<p>GC-globulin (GC), or vitamin D-binding protein, is a multifunctional protein involved in transport of circulating vitamin 25(OH)D and fatty acids, as well as actin-scavenging. In the pancreatic islets, the gene encoding GC, <em>GC</em>, is highly-localized to glucagon-secreting α cells. Despite this, the role of GC in α cell function is poorly understood. We previously showed that GC is essential for α cell morphology, electrical activity and glucagon secretion. We now show that loss of GC exacerbates α cell failure during metabolic stress. High fat diet-fed GC-/- mice have basal hyperglucagonemia, which is associated with decreased α cell size, impaired glucagon secretion and Ca2+ fluxes, and changes in glucose-dependent F-actin remodelling. Impairments in glucagon secretion can be rescued using exogenous GC to replenish α cell GC levels, increase glucagon granule area and restore the F-actin cytoskeleton. Lastly, GC levels decrease in α cells of donors with type 2 diabetes, which is associated with changes in α cell mass, morphology and glucagon expression. Together, these data demonstrate an important role for GC in α cell adaptation to metabolic stress.</p>
Article Figures and data Abstract Editor's evaluation Introduction Results and discussion Materials and methods Data availability References Decision letter Author response Article and author information Metrics Abstract The importance of pancreatic endocrine cell activity modulation by autonomic innervation has been debated. To investigate this question, we established an in vivo imaging model that also allows chronic and acute neuromodulation with genetic and optogenetic tools. Using the GCaMP6s biosensor together with endocrine cell fluorescent reporters, we imaged calcium dynamics simultaneously in multiple pancreatic islet cell types in live animals in control states and upon changes in innervation. We find that by 4 days post fertilization in zebrafish, a stage when islet architecture is reminiscent of that in adult rodents, prominent activity coupling between beta cells is present in basal glucose conditions. Furthermore, we show that both chronic and acute loss of nerve activity result in diminished beta–beta and alpha–beta activity coupling. Pancreatic nerves are in contact with all islet cell types, but predominantly with beta and delta cells. Surprisingly, a subset of delta cells with detectable peri-islet neural activity coupling had significantly higher homotypic coupling with other delta cells suggesting that some delta cells receive innervation that coordinates their output. Overall, these data show that innervation plays a vital role in the maintenance of homotypic and heterotypic cellular connectivity in pancreatic islets, a process critical for islet function. Editor's evaluation The role of islet innervation on endocrine cell activity is currently not well defined. Previously, Yang et al. described embryonic islet innervation dynamics in zebrafish and the role of neural activity in proper glucose homeostasis and δ-cell formation. In their new manuscript, the authors introduced a novel transgenic model for whole islet in vivo calcium imaging. By applying this tool in a series of innovative and technically challenging approaches, the authors provide novel insights into how neuronal inputs influence pancreatic endocrine cell connectivity and function. Overall, this is an important study that adds to our understanding for the role of neuronal interactions with the islet. https://doi.org/10.7554/eLife.64526.sa0 Decision letter eLife's review process Introduction Tight regulation of hormone release from pancreatic islets is critical for glucose homeostasis and its disruption can lead to diabetes mellitus (Noguchi and Huising, 2019). Pancreatic islets are composed of different cell types, including the hormone producing alpha, beta, and delta cells, peripheral nerves, and vascular endothelial and smooth muscle cells. Studies have implicated signaling from the vascular scaffold (Almaça et al., 2014; Mullapudi et al., 2019) and nerve networks (Rodriguez-Diaz et al., 2012; Taborsky et al., 1998; Borden et al., 2013; Yang et al., 2018; Makhmutova et al., 2019; Tarussio et al., 2014) during the development and function of pancreatic islet cells. However, it remains difficult to investigate the immediate effects of acute nerve modulation on islet cell function. Given the alterations in islet innervation architecture in some models of diabetes (Mundinger and Taborsky, 2016; Mundinger et al., 2016; Tang et al., 2018), it is imperative to understand whether disruption of nervous control can contribute to diabetes etiology. Different methods of assessing islet cell function have provided important clues into the role of autocrine and paracrine signaling in this process. Electrophysiological recordings have provided fundamental insights into isolated islet cell function (Vergari et al., 2020; Camunas-Soler et al., 2020; Hastoy et al., 2018), including functional connectivity studies that identified homotypic as well as heterotypic coupling between endocrine cells (Moreno et al., 2005; Briant et al., 2018). However, assessing islet function in live animals with undisrupted vascular and nerve networks remains challenging. Calcium dynamics is a good readout of the function of all islet cell types because its influx is critical for hormone release. However, no studies to date have been able to record simultaneously the activity of all islet endocrine cell types in the intact organ of a living animal, which is required to understand how the different endocrine cell types respond to physiological perturbations individually and interdependently. To this end, we established an in vivo imaging platform to visualize the activity of all the islet cell types by combining calcium imaging with cell type reporters. We investigated the functional connectivity between homotypic and heterotypic cell pairs by analyzing the correlation patterns in their intracellular calcium changes. Chronic and acute inhibition of nerve activity captured its dynamic control of the functional connectivity between islet endocrine cells. Results and discussion The activity of all pancreatic endocrine cell types can be studied simultaneously in vivo The zebrafish primary islet becomes highly innervated (Yang et al., 2018) and vascularized (Mullapudi et al., 2019; Hen et al., 2015; Toselli et al., 2019) early in development (Figure 1A). Fluorescent reporters for different pancreatic endocrine cell types, including beta, alpha, and delta cells, were used to study the establishment of islet cytoarchitecture (Figure 1B). By 100 hours post fertilization (hpf), a beta cell core and alpha cell mantle layout are observed (Figure 1B, C), in agreement with previous studies (Biemar et al., 2001), and reminiscent of adult rodent islets (Brereton et al., 2015) and small human islets (Bonner-Weir et al., 2015). Simultaneous functional assessment of all islet cell types in vivo required reporters for cell activity and cell identity. We used the Et(1121A:GAL4FF) enhancer trap line with the Tg(UAS:GCaMP6s) line for calcium imaging of all islet cells and a subset of peri-islet neurons (Figure 1D, E, Figure 1—video 1), as well as the Tg(ins:mCardinal) and Tg(sst2:RFP) lines to assign beta and delta cell identities, respectively; alpha cells were identified by their mantle localization and/or by immunostaining (Figure 1E). Thus, for the first time, we were able to assess the activity of all islet cells along with some peri-islet neurons in their native environment in an intact living animal (Figure 1F, Figure 1—video 2). Figure 1 with 2 supplements see all Download asset Open asset Pancreatic islet cell activity is visualized in vivo with preserved vascular and neural networks. (A) Wholemount immunostaining of wild-type zebrafish at 100 hours post fertilization (hpf) for acetylated Tubulin (nerves), Tg(kdrl:GFP) expression (vessels), and Insulin (beta cells), and counterstaining with DAPI (diamidino-2-phenylindole, DNA). (B) 100 hpf Tg(ins:mCardinal); Tg(sst2:RFP); Tg(gcga:GFP) zebrafish stained with DAPI (DNA). (C) Mean distance of pancreatic islet cells to islet core reveals a beta cell core and alpha cell mantle; mean ± SEM, n = 11 animals, p values from one-way analysis of variance (ANOVA) with Holm–Sidak’s multiple comparisons test; see Figure 1—source data 1. (D) 100 hpf Et(1121A:GAL4FF); Tg(UAS:GCaMP6s); Tg(ins:mCardinal); Tg(sst2:RFP) zebrafish stained with DAPI (DNA). (E) 100 hpf Et(1121A:GAL4FF); Tg(UAS:GCaMP6s); Tg(ins:mCardinal) zebrafish stained for Glucagon (alpha cells) and DNA. (F) Schematic of documented interactions between beta, delta, and alpha cells and of intracellular calcium recordings in each of these cell types. Maximum intensity projections or single planes are presented; A, anterior; D, dorsal; V, vagus nerve; P, pancreas. Figure 1—source data 1 Figure 1C. Mean distance of pancreatic islet cells to islet core reveals a beta cell core and alpha cell mantle. https://cdn.elifesciences.org/articles/64526/elife-64526-fig1-data1-v2.xlsx Download elife-64526-fig1-data1-v2.xlsx A subset of islet cells display activity coupling with peri-islet neurons Pancreatic islet innervation is in contact with all islet cell types (Figure 2A, B). However, both the beta and delta cells have a higher density of nerves in contact with their cell surfaces (Figure 2C). Prior to 120 hpf, this innervation is only from the vagus nerve (Yang et al., 2018). To investigate whether peri-islet neurons could actively modulate intra-islet coordination of activity, we first used the Et(1121A:GAL4FF); Tg(UAS:GCaMP6s) line which also labels a subset of peri-islet neurons (Figure 1—video 1) to simultaneously image the calcium dynamics in neurons and islet cells. While a higher number of neural activity connection to beta cells were observed, normalization to the number of cells imaged revealed no significant differences in the percentage of beta, delta, and alpha cells that display activity coupling with peri-islet neurons (Figure 2D, E). From the normalized single-cell calcium traces, correlation matrices, and average correlation coefficients (Ravg), we observed that homotypic coupling between beta cells is more prominent than those between delta and alpha cells (Figure 2F–H). Notably, we found a significant increase in homotypic coupling for the delta cells that display neural activity connection (Figure 2H). Future studies will determine whether direct neural activity connection is critical for the regulation of this delta cell subset. Figure 2 Download asset Open asset Pancreatic nerves display differential interactions with islet cell types. (A) 100 hpf Tg(ins:mCardinal), Tg(sst2:RFP), and Tg(gcga:GFP) zebrafish immuno-stained for acetylated Tubulin (nerves). (B) Segmentation and classification of islet nerves that are in contact with beta, delta, or alpha cell surfaces (magenta). All remaining islet nerves are colored in cyan. (C) Percentage of islet nerve density in contact with the specified pancreatic islet cell type; a majority of the nerves are in contact with beta and delta cells; mean ± standard error of the mean (SEM), n = 7–18 animals, p values from one-way analysis of variance (ANOVA) with Holm–Sidak’s multiple comparisons test; see Figure 2—source data 1. (D) Following exposure to elevated glucose and calcium imaging of pancreatic islet cells and peri-islet neurons at 105–110 hpf, correlation analysis was used to identify beta, delta, and alpha cells with neural activity connection. The percentage of cells of a given type with neural activity connection shows no significant difference between the different cell types; mean ± SEM, n = 6 animals, p values from one-way ANOVA with Holm–Sidak’s multiple comparisons test; see Figure 2—source data 2. (E) Correlation maps of a peri-islet neuron and beta, delta, and alpha cells. Individual cells are plotted with their coordinates. The strength of the correlation (Ravg) between cell pairs is drawn with a grayscale line and the number of connections for each cell is represented by the circle size. (F) Normalized calcium traces of pancreatic islet cells (including delta, beta, alpha, and unidentified cells) and a neuron (n). Individual islet cells were assigned to a cell type and given a cell id. (G) Correlation matrix of cell activity. Individual cells were assigned to a cell type (including delta, beta, alpha, and unidentified cells, and neurons) and average correlation coefficients for given cell pairs (matrix row-column intersects) were calculated. Areas displaying homotypic interactions are highlighted. (H) Average correlation coefficients from individual animals between homotypic cell pairs were divided into two groups (cells with or without neural connection); n = 6 animals, p values from paired t-tests. Figure 2—source data 1 Figure 2C. Percentage of islet nerve density in contact with the specified pancreatic islet cell type. https://cdn.elifesciences.org/articles/64526/elife-64526-fig2-data1-v2.xlsx Download elife-64526-fig2-data1-v2.xlsx Figure 2—source data 2 Figure 2D. The percentage of cells of a given type with neural activity connection. https://cdn.elifesciences.org/articles/64526/elife-64526-fig2-data2-v2.xlsx Download elife-64526-fig2-data2-v2.xlsx Homotypic and heterotypic coupling between endocrine cells requires pancreatic innervation Activity coupling between pancreatic endocrine cells can be mediated by autocrine and paracrine signaling, gap junctions, and other means. To investigate whether pancreatic innervation is critical for intra-islet coordination of activity, we used different approaches to chronically or acutely inhibit neural signaling. We used endoderm transplantation to generate chimeric zebrafish that express two GAL4/UAS systems in different germ layer-derived tissues and investigated the role of chronic neural inhibition on islet function (Figure 3A). Pan-neural expression of botulinum toxin (BoTx) chronically inhibits neurotransmitter release (Yang et al., 2018; Sternberg et al., 2016) and leads to elevated glucose levels at 100 hpf (Yang et al., 2018; Figure 3B). While primary islet volume was consistently greater in BoTx+ larvae at 100 hpf (Figure 3C; as we reported for earlier stages Yang et al., 2018), we did not observe changes in the architectural arrangement of the different islet cell types (Figure 3D). From the normalized single-cell calcium traces, correlation matrices, and average correlation coefficients (Ravg), we observed that the calcium dynamics in BoTx+ larvae were significantly disrupted, with impairment in beta cell coupling under both basal glucose and glucose stimulated conditions (Figure 3E–G, Figure 3—figure supplement 1). Our measure of Ravg over increasing intercellular distance revealed the expected decline in coupling over distance, and the significant difference in the elevation of the linear regression further confirmed the altered synchronicity between beta cells (Figure 3H). Figure 3 with 3 supplements see all Download asset Open asset Chronic inhibition of synaptic transmission disrupts islet cell activity. (A) Schematic of transplants to generate chimeras with endodermal organs derived entirely from donor embryos. (B) Whole larva-free glucose-level measurements at 100 hpf; mean ± standard error of the mean (SEM), n = 24–32 batches of 5 larvae per replicate, p value from t-test; see Figure 3—source data 1. (C) Quantification of primary islet mass; n = 21–29, p value from t-test; see Figure 3—source data 2. (D) Mean distance of pancreatic islet cells to islet core; mean ± SEM, n = 21–29 animals, p values from paired t-tests; see Figure 3—source data 3. (E) Normalized calcium traces of pancreatic islet cells (including delta, beta, alpha, and unidentified cells). Individual islet cells were assigned to a cell type and given a cell id; LG, basal condition; HG, glucose treated condition. (F) Correlation matrices of islet cell activity. Individual islet cells were assigned to a cell type and given a cell id, and average correlation coefficients for given cell pairs (matrix row-column intersects) were calculated for LG (basal condition; bottom left triangle) and HG (glucose treated condition; top right triangle). (G) Average beta cell correlation coefficients in individual larvae; n = 5–8 animals, p values from two-way analysis of variance (ANOVA) with Holm–Sidak’s multiple comparisons test; *, corresponding calcium traces and correlation matrices shown in panels E and F. (H) Average homotypic (beta–beta) and heterotypic (delta–beta and alpha–beta) cell correlation coefficients with cell distance distribution from 1 (close) to 10 (far), mean and linear regression (solid lines) with 95% confidence intervals; n = 5–8 animals, p values of slope and intercept from simple linear regression. (I–K) Fraction time analysis of heterotypic delta–beta, alpha–delta, and alpha–beta cell pairs for times when both are active (I), both are silent (J), and one is active and one is silent (K); mean ± SEM, n = 32–160 cell pairs, p values from two-way ANOVA with Holm–Sidak’s multiple comparisons test; magenta circle, active state; cyan circle, silent state. Figure 3—source data 1 Figure 3B. Whole larva-free glucose-level measurements at 100 hpf. https://cdn.elifesciences.org/articles/64526/elife-64526-fig3-data1-v2.xlsx Download elife-64526-fig3-data1-v2.xlsx Figure 3—source data 2 Figure 3C. Quantification of primary islet mass. https://cdn.elifesciences.org/articles/64526/elife-64526-fig3-data2-v2.xlsx Download elife-64526-fig3-data2-v2.xlsx Figure 3—source data 3 Figure 3D. Mean distance of pancreatic islet cells to islet core. https://cdn.elifesciences.org/articles/64526/elife-64526-fig3-data3-v2.xlsx Download elife-64526-fig3-data3-v2.xlsx To determine how perturbations in neural signaling influenced communication between different endocrine cell types, we conducted correlation analysis over increasing distance as well as fraction time analysis of heterotypic cell pairs that were in nearest proximity to each other (Figure 3H–K, Figure 3—figure supplement 2). Significant changes in the intercepts suggest impairments in delta–beta and alpha–beta heterotypic coupling (Figure 3H). Nearest neighbors have a greater likelihood of displaying coupling, as seen in our Ravg over increasing distance analysis. We analyzed single-cell calcium traces and determined the fraction of time a given nearest cell pair resides in a state when (1) both cells are active, (2) both cells are silent, and (3) one cell is silent, the other active. This analysis of activity patterns between nearest heterotypic cell pairs further supported the observed heterotypic coupling defects upon chronic neural inhibition (Figure 3I–K). Aside from the quiet phase, when both cell types are silent, we found changes in activity patterns between alpha–beta, delta–beta, and alpha–delta cell pairs (Figure 3I–K): upon chronic neural inhibition, the delta-silent/beta-active state was decreased while the delta-active/beta-silent state and the delta-active/alpha-silent state were both increased (Figure 3K). Although we cannot exclude potential defects in endocrine cell development, as reported in our previous study (Yang et al., 2018), these changes were not accompanied by alterations in delta cell calcium oscillation frequency nor peak height or duration (Figure 3—figure supplement 3). We also found a significant decrease in the alpha-active/beta-active state upon chronic neural inhibition (Figure 3I), suggesting that neural signaling is an important regulator of alpha–beta connectivity. Given the potential role of pancreatic innervation on islet cell maturation, we next investigated the effects of acutely blocking neural activity using two different approaches. By lineage tracing, we found that the neural crest-derived peri-islet neurons were also labeled by the Et(1121A:GAL4FF) enhancer trap (Figure 4A, B), thereby allowing us to investigate the effects of photo-ablating a subset of peri-islet neurons on islet cell activity (Figure 4C). The photo-ablation of peri-islet neurons reduced islet nerve density (Figure 4—figure supplement 1A, B). While the oscillatory pattern of calcium dynamics was maintained in beta cells upon this ablation (Figure 4D), the coupling between beta cells was significantly decreased (Figure 4E–G). Notably, we did not observe further impairment in beta cell coupling over increasing distance (Figure 4G), suggesting that upon ablation of peri-islet neurons, the signal that initiates beta cell coupling was blunted while beta cells maintained their propensity for coupling across the islet. Whether this beta cell coupling is due to gap junctional (Benninger et al., 2008) and/or soluble factors warrants further studies. Delta–beta coupling was also reduced (Figure 4—figure supplement 1C). Unlike in the chronic neural inhibition scenario, in the fraction time analysis, delta–beta and alpha–delta coupling was not affected upon ablating peri-islet neurons (Figure 4H–J). However, we observed a decrease in alpha–beta coupling and in the alpha-active/beta-active state (Figure 4G–H). The observed coupling defects are unlikely due to changes in individual calcium spike characteristics, as no significant differences were observed in calcium oscillation frequency, peak height, or peak duration (Figure 4—figure supplement 2). Overall, the ablation of peri-islet neurons significantly disrupted beta–beta and alpha–beta connectivity, while conclusions regarding other heterotypic interactions will require further investigation into the various neural subsets that were targeted. It is likely that our targeting of peri-islet neurons affected at least those that guide the activity coupling between alpha and beta cells. Figure 4 with 2 supplements see all Download asset Open asset Targeted ablation studies reveal the crucial role of peri-islet neurons for islet cell activity. (A) Schematic of lineage tracing of neural crest cells in Tg(sox10:CreERT2, myl7:GFP); Tg(ubb:loxP-CFP-loxP-nuc-mCherry); Tg(ins:mCardinal); Et(1121A:GAL4FF); Tg(UAS:GCaMP6s) zebrafish following 5 µM tamoxifen (TM) treatment from 16 to 24 hpf and staining at 108 hpf. (B) Wholemount immunostaining at 108 hpf for mCherry expression (neural crest-derived cells) and counterstaining with DAPI (DNA). Yellow arrowheads point to neural crest-derived cells positive for GCaMP6s expression. (C) Schematic of two-photon ablation experiment. (D) Normalized calcium traces of pancreatic islet cells (including delta, beta, alpha, and unidentified cells). Individual islet cells were assigned to a cell type and given a cell id; LG, basal condition; HG, glucose treated condition; HG a, ablation or mock ablation condition. (E) Correlation matrices of islet cell activity; LG, basal condition; HG, glucose treated condition; HG a, ablation or mock ablation condition. (F) Average beta cell correlation coefficients in individual larvae; n = 11–12 animals, p values from two-way analysis of variance (ANOVA) with Holm–Sidak’s multiple comparisons test. (G) Average homotypic (beta–beta) and heterotypic (alpha–beta) cell correlation coefficients with cell distance distribution from 1 (close) to 10 (far), mean and linear regression (solid lines) with 95% confidence intervals; n = 11–12 animals, p values of slope and intercept from simple linear regression. Fraction time analysis of heterotypic delta–beta, alpha–delta, and alpha–beta cell pairs for times when both are active (H), both are silent (I), and one is active and one is silent (J); mean ± standard error of the mean (SEM), n = 178–215 cell pairs, p values from two-way ANOVA with Holm–Sidak’s multiple comparisons test; magenta circle, active state; cyan circle, silent state. Next, we took an optogenetic approach by generating a transgenic line that allows one to acutely photo-inhibit the release of neurotransmitters with a single pulse of blue light. This method has previously been used in Drosophila (Makhijani et al., 2017) and C. elegans (Lin et al., 2013; Qi et al., 2012) for targeted photo-ablation and photo-inhibition. Pan-neural expression of a singlet oxygen generator, miniSOG2, tethered to synaptic granules resulted in a blue light inducible loss of swimming activity in 110 hpf larvae (Figure 5—figure supplement 1A–C). Following this confirmation of the effectiveness of the tool, we studied neural control of islet cell activity upon acute photo-inhibition (Figure 5—figure supplement 1D). Surprisingly, photo-inhibition decreased glucose levels compared with transgene-negative zebrafish exposed to the same light condition (Figure 5A). Similar to peri-islet neural ablation, pan-neural photo-inhibition decreased beta cell connectivity (Figure 5B–E). Changes in delta–beta and alpha–beta heterotypic interactions were also observed upon acute neural inhibition (Figure 5E–H). A significant decrease in delta-silent/beta-active state reflects what we observed upon chronic neural inhibition (Figure 5H). Like with the photo-ablation of peri-islet neurons, no changes in nearest alpha–delta interactions were observed (Figure 5F–H). Notably, following acute neural inhibition, alpha–beta coupling (Figure 5E) and alpha-active/beta-active states (Figure 5F) were significantly decreased. While we cannot exclude a role for soluble factors from other peripheral organs, these changes in alpha–beta interactions were consistently observed upon both acute pan-neural and peri-islet inhibition, possibly reflecting a role for neurons in the maintenance of alpha–beta coupling. Figure 5 with 2 supplements see all Download asset Open asset Acute optogenetic inhibition of neurotransmitter release disrupts islet cell activity. (A) Whole larva-free glucose-level measurements of Tg(elavl3:sypb-miniSOG2-P2A-mScarlet) zebrafish at 110 hpf; mean ± standard error of the mean (SEM), n = 22–31 batches of 5 larvae per replicate, p values from two-way analysis of variance (ANOVA) with Holm–Sidak’s multiple comparisons test; see Figure 5—source data 1. (B) Normalized calcium traces of pancreatic islet cells (including delta, beta, alpha, and unidentified cells). Individual islet cells were assigned to a cell type and given a cell id; LG, basal condition; HG, glucose treated condition. (C) Correlation matrices of islet cell activity; LG, basal condition; HG, glucose treated condition; HG λ, post-blue light treatment. (D) Average beta cell correlation coefficients in individual larvae; n = 10 animals, p values from two-way ANOVA with Holm–Sidak’s multiple comparisons test. (E) Average homotypic (beta–beta) and heterotypic (alpha–beta) cell correlation coefficients with cell distance distribution from 1 (close) to 10 (far), mean and linear regression (solid lines) with 95% confidence intervals; n = 10 animals, p values of slope and intercept from simple linear regression. Fraction time analysis of heterotypic delta–beta, alpha–delta, and alpha–beta cell pairs for times when both are active (F), both are silent (G), and one is active and one is silent (H); mean ± SEM, n = 141–220 cell pairs, p values from two-way ANOVA with Holm–Sidak’s multiple comparisons test; magenta circle, active state; cyan circle, silent state. Figure 5—source data 1 Figure 5A. Whole larva-free glucose-level measurements of Tg(elavl3:sypb-miniSOG2-P2A-mScarlet) zebrafish. https://cdn.elifesciences.org/articles/64526/elife-64526-fig5-data1-v2.xlsx Download elife-64526-fig5-data1-v2.xlsx Dissecting the complex interplay of local autocrine, paracrine, and gap junctional communication between different endocrine cells, in addition to vascular and nerve interactions, is often hindered by our inability to simultaneously study them in an intact organ within its innate environment. Imaging calcium dynamics with genetically encoded biosensors or calcium sensitive fluorescent indicators in individual islet cell types has been conducted in vitro with dispersed cells (Yang et al., 2013; Albrecht et al., 2015, whole islets Benninger et al., 2008; Johnston et al., 2016), and perfused pancreas slices (Stožer et al., 2013; Panzer et al., 2020), and in vivo with islets transplanted into the anterior chamber of the eye (Rodriguez-Diaz et al., 2012; Salem et al., 2019), as well as intravital imaging of the mouse pancreas (Adams et al., 2021). We report a noninvasive in vivo imaging strategy to study all the different pancreatic endocrine cell types within the same animal. Our three approaches to inhibit neural control, ranging in temporal and spatial specificity, provided useful insights into the role of neurons in regulating pancreatic islet function (Figure 6). Whether activity coupling between beta cells is in part mediated by gap junctions warrants further studies, but our data suggest that neural regulation is critical for the establishment and maintenance of beta cell connectivity as we consistently found decreased beta cell coupling upon chronic and acute neural inhibition. Given that our targeted neural ablation approach also led to this decline in beta cell coupling, it is likely that autonomic neural control is required for beta cell connectivity independently of possible indirect effects resulting from neural regulation of other organs. Whether this neural regulation is directly on beta cells or a bystander effect resulting from the regulation of other cell types, including delta and endothelial cells, requires further studies. It has been proposed that glucose sensing neurons regulate early postnatal beta cell proliferation and maintenance of beta cell function (Tarussio et al., 2014), and our data support the peri-islet localization of such neurons. Figure 6 Download asset Open asset Graphical abstract summarizing the research findings. Neuromodulation, with varying temporal and spatial specificity, provides useful insights into the role of neurons in regulating homotypic and heterotypic activity coupling between pancreatic islet cells. Green check marks indicate when significant defects were observed in correlation-based analysis across the whole islet. Blue check marks indicate when significant defects were observed in fraction time analysis between nearest neighbors. We have focused our studies on the pancreatic beta, alpha, and delta cells; however, it is important to note that there are other endocrine cell types (gamma and epsilon cells) that remain undefined, but do display glucose induced activity coupling with beta cells (Figure 3F). Correlation analysis allowed us to study heterotypic coupling and fraction time analysis further allowed us to study activity patterns of heterotypic cell pairs that are near each other, upon loss of neural signaling. We found changes in delta–beta activity coupling, supporting a role for gap j
This paper explores the influence of burst properties of the sympathetic nervous system on arterial contractility. Specifically, a mathematical model is constructed of the pathway from action potential generation in a sympathetic postganglionic neurone to contraction of an arterial smooth muscle cell. The differential equation model is a synthesis of models of the individual physiological processes, and is shown to be consistent with physiological data. The model is found to be unresponsive to tonic (regular) stimulation at typical frequencies recorded in sympathetic efferents. However, when stimulated at the same average frequency, but with repetitive respiratory-modulated burst patterns, it produces marked contractions. Moreover, the contractile force produced is found to be highly dependent on the number of spikes in each burst. In particular, when the model is driven by preganglionic spike trains recorded from wild-type and spontaneously hypertensive rats (which have increased spiking during each burst) the contractile force was found to be 10-fold greater in the hypertensive case. An explanation is provided in terms of the summative increased release of noradrenaline. Furthermore, the results suggest the marked effect that hypertensive spike trains had on smooth muscle cell tone can provide a significant contribution to the pathology of hypertension.
In diabetes, glucagon secretion from pancreatic α cells is dysregulated. The underlying mechanisms, and whether dysfunction occurs uniformly among cells, remain unclear. We examined α cells from human donors and mice using electrophysiological, transcriptomic, and computational approaches. Rising glucose suppresses α cell exocytosis by reducing P/Q-type Ca2+ channel activity, and this is disrupted in type 2 diabetes (T2D). Upon high-fat feeding of mice, α cells shift toward a "β cell-like" electrophysiological profile in concert with indications of impaired identity. In human α cells we identified links between cell membrane properties and cell surface signaling receptors, mitochondrial respiratory chain complex assembly, and cell maturation. Cell-type classification using machine learning of electrophysiology data demonstrated a heterogenous loss of "electrophysiologic identity" in α cells from donors with type 2 diabetes. Indeed, a subset of α cells with impaired exocytosis is defined by an enrichment in progenitor and lineage markers and upregulation of an immature transcriptomic phenotype, suggesting important links between α cell maturation state and dysfunction.
The importance of pancreatic endocrine cell activity modulation by autonomic innervation has been debated. To investigate this question, we established an in vivo imaging model that also allows chronic and acute neuromodulation with genetic and optogenetic tools. Using the GCaMP6s biosensor together with endocrine cell fluorescent reporters, we imaged calcium dynamics simultaneously in multiple pancreatic islet cell types in live animals in control states and upon changes in innervation. We find that by 4 days post fertilization in zebrafish, a stage when islet architecture is reminiscent of that in adult rodents, prominent activity coupling between beta cells is present in basal glucose conditions. Furthermore, we show that both chronic and acute loss of nerve activity result in diminished beta–beta and alpha–beta activity coupling. Pancreatic nerves are in contact with all islet cell types, but predominantly with beta and delta cells. Surprisingly, a subset of delta cells with detectable peri-islet neural activity coupling had significantly higher homotypic coupling with other delta cells suggesting that some delta cells receive innervation that coordinates their output. Overall, these data show that innervation plays a vital role in the maintenance of homotypic and heterotypic cellular connectivity in pancreatic islets, a process critical for islet function.
The α-, β- and δ-cells of the pancreatic islet exhibit different electrophysiological features. We used a large dataset of whole-cell patch-clamp recordings from cells in intact mouse islets ( N = 288 recordings) to investigate whether it is possible to reliably identify cell type (α, β or δ) based on their electrophysiological characteristics. We quantified 15 electrophysiological variables in each recorded cell. Individually, none of the variables could reliably distinguish the cell types. We therefore constructed a logistic regression model that included all quantified variables, to determine whether they could together identify cell type. The model identified cell type with 94% accuracy. This model was applied to a dataset of cells recorded from hyperglycaemic βV59M mice; it correctly identified cell type in all cells and was able to distinguish cells that co-expressed insulin and glucagon. Based on this revised functional identification, we were able to improve conductance-based models of the electrical activity in α-cells and generate a model of δ-cell electrical activity. These new models could faithfully emulate α- and δ-cell electrical activity recorded experimentally.
Sympathetic activity exhibits respiratory modulation that is amplified in hypertensive rats. Respiratory modulated sympathetic activity produces greater changes in vascular resistance than tonic stimulation of the same stimulus magnitude in normotensive but not hypertensive rats. Mathematical modelling demonstrates that respiratory modulated sympathetic activity may fail to produce greater vascular resistance changes in hypertensive rats because the system is saturated as a consequence of a dysfunctional noradrenaline reuptake mechanism. Respiratory modulated sympathetic activity is an efficient mechanism to raise vascular resistance promptly, corroborating its involvement in the ontogenesis of hypertension.Sympathetic nerve activity (SNA) exhibits respiratory modulation. This component of SNA is important - being recruited under cardiorespiratory reflex conditions and elevated in the spontaneously hypertensive (SH) rat - and yet the exact influence of this modulation on vascular tone is not understood, even in normotensive conditions. We constructed a mathematical model of the sympathetic innervation of an arteriole, and used it to test the hypothesis that respiratory modulation of SNA preferentially increases vasoconstriction compared to a frequency-matched tonic pattern. Simulations supported the hypothesis, where respiratory modulated increases in vasoconstriction were mediated by a noradrenergic mechanism. These predictions were tested in vivo in adult Wistar rats. Stimulation of the sympathetic chain (L3) with respiratory modulated bursting patterns, revealed that bursting increases vascular resistance (VR) more than tonic stimulation (57.8 ± 3.3% vs. 44.8 ± 4.2%; P < 0.001; n = 8). The onset of the VR response was also quicker for bursting stimulation (rise time constant = 1.98 ± 0.09 s vs. 2.35 ± 0.20 s; P < 0.01). In adult SH rats (n = 8), the VR response to bursting (44.6 ± 3.9%) was not different to tonic (37.4 ± 3.5%; P = 0.57). Using both mathematical modelling and in vivo techniques, we have shown that VR depends critically on respiratory modulation and revealed that this pattern dependency in Wistar rats is due to a noradrenergic mechanism. This respiratory component may therefore contribute to the ontogenesis of hypertension in the pre-hypertensive SH rat - raising VR and driving vascular remodelling. Why adult SH rats do not exhibit a pattern-dependent response is not known, but further modelling revealed that this may be due to dysfunctional noradrenaline reuptake.
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