Population averaging due to paracrine communication can arbitrarily reduce cellular response variability. Yet, variability is ubiquitously observed, suggesting limits to paracrine averaging. It remains unclear whether and how biological systems may be affected by such limits of paracrine signaling. To address this question, we quantify the signal and noise of Ca2+ and ERK spatial gradients in response to an in vitro wound within a novel microfluidics-based device. We find that while paracrine communication reduces gradient noise, it also reduces the gradient magnitude. Accordingly we predict the existence of a maximum gradient signal to noise ratio. Direct in vitro measurement of paracrine communication verifies these predictions and reveals that cells utilize optimal levels of paracrine signaling to maximize the accuracy of gradient-based positional information. Our results demonstrate the limits of population averaging and show the inherent tradeoff in utilizing paracrine communication to regulate cellular response fidelity.https://doi.org/10.7554/eLife.09652.001
The human body is made up of many different types of cell that are each specialized to perform particular roles. Although each cell type has the same set of genes, the level of activity (or “expression”) of these genes varies between each type. Additionally, gene expression in cells of the same type can vary due to randomness in the regulation of genes.
Although variation in gene expression between cells can allow populations of cells to adapt to a changing environment, variability can also cause problems when many different cells need to work together. A system called “paracrine signaling” allows cells to communicate with each other by releasing signaling molecules that bind to and activate surrounding cells. The distance that this molecule travels, or the “paracrine communication distance”, determines how many surrounding cells each cell can communicate with to coordinate their responses. However, it is not clear what impact paracrine signaling has on the variability between cells, or what limitations there are on the size of the paracrine communication distance.
Cells that are damaged during wounding immediately release a molecule called ATP, which acts as a danger signal to activate the wound healing process in the surrounding cells. The release of ATP from wounded cells forms a spatial gradient in the surrounding healthy cells and stimulates the release of molecules called growth factors that are required for the healing process.
Here, Handly et al. developed a new device to study the responses of human cells to a wound and used it in combination with a computational model to measure the impact of paracrine communication on these responses. The experiments show that paracrine signaling by the growth factor EGF reduces the variability in the responses of cells to the ATP signal. However, this reduction is limited by the size of the paracrine communication distance. Paracrine communication distances that are too small or too large either do not provide adequate reduction in variability or result in “over-averaging”. Handly et al.’s findings show that there is an optimal level of paracrine signaling during wounding that helps to coordinate the response in nearby cells without inappropriately over-averaging the signal.https://doi.org/10.7554/eLife.09652.002
Cellular variability is likely a biological trait with significant phenotypic consequences. Technological advances in single-cell measurement methodologies reveal substantial cellular variability. For instance, single-cell quantification of protein concentration variability between cells shows that the concentration of many signaling molecules can vary by ∼25% (coefficient of variation) (Sigal et al., 2006; Bar-Even et al., 2006; Spencer et al., 2009). Furthermore, a large and rapidly growing body of single-cell transcriptomics experiments further demonstrates that cells homogeneous in 'type' have substantially heterogeneous gene expression patterns (Junker and Van Oudenaarden, 2014). The origin of this cellular variability has been traced to fundamental properties of gene expression. Notably, single-molecule kinetics regulates gene expression and, as a result, is an inherently stochastic process (Sanchez and Golding, 2013).
While the costs and benefits of cellular variability are likely dependent on the specific physiological context, the functional significance of cellular variability suggests that cellular variability magnitude is regulated. Functional analysis of cellular response variability demonstrates that the observed cellular variability affects the core function of signaling networks. Despite a homogenous environment, cells respond in a heterogeneous manner due to biological variability. Response variability potentially degrades transmitted information and decreases downstream effector ability to reliably respond to environmental changes (Selimkhanov et al., 2014; Cheong et al., 2011; Voliotis et al., 2014; Hansen and O'Shea, 2015). The abundance of cellular variability throughout biological processes and the potential consequences of information degradation suggest that biological systems have developed mechanisms to regulate cellular variability. However, cellular variability is not necessarily detrimental to cellular function. In fact, cellular heterogeneity often plays a critical role in ensuring proper cellular response by mechanistically increasing the cellular response range to a constantly changing environment (Altschuler and Wu, 2010). For example, single-cell noise in NFκB dynamics creates robust population level responses to a wider range of inputs (Hughey et al., 2014; Kellogg and Tay, 2015).
Cells share information with each other via paracrine signaling, which effectively averages variable cellular responses and therefore reduces cellular variability. Overall population-level averaging decreases variability by following the statistical laws of the central limit theorem and the law of large numbers (Piras and Selvarajoo, 2014). Paracrine signaling averaging can decrease variability in a similar manner, but functions on a local population level. Specifically, paracrine signaling averaging functions such that the local concentration of the paracrine ligand, or the concentration of ligand a cell is exposed to, is the average ligand concentration secreted by local cells (Figure 1A). Indeed, the benefits from paracrine communication were previously demonstrated to increase post-paracrine cellular response fidelity (Rand et al., 2012; Shalek et al., 2014). The process of local population 'information averaging' by each cell enables increased accuracy of inherently single cell decisions such as proliferation and differentiation.
Despite promises of noise mitigation from paracrine averaging, parameters set by biological systems can limit these potential benefits. For example, population averaging due to paracrine communication may cause loss of information in a similar manner to the information loss of single-cell dynamics due to ‘population average’ bulk measurements (Elowitz et al., 2002; Newman et al., 2006; Bar-Even et al., 2006). The potential information loss due to ‘over-averaging’ of variable single-cell responses demonstrates a limitation to paracrine communication. Limitations to paracrine communication are also observed in post-paracrine single-cell responses that remain highly variable despite paracrine averaging. These limitations suggest an overall functional constraint to the potential benefits of paracrine communication. However, the identity and source of these limitations on paracrine communication benefits are unknown.
The initial paracrine signaling pathways that are activated in response to Damage Associated Molecular Patterns (DAMPs) are a good model system for investigating the influence and limits of paracrine communication on cellular response fidelity. Paracrine communication is pervasive during initial wound response. Wound healing begins as soon as the wound occurs and the initial cellular wound response provides the foundation for proper downstream healing. The initial cellular wound response relies on external environmental cues as well as programs inherent to the cell, including DAMPs as primary danger signals (Enyedi and Niethammer, 2015). DAMPs are released from necrotic cells and bind to extracellular receptors on surrounding cells. This binding initiates a signal in the surrounding cells to secrete a secondary set of cytokines and growth factors required to coordinate the wound healing process. Many DAMP signals, such as extracellular ATP, are transient and released in limited quantities. As a result, the initial wound response to such DAMPs shows high cellular variability and low fidelity. Despite the limited fidelity of the initial wound response, the wounded epithelium is able to establish a robust healing response. The complicated and multi-step wound healing process utilizes several paracrine communication mechanisms to share cellular information and coordinate the overall healing program.
Here we use the paracrine release of epidermal growth factor (EGF) ligands initiated by ATP binding to P2Y receptors as a model to investigate the limits of cellular information sharing through paracrine communication to mitigate biochemical noise (Figure 1A). We show that paracrine communication increases extracellular signal-regulated kinase (ERK) response fidelity using live single-cell quantitative fluorescent imaging of primary Ca2+ and secondary ERK responses downstream of P2YR and EGFR, respectively. Statistical analysis of the primary response signal-to-noise ratio (SNR) demonstrates that the increase in response fidelity is limited by paracrine communication distance (PCD). To analyze this pathway in the physiological context of wound response we developed a new microfluidics device to monitor the spatial propagation of initial wound response signaling. Our results demonstrate that the interplay between the wound induced spatial signaling gradient and the cellular noise pattern produces an optimal PCD. The optimal PCD balances the benefits of decreased noise from local averaging with the cost of reduced signal of the spatial signaling gradient due to over-averaging. Empirical measurements of the PCD reveal that cellular communication occurs at a distance to maximize cellular response fidelity.
Here we establish that the paracrine activation of ERK by ATP provides a suitable system to investigate signaling response fidelity changes due to paracrine communication. Extracellular ATP binding to P2YR results in EGF family ligand release to bind EGFR and activate ERK response as monitored by ERK activity following ATP addition. In the mammary epithelial cell line MCF-10A, addition of extracellular ATP increases ERK kinase activity in an EGFR dependent manner (Figure 1B) similar to results reported in other in vitro epithelial models (Yin et al., 2007). ERK, as measured by the genetically encoded FRET sensor EKAREV (Albeck et al., 2013; Komatsu et al., 2011), increases when stimulated with ATP. Inhibiting EGFR with tryphostin AG1478 prevents ERK activation upon ATP addition showing that ERK activation depends on secreted EGF binding to EGFR (Wetzker and Böhmer, 2003).
With our paracrine communication system established, we next confirmed the influence of paracrine communication on cellular response variability. Under conditions of low cell density we used a spatial clustering analysis to group cells such that the distance between groups effectively constrained communication to cells within groups (Figure 1C,D, Figure 1—figure supplement 1,2). In the case that cellular coordination is beneficial, we anticipated that the ERK response within groups of higher cellular density, that is cells have increased communication ability, would have reduced response variability than cell clusters with decreased communication ability. ERK response variability within clusters decreases with increasing cluster density indicating increased intercellular communication ability. Increased intercellular communication ability is not observed in the absence of paracrine communication such as with the primary Ca2+ response to ATP (Figure 1D, Figure 1—figure supplement 2). Furthermore, disrupting paracrine communication by partially inhibiting Src results in the loss of the observed benefit of paracrine communication in higher density clusters (Figure 1D, Figure 1—figure supplements 3,4). Together these observations support the hypothesis that paracrine communication decreases cellular variability by increasing cellular coordination.
Next we developed a computational model that mimics the coordination-effects of paracrine communication (see Materials and methods for details). This computational model quantifies the overall observed benefit of paracrine coordination and predicts the potential reduction in variability. Experimental single-cell dose response data of primary Ca2+ (prior to paracrine communication) response to ATP is used as an input to predict the secondary ERK response. We quantify cellular response fidelity by using a simple signal-to-noise analysis (SNR). In this analysis the cellular response magnitude of the input ligand (signal) is divided by the cellular response variability (noise). The signal is estimated by calculating the spread between the average cellular Ca2+ responses from multiple ATP concentrations using multi-well dose response data. Noise is calculated from the average variability between cellular responses to a single input ligand concentration. SNR is simply the ratio of these two estimates (Figure 1E). To mimic the benefit of paracrine communication our computational model performs a local, spatially weighted average (convolution) of the primary Ca2+ response to predict the variability of response post paracrine communication (ERK) (Figure 1F). In short, the convolution averages the signal for every cell with its associated surrounding cells by weighting the surrounding cells based on a Gaussian function parameterized with varying PCDs. The PCD represents how far the paracrine molecule travels from a single-cell to activate its associated surrounding cells. Local spatial averaging provides an upper bound of the possible benefit resulting from cellular communication in conditions where no additional noise exists in the paracrine pathway. This analysis indicates that paracrine averaging using a PCD of 100 μm increases response SNR from 0.9 to 20.2 by decreasing noise, or response variability, of the predicted ERK response (Figure 1E, gray/black). To investigate the limits of paracrine averaging, we repeated this analysis for multiple PCDs. Interestingly, our analysis estimates that the overall response SNR can increase up to eightyfold at PCDs of 500 μm when paracrine diffusion is not limiting, and up to twenty fivefold when diffusion of the paracrine ligand is limiting (Figure 1G). More sophisticated statistical measures, such as mutual information, produce similar results (Figure 1G, Figure 1—figure supplement 5). The large maximal SNR benefit suggests a potentially noise-free ERK response. However, experimental measurements of ERK response fidelity shows substantial ERK variability indicating potential factors that limit the benefit gained from paracrine communication (data not shown).
Extracellular ATP released from necrotic cells act as DAMPs to activate healthy cells proximal to the wound (Cordeiro and Jacinto, 2013). Given this role, the spatial component produced by the ATP concentration gradient and the resulting cellular positional information relative to the wound may be important in the analysis of paracrine communication that occurs over hundreds of microns from the wound. Our previous SNR analysis demonstrating an increasing SNR with increasing communication distance was done based on multi-well experiment data. However, the bolus addition of ATP creates a spatially uniform ligand concentration in the well and does not represent a physiologically relevant spatial component. To examine whether ATP spatial patterns influence the paracrine communication benefit we repeated the SNR analysis using single-cell wound response data.
In order to measure the spatial wound response for epithelial cells, we first developed a convection-free, small-volume wounding device. Scratch-assays, where a monolayer of cells is mechanically wounded using a pipet tip, are traditionally used for epithelial cell wounding (Sholley et al., 1977). Although the scratch-assay is useful for studying cell-migration following wounding, scratch-assays lack the ability to study paracrine signaling. The large volume above the cells and convection caused by the scratch present challenges to examine paracrine signaling due to the dilution and inadvertent mixing of any paracrine molecules released from a cell into the surrounding media. To circumvent these technical issues we developed a microfluidics based wounding device (Figure 2A,B). Our device has two components: an air channel (black) and a cell chamber with a ∼2.5 μL volume (orange). The ceiling of the cell chamber has a PDMS pillar that, when air pressure is increased in the upper air channel, lowers down on to the cells, thereby wounding the cells in the cell chamber in a highly controlled and reproducible manner (Figure 2B,C, Figure 2—figure supplement 1, Video 1).
We used our wounding device to monitor Ca2+ and ERK response to a 300 μm diameter wound using a stable, dual reporter MCF-10A cell line expressing the genetically encoded Ca2+ indicator RGECO (Akerboom et al., 2013; Zhao et al., 2011) and the EKAREV FRET reporter for ERK (Albeck et al., 2013; Komatsu et al., 2011) (Figure 2D,E; Video 2). We verified the key role of ATP in initial wound response by wounding in the presence of apyrase, an enzyme that rapidly hydrolyzes ATP. Wounding in the presence of apyrase inhibits both Ca2+ and ERK response (Figure 2D,E, insets). From each wound we quantified single-cell time traces for over 3000 cells. Notably, the maximum activity per cell shows a larger response in cells closer to the wound compared to cells farther away from the wound for both Ca2+ and ERK. These response gradients demonstrate the importance of the cellular position to determine the cellular response, or positional information (Figure 2D,E). We used coefficient of variation (CV) to measure the variability of the post-paracrine ERK response and the pre-paracrine Ca2+ response in the wound (Figure 2F). Indeed, the CV for Ca2+ wound response shows statistically higher variability than ERK wound response indicating that paracrine communication reduces response variability during initial wound response.
We adapted the computational SNR analysis to wound response data to determine the influence of spatial patterns on response fidelity. As opposed to the dose-response data, the wound response data uses the distance of each cell from the wound as the input rather than the concentration of activating ligand (Figure 3A). Similar to the dose-response data, noise is estimated by averaging the cellular response variability over all distances. The variability between the average response magnitude of each distance constituted the signal (Figure 3B). Other statistical measures of response fidelity such as mutual information were also adapted for the wound context (Figure 3—figure supplement 1).
The maximum primary Ca2+ response shows highly variable cellular response when plotted according to distance (Figure 3C, pink). This variability complicates the ability for a cell to distinguish its respective position to the wound based on its response We again mimicked paracrine communication to predict the post-paracrine ERK response by locally averaging the single-cell Ca2+ wound response using a Gaussian kernel (Figure 1F). Locally averaging the cellular Ca2+ response creates a smoother predicted ERK response pattern versus distance from the wound (Figure 3C, gray). However, the reduction in variability also decreases the overall response pattern trend. Locally averaging the Ca2+ signal using increasing PCDs decreases the magnitude of change of the average predicted ERK response between cells closest to the wound and farthest from the wound (Figure 3D). In other words, the response gradient becomes less obvious when cells are averaged over larger distances. Therefore, although the increase in PCD decreases response noise, the corresponding decrease in signal demonstrates the limit of PCD on the SNR benefit (Figure 3E). The difference in rates at which the signal and noise decrease results in a maximum SNR at a PCD of 91.0+/-6.3 μm (SEM, N = 5) (Figure 3F). This peak corresponds to a PCD where the amount of noise is decreased to the lowest amount possible without reducing the response gradient due to ‘over-averaging’. The predicted PCD with maximal benefit did not change when we expand the model to consider limitations due to diffusion (Figure 3F green curve, Materials and methods). Similar analysis using mutual information statistics shows a similar PCD with the maximal mutual information at the distance that showed maximal SNR (Figure 3E,F, Figure 3—figure supplement 1B). This analysis shows that the benefits from paracrine communication depend on how far a paracrine molecule travels which, in this specific case, has a maximal benefit at ∼100 μm, or approximately three cell diameters.
We next empirically measured the PCD in our experimental system to compare to the PCD predicted to maximize the SNR in the wound context. To measure the PCD of ERK activation we first established a co-culture system that allows us to separate the effects of autocrine and paracrine signaling. Our assay utilizes a synthetic GPCR: Designer Receptors Exclusively Activated by Designer Drugs (DREADD). The Gq human muscarinic derived GPCR DREADD is activated by a synthetic small molecule, clozapine-N-oxide (CNO), that has no known endogenous receptors (Armbruster et al., 2007). In addition, DREADD activates the Gq pathway similar to purinergic ATP receptors (Dong et al., 2010). Using a co-culture of DREADD expressing (activated by CNO) and non-expressing cells (not activated by CNO), we can determine which cells release EGF (DREADD expressing-red) and which cells accept EGF (non-expressing-gray) (Figure 4A). Using a synthetic system allows us to directly measure the average communication distance of EGF. CNO addition selectively activates Ca2+ response in DREADD expressing cells while the surrounding non-expressing cells show no response indicating a lack of paracrine activation of Ca2+ response in cells (Figure 4A). Although some systems show that Ca2+ response can propagate from cell-to-cell through gap junctions (Ross 2012), this does not appear to be the case in MCF-10A cells as non-expressing cells showed no cytosolic Ca2+ increase upon activation of DREADD cells. Alternatively, ERK response was found in both DREADD expressing and the surrounding non-expressing cells upon CNO addition but was inhibited in both cell types in the presence of the EGFR inhibitor tryphosphitin AG1478, confirming paracrine activation of ERK in the DREADD system (Figure 4B). The Ca2+ and ERK responses in the DREADD system suggest that local averaging takes place only at the EGF level between Ca2+ and ERK response. Additionally, increasing the ratio of DREADD cells to non-expressing cells shows an increasing ERK response magnitude in non-expressing cells, further supporting that paracrine communication locally activates ERK (Figure 4C).
We measured the PCD by monitoring local paracrine ERK activation with our DREADD co-culture assay. We co-cultured DREADD cells at a low concentration compared to non-expressing cells to ensure that neighboring non-expressing cells were activated only by a single DREADD cell. We then analyzed the ERK response of ∼1500 non-expressing cells neighboring a DREADD cell. (Figure 4D,E). Local ERK activation of non-expressing cells surrounding a DREADD cell show decreasing response with increasing distance from the DREADD cell. ERK response as a function of distance follows a Gaussian fit, consistent with how the concentration of diffusing molecules, like in paracrine signaling, changes over distance (Figure 4E) (Berg, 1993). The PCD was determined by calculating the spread, or sigma, of this Gaussian curve. According to our fit, the paracrine activation of ERK has a communication distance of 99.5+/-19.6 μm (SEM, N = 12 DREADD cells). This empirically measured value is statistically similar to the predicted communication distance value that maximizes the SNR of wound response (Figure 4F). In other words, the cellular communication distance is tuned to maximize the overall response fidelity during wound response signaling.
Multicellular organisms utilize cellular diversity for specialization and division of labor. However, the variability between cells can be detrimental due to the potential loss of response fidelity (Uda et al., 2013; Hansen and O'Shea, 2015; Voliotis et al., 2014; Cheong et al., 2011; Selimkhanov et al., 2014). Paracrine communication can serve to share information between cells to regulate cellular variability. In this study we analyzed the benefits and limitations of paracrine communication based information sharing between cells as a mechanism to control cellular response variability.
We analyzed the limits of paracrine communication on cellular response fidelity in two cases. First we analyzed the response to a spatially uniform ligand. Our analysis reveals that, under these conditions, the magnitude of single-cell response fidelity increases as a function of the PCD with no upper bound. In order for cells to facilitate larger PCDs, cells would need to synthesize larger amounts of paracrine signaling molecules or utilize fast diffusing paracrine ligands like H2O2 (Enyedi and Niethammer, 2015). The increased energy required to synthesize the additional molecules is likely to be minor in comparison to the overall energetic demand of a cell. Therefore cells could potentially take advantage of large PCDs to substantially mitigate biochemical noise. However, a spatially uniform input, while common in cell culture experiments, is likely an inadequate representation of physiological conditions. In the second case we analyzed the response of cells to spatially defined inputs in the form of a mechanical epithelial wound. We analyzed the cellular response to extracellular ATP gradients, a damage associated molecule, following a controlled wounding of an epithelial monolayer in vitro. Similar to developmental systems, an extracellular input ligand conveys positional information in wound response (Dubuis et al., 2013; Sonnemann and Bement, 2011). Analysis of the paracrine communication benefit in our novel quantitative wound response assay with defined spatial perturbations demonstrates that paracrine communication increased cellular response fidelity, but with limitations. Unlike the spatially uniform ligand in the first case, the magnitude of the response fidelity benefit varies with increasing PCD. The maximal increase of cellular response fidelity occurrs at a PCD of ∼100 μm, or approximately 3 cell diameters. In vivo work measuring ERK propagation using the same EKAREV FRET sensor also showed propagation extending ∼100 μm (Hiratsuka et al., 2015). Our results demonstrate that the paracrine information sharing benefit depends on the input ligand spatial scale, or PCD. Furthermore, empirical measurements of paracrine communication match the physiologically relevant spatial wound response maximum communication distance.
The process of wound healing is a complex multi-stage program that coordinates the action of multiple cell types over multiple timescales, from minutes to weeks, to address an acute need. The initial steps of wound healing programs propagate information concerning the wound in a manner that is appropriate to the magnitude of damage. Both inflammatory and fibrotic processes, critical steps in wound response signaling, are damaging when they go awry. Therefore, the initial cellular responses and the establishment of signaling gradients are key steps in wound healing. The mechanistic details underlying how tissues robustly match the wound response magnitude to the extent of wound-induced damage remain unknown. Our results demonstrate that intercellular communication during the initial wound response is optimized to increase overall response fidelity and provides the initial evidence that matching the wound response to wound damage is a critical aspect to wound healing programs. Future work is needed to further investigate tissue level response fidelity during wound healing programs.
Paracrine communication increases the fidelity of response at the single-cell level by mitigating biological noise at the single-cell level. Each cell integrates information from its local neighborhood to increase its individual response fidelity. Local averaging at the cellular level is a distinct mechanism compared to the benefit of global averaging at the population level. Without any paracrine communication, the reliability of the average of a cell population response can only increase with the size of the population. This is a consequence of the central limit theorem where the uncertainty of a sample average decreases with sample size. However, this increase in reliability is only true for the population average and not for individual cells in the population. Therefore, in cases where the biologically significant output is the collective action of the population, for example the secretion of a cytokine, intercellular information sharing is not required. However, when biologically significant output requires single-cell action, local information sharing via paracrine communication increases cellular response fidelity. Therefore, whether paracrine communication is required remains context dependent. It is possible that paracrine information sharing is more prevalent in signaling networks that support individual cellular decisions and less prevalent in cases where biologically meaningful outcomes result from population averages.
In cases where paracrine information sharing is used as a method to mitigate biological noise, the breakdown of this system could be detrimental. In vivo studies of ERK response in mammary tumor cells using the same EKAREV FRET sensor utilized here show highly variable ERK response that may lead to the survival and propagation of cancer cells (Kumagai et al., 2014). Although the cause for this heterogeneity is unknown, one possible mechanism may be the breakdown of paracrine communication between cells similar to how our partial inhibition of paracrine communication showed no decrease in ERK variability (Figure 1—figure supplement 4).
The abundance of paracrine communication in mammals, that is the activation of a receptor by a ligand synthesized by another cell, demonstrates the heavy utilization of intercellular communication (Ben-Shlomo et al., 2003; 2007). Paracrine averaging demonstrates how intercellular communication enables cellular collective decision making where the 'wisdom of the crowd' is greater than the individual cell. Theoretical and empirical work in humans and animal collectives has shown that the benefit of collective decision making depends on the size of the group; big crowds are not always better than small crowds (Sasaki et al., 2013; Kao et al., 2014; Hoare et al., 2004; Sueur et al., 2011). Therefore, it is likely that the extent of secretion of each paracrine ligand is adjusted to the level of cellular information sharing to ensure an effective collective decision.
The optimal PCD we identified is not universal. Rather, the optimal distance depends on the specific shape of the spatial pattern of the initial activating ligand and the noise pattern of the primary response. Additionally, propagation patterns of the same activating ligand can depend on the physiological signaling context as demonstrated by differences found during in vivo ERK propagations under wound and normal conditions (Hiratsuka et al., 2015). The effective PCD can be regulated at the cellular level by several possible factors to optimize the benefit of paracrine communication to the specific noise and spatial patterns characteristic to each signaling system (Batsilas et al., 2003; Muratov and Shvartsman, 2003a; 2003b). PCD also depends on the effective diffusion coefficient of the secreted molecule, transmitted signal strength (e.g. number of secreted molecules), and receiver cell sensitivity (e.g. receptor Kd). The diffusion coefficients of paracrine signaling molecules can vary by two orders of magnitude, let alone differences in signal strength and receptor sensitivity in individual paracrine signaling pathways (Kreuz et al., 1965; Gregor et al., 2007). Fine-tuning each of these factors provides a possible mechanism for cells to regulate the PCD and thereby the extent a cell locally communicates. The ability to specifically tune PCD raises the possibility that evolutionary pressures can tune paracrine communication to provide the optimal benefit in many other paracrine communication systems.
MCF-10A cells were cultured following established protocols (Debnath et al., 2003). Before plating cells, each surface was first treated with a collagen (Life Technologies, Carlsbad, CA), BSA (New England Biolabs), and fibronectin (Sigma-Aldrich) solution in order for cells to completely adhere, according to established methods. In order to maintain a viable environment, cells were imaged at 32°C and 5% CO2. All EGF (PeproTech) titrations and DREADD experiments were conducted in 96-well plates using extracellular hepes buffer (ECB) to reduce background fluorescence (5 mM KCl, 125 mM NaCl, 20 mM Hepes, 1.5 mM MgCl2, and 1.5 mM CaCl2, pH 7.4). All imaging for wounding was done in MCF-10A assay media (Debnath et al., 2003).
Cells were plated at a density of 2,000,000 cells/100mm plate and allowed to adhere overnight. Cells were transfected with the Gq-coupled DREADD HA-tagged hM3D with an mCherry tag using a 3:1 ratio of FuGene HD (Promega) to DNA and allowed to incubate overnight (Dong et al., 2010). In order to measure the paracrine signal from a single-cell, non-transfected cells were mixed with DREADD-transfected cells at ratios of 1:0, 1:1, 1:2, 1:5, 1:7, and 0:1 (non-transfected:DREADD) and plated in 96-well plates at a density of 30,000 cells/well. The following day, cells were loaded with 1 μM Hoechst dye for nuclear imaging for 30 min for cell segmentation purposes. 5 μM clozapine-N-oxide (CNO) (Enzo Life Sciences) was added to each well to specifically activate DREADD cells. ERK activation was monitored using the EKAREV FRET reporter (Albeck et al., 2013; Komatsu et al., 2011) and Ca2+ activation was monitored using the Ca2+ indicator dye Fluo-4 using the published protocol (Invitrogen).
In order to measure the standard deviation of Ca2+ and ERK activity within a small group of cells, MCF-10A cells were plated at densities of 1000, 2000, and 3000 cells per well in a 96-well plate, taking advantage of the natural tendency for MCF-10A cells to cluster together. Cells were stimulated with 10 μM or 100 μM ATP and imaged for 5 min every 3 s (Ca2+ ) or 30 min every minute (ERK).
Standard deviation and average expression of Ca2+ and ERK were analyzed by grouping cells in to clusters based on the distances between cells and clusters (Figure 1—figure supplement 1). Following the cluster analysis, the average and standard deviation of Ca2+ and ERK activation were calculated for each cluster. ERK activation was measured using the ERK FRET reporter (Albeck et al., 2013; Komatsu et al., 2011) and Ca2+ activation was monitored using the genetically encoded sensor R-GECO (Zhao et al., 2011).
Master molds for the microfluidics based wounding device were created using silicon wafers and layer-by-layer photolithography using established methods (Ferry et al., 2011). A separate mold for both the air layer and cell layer were made using negative photoresists and masks. Chips were made by pouring uncured polydimethylsiloxane (PDMS) onto each mold, allowing the PDMS to harden, and bonding the layers together and subsequently to a glass slide. Cells were loaded into the devices through the inlet port using a 20G needle. During wounding the outlet port was plugged using tape and the inlet port held a reservoir of media to prevent evaporation in the chamber. Wounding was accomplished by increasing the air pressure in the top layer of the device until the pillar made contact with the bottom of the device after which the air pressure was released to raise the pillar back up. Cells were loaded in to the wounding device at a density of 15,000,000 cells/mL using a 20G needle. Following trypsinization and resuspension, cells were put on ice to prevent aggregation. Two o-rings were attached to the device surrounding both the inlet and outlet ports for media reservoirs. Each o-ring was attached using a thin film of vacuum grease. Wounding devices were kept in an empty pipet box filled with water to prevent media evaporation. Cells were allowed to adhere for 18–24 hr before wounding.
Imaging was accomplished using a Nikon Plan Apo λ 10X/0.45objective with a 0.7x demagnifier and Nikon Eclipse Ti microscope with a sCMOS Zyla camera. All imaging was accomplished using custom automated software written using MATLAB and Micro-Manager (Edelstein et al., 2010). Image analysis was accomplished using a custom MATLAB code published previously (Selimkhanov et al., 2014) and is available through GitHub repository https://github.com/rwollman/CellSegmentation.git.
The paracrine ligand concentration (P) for a cell at position (x,y) observed by (P[x,y]) is the local average of the concentration of ligand released by cells in the local neighborhood (Figure 1A). We modeled this paracrine ligand local average using a convolution of two functions: S(x,y) that represents the amount of ligand secreted by each cell and D(x,y) that represents the expected diffusion of the paracrine ligand during the timescale of paracrine signal integration:
The function S(x,y) was estimated using experimental cellular Ca2+ response data according to:
The function D(x,y) was approximated to follow Gaussian weights with a length-scale we named the Paracrine Communication Distance (PCD):
Detailed analysis of how PCD depends on diffusion, number of secreted paracrine molecules, sensitivity of detection, physiological levels of fluid flow (Polacheck et al., 2011), and cellular decoding of time varying paracrine signal are presented in Materials and methods. In cases where biologically relevant integrations times may influence the predicted paracrine communication response, the PCD did not exceed the approximate distance EGF could travel before the first ERK response (Figure 1G, Figure 3F, Materials and methods). Based on single-cell ERK data to ATP stimulation, this time was found to be ∼5 min which resulted in a maximum PCD of ∼300 μm (data not shown) based on EGF diffusion coefficient of 50 μm2/s.
Signal to Noise ratio analysis on Ca2+ response to ATP titration data was estimated as was done previously (Selimkhanov, 2014). Briefely, the signal S was calculated using:
The noise N was calculated by:
Where Ca2+ (t) is the temporal time series of Ca2+ response measured experimentally. Cells are separated into bins according to either different dosages of ATP added to multiple wells (Figure 1) or different distances from the wound source (Figure 3). SNR was then simply: SNR = S/N.
In this section we analyze how the Paracrine Communication Distance (PCD), the characteristic length-scale of paracrine communication, depends on factors related to the paracrine signal. Specifically we look into how the PCD depends on the diffusion coefficient D, the number of molecules released from a cell , the number of molecules needed for detection , and the total integration time T.
To understand how PCD depends on the factors mentioned above, we considered the diffusion of a paracrine ligand from a single cell to its surrounding neighbors. We considered a 2D-like geometry where cylindrical cells, each of height and radius , grow in a chamber of total height. We simplify the below analysis by approximating the cell monolayer geometry to a series of 'cell cylinders'. The key results of the scaling of PCD and required integration time are similar for other comparable geometries (data not shown). Under these conditions one could write the analytical solution of the diffusion equations:
Where is the concentration of paracrine ligand for distance r and time t. For a neighboring cell to respond to this paracrine signal, a critical number of molecules needs to reach the volume surrounding the cell. We assume that a cell ‘senses’ a volume comparable to the volume of a cell itself. For a cylindrical cell of area and height the critical concentration required for cellular response will be:
This is simply the required number of molecules divided by the cell volume. Combining equations 6,7 we can solve for the distance and time of where the critical concentration will be reached. Solving for distance we get that
The concentration of the paracrine ligand is diluted as it diffuses from the source. Therefore, there is a point in space which is the maximal distance from the source that the critical detection concentration will be reached at some point in time. Distances that are greater than the critical distance will only experience concentrations lower than the critical detection concentration . The existence of such maximum can also be seen by the non-monotonous dependency of rdetect on t in equation 8. To find the maximal distance we can simply find the maximum of 1.3 in respect to t. Doing so we get that:
We can simplify the analysis by the introduction of two dimensionless variables: 1) represents the strength of the signal and is defined as the ratio of released molecules and the number of molecules needed to detect the signal . 2) represents the fraction of the height of the flow chamber that cells occupy. When we substitute the new variables into Equation 1,4 we get that:
Interestingly this shows that the value of PCD does not depend on the diffusion coefficient. Rather, PCD scales as a function of the square root of the strength of the signal S with a multiplicative constant that depends on the specific cell geometry. PCD also depends on cell geometry with the cell radius and the relative height of a cell in the effective environment . Figure 1—figure supplement 6 shows equation 10 graphically.
While the analysis above shows that the diffusion coefficient has no influence on the overall PCD, the time required to reach this maximal distance has important biological implications. 'Paracrine averaging' requires cells to integrate the signal. However, the time required for signal integration must be biologically feasible given the cellular response time and diffusion coefficient.
From equation 8 we can identify the time by which the PCD is maximal to be:
The integration time grows linearly with signal strength S. This is because the PCD itself scales as a square root of S and the diffusion time grows with the square of the distance. The integration time decreases with increasing diffusion coefficient as expected. Figure 1—figure supplement 7 shows the scaling of the integration time with the diffusion coefficient for a few PCD values.
For diffusion coefficient values of ∼10–100 μm2/s and a PCD of 100 μm (similar to the distance measured in Figure 3) integration times ranged between 0.5 to 5 min. Given that ERK activation is observed only after 5 min post-activation, the required integration time does not pose an issue. However, larger PCDs will require higher diffusion coefficients to allow proper integration of the paracrine signal. Interestingly, H2O2, another key paracrine signaling molecule critical to initial wound response signaling, has a diffusion coefficient of ∼2000 μm2/s. A larger diffusion coefficient could allow for a much longer PCD with reasonable biological integration times.
All the analysis above assumed static conditions, that is no fluid mixing or advection of any kind. In this section we analyze the degree to which the principles of paracrine communication are applicable in non-static conditions.
Non-static fluid conditions potentially have two effects on mass transport. 1) Non-static fluid conditions can create mixing due to turbulence and 2) Laminar advection can transport secreted molecules away from the secretion source. Since the extracellular environment is characterized by a low Reynold’s number there is effectively no turbulent mixing in biologically relevant parameters.
To analyze the relative contribution of advection and diffusive transport we utilize a dimensionless number, the Péclet number (P), that represents the ratio between the contribution of advection and diffusion:
Where v is the interstitial flow rate, D is the diffusion coefficient and L is the characteristic length scale. In our case, the characteristic length scale is the PCD, which depends on the signal strength as described above (equation 10 and Figure 1—figure supplement 6). Therefore, the P number can be expressed as a function of the signal strength S and diffusion coefficient:
Graphical representation of this expression is shown in Figure 1—figure supplement 8 where the map of D and S is color coded by the Péclet number with three highlighted regions: A red region where flow will dominate, a cyan region where diffusion will dominate, and the region in between where both advection and diffusion contribute to paracrine communication.
To gain further insight into the relative contribution of advection and diffusion we looked at the distance molecules will travel via advection for a specific signal strength (S = 1000). As can be seen in Figure 1—figure supplement 8b, for diffusion coefficients of small protein ligands advection will contribute minimally.
When considering positional accuracy of cellular response, an important consideration is that advection can potentially 'shift' the effects of paracrine signaling downstream of the flow. Even if the shift is characterized by low Péclet number, advection can interfere with positional information accuracy (as analyzed in Figure 3). To estimate the potentially degrading effects of flow we calculate the expected level of positional accuracy error induced by flow. We estimate that the wound induced signaling gradient (Figure 3C) to be >500 μm. Therefore the effect on positional accuracy will be minimal (<10%) at advection distances up to 50 μm, or for a PCD of 100 μm, a Péclet number up to 0.5. The isocline of a Péclet number of 0.5 is shown in Figure 1—figure supplement 8a as a dotted black line. This shows that for paracrine ligands with a diffusion coefficient >40 μm2/sec, advection will have little effect on positional accuracy of initial wound response signaling.
The analysis in the previous two sections assumes that the concentration of the paracrine ligand decreases over increasing distance from the source of secretion according to a Gaussian fit where the diffusion length-scale represents the PCD. The cellular response to a paracrine ligand depends on cellular decoding of the temporal paracrine concentration profile a cell observes. As both the temporal profile of the secreted paracrine molecule and the temporal cellular decoding are unknown, we consider the simple assumption of a Gaussian profile reasonable. To quantitatively test this assumption we compared the Gaussian profile to an alternative model that could be addressed analytically. In the alternative model, we assume that all paracrine molecules are released at T = 0 and that cellular decoding of the paracrine signal is simple temporal averaging. Under these assumptions one can write an expression of the temporal average of the paracrine concentration at a distance r from the source as:
Where all symbols follow Equation 6 and ei represent the exponential integral:
Comparison of the two models can be seen in Figure 1—figure supplement 9. Overall, the two models generate very similar Paracrine Averaging Weights (the effect of cellular decoding of paracrine signal). There is a small discrepancy between the two models at very low distances (<50 μm). However, this discrepancy is most likely a result of the assumption in the alternative model that all the paracrine molecules are released at once. Under the more realistic assumption where paracrine molecule release duration is not much smaller than the time to diffuse 50 μm (12.5 s at D = 50 μm2/s) we anticipate that the similarity between these two profiles will further increase.
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Sarah A TeichmannReviewing Editor; EMBL-European Bioinformatics Institute & Wellcome Trust Sanger Institute, United Kingdom
eLife posts the editorial decision letter and author response on a selection of the published articles (subject to the approval of the authors). An edited version of the letter sent to the authors after peer review is shown, indicating the substantive concerns or comments; minor concerns are not usually shown. Reviewers have the opportunity to discuss the decision before the letter is sent (see review process). Similarly, the author response typically shows only responses to the major concerns raised by the reviewers.
Thank you for submitting your work entitled "Paracrine Communication Maximizes Cellular Response Fidelity in Wound Signaling" for peer review at eLife. Your submission has been favorably evaluated by Naama Barkai (Senior Editor), a Reviewing Editor, and two reviewers.
The reviewers have discussed the reviews with one another and the Reviewing Editor has drafted this decision to help you prepare a revised submission.
In this report, Handly et al. analyzed the impact of paracrine communication on the cellular response fidelity in an epithelial cell line during wound healing. Through single cell live imaging they quantified signal and noise of Ca2+ and ERK responses following treatment with ATPs (which recapitulates an event happening in wound context). They first validated the system (paracrine activation of ERK by ATP) and then they analyzed the effect of differential spatial density of cell clusters on the responses. They identified that higher density correlates with lower response variability, suggesting that paracrine communication decreases cellular variability response. To quantify the observed benefit of paracrine communication they performed a computational analysis based on signal-to-noise ratio (SNR). This analysis showed that paracrine communication can increase the response SNR.
To measure the spatial wound response they developed and used a new microfluidics-based device. The single cell analysis of Ca2+ and ERK showed the importance of cellular position for the determination of cellular response. Applying the same computational strategy as before in a better-controlled environment, they showed again that the paracrine communication distance decreases the noise of the response. However they also identified a limit of paracrine communication, which consist in reducing the gradient magnitude.
To directly measure the paracrine communication, the authors used a co-culture system in which they can distinguish "sender" and "receiver" cells. They measured the ERK level in "receiver" cells in relation of the distance from a sender cell. The authors determined the paracrine communication distance and compared it with their predicted distance value that maximizes the SNR. Therefore they concluded that the distance between communicating cells maximize cellular response fidelity.
1) Although the new microfluidics-based device represents a great tool to study wound healing in vitro in a highly controlled manner and already provided intriguing results, it would be important to see if some of the principles of paracrine communication observed in a static media condition can also be identified in a non-static condition (Figure 2–figure supplement 1).
2) The data collected and the analysis are interesting, however they refer to an in vitro setting (this should be more clear in the Abstract). Please discuss these data in the light of in vivo data present in literature (i.e. ERK reporter has been used in vivo).
3) The analyses are largely described in the text without any equations; having the equations in the Methods or supplements would be much better, and several of the quantitative figures are described quite vaguely (Figure 1G, Figure 2H, I, J, and Figure 3F).
4) At a number of points, the meaning of error bars and p-values are not explicitly stated, and these need to be fixed.
5) Given the setup in Figure 1A, please show some quantification of ERK variability in Figures 1 and 2. This omission seems odd given that ERK is the signal that is ultimately being affected by the averaging, and which is being predicted by the analysis. Is it in fact less variable than the Ca2+ signal in these systems? There also seems to be a logical disconnect – the optimum communication distance shown in Figure 2J is calculated based on Ca2+ responses, but then compared to the ERK response in Figure 3.
6) In Figure 1F (and in general), what is the expected role of diffusion? The authors conclude that there is no upper bound on SNR as distance is increased, but their analysis doesn't appear to take diffusion into account, which would presumably limit the distance over which averaging could be effective. This should be clarified. It would also be helpful to comment on the role of the integration time over which the cellular response operates.https://doi.org/10.7554/eLife.09652.020
Essential revisions:1) Although the new microfluidics-based device represents a great tool to study wound healing in vitro in a highly controlled manner and already provided intriguing results, it would be important to see if some of the principles of paracrine communication observed in a static media condition can also be identified in a non-static condition (Figure 2–figure supplement 1).
We now include a section in Material and methods (“Analysis of the effect of fluid flow on paracrine communication”) with an additional figure (Figure 1–figure supplement 7) where we present an analysis of the relative contribution of diffusion (i.e. static) and advection (i.e. non-static) conditions. Our analysis shows that at physiological levels of interstitial flow, the principles of paracrine communication can also be identified.
2) The data collected and the analysis are interesting however they refer to an in vitro setting (this should be more clear in the Abstract).
We now clarify that our data was collected in an in vitro setting in the Abstract as well as within the main text (subsection “Paracrine signaling reduces response variability” and Discussion, second paragraph).
Please discuss these data in the light of in vivo data present in literature (i.e. ERK reporter has been used in vivo).
The in vitro data presented here is now discussed in light of in vivo data using the same ERK FRET reporter from 2 different papers (Hiratsuka et al. and Kumagai et al.). Please see the Discussion.
3) The analyses are largely described in the text without any equations; having the equations in the Methods or supplements would be much better, and several of the quantitative figures are described quite vaguely (Figure 1G, Figure 2H, I, J, and Figure 3F).
We now include 14 equations to better describe the analyses used throughout the paper. Equations describing the paracrine model were added to the Methods section. In addition, multiple new sections were added to the Material and methods section including:
a) Model for paracrine communication based on local isotropic diffusion;
Signal to Noise Analysis;
b) Analysis of the effects of diffusion, secretion and integration time on paracrine communication;
c) Analysis of the effect of fluid flow on paracrine communication;
d) Analysis of the effect of cellular decoding schemes on paracrine communication.
These sections describe our model in details and include detailed analytical derivations that justify the assumption behind the model. Four new figure supplements to Figure 1 are presented to better describe the results of the additional analysis graphically. In order to better clarify Figure 1G, Figure 2H, I, J, and Figure 3F, the figure legends were modified to indicate which analyses took place.
4) At a number of points, the meaning of error bars and p-values are not explicitly stated, and these need to be fixed.
The meaning of error bars, shaded regions, and p-values are now explicitly stated throughout the figure legends.
5) Given the setup in Figure 1A, please show some quantification of ERK variability in Figures 1 and 2. This omission seems odd given that ERK is the signal that is ultimately being affected by the averaging, and which is being predicted by the analysis. Is it in fact less variable than the Ca2+ signal in these systems?
We added additional experimental data and additional analysis related to variability of ERK. Specifically, we added the following quantifications:
a) Figure 1–figure supplement 3-4: Quantification of ERK variability when the paracrine signaling length-scale is manipulated;
b) Figure 2 was divided in to Figure 2 and Figure 3. Additional ERK wound response data is shown in Figure 2E and the variability of the Ca2+ response compared to the ERK response, shown as coefficient of variation, to wounding is shown in 2F. As expected from our model, Ca2+ response shows higher variability than ERK response.
Collectively the additional data demonstrates that the wound induced ERK response has lower variability than Ca2+ response. Because Ca2+ response is prior to paracrine communication and ERK response is post paracrine communication, this reduction in variability provides direct support to our paracrine communication model.
To prevent potential perceived logical disconnect we now clarify the difference between the Ca2+ response, the predicted ERK response from locally averaging the Ca2+ response, and the actual ERK response in both the text (subsection “Cellular response fidelity depends on the extent of paracrine signaling during wound response”) and Figure 3.
6) In Figure 1F (and in general), what is the expected role of diffusion? The authors conclude that there is no upper bound on SNR as distance is increased, but their analysis doesn't appear to take diffusion into account, which would presumably limit the distance over which averaging could be effective. This should be clarified. It would also be helpful to comment on the role of the integration time over which the cellular response operates.
We thank the reviewer for bringing up this important point. We now extended our model to explicitly take into account the effects of diffusion under conditions of limited integration time. We show an extended model that explicitly takes into account integration time in both Figure 1G and 3F. The equations that are part of the derivation of this extended model are presented in Material and methods section: “Analysis of the effects of diffusion, secretion and integration time on paracrine communication”. In this section we analytically derive key expressions that show the dependency of the Paracrine Communication Distance (PCD) on the diffusion coefficient and the ratio between the number of released molecules to the sensitivity of detection. We show under what regimes integration time could become limiting and therefore extend our model to include such limitations to the potential benefit of paracrine communication.https://doi.org/10.7554/eLife.09652.021
- Roy Wollman
- L Naomi Handly
- Roy Wollman
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
We thank Jeff Hasty, Ryan Johnson, and Megan Dueck from the San Diego Center for Systems Biology Cell Dynamics core for their technical assistance. The work was supported by GM111404 & EY024960 (RW), and a training grant (GM007240) for LNH.
- Sarah A Teichmann, EMBL-European Bioinformatics Institute & Wellcome Trust Sanger Institute, United Kingdom
© 2015, Handly 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.
How cells control gene expression is a fundamental question. The relative contribution of protein-level and RNA-level regulation to this process remains unclear. Here, we perform a proteogenomic analysis of tumors and untransformed cells containing somatic copy number alterations (SCNAs). By revealing how cells regulate RNA and protein abundances of genes with SCNAs, we provide insights into the rules of gene regulation. Protein complex genes have a strong protein-level regulation while non-complex genes have a strong RNA-level regulation. Notable exceptions are plasma membrane protein complex genes, which show a weak protein-level regulation and a stronger RNA-level regulation. Strikingly, we find a strong negative association between the degree of RNA-level and protein-level regulation across genes and cellular pathways. Moreover, genes participating in the same pathway show a similar degree of RNA- and protein-level regulation. Pathways including translation, splicing, RNA processing, and mitochondrial function show a stronger protein-level regulation while cell adhesion and migration pathways show a stronger RNA-level regulation. These results suggest that the evolution of gene regulation is shaped by functional constraints and that many cellular pathways tend to evolve one predominant mechanism of gene regulation at the protein level or at the RNA level.
Synaptic communication relies on the fusion of synaptic vesicles with the plasma membrane, which leads to neurotransmitter release. This exocytosis is triggered by brief and local elevations of intracellular Ca2+ with remarkably high sensitivity. How this is molecularly achieved is unknown. While synaptotagmins confer the Ca2+ sensitivity of neurotransmitter exocytosis, biochemical measurements reported Ca2+ affinities too low to account for synaptic function. However, synaptotagmin’s Ca2+ affinity increases upon binding the plasma membrane phospholipid PI(4,5)P2 and, vice versa, Ca2+ binding increases synaptotagmin’s PI(4,5)P2 affinity, indicating a stabilization of the Ca2+/PI(4,5)P2 dual-bound state. Here, we devise a molecular exocytosis model based on this positive allosteric stabilization and the assumptions that (1.) synaptotagmin Ca2+/PI(4,5)P2 dual binding lowers the energy barrier for vesicle fusion and that (2.) the effect of multiple synaptotagmins on the energy barrier is additive. The model, which relies on biochemically measured Ca2+/PI(4,5)P2 affinities and protein copy numbers, reproduced the steep Ca2+ dependency of neurotransmitter release. Our results indicate that each synaptotagmin engaging in Ca2+/PI(4,5)P2 dual-binding lowers the energy barrier for vesicle fusion by ~5 kBT and that allosteric stabilization of this state enables the synchronized engagement of several (typically three) synaptotagmins for fast exocytosis. Furthermore, we show that mutations altering synaptotagmin’s allosteric properties may show dominant-negative effects, even though synaptotagmins act independently on the energy barrier, and that dynamic changes of local PI(4,5)P2 (e.g. upon vesicle movement) dramatically impact synaptic responses. We conclude that allosterically stabilized Ca2+/PI(4,5)P2 dual binding enables synaptotagmins to exert their coordinated function in neurotransmission.