears to have a beneficial effect on pneumonia risk and mortality (Colón-Emeric et al., 2010; Sing et al., 2020; Reid et al., 2021).

Figure 4
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Potential routes of antimicrobial activity of nitrogen-containing bisphosphonate (N-BP) via effects on the mevalonate pathway in alveolar macrophages.

Inhibition of farnesyl diphosphate (FPP) synthase by N-BP prevents the biosynthesis of isoprenoid lipids required for normal protein prenylation (step 1). Lack of prenylation leads to enhanced inflammasome activation and increased IL-1β release in response to bacterial endotoxin, boosting the initial inflammatory response and pathogen clearance. Lack of isoprenoid biosynthesis may also hinder the propagation of intracellular pathogens that depend on the host cells' mevalonate pathway. Inhibition of FPP synthase by N-BP causes the accumulation of isopentenyl diphosphate (IPP)/dimethylallyl diphosphate (DMAPP) phosphoantigens (step 2) capable of triggering activation and proliferation of human Vγ9VδT cells with antimicrobial activity. Inhibition of FPP synthase by N-BP may also mimic the endogenous antiviral effect of 25-hydroxycholesterol (25HC), one of the routes by which IFN signalling suppresses the flux through the mevalonate pathway.

Finally, it is noteworthy that ZOL was recently identified, using computational biology approaches, as one of the 200 clinically approved drugs that are predicted to target pathways induced by SARS-CoV-2 and could be suitable for drug repurposing against COVID-19 (Han et al., 2021). Epidemiological studies are therefore urgently needed to determine whether N-BP therapy alters the incidence, severity, or risk of mortality from SARS-Cov-2 infection.

Conclusions

We show that systemically administered N-BP drug can act outside the skeleton, inhibiting the mevalonate pathway and preventing protein prenylation in tissue-resident macrophages, which in turn enhances macrophage responsiveness to bacterial endotoxin. Our observations in mice, together with data from clinical studies in humans (Colón-Emeric et al., 2010; Sing et al., 2020; Reid et al., 2021), suggest that the beneficial effects of these drugs against pneumonia infection and mortality are, at least in part, mediated by targeting AMΦ, thereby boosting early immune responses in the lung. These findings add further weight to the view that N-BP therapy has benefits beyond just preventing bone loss and could be considered as prophylactic treatment to reduce the risk of pneumonia in individuals with osteopenia or osteoporosis, who are already eligible for bisphosphonate treatment under standard clinical guidelines.

Materials and methods

Key resources table
Reagent type (species) or resourceDesignationSource or referenceIdentifiersAdditional information
AntibodyBUV395 anti-CD11b (rat monoclonal)BD BiosciencesClone M1/70Flow cytometry (1:200)
AntibodyBiotin anti-F4/80(rat monoclonal)BioLegendClone BM8Flow cytometry(1:200)
AntibodyFITC anti- I-A/I-E (MHC-II) (rat monoclonal)BD BiosciencesClone 2G9Flow cytometry (1:200)
AntibodyBB515 anti-Siglec-F (rabbit monoclonal)BD BiosciencesCloneE50-2440Flow cytometry(1:200)
AntibodyPE anti-CD11c(hamster monoclonal)BD BiosciencesClone N418Flow cytometry(1:200)
AntibodyPerCP-Cy5.5 anti-Ly6G(rat monoclonal)BioLegendClone IA8Flow cytometry(1:200)
AntibodyBUV737 anti-B220(rat monoclonal)BD BiosciencesCloneRA3-6B2Flow cytometry (1:300)
AntibodyPE-Cy7 anti-Ly6C(rat monoclonal)BD BiosciencesClone AL-21Flow cytometry(1:200)
AntibodyAPC-Cy7 anti- TCRb(hamster monoclonal)BD BiosciencesCloneH57-597Flow cytometry(1:300)
AntibodyAnti-CD16/CD32 (rat monoclonal Fc block)BD BiosciencesClone 2.4G2Flow cytometry(1:200)
Peptide, recombinant proteinStreptavidinBD BiosciencesBV421-streptavidinFlow cytometry (1:400)
Chemical compound, drugZombie AquaBioLegendCat#: 423101Flow cytometry(1:700)
Chemical compound, drugAF647-ZOLBioVinc, CACat#: SKU BV501001Flow cytometry(47.5 μg/40 nmoles per mouse i.v. dose)
Chemical compound, drugZoledronic acidSigma-AldrichCat#: SML0223500 μg/kgi.v. dose
Chemical compound, drugLPS (Escherichia coli)Sigma-AldrichO111:B410 μg i.n. or 100 μg i.p. per mouse
Chemical compound, drugBiotin-GPPdoi.org.10.1080/21541248.2015.1085485Prof Kirill Alexandrov
Peptide, recombinant proteinREP-1(zebrafish)doi.org.10.1080/21541248.2015.1085485Prof Kirill Alexandrov
Peptide, recombinant proteinGGTase-II(rat)doi.org.10.1080/21541248.2015.1085485Prof Kirill Alexandrov
Peptide, recombinant proteinStreptavidin-680RDLiCORP/N: 925-68079Western blotting (1:20,000)
AntibodyAnti-IL-1β(goat polyclonal)R&D SystemsCat#:AF-401-NAWestern blotting (1:1000)
AntibodyHRP anti-goat IgG(donkey polyclonal)Thermo FisherCat#:A15999Western blotting (1:5000)
Commercial assay or kitSuperSignal West Pico substrateThermo FisherCat#: 34580Western blotting
Commercial assay or kitBio-Plex immunoassay kitBio-RadCat#: M60009RDPDCytokine and chemokine assay
Recombinant proteinM-CSF (human)Sino BiologicalCat#: 11792-HNAHCell culture supplement (50 ng/mL)
Chemical compoundNigericinSigma-AldrichCat#: N7143
Chemical compoundIPP triammonium saltSigma-AldrichCat#: I0503-1VLLC-MS/MS standard
Chemical compoundDMAPP triammonium saltToronto Research ChemicalsCat#: 63180-1MGLC-MS/MS standard
Software, algorithmFlowJo softwareBecton DickinsonRRID:SCR_008520Version 10.6.2
Software, algorithmMassHunter Quantitative Analysis softwareAgilentVersion B08.00.00

Animals and tissue collection

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Studies involving mice were performed in strict accordance with the Australian Code for the care and use of animals for scientific purposes (2013). All of the animals were handled according to Animal Ethics Committee protocols (Animal Research Authority: 18/40) approved by the Garvan Institute/ St Vincent’s Hospital Animal Ethics Committee. Procedures were performed under appropriate anaesthesia, with animal welfare consideration underpinned by the principles of Replacement, Reduction, and Refinement.

All experiments involved adult female C57BL/6JAusb mice, and group sizes were based on previous studies using the same methodologies. Animals were purchased from Australian BioResources, housed with standard chow diet in specific pathogen-free conditions, and randomly allocated to experimental groups. Mice were anaesthetised with isoflurane prior to retro-orbital i.v., i.n., or i.p. drug administration. Mice were euthanised by CO2 inhalation, and peritoneal and bronchoalveolar cells were isolated by lavage using 2 mM EDTA/magnesium- and calcium-free DPBS (Gibco). PL cells were collected by injecting 5 mL of solution into the peritoneal cavity, and BAL cells by pooling three consecutive 1.5 mL washes administered via an insertion in the trachea. To generate BMDM, the femora and tibiae of adult mice were flushed with sterile PBS. Bone marrow cells were cultured for 4 days in Petri dishes in RPMI supplemented with 10% heat-inactivated foetal calf serum, 50 units/mL penicillin; 50 μg/mL streptomycin (Gibco) and 50 ng/mL rhM-CSF (Sino Biological), in a humidified incubator with 5% CO2 at 37°C.

Flow cytometry

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A single dose (47.5 μg /40 nmoles) of AF647-ZOL (BioVinc, CA) or 500 μg/kg ZOL (or saline vehicle) was administered i.v. in a final volume of 100 μL. Uptake of AF647-ZOL was assessed in BAL and PL cells 4 hr later. For LPS challenge, mice were treated with i.v. ZOL 48 hr prior to administration of i.n. LPS (10 μg LPS in 20 μL saline) or i.p. LPS (100 μg in 200 μL saline). Cell viability and total cell numbers in BAL and PL were assessed by trypan blue staining using a Corning CytoSMART cell counter. For flow cytometric analysis, cells were pre-incubated with mouse-Fc block and viability marker (Zombie Aqua viability stain, 1:700), prepared in calcium/magnesium-free PBS (Gibco), before staining with fluorescently conjugated antibodies prepared in staining buffer (2 mM EDTA, 0.02% azide; 0.5% foetal calf serum, in calcium/magnesium-free PBS). Antibodies and dilutions are listed in the Key resources table. Samples were analysed using a BD LSRII SORP flow cytometer/DIVA software. The post-acquisition analysis was performed using FlowJo 10.6.2 (BD).

LC-MS/MS analysis of IPP/DMAPP

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10-week-old female mice were administered a single 100 μL retro-orbital i.v. dose of 500 μg/kg ZOL (or saline control). Animals were culled 48 hr later, and bronchoalveolar cells and peritoneal cells were collected by pooling the BAL or PL lavages from n = 8 mice (BAL) or n = 5 mice (PL). Cell pellets were then stored at –80°C. For analysis of IPP/DMAPP, 1 mL cold extraction solvent (80:20 methanol:water) was added to the cell pellets, then vortexed for 10 s and incubated in a ultrasonic bath filled with ice water for 1 hr, then centrifuged at 3000 rpm for 30 min at 4°C. Aliquots (850 μL) of supernatant were dried under vacuum in an Eppendorf Concentrator Plus then reconstituted in 42.5 μL 70% methanol, 30% 10 mM ammonium acetate. Samples (injection volume 1 μL) were analysed by targeted LC-MS/MS using an Agilent 1290 Infinity II UHPLC system coupled to an Agilent 6495B triple quadrupole mass spectrometer. Separation was achieved using an Agilent Infinity Poroshell 120 EC-C18 column (3.0 × 150 mm, 2.7 μm) fitted with an Agilent Infinity Poroshell 120 EC-C18 UHPLC guard column (3.0 × 150 mm, 2.7 μm), maintained at 20°C. The mobile phases were 10 mM ammonium acetate in water (A) and methanol (B), both containing 5 μM medronic acid (Sigma-Aldrich) to chelate metal ions (gradient 98% A from 0 to 3 min, decreased to 2% A from 3.5 to 6.5 min at 0.5 mL/min, then increased to 98% A at 0.4 mL/min from 6.5 to 12 minutes; total run time 12 min). Autosampler temperature was 4°C. The mass spectrometer was operated in negative electrospray ionisation mode: source gas temperature was 250°C with flow at 17 L/min, sheath gas temperature was 400°C with flow at 12 L/min, and nebuliser pressure was 45 psi. Data were acquired in Multiple Reaction Monitoring (MRM) mode and were processed using Agilent MassHunter Quantitative Analysis software version B08.00.00. By comparison with pure standard compounds (Sigma-Aldrich), the isomers IPP and DMAPP eluted at the same retention time (approximately 2.4 min) and were calculated as total area under the curve. The limit of detection in cell extracts was 20 nM.

Detection of unprenylated Rab proteins

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To assess the accumulation of unprenylated Rab GTPase proteins, we used an in vitro prenylation assay as previously described (Ali et al., 2015). Mice were treated with i.v. ZOL or saline as described above, then cell pellets were obtained by BAL or PL (each pooled from n = 5 mice) and lysed by sonication in prenylation buffer (50 mM HEPES, pH 7.2, 50 mM NaCl, 2 mM MgCl2, 100 μM GDP, 1× Roche cOmplete EDTA-free protease inhibitor cocktail). To compare the effect of ZOL and AF647-ZOL, BMDMs were treated with 1, 5, or 10 μM ZOL or AF647-ZOL for 24 hr before cells were collected and lysed in prenylation buffer.

For the in vitro prenylation assay, 10 μg of protein were incubated with recombinant GGTase II, REP-1, and biotin-conjugated GPP (a synthetic isoprenoid lipid) for the labelling of unprenylated Rab proteins (Ali et al., 2015). The resulting biotinylated Rabs were then detected on PVDF blots using streptavidin-680RD (LiCOR). A narrow doublet (often appearing as a broad singlet) of endogenous biotinylated 75 kDa proteins was used as a sample loading control.

Immune responses to LPS in vivo

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10-week-old female mice were administered a single retro-orbital i.v. dose of 500 μg/kg ZOL (or saline control), 48 hr before immune challenge with LPS (Escherichia coli O111:B4, Sigma-Aldrich) administered either i.n. (10 μg LPS in 20 μL saline) or i.p. (100 μg in 200 μL saline). Mice were culled 2 hr later, and BAL or PL fluid were collected by injecting 500 μL or 1 mL PBS into the lungs or peritoneal cavity, respectively. Cytokines and chemokines in BAL, PL, and serum were measured using a Bio-Plex multiplex immunoassay (Bio-Rad) and a MAGPIX (Luminex) multiplex reader according to the manufacturer’s instructions.

IL-1β release by peritoneal cells ex vivo

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PL samples were obtained from ZOL- or saline-treated mice as described above. PL cells were placed in 96-well plates (400,000 cells/well) and treated at 37°C for 5.25 hr with 200 ng/mL LPS, in a final volume of 200 μL serum-free Opti-MEM medium (Gibco), followed by stimulation for 45 min with 10 μM nigericin (Sigma-Aldrich). The level of mature (17 kDa) IL-1β in conditioned medium was analysed by western blotting on nitrocellulose membrane with a goat anti-mouse IL-1β antibody (AF-401-NA, R&D Systems, 1:1000 dilution), donkey anti-goat horseradish peroxidase-conjugated secondary antibody (A15999, Thermo Fisher, 1:5,000 dilution), and enhanced chemiluminescence using SuperSignal West Pico chemiluminescent substrate (Thermo Fisher). The signal was detected using a Fusion FX7 imaging system (Etablissements Vilber Lourmat SAS), and densitometry was performed on blots using ImageJ (v2.0.0).

Data availability

All data generated or analysed during this study are included in the manuscript and measurements obtained from individual mice are shown as separate data points in the figures. Source data files are provided for the protein blots shown in Figure 1a, Figure 2c and Figure 3d.

References

    1. Dunford JE
    2. Thompson K
    3. Coxon FP
    4. Luckman SP
    5. Hahn FM
    6. Poulter CD
    7. Ebetino FH
    8. Rogers MJ
    (2001)
    Structure-activity relationships for inhibition of farnesyl diphosphate synthase in vitro and inhibition of bone resorption in vivo by nitrogen-containing bisphosphonates
    The Journal of Pharmacology and Experimental Therapeutics 296:235–242.

Decision letter

  1. Dolores Shoback
    Reviewing Editor; University of California, San Francisco, United States
  2. Carlos Isales
    Senior Editor; Medical College of Georgia at Augusta University, United States
  3. T John Martin
    Reviewer; St. Vincent's Institute of Medical Research, Melbourne, Australia
  4. Massimo Massaia
    Reviewer; University of Turin, Turin, Italy
  5. Lilian Plotkin
    Reviewer; Indiana University School of Medicine, Indianapolis, United States

Our editorial process produces two outputs: (i) public reviews designed to be posted alongside the preprint for the benefit of readers; (ii) feedback on the manuscript for the authors, including requests for revisions, shown below. We also include an acceptance summary that explains what the editors found interesting or important about the work.

Decision letter after peer review:

Thank you for submitting your article "Bisphosphonate drugs have actions outside the skeleton and inhibit the mevalonate pathway in alveolar macrophages" for consideration by eLife. Your article has been reviewed by 3 peer reviewers, and the evaluation has been overseen by a Reviewing Editor and Carlos Isales as the Senior Editor. The following individuals involved in review of your submission have agreed to reveal their identity: T. Jack Martin (Reviewer #1); Massimo Massaia (Reviewer #2); Lilian Plotkin (Reviewer #3).

The reviewers have discussed their reviews with one another, and the Reviewing Editor has drafted this to help you prepare a revised submission.

Essential revisions:

The Reviewing Editor believes that there are very few time-consuming requests in the 3 reviews above, unless I am incorrect. I believe the authors can respond to each Reviewer in a succinct manner as they are enthusiastic overall regarding the data, the paper and the topic.

Reviewer #1 (Recommendations for the authors):

1. Figure 1. AF647ZOL after IV injection in the mouse was clearly localized in pulmonary alveolar and in peritoneal macrophages. AF647-ZOL is a fluorescent-labelled zoledronate. The authors should provide more details in Methods about this reagent, its preparation and properties. There is nothing published about it of which I am aware. The literature on the corresponding risedronate analog, AF647-RIS, is confusing. It was used in Junankar et al., where it was described as bone-seeking but pharmacologically inactive , but this appears to differ from the original description, in Roelofs et al., (JBMR 2010 ). Perhaps the authors could clarify.

2. The AF647-ZOL was used only in the work of Figure 1, where the localization in macrophages is clearly shown. A couple of questions arise. First, if the labelled compound is active, sufficient was injected in Figure 1 to show a pharmacological effect as was studied in Figure 2 – was there any biological activity of AF647ZOL – or a reduced activity?? Second, it is assumed, but not shown, that the labelled ZOL behaves as unlabelled. As one would do with any binding or "receptor" study, one would see if it were possible to block the label from entering cells. This could be done, for example, by examining mice co-injected with an increased amount of unlabelled ZOL. The question is being asked to increase confidence that the pharmacological effects shown in Figures2 and 3 are indeed the result of direct action of the unlabelled ZOL.

3. The present experiments were carried out with one N-BP, the most potent of all those in common use. Much higher doses of that drug are required in mice than in human subjects, but it would be very helpful to know what is needed to produce the pharmacologic effects that are shown. The impracticality of of dose responses is obvious, but what about repeating the Figure 2 experiment with less active N-BPs/ – e.g. risedronate, alendronate, pamidronate?

4. Given that ZOL is active on bone in human studies when given with as little as 1 microgram intermittent doses, the authors would do well to discuss how this question of bioavailability is to be addressed. It might well be beyond the scope of this paper, but it surely should be discussed.

Reviewer #2 (Recommendations for the authors):

1. I would recommend a more cautious approach before stating that "these findings demonstrate unequivocally for the first time that systemic administration of N-BP has pharmacological activity outside the skeleton" (page 5, line 10, and thereafter). Similar results have already been reported by several groups (Rogers TL et al., Macrophages as potential targets for zoledronic acid outside the skeleton-evidence from in vitro and in vivo models. Cell Oncol (Dordr). 2013 Dec;36(6):505-14; Comito G et al., Zoledronic acid impairs stromal reactivity by inhibiting M2-macrophages polarization and prostate cancer-associated fibroblasts. Oncotarget. 2017 Jan 3;8(1):118-132; Coscia et al., J Cell Mol Med. 2010 Dec;14(12):2803-15). The paper by Coscia et al., was the first one to demonstrate that ZOL at clinically achievable doses targets the mevalonate pathway of tumor-associated macrophages (TAM) and tumor cells in a mouse model of primary tumor not located in the bone. In the same paper, it was shown a marked inhibition of the Mev pathway of peritoneal macrophages after ZOL treatment, as shown by the intracellular decrease of FPP, cholesterol, and ubiquinone, and the concurrent increase of IPP. As expected, protein prenylation was also affected as shown by the decreased intracellular contents of prenylated Ras and Ras-GTP. The Authors should reconsider and discuss again their results in light of these published data.

2. Interestingly, the uptake of the fluorescently-labelled ZOL analog (AF647-ZOL) is mostly restricted to large peritoneal (LP) macrophasegs sparing small peritoneal (SP) macrophages. The Authors should explain the functional difference between these 2 subsets and provide some hypotheses why uptake is restricted to the former (i.e, activated macrophages?). Is AF647-ZOL uptake specific or is this the consequence of a general increased phagocytic activity of LP macrophages (control expts with FITC-dextran could answer the question).

3. Another interesting set of data is represented by the enhanced cytokines and chemokines production induced by LPS after in vivo ZOL priming. These results confirm previous findings (Coscia et al., J Cell Mol Med. 2010 Dec;14(12):2803-15) that ZOL repolarizes TAM from M2 (protumoral) to M1 (antitumoral) activity by inhibiting intracellular protein prenylation. iNOS is considered a hallmark of M1 polarized macrophages and an important player of the M1-mediated tumoricidal activity. Do the Authors believe that some sort of M1 polarization and iNOS induction can play a role in the improved capacity of ZOL-primed to resist to LPS challenge and survive pneumonia?

4. As reported by the Authors, clinical data associating improved pneumonia outcome with ZOL treatment have been generated in aged patients. Have the Authors any evidence that age can influence the ability to prime alveolar or peritoneal macrophages in C57BL/6J mice in relation to age? Do the Authors have any explanation about a possible selective effect of ZOL in the elderly, or the possible association is simply because ZOL is used in the elderly to treat hip fractures or osteoporosis? Is any evidence about a protective effect of ZOL in young cancer patients treated with ZOL for bone disease (i.e., myeloma, breast cancer, prostate cancer, etc)?

5. It is very exciting that ZOL has been identified, using computational biology approaches, as one of 200 clinically-approved drugs that are predicted to target pathways induced by SARS-CoV-2 and could be suitable for drug repurposing against COVID-19 (page 7, line 11 onwards). However, one major cause of Sars-CoV-2 induced morbidity and mortality is the exaggerated inflammatory response in the lung. How do the Authors reconcile a protective effect against SARS-CoV-2 infection with the capacity of ZOL to boosts the reactivity of alveolar macrophages? Is LPS challenge a suitable surrogate to mimic viral infection? My personal feeling is that the concurrent activation of Vg9Vd2 T cells can be more important in viral infections. The Authors should comment on a possible difference between ZOL and statins in regulating inflammatory and immune responses against bacteria and viruses. I am also wondering whether statins (that induce and accumulate unprenylated small GTPase proteins like ZOL, but do not activate Vg9Vd2 T cells) have the same ability to prime alveolar macrophages reactivity to LPS challenge.

Reviewer #3 (Recommendations for the authors):

The manuscript is clearly written, and the data are properly presented. While the conclusions and potential relevance of the studies are clear and appropriate, the authors should also discuss the potential implications of their finding on the acute phase response observed in patients receiving bisphosphonates. Further, the potential of eliciting an exacerbated response that could be deleterious to the patients should also be noted.

https://doi.org/10.7554/eLife.72430.sa1

Author response

Reviewer #1 (Recommendations for the authors):

1. Figure 1. AF647ZOL after IV injection in the mouse was clearly localized in pulmonary alveolar and in peritoneal macrophages. AF647-ZOL is a fluorescent-labelled zoledronate. The authors should provide more details in Methods about this reagent, its preparation and properties. There is nothing published about it of which I am aware. The literature on the corresponding risedronate analog, AF647-RIS, is confusing. It was used in Junankar et al., where it was described as bone-seeking but pharmacologically inactive , but this appears to differ from the original description, in Roelofs et al., (JBMR 2010 ). Perhaps the authors could clarify.

We appreciate the Reviewer raising these questions, and realise that AF647-ZOL does indeed lack description in the literature. It is a commercially-available reagent and was sourced from BioVinc (as stated in the Methods). We now include an additional panel (a) in Figure 1 showing that AF647-ZOL, like AF647-RIS (described in Roelofs et al., 2010) does not inhibit protein prenylation in cultured macrophages at equimolar concentrations to unlabelled ZOL. AF647-ZOL is therefore a valuable tool to examine the distribution of bisphosphonate compounds in vivo but lacks pharmacologic activity. This is now made clear in the revised text (1st paragraph of Results and Discussion). To clarify, the study by Roelofs et al., (JBMR 2010) demonstrates that FAM-RIS is pharmacologically active but clearly states that, unlike FAM-RIS, “AF647-RIS did not inhibit Rap1A prenylation in J774.2 cells in vitro”.

2. The AF647-ZOL was used only in the work of Figure 1, where the localization in macrophages is clearly shown. A couple of questions arise. First, if the labelled compound is active, sufficient was injected in Figure 1 to show a pharmacological effect as was studied in Figure 2 – was there any biological activity of AF647ZOL – or a reduced activity?? Second, it is assumed, but not shown, that the labelled ZOL behaves as unlabelled. As one would do with any binding or "receptor" study, one would see if it were possible to block the label from entering cells. This could be done, for example, by examining mice co-injected with an increased amount of unlabelled ZOL. The question is being asked to increase confidence that the pharmacological effects shown in Figures2 and 3 are indeed the result of direct action of the unlabelled ZOL.

As described above (and in the revised text and Figure 1a), we now explain that AF647-ZOL is pharmacologically inactive and was only used in Figure 1 to reveal cellular uptake by macrophages in vivo. In Figures 2 and 3, only unlabelled ZOL was used. Given that ZOL is a well-described, potent bisphosphonate inhibitor of the mevalonate pathway, and that the only cells in BAL and PL samples that internalised bisphosphonate were macrophages, we cannot think of any other explanation for the results in Figure 2 other than a direct effect of ZOL on the mevalonate pathway in AMφ and PMφ. We do not suggest that all of the cytokines and chemokines measured in Figure 3 are derived solely from macrophages, and the exact source and mechanism for the increase remains to be determined. Single cell RNA sequencing experiments are underway in a follow-up study to examine this in more detail but we feel that this is beyond the scope of the current Short Report. Nevertheless, intranasal or intraperitoneal administration of LPS is an established method for activating AMφ and PMφ and inducing IL-1β release from these cells. We state (page 7) that: “IL-1β is a central mediator of the innate immune response that orchestrates the production of a cascade of cytokines and chemokines (Garlanda et al., 2013)” therefore it is reasonable to expect that at least some of the acute increase in IL1-β and other cytokine/chemokines in BAL fluid and PL fluid occurs directly from AMφ and PMφ respectively. Furthermore, cytokine/chemokine release in BAL and PL fluid was measured just 2 hours after LPS administration, before infiltration by other immune cells occurs.

3. The present experiments were carried out with one N-BP, the most potent of all those in common use. Much higher doses of that drug are required in mice than in human subjects, but it would be very helpful to know what is needed to produce the pharmacologic effects that are shown. The impracticality of of dose responses is obvious, but what about repeating the Figure 2 experiment with less active N-BPs/ – e.g. risedronate, alendronate, pamidronate?

The single dose of ZOL that was used in the studies in Figures 2 and 3 is reasonably comparable (in terms of µg ZOL/kg body weight) to the clinical dose used in humans. Because of the bone-targeting property of bisphosphonates such as ZOL the exact concentration that is present in soft tissues such as lung is extremely low (see Green and Rogers, Drug Dev Res 55:210–224, 2002). As we suggest in the text (page 3), the ability of macrophages to internalise bisphosphonate in tissues outside the skeleton presumably reflects their enormous capacity for rapid endocytosis. We agree that it will be important to assess the ability of orally-administered bisphosphonates to have effects on AMφ, but we respectfully consider this to be beyond the scope of this initial Short Report.

4. Given that ZOL is active on bone in human studies when given with as little as 1 microgram intermittent doses, the authors would do well to discuss how this question of bioavailability is to be addressed. It might well be beyond the scope of this paper, but it surely should be discussed.

With respect, we are unsure what the Reviewer is asking. Despite the rapid bone-targeting property of bisphosphonates it has been shown in rodents that small amounts of ZOL can accumulate in soft tissues (Green and Rogers, Drug Dev Res 55:210–224, 2002) but the concentrations that can be achieved are unknown. This has now been stated in the text (page 4). The randomised clinical trial by Grey et al., (J Bone Miner Res 2014) showed that ZOL is pharmacologically active in humans when administered intravenously at intermittent doses of 1 milligram (not 1 microgram). In our study in mice we used a single dose of 500 micrograms/kg, which is equivalent to about 10 micrograms per mouse, and was delivered intravenously (as in humans). As discussed in response to point 3 above, it will be important to determine in future studies whether orally-administered N-BP is sufficiently bioavailable to affect tissue-resident macrophage populations such as AMφ, but this is beyond the scope of the current study in which we clearly show an effect of a single dose of intravenous ZOL.

Reviewer #2 (Recommendations for the authors):

1. I would recommend a more cautious approach before stating that "these findings demonstrate unequivocally for the first time that systemic administration of N-BP has pharmacological activity outside the skeleton" (page 5, line 10, and thereafter). Similar results have already been reported by several groups (Rogers TL et al., Macrophages as potential targets for zoledronic acid outside the skeleton-evidence from in vitro and in vivo models. Cell Oncol (Dordr). 2013 Dec;36(6):505-14; Comito G et al., Zoledronic acid impairs stromal reactivity by inhibiting M2-macrophages polarization and prostate cancer-associated fibroblasts. Oncotarget. 2017 Jan 3;8(1):118-132; Coscia et al., J Cell Mol Med. 2010 Dec;14(12):2803-15). The paper by Coscia et al., was the first one to demonstrate that ZOL at clinically achievable doses targets the mevalonate pathway of tumor-associated macrophages (TAM) and tumor cells in a mouse model of primary tumor not located in the bone. In the same paper, it was shown a marked inhibition of the Mev pathway of peritoneal macrophages after ZOL treatment, as shown by the intracellular decrease of FPP, cholesterol, and ubiquinone, and the concurrent increase of IPP. As expected, protein prenylation was also affected as shown by the decreased intracellular contents of prenylated Ras and Ras-GTP. The Authors should reconsider and discuss again their results in light of these published data.

We appreciate the Reviewer’s comment. Our intention was to make the point that a single dose of ZOL can affect cells outside the skeleton under benign conditions i.e. not in mice bearing tumours and with potentially tumour-influenced immune systems, but we realise that this was not clear. We propose to rephrase the title, from “Bisphosphonate drugs have actions outside the skeleton and inhibit the mevalonate pathway in alveolar macrophages” to “Bisphosphonate drugs have actions in the lung and inhibit the mevalonate pathway in alveolar macrophages”. This more specifically reflects the novel findings that we present in the Short Report. As suggested, we have also modified the sentence on page 5 and added an additional short section toward the end of the Results and Discussion (page 7) to acknowledge previous findings in tumour-bearing mice.

2. Interestingly, the uptake of the fluorescently-labelled ZOL analog (AF647-ZOL) is mostly restricted to large peritoneal (LP) macrophasegs sparing small peritoneal (SP) macrophages. The Authors should explain the functional difference between these 2 subsets and provide some hypotheses why uptake is restricted to the former (i.e, activated macrophages?). Is AF647-ZOL uptake specific or is this the consequence of a general increased phagocytic activity of LP macrophages (control expts with FITC-dextran could answer the question).

This is indeed an interesting question. An explanation for the specific uptake of bisphosphonate by large PMφ compared to small PMφ requires further detailed studies (both subsets are capable of phagocytosis and endocytosis). Since our studies were more focused on AMφ rather than PMφ we consider this to be beyond the scope of this Short Report. However, we now indicate (page 4) that these two PMφ subsets differ in their origin, phenotype and function, which is explained in detail in the cited review.

3. Another interesting set of data is represented by the enhanced cytokines and chemokines production induced by LPS after in vivo ZOL priming. These results confirm previous findings (Coscia et al., J Cell Mol Med. 2010 Dec;14(12):2803-15) that ZOL repolarizes TAM from M2 (protumoral) to M1 (antitumoral) activity by inhibiting intracellular protein prenylation. iNOS is considered a hallmark of M1 polarized macrophages and an important player of the M1-mediated tumoricidal activity. Do the Authors believe that some sort of M1 polarization and iNOS induction can play a role in the improved capacity of ZOL-primed to resist to LPS challenge and survive pneumonia?

We take a more cautious approach and have now stated in the revised text that:

“Our findings are also consistent with previous reports suggesting that ZOL treatment causes polarisation of tumour-associated macrophages towards an M1-like, pro-inflammatory phenotype….”

We do not wish to state that our findings confirm this suggestion because this requires detailed analysis of the phenotype of AMφ and PMφ. As indicated to Reviewer #1, single cell RNA sequencing studies (not just iNOS expression) are underway to address this question in far more detail and to provide a complete explanation for the effect of ZOL, but we feel that this is beyond the scope of the current Short Report.

4. As reported by the Authors, clinical data associating improved pneumonia outcome with ZOL treatment have been generated in aged patients. Have the Authors any evidence that age can influence the ability to prime alveolar or peritoneal macrophages in C57BL/6J mice in relation to age? Do the Authors have any explanation about a possible selective effect of ZOL in the elderly, or the possible association is simply because ZOL is used in the elderly to treat hip fractures or osteoporosis? Is any evidence about a protective effect of ZOL in young cancer patients treated with ZOL for bone disease (i.e., myeloma, breast cancer, prostate cancer, etc)?

We are not aware of any studies to suggest that there is a selective effect of ZOL in the elderly and this could be a topic to address in future work. Of course, the elderly population are the most likely to receive bisphosphonate therapy for age-associated bone disorders such as osteoporosis, and are also more susceptible to pulmonary infections and pneumonia. We have now rephrased the last sentence of the Conclusion to make the clinical significance of our findings clearer:

“These findings add further weight to the view that N-BP therapy has benefits beyond just preventing bone loss and could be considered as prophylactic treatment to reduce the risk of pneumonia in individuals with osteopenia or osteoporosis, who are already eligible for bisphosphonate treatment under standard clinical guidelines”.

5. It is very exciting that ZOL has been identified, using computational biology approaches, as one of 200 clinically-approved drugs that are predicted to target pathways induced by SARS-CoV-2 and could be suitable for drug repurposing against COVID-19 (page 7, line 11 onwards). However, one major cause of Sars-CoV-2 induced morbidity and mortality is the exaggerated inflammatory response in the lung. How do the Authors reconcile a protective effect against SARS-CoV-2 infection with the capacity of ZOL to boosts the reactivity of alveolar macrophages? Is LPS challenge a suitable surrogate to mimic viral infection? My personal feeling is that the concurrent activation of Vg9Vd2 T cells can be more important in viral infections. The Authors should comment on a possible difference between ZOL and statins in regulating inflammatory and immune responses against bacteria and viruses. I am also wondering whether statins (that induce and accumulate unprenylated small GTPase proteins like ZOL, but do not activate Vg9Vd2 T cells) have the same ability to prime alveolar macrophages reactivity to LPS challenge.

It is worth re-emphasising that ZOL is only predicted to target pathways important for SARS-CoV-2 infection and there is no evidence yet, to our knowledge, that ZOL has any clinical benefit against COVID-19. Whether there is any clinical benefit, or indeed a deleterious effect, of ZOL therapy remains to be determined. We state (towards the end of the Results and Discussion) that there is evidence from epidemiological studies for only a beneficial effect of bisphosphonates on pneumonia and no evidence for a deleterious effect, despite the apparent pro-inflammatory actions of ZOL. The possible mechanisms underlying the beneficial effect on pneumonia are described in the text and in Figure 4. It is important to bear in mind that a rapid response to pathogens may lead to a better resolution of the infection. Hence an improved acute and early immune response in the lung may lead to overall better outcomes. The findings that we present in this Short Report reveal a possible explanation for the apparent beneficial effects of bisphosphonates against pneumonia and open a whole new area of research – the questions raised by the Reviewer remain to be explored. We do not suggest that LPS administration is a model of viral infection and we cite the studies that have previously reported anti-viral effects of ZOL. We totally agree that activation of Vγ9Vծ2 T cells is likely to be a major component of any effect of bisphosphonates to combat infection (both viral and bacterial) and discuss this in the text and in Figure 4, but naturally this cannot be examined in normal mice because they lack this subset of γ,ծ-T cells. Whether statins, or other pharmacologic agents that are capable of inhibiting steps of the mevalonate pathway, can also prime alveolar macrophages in vivo remains to be determined and is beyond the scope of this Short Report, but we cite key references that describe the effects of statins on infection (e.g. Parihar et al., 2019; Sapey et al., 2019).

Reviewer #3 (Recommendations for the authors):

The manuscript is clearly written, and the data are properly presented. While the conclusions and potential relevance of the studies are clear and appropriate, the authors should also discuss the potential implications of their finding on the acute phase response observed in patients receiving bisphosphonates. Further, the potential of eliciting an exacerbated response that could be deleterious to the patients should also be noted.

We thank the Reviewer for this comment and to address it we have added a sentence (page 5) that states:

“Our findings also shed new light on the commonest side-effect of N-BP therapy, a transient acute phase response. This was previously thought to be caused by the accumulation of IPP in circulating monocytes, which then activates Vγ9Vծ2 cells to produce TNFα and IFNγ (Roelofs et al., 2009). Our findings suggest that tissue-resident macrophages, such as AMφ and large PMφ, are in fact the more likely source of IPP responsible for the activation of Vγ9Vծ2 cells”.

As described in the response to Reviewer #2, we already state that there is no evidence that enhanced cytokine production caused by N-BP therapy worsens lung inflammation in pneumonia patients, and on the contrary, N-BP treatment appears to have a beneficial effect on pneumonia risk and mortality. We have now emphasised this further in the revised text (page 7) by stating:

“Further studies are necessary to determine exactly how ZOL alters the phenotype of AMφ. Importantly however, despite the ability of ZOL to enhance cytokine and chemokine production, to our knowledge there is no evidence that N-BP therapy exacerbates lung inflammation in pneumonia patients, and on the contrary, treatment appears to have a beneficial effect on pneumonia risk and mortality (Colon-Emeric et al., 2010, Sing et al., 2020, Reid et al., 2021)”.

https://doi.org/10.7554/eLife.72430.sa2

Article and author information

Author details

  1. Marcia A Munoz

    Garvan Institute of Medical Research and St Vincent’s Clinical School, UNSW Sydney, Sydney, Australia
    Contribution
    Conceptualization, Funding acquisition, Investigation, Project administration, Writing – review and editing
    Competing interests
    FHE is an employee of BioVinc (Pasadena, CA, USA). SS also co-affiliates with BioVinc. JRC participates on advisory boards of Amgen and Bayer and receives payment from Amgen for educational activities
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-7603-0351

  2. Emma K Fletcher

    Garvan Institute of Medical Research and St Vincent’s Clinical School, UNSW Sydney, Sydney, Australia
    Contribution
    Investigation, Methodology
    Competing interests
    No competing interests declared

  3. Oliver P Skinner

    Garvan Institute of Medical Research and St Vincent’s Clinical School, UNSW Sydney, Sydney, Australia
    Contribution
    Investigation, Methodology
    Competing interests
    No competing interests declared

  4. Julie Jurczyluk

    Garvan Institute of Medical Research and St Vincent’s Clinical School, UNSW Sydney, Sydney, Australia
    Contribution
    Investigation, Methodology
    Competing interests
    No competing interests declared

  5. Esther Kristianto

    Victor Chang Cardiac Research Institute Innovation Centre, Sydney, Australia
    Contribution
    Investigation, Methodology
    Competing interests
    No competing interests declared

  6. Mark P Hodson

    1. Victor Chang Cardiac Research Institute Innovation Centre, Sydney, Australia
    2. School of Pharmacy, University of Queensland, Woolloongabba, Australia
    Contribution
    Investigation, Methodology
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-5436-1886

  7. Shuting Sun

    1. BioVinc, Pasadena, United States
    2. University of Southern California, Los Angeles, United States
    Contribution
    Methodology
    Competing interests
    FHE is an employee of BioVinc (Pasadena, CA, USA). SS also co-affiliates with BioVinc. JRC participates on advisory boards of Amgen and Bayer and receives payment from Amgen for educational activities

  8. Frank H Ebetino

    BioVinc, Pasadena, United States
    Contribution
    Methodology
    Competing interests
    FHE is an employee of BioVinc (Pasadena, CA, USA). SS also co-affiliates with BioVinc. JRC participates on advisory boards of Amgen and Bayer and receives payment from Amgen for educational activities

  9. David R Croucher

    Garvan Institute of Medical Research and St Vincent’s Clinical School, UNSW Sydney, Sydney, Australia
    Contribution
    Methodology
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-4965-8674

  10. Philip M Hansbro

    Centre for Inflammation, Centenary Institute and University of Technology Sydney, Sydney, Australia
    Contribution
    Methodology, Writing – review and editing
    Competing interests
    No competing interests declared

  11. Jacqueline R Center

    Garvan Institute of Medical Research and St Vincent’s Clinical School, UNSW Sydney, Sydney, Australia
    Contribution
    Writing – review and editing
    Competing interests
    FHE is an employee of BioVinc (Pasadena, CA, USA). SS also co-affiliates with BioVinc. JRC participates on advisory boards of Amgen and Bayer and receives payment from Amgen for educational activities
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-5278-4527

  12. Michael J Rogers

    Garvan Institute of Medical Research and St Vincent’s Clinical School, UNSW Sydney, Sydney, Australia
    Contribution
    Conceptualization, Funding acquisition, Project administration, Supervision, Writing – original draft
    For correspondence
    m.rogers@garvan.org.au
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-1818-9249

Funding

NHMRC (1079522)

  • Michael J Rogers

Perpetual IMPACT

  • Marcia A Munoz

NHMRC (1175134)

  • Philip M Hansbro

Australian Government Research Training Program Scholarship

  • Emma K Fletcher

Mrs Janice Gibson and the Ernest Heine Family Foundation

  • Michael J Rogers

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Acknowledgements

We thank Prof Kirill Alexandrov (Queensland University of Technology) and Dr Zakir Tnimov (MRC Laboratory of Molecular Biology) for providing reagents for the Rab prenylation assay. This work was supported in part by the National Health and Medical Research Council (NHMRC) of Australia project grant 1079522 to MJR, by Mrs Janice Gibson and the Ernest Heine Family Foundation, and a Perpetual IMPACT grant to MAM. EKF was supported through an Australian Government Research Training Program Scholarship. PMH was funded by a Fellowship and grants from the NHMRC (1175134) and by the University of Technology Sydney (UTS). We gratefully acknowledge funding by the New South Wales Government for the Victor Chang Cardiac Research Institute Innovation Centre, as well as funding from the Freedman Foundation for the Metabolomics Facility.

Ethics

Studies involving mice were performed in strict accordance with the Australian Code for the care and use of animals for scientific purposes (2013). All of the animals were handled according to Animal Ethics Committee protocols (Animal Research Authority: 18/40) approved by the Garvan Institute/ St Vincent's Hospital Animal Ethics Committee. Procedures were performed under appropriate anaesthesia, with animal welfare consideration underpinned by the principles of Replacement, Reduction and Refinement.

Senior Editor

  1. Carlos Isales, Medical College of Georgia at Augusta University, United States

Reviewing Editor

  1. Dolores Shoback, University of California, San Francisco, United States

Reviewers

  1. T John Martin, St. Vincent's Institute of Medical Research, Melbourne, Australia
  2. Massimo Massaia, University of Turin, Turin, Italy
  3. Lilian Plotkin, Indiana University School of Medicine, Indianapolis, United States

Version history

  1. Received: July 23, 2021
  2. Preprint posted: August 10, 2021 (view preprint)
  3. Accepted: December 19, 2021
  4. Version of Record published: December 30, 2021 (version 1)

Copyright

© 2021, Munoz et al.

This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

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  1. Marcia A Munoz
  2. Emma K Fletcher
  3. Oliver P Skinner
  4. Julie Jurczyluk
  5. Esther Kristianto
  6. Mark P Hodson
  7. Shuting Sun
  8. Frank H Ebetino
  9. David R Croucher
  10. Philip M Hansbro
  11. Jacqueline R Center
  12. Michael J Rogers
(2021)
Bisphosphonate drugs have actions in the lung and inhibit the mevalonate pathway in alveolar macrophages
eLife 10:e72430.
https://doi.org/10.7554/eLife.72430

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