The pelvic organs receive no parasympathetic innervation
eLife assessment
This useful study compares gene expression patterns among different autonomic ganglia and will be of interest to developmental neuroscientists and neurophysiologists. The study expands the database of genes expressed by subpopulations of autonomic neurons in ganglia, a key step in decoding their developmental origins and physiological functions. The evidence supporting the alternative view that the pelvic ganglionic neurons are actually modified sympathetic neurons is incomplete and may cause confusion, given the enrichment of cholinergic neurons, as well as the large number of molecular and functional differences known to be present between cranial and sacral neurons.
https://doi.org/10.7554/eLife.91576.3.sa0Useful: Findings that have focused importance and scope
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Abstract
The pelvic organs (bladder, rectum, and sex organs) have been represented for a century as receiving autonomic innervation from two pathways – lumbar sympathetic and sacral parasympathetic – by way of a shared relay, the pelvic ganglion, conceived as an assemblage of sympathetic and parasympathetic neurons. Using single-cell RNA sequencing, we find that the mouse pelvic ganglion is made of four classes of neurons, distinct from both sympathetic and parasympathetic ones, albeit with a kinship to the former, but not the latter, through a complex genetic signature. We also show that spinal lumbar preganglionic neurons synapse in the pelvic ganglion onto equal numbers of noradrenergic and cholinergic cells, both of which therefore serve as sympathetic relays. Thus, the pelvic viscera receive no innervation from parasympathetic or typical sympathetic neurons, but instead from a divergent tail end of the sympathetic chains, in charge of its idiosyncratic functions.
Introduction
The pelvic ganglion is a collection of autonomic neurons, close to the walls of the bladder, organized as a loose ganglionated plexus (as in humans) or a bona fide ganglion (as in mouse). It receives input from preganglionic neurons of the thoracolumbar intermediate lateral motor column, a sympathetic pathway that travels through the hypogastric nerve. A second input is from the so-called ‘sacral parasympathetic nucleus’ that projects through the pelvic nerve. The assignment of these two inputs to different divisions of the autonomic nervous system by Langley, 1921; Langley, 1899, largely based on physiological observation on external genitals which were never generally accepted (reviewed in Espinosa-Medina et al., 2018), has led, in turn, to propose that the pelvic ganglion, targeted by both pathways, is of a mixed sympathetic/parasympathetic nature (Kuntz and Moseley, 1936). Of note, this unique case of anatomic promiscuity between the two types of neurons poses a challenge for the schematic representation of the autonomic nervous system, so that the pelvic ganglion is most often omitted from such representations (Espinosa-Medina et al., 2018). A duality of the pelvic ganglion was also suggested by the coexistence of noradrenergic and cholinergic neurons, which elsewhere in the autonomic nervous system form, respectively, the vast majority of sympathetic ganglionic cells and the totality of parasympathetic ones. Here, we directly explore the composition of the mouse pelvic ganglion in cell types, using single-cell transcriptomics, and compare it to sympathetic and parasympathetic ganglia.
Results
We isolated cells from several autonomic ganglia of postnatal day 5 mice: the stellate ganglion and the lumbar chain (both belonging to the paravertebral sympathetic chain), the coeliac-superior mesenteric complex (belonging to the prevertebral sympathetic ganglia, later refered to as "coeliac"), the sphenopalatine ganglion (parasympathetic) and the pelvic ganglion, and processed them for single-cell RNA sequencing (cf Materials and methods). Neuronal cells segregated in three large ensembles (Figure 1A; Figure 1—figure supplement 1A and B): one that contained all sympathetic neurons, one that contained all parasympathetic neurons, and the third that contained most pelvic neurons – except one subset that segregated close to the sympathetic cluster. Thus, no pelvic neuron segregates with parasympathetic neurons, but the great majority of them do not segregate with sympathetic neurons either.
The separation, on the Uniform Manifold Approximation and Projection (UMAP), of most pelvic from all other ganglionic cells contrasts with the suite of five developmental transcription factors that we previously reported as differentially expressed between the sympathetic and pelvic ganglia on one hand, and parasympathetic ganglia on the other (Espinosa-Medina et al., 2016). To explore this conundrum, we searched for more genes that would help place the pelvic ganglion relative to the sympatho-parasympathetic dichotomy: additional genes that would put the pelvic ganglion in the sympathetic category (as per our previous findings), genes that would put it in a class by itself (as the UMAP suggests), or genes that would split pelvic neurons into parasympathetic-like and sympathetic-like clusters (as the current dogma implies).
In an unbiased approach, we sought genes expressed in a higher proportion of cells in any set of ganglia compared to its complementary set (see ‘Materials and methods’). To do justice to the classical notion that the pelvic ganglion is heterogeneous, i.e., mixed sympatho/parasympathetic, we treated the clusters of pelvic ganglionic cells, four in our conservative estimate (P1–4) (Figure 1A; Figure 1—figure supplement 1B) as four ganglia, alongside the four other ganglia (sphenopalatine, stellate, coeliac, and lumbar) – i.e., we made (28-2)=254 comparisons and analyzed the 100 ‘top’ genes, i.e., with the highest discrimination score, irrespective of the comparison scored (Supplementary files 1–3).
The vast majority of the top 100 genes fell into 7 of the 254 possible dichotomized expression patterns, visualized on a heatmap (patterns I–VI, Figure 1B and C; pattern VII, Figure 1—figure supplement 2) where cells are grouped by ganglion, and genes by expression pattern (i.e. disregarding their score). These seven patterns can be consolidated into three, among which only the first is informative about a sympathetic or parasympathetic identity of pelvic neurons:
Patterns I–IV comprise 39 genes with an opposite status in sympathetic and parasympathetic cells, among which 20 (I+III) are sympathetic-specific and 19 (II+IV) parasympathetic-specific (Figure 1B and C). Those which are also expressed in pelvic clusters (I and IV) argue for their sympathetic (respectively parasympathetic) identity, and against the opposite identity; those which are not expressed in pelvic clusters (II and III) argue solely against such an identity. Overall, 32 genes (I+II) argue against a parasympathetic identity of all pelvic clusters, among which 16 genes (I) argue for their sympathetic identity; 7 genes (III +IV) argue against a sympathetic identity of all clusters, among which 3 genes (IV) argue for a parasympathetic identity of P1 or P4 (which are otherwise not parasympathetic by the criterion of 31 and 32 genes, respectively). We verified expression of 7 sympathetic and 7 parasympathetic markers by in situ hybridization on the pelvic ganglion at E16.5 (Figure 2).
Patterns V+VI comprise 12 genes that correlate with neurotransmitter phenotype (cholinergic or noradrenergic) by being expressed in the sphenopalatine ganglion and P1, P2, and P4 (5 genes (V), including ChAT) or, conversely, in all sympathetic ganglia and P3 (7 genes (VI), including Th) (Figure 1B and C). These genes point to noradrenergic and cholinergic ‘synexpression groups’ (Niehrs and Pollet, 1999) broader than the defining biosynthetic enzymes and transporters. Neurotransmitter phenotype has been suggested to largely coincide with origin of input, lumbar, or sacral (Keast, 1995) which currently defines, respectively, sympathetic versus parasympathetic identity (Keast, 2006). However, we find that the lumbar sympathetic pathway targets both cholinergic and noradrenergic pelvic ganglionic cells (in a proportion that reflects their relative abundance), by anterograde tracing (Figure 3). Thus, noradrenergic and cholinergic genes are excluded from a debate on the sympathetic or parasympathetic identity of pelvic neurons.
Pattern VII involves 42 genes that place all or some pelvic clusters in a class by themselves (Figure 1—figure supplement 2), thus neither sympathetic nor parasympathetic (as does the whole transcriptome, as evidenced by the UMAP (Figure 1A)), by being expressed, or not expressed, exclusively in them. The cholinergic cluster P4 was particularly rich in genes with such idiosyncratic expression states (20 genes). Figure 1—figure supplement 3 provides the five top genes of each pelvic cluster.
In the aggregate, the pelvic ganglion is best described as a divergent sympathetic ganglion, devoid of parasympathetic neurons. The fact that few of the top 100 genes (4 genes, III) marked sympathetic neurons to the exclusion of pelvic ones (Figure 1B), while many (40 genes, VII) did the opposite (Figure 1—figure supplement 2), argues that the pelvic identity is an evolutionary elaboration of a more generic, presumably more ancient, sympathetic one.
A third of the top 100 genes (32 genes) are transcription factors: 6 define a parasympathetic/non{sympathetic+pelvic} identity (Hmx2, Hmx3, Dlx5, Dlx6, Ebf3, Satb2); 12 define a {pelvic+sympathetic}/non-parasympathetic identity (Isl1, Gata2, Gata3, Hand1, Hmx1, Tbx20 plus 6 Hox genes); 3 correlate with the noradrenergic phenotype (Tfap2b, Insm2, and Zfpm2); 8 (including 6 Hox genes) are specific to the pelvic ganglion or some of its clusters (Figure 1—figure supplement 2) and 3 Hox genes are specific to the pelvic+lumbar ganglia (Figure 1B). Nothing is known of the function of the 6 parasympathetic transcription factors, but most of the non-Hox {sympathetic+pelvic} ones are implicated in sympathetic differentiation: Islet1 (Huber et al., 2013), Hand1 (Doxakis et al., 2008), Gata2 (Tsarovina et al., 2004), Gata3 (Lim et al., 2000), and Hmx1 (Furlan et al., 2013).
Expression of a shared core of 12 transcription factors by pelvic and sympathetic ganglia, yet of divergent transcriptomes overall, logically calls for an additional layer of transcriptional control to modify the output of the 12 sympathetic transcription factors. Obvious candidates are the 6 Hox genes restricted to the pelvic ganglion (Hoxd9, Hoxa10, Hoxa5, Hoxd10, Hoxc11, and Hoxb3) (Figure 1—figure supplement 2) and 6 more beyond the 100 top genes, mostly Hoxb paralogues (Figure 1—figure supplement 4). Given that the parasympathetic and sympathetic ganglia are deployed according to a rostro-caudal pattern (parasympathetic ganglia in register with cranial nerves, sympathetic ganglia with thoraco-lumbar nerves, and the pelvic ganglion with lumbar and sacral nerves; Figure 4), the entire taxonomy of autonomic ganglia could be a developmental readout of Hox genes (whose multiplicity makes this conjecture hard to test). A role for Hox genes in determining types of autonomic neurons would be reminiscent of their specification of other neuronal subtypes in Drosophila (Suska et al., 2011), Caenorhabditis elegans (Zheng et al., 2015), and Mus (Coughlan et al., 2019).
Discussion
The notion that the pelvic ganglion is a caudal elaboration of the sympathetic ganglionic chains echoes the situation of its preganglionic neurons, in the lumbar and sacral spinal cord. We showed that lumbar and sacral preganglionics are indistinguishable by several criteria, including the expression state of six transcription factors (Phox2a, Phox2b, Tbx3, Tbx2, Tbx20, FoxP1) and their dependency on the bHLH gene Olig2, in addition to their well-known location (the intermediate lateral column) and the ventral exit point of their axon (Espinosa-Medina et al., 2016). Recent surveys of spinal preganglionic neurons by single-cell transcriptomics (Blum et al., 2021; Alkaslasi et al., 2021) discovered many subtypes, most of them evenly distributed from thoracic to sacral levels, and a few enriched at, or specific to the sacral level, confirming that the sacral preganglionic neurons are sympathetic, yet represent a caudal modification of the thoraco-lumbar intermediate lateral column.
In conclusion, the genetic signatures of neither pre- nor post-ganglionic neurons of the sacral autonomic outflow support its century-old assignment to the parasympathetic division of the visceral nervous system. Importantly, we have argued (Espinosa-Medina et al., 2018) that the supposed parasympathetic identity was unnecessary at best to understand the physiology of the pelvis, at worst incongruent with it, at least concerning sex organs and the bladder. The antagonism between an anti-erectile lumbar and a pro-erectile sacral autonomic pathways on the blood vessels of the external genitals – the key argument that Langley advanced for making the sacral pathway parasympathetic, even before he coined the term (Langley, 1899) – was repeatedly challenged by the evidence of a lumbo-sacral pro-erectile synergy (reviewed in Espinosa-Medina et al., 2018). And experimental support for a lumbo-sacral antagonism on the bladder is scant, despite common perception from textbooks and reviews (reviewed in Espinosa-Medina et al., 2018). It is thus remarkable that the cell type-based anatomy that we uncover in no way contradicts the physiology. There is no need to posit that the sympathetic-like neurons we describe in the pelvic region display a type of physiology common with that of parasympathetic ones in the head or thorax, which would deserve a common name. The classical parasympathetic label is thus best dropped and replaced by the genetic (i.e. embryological and evolutionary) notion of a sympathetic one, modified to suit the unique demands of pelvic physiology. The division of the autonomic nervous system that encompasses the pelvic ganglion and both its lumbar and sacral afferents (which could be termed ‘pelvo-sympathetic’ and includes whatever antagonistic pathways operate in the region – e.g. on genital blood vessels) is now ripe for finer grain analysis, anatomical and physiological, at the level of neuron types, defined by their gene expression patterns.
Materials and methods
Mice
Phox2b::Cre (D’Autréaux et al., 2011): a BAC transgenic line expressing Cre under the control of the Phox2b promoter.
Rosalox-stop-lox-tdTomato (RosatdT) (Madisen et al., 2010): Knock-in line expressing the reporter gene tdTomato from the Rosa locus in a Cre-dependent manner.
Obtainment of ganglionic cells
Request a detailed protocolSphenopalatine, stellate, coeliac, lumbar, and pelvic ganglia were dissected from Phox2bCre;RosatdT P5 pups representing both sexes and placed in artificial cerebrospinal fluid oxygenated with carbogen (4°C). Fat tissue was carefully removed and nerves emanating from the ganglia were cut. Ganglia were transferred into a 1.5 ml Eppendorf tube containing 1 ml PBS-glucose (1 mg/ml glucose), 20 µl papain solution (Worthington LS003126; 25.4 units/mg) and 20 µl DNAse (2 mg/ml in PBS) and incubated at 37°C for 15 min. The ganglia were collected by centrifugation (300×g, 1 min), the supernatant replaced by 1 ml PBS-glucose supplemented with 50 µL Collagenase/Dispase (Worthington CLS-1 345 U/mg; Dispase II Roche 1.2 U/mg; 80 mg Collagenase and 92 mg Dispase II dissolved in 1 ml PBS-glucose) and 20 µl DNAse solution and the ganglia incubated at 37°C for 8 min. After collecting the ganglia by centrifugation for 3 min at 300×g they were dissociated in 1 ml PBS-glucose supplemented with 0.04% bovine serum albumin (BSA) and DNAse (20 µl) by trituration, using a fire-polished, siliconized Pasteur pipette. The cell suspension was then filtered through a 40 µm cell strainer. To eliminate cell debris, the cell suspension was centrifuged through a density step gradient by overlaying the cell suspension onto 1 ml OptiPrep solution (80 µl OptiPrep [Sigma], 900 µl PBS supplemented with 0.04%BSA, 20 µl DNAse) for 15 min, 100×g at 5°C. After removal of the supernatant from the soft cell pellet, the cells were suspended in 100 µl PBS-glucose/0.04% BSA and collected again in a 500 µl Eppendorf tube for 15 min, 100×g at 5°C. The supernatant was carefully removed (under control by fluorescence microscope). After addition of 40 µl PBS-glucose/0.04% BSA, the cell density was adjusted to 1000 cells/μl and transferred to the 10x Genomics platform.
Library construction and sequencing
Request a detailed protocolSingle-cell RNA sequencing was performed in two separate experimental rounds, one for the stellate, sphenopalatine, and pelvic ganglia (pelvic_1) performed at the École normale supérieure GenomiqueENS core facility (Paris, France), and one for the celiac, lumbar and pelvic ganglia (pelvic_2) performed at the ICGex NGS platform of the Institut Curie (Paris, France). Cellular suspensions (10,000 cells for the first round, 5300 cells for the second) were loaded on a 10x Chromium instrument (10x Genomics) to generate single-cell GEMs (5000 for the first round, 3000 for the second). Single-cell RNA sequencing libraries were prepared using Chromium Single Cell 3' Reagent Kit (v2 for the first round, v3 for the second) (10x Genomics) according to the manufacturer’s protocol based on the 10x GEMCode proprietary technology. Briefly, the initial step consisted in performing an emulsion where individual cells were isolated into droplets together with gel beads coated with unique primers bearing 10x cell barcodes, UMI (unique molecular identifiers) and poly(dT) sequences. Reverse transcription reactions were applied to generate barcoded full-length cDNA followed by disruption of the emulsions using the recovery agent and the cDNA was cleaned up with DynaBeads MyOne Silane Beads (Thermo Fisher Scientific). Bulk cDNA was amplified using a GeneAmp PCR System 9700 with 96-Well Gold Sample Block Module (Applied Biosystems) (98°C for 3 min; 12 cycles: 98°C for 15 s, 63°C for 20 s, and 72°C for 1 min; 72°C for 1 min; held at 4°C). The amplified cDNA product was cleaned up with the SPRIselect Reagent Kit (Beckman Coulter). Indexed sequencing libraries were constructed using the reagents from the Chromium Single Cell 3' Reagent Kit v3, in several steps: (1) fragmentation, end repair, and A-tailing; (2) size selection with SPRI select; (3) adaptor ligation; (4) post-ligation cleanup with SPRI select; (5) sample index PCR and cleanup with SPRI select beads (with 12–14 PCR cycles depending on the samples). Individual library quantification and quality assessment were performed using the Qubit fluorometric assay (Invitrogen) with the dsDNA HS (High Sensitivity) Assay Kit and a Bioanalyzer Agilent 2100 using a High Sensitivity DNA chip (Agilent Genomics). Indexed libraries were then equimolarly pooled and quantified by qPCR using the KAPA library quantification kit (Roche). Sequencing was performed on a NextSeq 500 device (Illumina) for the first round and a NovaSeq 6000 (Illumina) for the second, targeting around 400M clusters per sample and using paired-end (26/57 bp for the first round, 28×91 bp for the second).
Bioinformatic analysis
Request a detailed protocolFor each of the six samples (pelvic_1, stellate, sphenopalatine, pelvic_2, coeliac, and lumbar) we performed demultiplexing, barcode processing, and gene counting using the Cell Ranger software (v. 6.0.1). The ‘filtered_feature_bc_matrix’ files (uploaded at https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE232789) were used as our starting points for defining cells. For each dataset, only droplets that expressed more than 1500 genes, less than 11,000 genes, and a percentage of mitochondrial genes below 15% were retained. This resulted in the selection of 4404 pelvic_1 cells, 7225 stellate cells, 4630 sphenopalatine cells, 1643 pelvic_2 cells, 1428 coeliac, and 2120 lumbar cells.
We used Seurat version 3 (Stuart et al., 2019) to read, manipulate, assemble, and normalize (Hafemeister and Satija, 2019) the datasets. Specifically, we concatenated cells from all six datasets and normalized the data using the sctransform (SCT) method for which we fitted a Gamma-Poisson generalized linear model (‘glmGamPoi’ option). Using the Seurat framework, we then performed a PCA on the normalized dataset.
Next, we integrated all six datasets using Batchelor (Haghverdi et al., 2018) (a strategy for batch correction based on the detection of mutual nearest neighbors), and we visualized all cells, including neurons, in two dimensions using the UMAP method (Becht et al., 2018) on the first 50 components from the PCA.
We selected neurons based on their mean expression of a set of neuronal marker genes (Stmn2, Stmn3, Gap43, and Tubb3). Specifically, cells were classified as neurons if their mean marker SCT-normalized gene expression exceeded a threshold of 3, that best separated the bimodal distribution of the higher and lower values of the mean expression of neuronal markers. Likewise, we excluded glial-containing doublets using the following markers: Plp1, Ttyh1, Fabp7, Cryab, and Mal. The number of neurons thus selected was 862 for Pelvic_1, 2689 for the stellate, 1857 for the sphenopalatine, 361 for Pelvic_2, 236 for celiac, and 925 for the lumbar chain.
We then clustered pelvic neurons based on the first two components from the UMAP generated from the 50 batch-corrected components, using the graph-based clustering method Louvain (Blondel et al., 2008) implemented in the Seurat framework, with a resolution of 0.3. This procedure defined 24 clusters and split the pelvic ganglion into four clusters 1, 7, 15, and 19 (Figure 1—figure supplement 1B), that we renamed P1, P2, P3, P4 (Figure 1A). The efficiency of batch correction is attested by the equal contribution from both batches of pelvic ganglia to all four defined pelvic clusters (P1–4) (Figure 1—figure supplement 1A), and the comparable expression level of the top 100 genes across both pelvic batches in the violin plots (Supplementary file 2).
To search in an unbiased manner for gene expression similarities between pelvic neurons and either sympathetic or parasympathetic ones, we systematically compared the expression of every gene of the dataset across all possible splits among ganglia, i.e., between every subset of ganglia (‘subset_1’), and its complementary subset (‘subset_2’). Because we treated each of the 4 pelvic clusters as a ganglion, there were 2^8=256 such splits (2 of them, defined by ‘all_8_groups vs none’ and ‘none vs all_8_groups’, being meaningless). For every split and every gene, we devised a score that would best reflect how higher the proportion is of cells expressing the gene (i.e. one read of the gene or more) in subset_1 than in subset_2. We used a metric based on the product of the proportions of cells expressing the gene in each ganglion of subset_1 or subset_2 (rather than throughout subset_1 or subset_2), to give an equal weight to each ganglion (irrespective of its size), and to penalize splits that contain outliers (i.e. ganglia that contain much fewer cells positive for that gene than other ganglia in subset_1, or ganglia that contain much more cells positive for that gene than other ganglia in subset_2).
Specifically, for a given split and a given gene, the score (here defined by the variable score, in the R programming language) is defined as:
where:
S1 and S2 are the ganglion subsets subset_1 and subset_2 as described above.
nS1 and nS2 are the number of ganglion clusters that belong to subset_1 and subset_2.
and are the proportion of cells from ganglion or pelvic cluster i and j (i belonging to subset_1 and j to subset_2) which express the given gene.
epspos=0.9 and epsnega=0.02 are parameters controlling a tradeoff between favoring genes expressed in subset_1 and penalizing genes expressed in subset_2.
Note that when epspos=0.9 (the parameter value used here) the quantity can be negative, in which case the expression becomes equal to -Inf and the gene gets the lowest possible score for that given split. This means that with these settings all dichotomies involving a ganglion or pelvic cluster in which less than 10% of cells express the gene (p=0.1) will get the minimal possible score.
In vivo gene expression
Tissue preparation
Request a detailed protocolEmbryo sections: E16.5 WT embryos were freshly dissected, washed with 1× PBS, and fixed overnight in 4% PFA at 4°C. Tissues were washed a few times in 1× PBS and treated in 15% sucrose to cryopreserve the tissues for frozen tissue sections. Tissues were then embedded in the optimal cutting temperature compound and snap-frozen. Tissues were cut at 14 μm on a cryostat. Tissue sections were stored at –80°C until use for staining.
In situ hybridization
Request a detailed protocolFrozen tissue sections were washed in 5× SSC buffer 15 min at room temperature (RT) and treated in the pre-hybridization solution (50% formamide, 5× SSC buffer, and 40 μg/ml Herring sperm DNA in H2O) for 1 hr at 60°C. Then, slides were put in the hybridization solution (50% formamide, 5× SSC buffer, 5× Denhardt’s, 500 μg/ml Herring sperm DNA, 250 μg/ml yeast RNA, and 1 mM DTT in H2O) containing the probe (100 ng/ml), at least two overnights at 60°C. Slides were washed two times in 5× SSC buffer (5 min) and two times in 0.2× SSC buffer (30 min) at 70°C, and then, three times in TBS at RT (10 min). Then, tissues were put in the blocking solution (TBS+10% FCS) for 1 hr in the dark, at RT and in humid atmosphere (250 μl/slide) and incubated 1 hr with the primary antibody (anti-DIG) diluted 1/200 in blocking solution (250 μl/slide). Then, slides were washed again three times in TBS (10 min) and treated 5 min in the AP buffer solution (100 nM Tris pH 9.5, 50 nM MgCl2, and 100 nM NaCl in H2O). The revelation was made by the NBT-BCIP solution (Sigma) in the dark (250 μl/slide). The reaction was stopped in PBS-Tween (PBST).
Immunohistochemistry
Request a detailed protocolAfter in situ hybridization, frozen tissues were fixed 15 min in 4% PFA at RT and washed in PBST. Then, tissues were incubated in PBST+10% FCS in the dark for 1 hr (500 μl/slide, without coverslip) and incubated overnight with the primary antibody in the same solution at 4°C (250 μl/slide). Slides were washed in PBST three times (10 min) and incubated for 2 hr at RT with the secondary antibody in the same solution again. Tissues were washed three times in PBST and then incubated at RT with avidin/biotin solution diluted 1/100 in 1× PBS. Then, tissues were washed three times and the revelation was made in 3,3’-diaminobenzidine (DAB) solution containing DAB and urea in H2O (Sigma). The reaction was stopped in PBST, and slides were washed in PBST and in ultra-pure H2O. Slides were mounted in Aquatex mounting medium (Merck).
Imaging
Request a detailed protocolTissues processed by an in situ hybridization and immunohistochemistry were photographed on a Leica bright-field microscope with a 40× oil immersion objective. Images were then treated by Photoshop v. 24.1.0.
Anterograde tracing
Tracer injections
Request a detailed protocolSurgeries were conducted under aseptic conditions using a small animal digital stereotaxic instrument (David Kopf Instruments). Male, C57bl mice (2–4 months of age) were anesthetized with isoflurane (3.5% at 1 l/min for induction and 2–3% at 0.3 l/min for maintenance). Carprofen (0.5 mg/kg) was administered subcutaneously for analgesia before surgery. A feedback-controlled heating pad was used to maintain the animal temperature at 36°C. Anesthetized animals were shaved along the spine and placed in a stereotaxic frame. The skin overlying the spine was sterilized with alternating scrubs of Vetadine and 80% (wt/vol) ethanol and a 100 μl injection of lidocaine (2%) was made subcutaneously along the spine before an incision was made from the iliac crest to the T9 vertebral spinous process. The T10 and T11 spinous processes were identified by counting rostrally from the L6 spinous process (identified relative to the iliac crest). Two small rostro-caudal incisions were made on each side of the vertebral column through the superficial-most layer of muscle. Parallel clamps were then placed within these incisions until firm contact was made with the transverse process of the T11 vertebra. The T11 vertebra was then raised upward via the clamps until no respiratory movement was observed. The muscles connecting the T10 spinous process to transverse processes of caudal vertebra were dissected to expose the T10/T11 intervertebral space. A lateral incision was made across the dura to expose the underlying L1 spinal segment and 150 nl injections of 4% lysine fixable, tetramethylrhodamine or Alexa-488-conjugated dextran, 3000 MW (Thermo Fisher) were made bilaterally, into the intermediolateral nucleus and intermedio-medial nucleus (0.600 mm lateral, 0.600 mm deep and 0.150 mm lateral and 0.700 mm deep) using a narrow-tapered glass pipette and a Nanoject III injector (Drummond Scientific). Injections were made at 5 nl per second and left in place for 5 min following injection to prevent dextran leakage from the injection site. The pipette was then retracted, and the intervertebral space bathed with sterile physiological saline. A small piece of sterile gel foam hemostat (Pfizer) was then placed within the intervertebral space and the incision overlying the spine was sutured closed.
Histology
Request a detailed protocol7–14 days after injection the mice were intracardially perfused with cold PBS until exsanguinated and subsequently fixed by perfusion with cold 4% PFA until the carcass became stiff. The bladder, prostate, and pelvic ganglia were immediately dissected as an intact bloc and post-fixed in 4% PFA overnight at 4 °C. The intact spinal column was also dissected out and the dorsal surface of the spinal cord exposed before post-fixation overnight in 4% PFA at 4 °C. The fixed tissues were then rinsed in PBS 3×30 min the following day. The ‘bladder block’ was then cryopreserved in 15% sucrose (wt/vol) in PBS until non-buoyant. The dorsal aspect of the injection site was imaged in situ using fluorescence stereoscope. The spinal cord was then dissected out and cryopreserved as described above.
The bladder block was sectioned on a cryostat in a sagittal orientation to capture serial sections of the entire pelvic ganglion. Sections were cut at a thickness of 30 µm and collected as a 1 in 4 series on Superfrost Plus glass slides. The spinal cord was sectioned coronally at a thickness of 60 µm as a 1 in 2 series. On slide immunohistochemistry was performed against tyrosine hydroxylase (TH) and choline acetyltransferase (CHAT) for the bladder block sections, primary incubation: 4–6 hr at RT, secondary incubation: 2 hr at RT, with 3×5 min washes in PBS after each incubation. Sections were then mounted with dako fluorescence mounting medium and coverslipped.
Imaging
Request a detailed protocolSections were imaged on a Leica Stellaris 5 confocal microscope (Leica microsystems). Images of the pelvic ganglia were captured as Z-stacks with 1 µm interslice distances, with a 20× objective at 2000 mp resolution.
Counting
Request a detailed protocolAll ganglionic cells and cells surrounded by dextran labeled varicosities were identified as either CHAT or TH positive and counted, on a total of 4 animals, 48 sections, and 3186 cells.
Probes
Request a detailed protocolPrimers were designed to amplify by PCR probe templates for the following genes:
Probe | Forward primer | Reverse primer |
---|---|---|
Dlx5 | 5’-GACGCAAACACAGGTGAAAATCTGG-3’ | 5’-GGGCGGGGCTCTCTGAAATG-3’ |
Gata2 | 5’-TTGTGTTCTTGGGGTCCTTC-3’ | 5’-GCTTCTGTGGCAACGTACAA-3’ |
Hmx1 | 5’-CGTTCGCCACTATCCAAACGGG-3’ | 5’-TGTCAGGACTTAGACCACCTCCG-3’ |
Ntn1 | 5’-CTTCCTCACCGACCTCAATAAC-3’ | 5’-GCGATTTAGGTGACACTATAGTTGTGCCTACAGTCACACACC-3’ |
Syt6 | 5’-GTGGTCTTCTTGTCCCGTGT-3’ | 5’-CATGTGCTTACAGGGTGTGG-3’ |
Zbtb16 | 5’-ATGAAAACATACGGGTGTGAA-3’ | 5’-CCAAGGCCAAGTAACTATCAGG-3’ |
The PCR fragment were ligated into a pGEM-T Easy Vector System (Promega), transformed into chemically competent cells and sequenced. The other plasmid templates were Ebf3 (gift of S Garel), Gata3 (gift of JD Engel), Hand1 (gift of P Cserjesi), Hmx2 (gift of EE Turner), Hmx3 (gift of S Mansour), Islet1 (Tiveron et al., 1996), Tbx20 (Dufour et al., 2006) and Sst (Clone Image ID #4981984).
Plasmids were digested by restriction enzymes and purified using a DNA Clean & Concentrator kit (Zymo Research). Antisense probes were synthesized with RNA polymerases and a DIG RNA labeling mix, and purified by the ProbeQuant G-50 micro columns kit (GE Healthcare). Probes were stored at –20°C.
Antibodies
Primary antibodies were α-PHOX2B rabbit (1:500 or 1:1000, Pattyn et al., 1997). α-TH (Invitrogen: OPA1-04050, 1:1000) and α-CHAT (Thermo Fisher: PA1-9027, 1:100).
Secondary antibodies were goat α-rabbit (PK-4005, Vector Laboratories), donkey anti-goat 647 (A-21447, Thermo Fisher), donkey anti-rabbit 488 (A-21206, Thermo Fisher), and donkey α-rabbit Cy3 (711-165-152, Jackson).
Data availability
The data can be accessed at: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE232789.
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NCBI Gene Expression OmnibusID GSE232789. The pelvic ganglion is a divergent outpost of the sympathetic chains.
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ConferencePresidential address, Physiological sectionReport of the Meetings of the British Association for the Advancement of Science. pp. 881–892.
Article and author information
Author details
Funding
Agence Nationale de la Recherche (ANR-19-CE16- 0029-01)
- Jean-François Brunet
Agence Nationale de la Recherche (ANR-17-CE16-0006-01)
- Jean-François Brunet
Fondation pour la Recherche Médicale (FRM EQU202003010297)
- Jean-François Brunet
National Health and Medical Research Council (APP2001128)
- Bowen Dempsey
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Acknowledgements
We thank Nicolas Narboux-Nême for help with the analysis of Dlx5 expression, Sonia Garel for the gift of the Ebf3 probe, Amandine Delecourt and Gwendoline Firmin for help with the mouse colonies. The Brunet laboratory is supported by INSERM, CNRS, ANR-19-CE16-0029-01, ANR-17-CE16-0006-01, FRM EQU202003010297. MA is a recipient of a doctoral fellowship from Labex MemoLife. BD was funded by grant APP2001128 from the National Health & Medical Research Council, Australia. HR has been supported by a grant from the Wilhelm Sander Foundation and from Labex MemoLife. High-throughput sequencing was performed by (1) the GenomiqueENS core facility supported by the France Génomique national infrastructure, funded as part of the 'Investissements d'Avenir' program managed by the Agence Nationale de la Recherche (contract ANR-10-INBS-0009); (2) the ICGex NGS platform of the Institut Curie supported by the grants ANR-10-EQPX-03 (Equipex) and ANR-10-INBS-09–08 (France Génomique Consortium) from the Agence Nationale de la Recherche ('Investissements d’Avenir' program), by the ITMO-Cancer Aviesan (Plan Cancer III) and by the SiRIC-Curie program (SiRIC Grant INCa-DGOS-465 and INCa-DGOS- Inserm_12554). Data management, quality control, and primary analysis were performed by the Bioinformatics platform of the Institut Curie.
Ethics
Breeding of mice, obtainment of mouse embryos and of cells from mouse pups were performed in strict accordance with the recommendations of the French Ministry of Agriculture and have been approved by the Direction Départementale des Services Vétérinaires de Paris. Tracer injection experiments were approved by the Macquarie University Animal Ethics Committee (animal research authority# 2018-024) and conformed to the Australian Code of Practice for the Care and Use of Animals for Scientific Purposes 2013.
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You can cite all versions using the DOI https://doi.org/10.7554/eLife.91576. This DOI represents all versions, and will always resolve to the latest one.
Copyright
© 2023, Sivori, Dempsey 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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