The glucagon-like peptide-1 receptor (GLP1R) is a class B G protein-coupled receptor (GPCR) involved in metabolism. Presently, its visualization is limited to genetic manipulation, antibody detection or the use of probes that stimulate receptor activation. Herein, we present LUXendin645, a far-red fluorescent GLP1R antagonistic peptide label. LUXendin645 produces intense and specific membrane labeling throughout live and fixed tissue. GLP1R signaling can additionally be evoked when the receptor is allosterically modulated in the presence of LUXendin645. Using LUXendin645 and LUXendin651, we describe islet, brain and hESC-derived β-like cell GLP1R expression patterns, reveal higher-order GLP1R organization including membrane nanodomains, and track single receptor subpopulations. We furthermore show that the LUXendin backbone can be optimized for intravital two-photon imaging by installing a red fluorophore. Thus, our super-resolution compatible labeling probes allow visualization of endogenous GLP1R, and provide insight into class B GPCR distribution and dynamics both in vitro and in vivo.
The glucagon-like peptide-1 receptor (GLP1R) is a secretin family class B G protein-coupled receptor (GPCR) characterized by hormone regulation1. Due to its involvement in glucose homeostasis, the GLP1R has become a blockbuster target for the treatment of type 2 diabetes mellitus2. The endogenous ligand, glucagon-like peptide-1 (GLP-1) is released from enteroendocrine L-cells in the gut in response to food intake3, from where it travels to the pancreas before binding to its cognate receptor expressed in β-cells. Following activation, the GLP1R engages a cascade of signaling pathways including Ca2+, cAMP, ERK and β-arrestin, which ultimately converge on β-cell survival and the glucose-dependent amplification of insulin release4,5. GLP1R is also expressed in the brain6,7, where it further contributes to metabolism via effects on food intake, energy expenditure, locomotion, and insulin sensitivity. Despite this, GLP1R localization remains a challenge and is impeding functional characterization of GLP-1 and drug action.
Chemical biology and recombinant genetics have made available a diverse range of methods for the visualization of biological entities. Thus, classical fluorescent protein-fusions8, self-labeling suicide enzymes (SNAP-, CLIP-, and Halo-tag)9,10,11, “click chemistry”12,13 and fluorogenic probes14,15,16 have provided insight into the localization and distribution of their respective targets in living cells. In particular, current approaches for visualizing the GLP1R have so far relied on monoclonal antibodies (mAbs) directed against GLP1R epitopes17,18, SNAP-tags19,20,21, or fluorescent analogues of Exendin4(1–39), Exendin4(9–39), and Liraglutide22,23,24,25. Moreover, mouse models exist in which Cre recombinase is driven by the Glp1r promoter, allowing labeling of GLP1R-expressing cells when crossed with reporter mice6,7.
Such methods have a number of shortcomings. Antibodies possess variable specificity17 and tissue penetration, and GLP1R epitopes might be hidden or preferentially affected by fixation in different cell types and tissues. Enzyme self-labels allow GLP1R to be visualized in living cells without affecting ligand binding, but require heterologous expression and have therefore not yet been able to address endogenous receptor. Moreover, fluorescent analogues of Exendin4(1–39) and Liraglutide activate and internalize the receptor, which could confound results in live cells, particularly when used as a tool to sort purified populations (i.e. β-cells)26,27. Antagonist-linked fluorophores circumvent this issue, but the majority lack thorough pharmacological validation, or possess near infrared tags which require sophisticated confocal imaging modalities. On the other hand, reporter mouse strategies possess high fidelity, but cannot account for lineage-tracing artefacts, post-translational processing, protein stability and trafficking of native receptor28. Lastly, none of the aforementioned approaches are amenable to super-resolution imaging of endogenous GLP1R.
Given the wider reported roles of GLP-1 signaling in the heart29, liver30, immune system2, and brain31, it is clear that new tools are urgently required to help identify GLP-1 target sites, with repercussions for drug treatment and its side effects. In the present study, we therefore set out to generate a specific probe for endogenous GLP1R detection in its native, surface-exposed state in live and fixed tissue, without receptor activation. Herein, we report LUXendin645 and LUXendin651, Cy5- and silicon rhodamine (SiR)- conjugated far-red fluorescent antagonists with excellent specificity, live tissue penetration, and super-resolution capability. Using our tools, we provide an updated view of GLP1R expression patterns in pancreatic islets, brain, and hESC-derived β-like cells, show that endogenous GLP1Rs form nanodomains at the membrane, and reveal receptor subpopulations with distinct diffusion modes in their non-stimulated state. Lastly, installation of a tetramethylrhodamine (TMR) fluorophore allows in vivo multiphoton imaging. As such, the LUXendins provide the first nanoscopic characterization of a class B GPCR, with wider flexibility for detection and interrogation of GLP1R in the tissue setting both in vitro and in vivo.
Design of LUXendin555, LUXendin645, and LUXendin651
Ideally, a fluorescent probe to specifically visualize a biomolecule should have the following characteristics: straightforward synthesis and easy accessibility, high solubility, relatively small size, high specificity and affinity, and a fluorescent moiety that exhibits photostability, brightness and (far-)red fluorescence with an additional two-photon cross-section. Moreover, the probe should be devoid of biological effects when applied to live cells and show good or no cell permeability, depending on its target localization. While some of these points were addressed in the past, we set out to achieve this high bar by designing a highly specific fluorescent GLP1R antagonist using TMR, Cy5, and SiR fluorophores. As no small molecule antagonists for the GLP1R are known, we turned to Exendin4(9–39), a potent antagonistic scaffold amenable to modification (Fig. 1)32. We used solid-phase peptide synthesis (SPPS) to generate an S39C mutant21, which provides a C-terminal thiol handle for late-stage installation of different fluorophores. As such, TMR-, Cy5- and SiR-conjugated versions were obtained by means of cysteine-maleimide chemistry, termed LUXendin555, LUXendin645, and LUXendin651, respectively, with spectral properties shown in Table 1 (characterization of and purity of compounds in Supplementary Figs. 1–11) (Fig. 1).
LUXendin645 intensely labels GLP1R in cells and tissue
GLP-1-induced cAMP production was similarly blocked by Exendin4(9–39) and its S39C mutant (Fig. 2a). Installation of Cy5 to produce LUXendin645 did not affect these antagonist properties (Fig. 2a) (Supplementary Fig. 12). No agonist or partial agonist activity was detected for Exendin4(9–39), S39C_Exendin4(9–39), or LUXendin645 (Fig. 2a) (Supplementary Fig. 12). As expected, addition of the GLP1R-positive allosteric modulator (PAM) BETP33 conferred weak agonist activity on LUXendin645 (EC50(cAMP) = 192 nM) (Fig. 2b).
As a first assessment of GLP1R-labeling efficiency, we probed YFP-AD293-SNAP_GLP1R cells with increasing concentrations of LUXendin645. Maximal LUXendin645 labeling occurred at 250–500 nM (Fig. 2c), with no signal detected in control YFP-AD293 cells lacking GLP1R (Fig. 2d). We next examined whether LUXendin645 would allow labeling of endogenous GLP1R in primary tissue. Following 60 min application of LUXendin645, isolated islets demonstrated intense and clean labeling, which was restricted to the membrane (Fig. 2e). To minimize background fluorescence, slightly lower concentrations of LUXendin645 were used in islets (50–100 nM) vs. plated cells (250 nM). Using conventional confocal microscopy, we were able to detect bright staining even 60 µm into the islet (Fig. 2e). Given these results, we next attempted to penetrate deeper into the islet by taking advantage of the superior axial resolution of two-photon excitation (Fig. 2f). Remarkably, this imaging modality revealed LUXendin645 labeling at high resolution throughout the entire volume of the islet (170 µm in this case) (Fig. 2f). Consistent with the cAMP assays, GLP1R internalization was detected following co-application of LUXendin645 and BETP to MIN6 β-cells, which endogenously express the receptor (Fig. 2g, h).
LUXendin645 allows multiplexed GLP1R detection
Demonstrating flexibility, LUXendin645 labeling was still present following formaldehyde fixation (Fig. 2i, j). Immunostaining using a specific primary monoclonal antibody against the GLP1R revealed strong co-localization with LUXendin645 in both islets (Fig. 2i) and MIN6 cells (Fig. 2j). Notably, LUXendin645 displayed superior signal-to-noise-ratio and membrane resolution compared to the antibody (Fig. 2k), expected to be even better in live tissue where auto-fluorescence is less. Likewise, LUXendin645 co-localized with SNAP-Surface 488 in SNAP_GLP1R-INS1 rat β-cells generated on an endogenous null background (Fig. 2l). Suggesting that LUXendin645 requires the presence of surface GLP1R, labeling was markedly reduced following prior internalization with Exendin4(1–39) (94.1 ± 2.0% decrease in surface LUXendin645 labelling with Exendin4(1–39) treatment, mean ± s.d.; n = 3 independent repeats) (Fig. 2l, m).
LUXendin645 specifically binds the GLP1R
To further validate the specificity of LUXendin645 labeling in primary tissue, we generated Glp1r knock-out mice. This was achieved using CRISPR-Cas9 genome editing to introduce a deletion into exon 1 of the Glp1r. The consequent frameshift was associated with absence of translation and therefore a global GLP1R knockout, termed Glp1r(GE)−/−, in which all intronic regions, and thus regulatory elements, are preserved (Fig. 3a, b). Wild-type (Glp1r+/+), heterozygous and homozygous littermates were phenotypically normal and possessed similar body weights (Fig. 3c).
Confirming successful GLP1R knock-out, insulin secretion assays in islets isolated from Glp1r(GE)−/− mice showed intact responses to glucose, but absence of Exendin4(1–39)-stimulated insulin secretion (Fig. 3d). Reflecting this finding, the incretin-mimetic Liraglutide was only able to stimulate cAMP rises in islets from wild-type (Glp1r+/+) littermates, measured using the FRET probe Epac2-camps (Fig. 3e, f). As expected, immunostaining with monoclonal antibody showed complete absence of GLP1R protein (Fig. 3g). Suggesting that LUXendin645 specifically targets GLP1R, with little to no cross-talk from glucagon receptors34, signal could not be detected in Glp1r(GE)−/− islets (Fig. 3g).
Together, these data provide strong evidence for a specific mode of LUXendin645 action via the GLP1R.
LUXendin645 highlights weak GLP1R expression
Previous approaches have shown low abundance of Glp1r transcripts in the other major islet endocrine cell type, i.e. glucagon-secreting α-cells7,35. This is associated with detection of GLP1R protein in ~1–10% of cells7,36, providing an excellent testbed for LUXendin645 sensitivity and specificity. Studies in intact islets showed that LUXendin645 labeling was widespread in the islet and well co-localized with insulin immunostaining (Fig. 4a). However, LUXendin645 could also be seen on membranes very closely associated with α-cells and somatostatin-secreting δ-cells (Fig. 4b, c), similarly to results obtained with GLP1R mAb. Due to the close apposition of β-, δ- and α–cell membranes, we were unable to accurately assign cell-type specificity to LUXendin645. Instead, using cell clusters plated onto coverslips, we could better discern LUXendin645 labeling, revealing GLP1R expression in 12.3 ± 3.3% of α-cells (mean ± s.d.; n = 18 cell clusters, ten animals, three separate islet preparations) (Fig. 4d–f). Notably, GLP1R-expressing α-cells tended to adjoin, whereas those without the receptor were next to β-cells. Confirming previous findings, a majority (85.1 ± 16.3%) (mean ± s.d.; n = 18 cell clusters, ten animals, three separate islet preparations) of β-cells were positive for LUXendin645 (Fig. 4d–f)7,25.
We wondered whether fixation required for immunostaining might increase background fluorescence such that GLP1R detection specificity was reduced. To circumvent this, studies were repeated in live islets where LUXendin645 signal was found to be much brighter and background almost non-existent. GLP1R was detected in 24.6 ± 5.0% (mean ± s.d.; n = 31 islets, six animals, three separate islet preparations) of non-β-cells (Fig. 4g, h) using Ins1CreThor;R26mTmG reporter mice in which β-cells are labeled green and all other cell types are labeled red following Cre-mediated recombination. Once adjusted for the previously reported GLP1R expression in δ-cells (assuming 100%), which constitute ~20% of the insulin-negative islet population37, this leaves ~5% of GLP1R+ α-cells. This was not an artefact of optical section, since two-photon islet reconstructions showed similar complete absence of LUXendin645 staining in discrete regions near the surface (where α-cells predominate) (Supplementary Movie 1).
LUXendins reveal higher-order GLP1R organization
By combining LUXendin645 with super-resolution radial fluctuations (SRRF) analysis38, GLP1R could be imaged at super-resolution using streamed images (~500) from a conventional widefield microscope (Fig. 5a). To image endogenous GLP1R at <100 nm lateral resolution, we combined STED nanoscopy with LUXendin651, which bears SiR instead of Cy5. LUXendin651 displayed antagonist behavior, with no evidence of partial agonism, and produced bright labeling of wild-type but not Glp1r(GE)−/− islets, with an identical distribution to LUXendin645 (Supplementary Figs. 12 and 13). Incubation of MIN6 cells with LUXendin651 and subsequent fixation allowed STED imaging of the endogenous GLP1R with a FWHM = 70 ± 10 nm (mean ± s.d.; n = 15 line profiles measured on the raw data, from two independent repeats) (Fig. 5b–d). STED snapshots of MIN6 β-cells revealed detailed GLP1R distribution: receptors were not randomly arranged but rather tended to organize into nanodomains with neighbors (Fig. 5b–d). This was confirmed using the F- and G-functions, which showed a non-random and more clustered GLP1R distribution (Fig. 5e, f). Differences in GLP1R expression level and pattern could clearly be seen between neighboring cells with a subpopulation possessing highly concentrated GLP1R clusters (Fig. 5g). LUXendin651 even allowed GLP1R to be imaged in living MIN6 cells using SRRF and STED, although nanodomains were more difficult to resolve due to the lateral diffusion of receptors (Fig. 5h, i).
LUXendin645 and Luxendin651 label single GLP1R molecules
To test whether LUXendin645 and LUXendin651 would be capable of tracking single GLP1Rs in live cells, we performed single-molecule microscopy experiments in which individual receptors labeled with either fluorescent probe were imaged by total internal reflection fluorescence (TIRF) microscopy39,40. Both probes allowed GLP1R to be tracked at the single-molecule level in CHO-K1-SNAP_GLP1R cells, but bleaching precluded longer recordings with LUXendin645 (Fig. 6a and Supplementary Movies 2, 3). By combining single-particle tracking with LUXendin651, we were able to show that GLP1Rs diffuse at the membrane in their non-stimulated or antagonized state (Fig. 6a and Supplementary Movie 4). However, a mean square displacement (MSD) analysis40 revealed a high heterogeneity in the diffusion of GLP1Rs on the plasma membrane, ranging from virtually immobile receptors to some displaying features of directed motion (superdiffusion) (Fig. 6b, c). GLP1R diffusion properties were not ligand-dependent, since similar profiles were detected for both LUXendin645 and LUXendin651 (Fig. 6c).
LUXendin645 allows visualization of central GLP1 targets
To further show the utility of LUXendin645 for visualizing endogenous GLP1R, we extended studies to the brain in which mAbs do not work reliably and where peripheral GLP1 targets still remain poorly characterized. Two hours following subcutaneous injection of LUXendin645, perfuse-fixed brains were retrieved for analysis. Intense labelling could be detected in the arcuate nucleus (ARC), area postrema (AP) and choroid plexus (CP) (Fig. 7a, b), all regions known to express GLP1R using reporter or fluorescent agonist approaches6,22. Notably, LUXendin645-labeled neurons overlapped with areas receiving innervation from GLP1-producing neurons41, with GLU-YFP synaptic boutons closely abutting GLP1R+ areas (Fig. 7a, b). LUXendin645 labeling co-localized with GLP1R-expressing neurons in the ARC/median eminence (ME) and AP/nucleus tractus solitarius (NTS), shown using GLP1RCre;LSL-GCaMP3 reporter mice (Fig. 7c–e).
Super-resolution imaging (~140 nm lateral resolution) revealed the presence of LUXendin645 on the cell membranes of GLP1R+ neuron cell bodies, as well as dendrites. Moreover, GLP1R were found to accumulate into nanodomains on the membranes of ARC and AP neuron membranes, as well as ependymal cells of the CP (Fig. 7f). Lastly, optical projection tomography allowed entire LUXendin645-labelled brains to be imaged and mapped in three-dimensions, confirming the above results and also extending probe localization to the subfornical organ (SFO), organum vasculosum of the lamina terminalis (OVLT), and ventricles (Fig. 7g).
LUXendin645 labels GLP1R in hESC-derived β-cells
Since GLP1R are expressed in mature β-cells42, we wondered whether LUXendin645 would serve as a useful surface marker for assessing differentiation of human embryonic stem cell (hESC)-derived β-like cells. LUXendin645 was unable to label undifferentiated ES cells (Fig. 8a). Following differentiation and 21 days’ culture, LUXendin645 labeling was clearly visible in spheroids, in line with increasing levels of GLP1R expression (Fig. 8b). As for mouse islets, LUXendin645 co-localized with insulin, with minimal signal in areas strongly positive for glucagon (Fig. 8c), shown using Manders’ split coefficients (Fig. 8d). Not all insulin-containing cells stained for GLP1R, however (Fig. 8c). Confirming a β-like cell phenotype, spheroids were fixed and sliced before staining for insulin and NKX6-1 (Fig. 8e).
We next investigated whether LUXendin645 would allow β-like cells to be purified according to GLP1R expression. To this end, LUXendin645-labelled spheroids were subjected to fluorescence-activated cell sorting (FACS), before gene expression analyses of LUXendin645+ and LUXendin645− populations. Notably, the LUXendin645+ population expressed higher levels of GLP1R and NKX6-1, with a tendency toward increased INS (Fig. 8f). As expected from the imaging data, GCG expression was significantly decreased in the LUXendin645+ β-like cells (Fig. 8f).
LUXendin555 allows labeling of islets in vivo
Lastly, we explored whether swapping the far-red Cy5/SiR for a TMR dye would be tolerated to obtain a spectrally orthogonal probe, termed LUXendin555. Labeling was detected in YFP-AD293-SNAP_GLP1R (Fig. 9a) but not in YFP-AD293 cells (Fig. 9b), with max labeling at 600 nM (Fig. 9c). A slightly lower concentration (250 nM) of LUXendin555 was found to produce bright staining in both cells and islets, whilst minimizing background fluorescence. However, we noticed a more punctate LUXendin555 staining pattern when viewed at high-resolutions (Fig. 9a). To determine whether the appearance of puncta was due to receptor internalization, or alternatively accumulation of cleaved, charged TMR in organelles, labeling was repeated in islets co-stained with GLP1R monoclonal antibody (Supplementary Fig. 14). In these experiments, no differences in GLP1R surface expression could be seen between LUXendin555, LUXendin645, and Ex9 (Fig. 9d), suggesting that puncta are unlikely to be internalized receptor. In line with this, LUXendin555 was found to display antagonist properties using HTRF-based cAMP assay (Fig. 9e). However, a second independent detection method (luciferase) showed the opposite result, raising the possibility that the installed TMR might influence assay readout (Fig. 9f). As for the other probes, LUXendin555 was unable to label Glp1r(GE)−/− islets (Supplementary Fig. 14).
We thought that the relatively high quantum yield of TMR, coupled with good two-photon cross-section might suit LUXendin555 well to in vivo imaging. Two-photon imaging was applied to anaesthetized mice to allow visualization of the intact pancreas, exposed through an abdominal incision (Fig. 9g). Vessels and nuclei were first labeled using FITC-dextran and Hoechst before injecting LUXendin555 intravenously. The following observations support that LUXendin555 displays antagonist activity in vivo: (1) labeling occurred rapidly within 5 min post-injection; (2) staining was confined to the cell membrane with no apparent internalization (Fig. 9h); and (3) normoglycemia was not significantly altered over 30 min (173.0 ± 21.1 vs. 215.3 ± 41.4 mg/dl, 0 and 30 min post-injection, respectively; mean ± s.d.; n = 3 mice; non-significant, paired t-test).
In the present study, we synthesize and validate far-red fluorescent labels, termed LUXendins for the real-time detection of endogenous GLP1R in live cells. Nanomolar concentrations of LUXendin645 and LUXendin651 lead to intense membrane-labeling of the GLP1R, with best in class tissue penetration and signal-to-noise ratio, as well as super-resolution capability. Notably, LUXendin645 and LUXendin651 do not activate the GLP1R unless agonist activity is conferred with the widely available PAM BETP. LUXendin645 and LUXendin651 are highly specific, as shown using a CRISPR-Cas9 mouse line lacking GLP1R expression. Lastly, the analogous compound LUXendin555, bearing a different fluorophore, expands the color palette without changing the peptidic pharmacophore.
Compared to present chemical biology approaches, LUXendins possess a number of advantages for GLP1R labeling, which generally rely on Exendin4(1–39) or Exendin4(9–39) peptides labeled with for instance FITC, Cy3, Alexa594, Cy5, or VT75019,22,23,24,25,33. Firstly, the use of an antagonist retains more receptor at the cell surface, which likely increases detection capability. Secondly, the GLP1R is not fully activated, meaning that results can be interpreted in the absence of potentially confounding cell signaling or internalization, such as that expected with agonists25. Thirdly, Cy5 and SiR occupy the far-red range, leading to less background fluorescence, increasing depth penetration in confocal microscopy due to reduced scatter, and avoiding the use of more phototoxic wavelengths43. Fourthly, LUXendin pharmacology and labelling specificity has been validated in-depth. Lastly, LUXendins are well-adapted for super-resolution imaging through the use of optimally suited fluorescent moieties. Together, these desirable properties open up the possibility to image expression and distribution of native GLP1R over extended periods of time using multiple imaging modalities.
While LUXendins also allowed GLP1R trafficking to be monitored, this required the presence of a PAM to allosterically activate the receptor. Due to the probe-dependent nature of PAMs, LUXendins with a number of different pharmacophores would need to be generated to fully assess the ligand-dependency of GLP1R trafficking. In some experiments, we also noticed the presence of punctate LUXendin645 and LUXendin651 labelling. Suggesting that this staining pattern reflects cleaved fluorophore rather than internalized GLP1R are the following observations: (1) succinimide exchange with reactive thiols can lead to linker loss44, allowing free fluorophore to cross the membrane and accumulate in organelles; and (2) puncta were not apparent in the same samples co-stained with GLP1R mAb.
To test the specificity of LUXendins, we used CRISPR-Cas9 genome-editing to globally knock out the GLP1R in mice. Protein deletion was confirmed by absence of detectable GLP1R signal following labeling with monoclonal antibody, LUXendin555, LUXendin645, and LUXendin651. While Glp1r−/− animals already exist, and have made important contributions to our understanding of incretin biology, they were produced using a mutation to replace exons encoding transmembrane regions 1 and 3 (encoded by exons 5 and 7), presumably leading to deletion of the introns in between (~6.25 kb)45. By contrast, Glp1r(GE)−/− mice possess intact introns. Since introns contain regulatory elements, such as distant-acting enhancers46, miRNAs47, and lncRNAs48, their loss in transgenic knockouts could have wider influence on the transcriptome. GLP1R knock-out mice might therefore be useful alongside conventional approaches for validating GLP1R reagents, including antibodies, agonist and antagonist, and derivatives thereof.
Demonstrating the excellent sensitivity of the Cy5-linked LUXendin645 in particular, we were able to detect GLP1R expression in ~5% of α-cells. Understanding α-cell GLP1R expression patterns is important because incretin-mimetics reduce glucagon secretion49, which would otherwise act to aggravate blood glucose levels. Previous studies using antibodies, reporter animals and agonist-fluorophores have shown that ~1–10% of mouse and rat α-cells express GLP1R, in line with the low transcript abundance7,25,35,50, despite reports that GLP-1 can directly suppress glucagon release36. Our data are in general concordance with these findings, but demonstrate an increase in sensitivity compared to other approaches capable of detecting native GLP1R protein, namely mAb and agonist-fluorophore. This improvement is likely related to the superior signal-to-noise ratio (SNR) and selectivity of LUXendin645, increasing the ability to resolve relatively low levels of endogenous GLP1R. A recent report showed GLP1R expression in ~80% of α-cells using an antibody raised against the N-terminal region, with both membrane and cytosolic staining evident51. While the reasons for this discrepancy are unknown, it should be noted that LUXendin645 binds the orthosteric site and so reports the proportion of GLP1R that is “signaling competent”7,19,32.
In addition to islets, LUXendin645 was also able to label brain tissue. 3D rendering of entire cleared brains using optical projection tomography showed strong LUXendin645 staining in the circumventricular organs and their directly neighboring regions, including the NTS and ARC. We also detected LUXendin645-labelling in the CP, an epithelial-vascular structure that secretes cerebrospinal fluid (CSF). Rat CP has recently been shown to express GLP1R ex vivo, with Ex4 reducing intracranial pressure in hydrocephalic models52. Notably, super-resolution snapshots showed that GLP1R in the ARC, AP, and CP were organized as nanodomains at the membrane. Such higher organization has not been previously appreciated in the brain and it will now be interesting to understand the functional relevance for GLP1 signaling. A number of central GLP1R-expressing regions remained obscure, likely reflecting the pharmacokinetic properties of peripherally administered agonist/antagonist. However, we anticipate that LUXendin645 will be useful for the study of these regions following targeted injections. Taken together, these data show that LUXendin645 allows endogenous GLP1R to be visualized in extrapancreatic tissue using both conventional and super-resolution-imaging approaches.
We could also extend studies to hESC-derived β-like cells, where GLP1R expression was detected in spheroids following induction of differentiation and 21 days’ culture. LUXendin645 labeling was seen almost exclusively in the β-like cell compartment, reflecting known distributions in mouse7,25 and human53 islets. While not all β-like cells were visibly labelled, this likely reflects GLP1R expression levels, which were ~50% lower in spheroids than adult human islets. Pertinently, LUXendin645 allowed more mature/differentiated β-like cells to be identified and purified according to GLP1R, which increases almost 20-fold in adult vs. neonatal rat β-cells42. Thus, these studies show the potential of LUXendins to understand GLP1R expression patterns in regenerated β-like cells, as well as rapidly mark differentiation/maturity status using a simple one-step surface marker.
Since LUXendin645 showed excellent SNR using conventional epifluorescence, it was highly amenable to SRRF analysis. As such, LUXendin645 and its congeners open up the possibility to image the GLP1R at super-resolution using simple widefield microscopy available in most laboratories. For stimulated emission depletion (STED) microscopy experiments, Cy5 was replaced with SiR to give LUXendin651. STED imaging showed that endogenous GLP1R possess a higher structural order in the presence of LUXendin651 binding: namely organization into nanodomains at the cell membrane. Since GLP1R plasma membrane distribution is ligand-dependent, for example via effects on palmitoylation and clustering into cholesterol-rich nanodomains20 it will be interesting to repeat these experiments using a range of agonists/antagonists. Indeed, LUXendins provide an ideal template for the production of fluorescent ligands that would allow super-resolution examination of nanodomain architecture in response to different activation modes.
Notably, a subpopulation of β-cells appeared to possess concentrated GLP1R clusters even in unstimulated conditions. It will be important in the future to investigate whether this is a cell autonomous heterogenous trait, or instead reflects biased distribution of receptors in membranes of specific β-cells. Lastly, both LUXendin645 and LUXendin651 allowed GLP1Rs to be imaged in live cells by single molecule microscopy, revealing variability in diffusion at the plasma membrane. Particle tracking analyses segregated GLP1R into four different populations based upon diffusion mode, in keeping with data from a class A GPCR, the beta adrenergic receptors40. Together, these experiments provide the first super-resolution characterization of a class B GPCR and suggest a degree of complexity not readily appreciated with previous approaches.
LUXendin555 showed antagonist activity in terms of cAMP generation using a HTRF approach. However, we could not confirm this result using a luciferase-based detection method. The reasons for this are unclear, but might include interference of the red fluorescent TMR with either assay, or alternatively different GLP1R coupling strength between cell lines. As such, use of LUXendin555 should consider the possibility that the ligand is an antagonist or agonist. Nonetheless, LUXendin555 retained GLP1R at the membrane, and possesses advantageous properties for in vivo imaging including good two-photon cross-section and high quantum yield.
In summary, we provide a comprehensively tested and unique GLP1R detection toolbox consisting of far-red antagonist labels, LUXendin645 and LUXendin651, an agonist/antagonist LUXendin555, and knockout Glp1r(GE)−/− animals. Using these freely available probes, we provide an updated view of GLP1R organization, with relevance for the treatment of complex metabolic diseases such as obesity and diabetes. Thus, the stage is set for visualizing GLP1R in various tissues using a range of imaging techniques, as well as the production of peptidic labels and agonists.
A free cysteine bioconjugation handle was installed on Exendin4(9–39) using solid-phase synthesis to give the derivatized S39C-Exendin4(9–39)21. Maleimide-conjugated-6-TMR, -6-SiR and -Cy5 were obtained by TSTU activation of the corresponding acids and reaction with 1-(2-amino-ethyl)-pyrrole-2,5-dione (TFA salt, Aldrich). Fluorophore coupling via thiol-maleimide chemistry to peptides was performed in PBS. All compounds were characterized by HRMS and purity was assessed to be >95% by HPLC. Extinction coefficients were based upon known manufacturer bulk material measures for TMR-Mal, Cy5-Mal (both Lumiprobe), and SiR-Mal (Spirochrome). Details for synthesis including characterization of all LUXendins are detailed in the Supplementary Methods and Supplementary Figs. 1–11. LUXendin555, LUXendin645, and LUXendin651 are freely available for academic use upon request.
AD293 cells (Agilent) were maintained in Dulbecco’s Modified Eagles medium (DMEM; D6546, Sigma) supplemented with 10% fetal calf serum (FCS), 1% l-glutamine, and 1% penicillin/streptomycin. CHO-K1 cells stably expressing the human SNAP_GLP1R (Cisbio) (CHO-K1-SNAP_GLP1R) were maintained in DMEM supplemented with 10% FCS, 1% penicillin/streptomycin, 500 μg/mL G418, 25 mM HEPES and 1% nonessential amino acids and 2% l-glutamine. MIN6 β-cells (a kind gift from Prof. Jun-ichi Miyazaki, Osaka University) were maintained in DMEM (D6546, Sigma) supplemented with 15% FCS, 25 mM d-glucose, 71 μM BME, 2 mM l-glutamine, 100 U/mL penicillin, 100 μg/mL streptomycin, and 25 mM HEPES. INS1 832/3 CRISPR-deleted for the endogenous GLP1R locus (a kind gift from Dr. Jacqui Naylor, MedImmune)54 were transfected with human SNAP_GLP1R, before FACS of the SNAP-Surface488-positive population and selection using G41820. The resulting SNAP_GLP1R_INS1GLP1R−/− cells were maintained in RPMI-1640 supplemented with 10% FBS, 10 mM HEPES, 2 mM l-glutamine, 1 mM pyruvate, 72 µM β-mercaptoethanol, 1% penicillin/streptomycin, and 500 μg/mL G418.
Glp1r(GE)-/-: CRISPR-Cas9 genome-editing was used to introduce a single base pair deletion into exon 1 of the Glp1r locus. Fertilized eggs of female Cas9-overexpressing mice (strain Gt(ROSA)26Sortm1.1(CAG-cas9*,–EGFP)Fezh/J; JAX stock no. 024858) were harvested following super-ovulation. Modified single-guide RNA (Synthego) targeting exon 1 of Glp1r and a single-stranded repair-template were injected at 20 ng/µl into the pronucleus of embryos at the 1-cell stage. In culture, 80% of embryos reached the 2-cell stage and were transplanted into surrogate mice. Glp1r(GE)−/− mice did not integrate the repair-template (confirmed by genotyping PCR), but instead harbored a single nucleotide deletion leading to a frame-shift mutation and loss of GLP1R protein. Knock-in mice that integrated the repair template were not used in the present studies and will be described elsewhere. The targeted locus of Glp1r(GE)−/− offspring was analyzed by PCR and sequencing. Off-target sites were predicted using the CRISPR Guide Design Tool (crispr.mit.edu). Loci of the top 10 off-target hits were amplified by PCR and analyzed via Sanger sequencing (Supplementary Table 1). Founder animals carrying alleles with small deletions were backcrossed to wild type animals (strain C57BL/6J) for 1–3 generations to outbreed affected off-targets and then bred to homozygosity (Supplementary Figs. 15 and 16). Animals were born in Mendelian ratios, genotyping was performed using Sanger sequencing or PCR. Genotyping PCRs were performed with Glp1r forward primer 5′-CAGGCGCTCAGAGCTAGAAGC-3′ and with Glp1r wild-type reverse primer 5′-CCAGGGCTCACCTGAGGG-3′ or Glp1r knockout 5′-CCAGGGCTCACCTGAGGC-3′ to amplify and detect the WT or mutant allele, respectively. Animals were bred as heterozygous pairs to ensure Glp1r+/+ littermates. Glp1r(GE)−/− animals are freely available for academic use, subject to a Material Transfer Agreement.
Ins1CreThor;R26mT/mG: To allow identification of β- and non-β-cells, Ins1CreThor animals with Cre knocked-in at the Ins1 locus (strain B6(Cg)-Ins1tm1.1(cre)Thor/J; JAX stock no. 026801) were crossed with R26mT/mG reporter mice (strain B6.129(Cg)-Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/J; JAX stock no. 007676). Cre-dependent excision of the floxed allele results in deletion of tdTomato, expression of membrane-localized GFP and thus identification of recombined and non-recombined cells.
GLU-YFP: Animals harboring YFP under the control of the glucagon promoter were generated and bred as previously described55.
GLP1RCre;LSL-GCaMP3: To identify GLP1R-expressing cells in the brain, mice with Glp1r promoter-drive Cre7 were bred with stop-flox’d GCaMP3 animals (JAX stock no. 014538).
CD1 wild-type animals were purchased from Charles River Laboratories UK.
All studies were performed with 6–12-week-old male and female animals,
All animal research complied with the Animals (Scientific Procedures) Act 1986 of the U.K. Approval was granted by the University of Birmingham’s Animal Welfare and Ethical Review Body. Procurement of human islets was approved by the Human Research Ethics Board (Pro00013094; Pro00001754) at the University of Alberta and all families of organ donors provided written informed consent. hESC (WA01/H1; hPSCreg name WAe001-A) (obtained from WiCell) were generated by the originating institute with informed consent and ethical approval from the Robert-Koch Institut, Berlin (Az.3.04.02/0101) and NIH (NIHhESC-10-0043). Studies with hESC (WA01/H1) were approved by the BC Children’s and Women’s Hospital Human Research Ethics Board (Approval #H09-00676). Studies with human tissue were approved by the BC Children’s and Women’s Hospital Human Research Ethics, University of Birmingham Ethics Committee and the National Research Ethics Committee (REC reference 16/NE/0107, Newcastle and North Tyneside, UK).
Animals were humanely euthanized before injection of collagenase 1 mg/mL (Serva NB8) into the bile duct. Following removal of the inflated pancreas and digestion for 12 min at 37 °C, islets were separated using a Histopaque (Sigma-Aldrich) gradient. Islets were cultured in RPMI medium containing 10% FCS, 100 units/mL penicillin, and 100 μg/mL streptomycin.
Binding and potency assays
Binding assays were performed in transiently transfected YFP-AD293-SNAP_GLP1R cells (using PolyJet reagent; SignaGen). Increasing concentrations of compound were applied for 60 min, before imaging using a Zeiss LSM880 meta-confocal microscope configured with GaAsP detectors and ×10/0.45W, ×40/1.00W and ×63/1.20W objectives. YFP, TMR (LUXendin555), and Cy5 (LUXendin645) were excited using λ = 514 nm, λ = 561 nm, and λ = 633 nm lasers, respectively. Emitted signals were captured at λ = 519–574 nm, λ = 570–641 nm, and λ = 638–759 nm for YFP, TMR (LUXendin555), and Cy5 (LUXendin645), respectively. Control experiments were performed in YFP-AD293-SNAP cells, as above.
Potency for cAMP generation and inhibition was tested in heterologous expression systems, comprising either stable CHO-K1-SNAP_GLP1R or HEK-SNAP_GLP1R cells, or transiently transfected YFP-AD293-SNAP_GLP1R cells21. Briefly, cells were incubated with increasing concentrations of compound with and without allosteric modulator for 30 min, before harvesting, lysis and measurement of cAMP using either cAMP-GloTM (Promega) or HTRF (Cisbio) assays, according to the manufacturer’s instructions. All assays were performed in the presence of 100–500 µM IBMX to inhibit phosphodiesterase activity. EC50 values were calculated using log concentration–response curves fitted with a three-parameter or four-parameter equation.
Islets were incubated for 1 h at 37 °C in culture medium supplemented with either 100–250 nM LUXendin555, 50–100 nM LUXendin645, or 100 nM LUXendin651. Islets were imaged using either a Zeiss LSM780 or LSM880 microscope, as above (LUXendin651 was imaged as for LUXendin645). Ins1CreThor;R26mT/mG islets were excited at λ = 488 nm (emission, λ = 493–555 nm) and λ = 561 nm (emission, λ = 570–624 nm) for mGFP and tdTomato, respectively. Two-photon imaging of LUXendin645 was performed using a Zeiss LSM 880 NLO equipped with a Spectra-Physics Insight X3 femtosecond-pulsed laser and ×20/1.00W objective. Excitation was performed at λ = 800 nm and emitted signals detected at λ = 638–759 nm.
Islets were transduced with adenovirus harboring the FRET sensor, Epac2-camps56 (a kind gift from Prof. Dermot Cooper, University of Cambridge), before imaging using a Crest X-Light spinning disk system coupled to a Nikon Ti-E base and ×10/0.4 NA objective. Excitation was delivered at λ = 430–450 nm using a Lumencor Spectra X light engine. Emitted signals were detected at λ = 460–500 and λ = 520–550 nm for Cerulean and Citrine, respectively, using a Photometrics Delta Evolve EM-CCD. Imaging was performed in HEPES–bicarbonate buffer, containing (in mmol/L) 120 NaCl, 4.8 KCl, 24 NaHCO3, 0.5 Na2HPO4, 5 HEPES, 2.5 CaCl2, 1.2 MgCl2, and 3–17 d-glucose. Vehicle (H2O), Exendin4(1–39) (10–20 nM), or Liraglutide (10 nM) were applied at the indicated time points, with forskolin (10 µM) acting as a positive control.
LUXendin555 (250 nM) or LUXendin645 (50–250 nM) were applied to cells or tissue for 60 min, before fixation in 4% formaldehyde. Primary antibodies were applied overnight at 4 °C in PBS + 0.1% Triton + 1% BSA. Secondary antibodies were applied in the same buffer for 1 h at room temperature, before mounting on slides using Vectashield Hardset containing DAPI. Primary antibodies were mouse monoclonal anti-GLP1R 1:30 (Iowa DHSB; mAb #7F38), rabbit anti-insulin 1:500 (Cell Signaling Technology, #3014), mouse monoclonal anti-glucagon 1:2000 (Sigma-Aldrich, #G2654), and mouse anti-somatostatin 1:5000 (Invitrogen, #14-9751-80). Secondary antibodies were goat anti-mouse DyLight488, goat anti-mouse Alexa Fluor 568, and donkey anti-rabbit DyLight 488 1:1000. Images were captured using an LSM880 meta-confocal microscope. DyLight488 and Alexa Fluor 568 were excited at λ = 488 nm and λ = 568 nm, respectively. Emitted signals were detected at λ = 500–550 nm (DyLight 488) and λ = 519–574 nm (Alexa Fluor 568). GLP1R surface expression was quantified vs. total GLP1R expression, and normalized against Exendin4(1–39) controls.
SRRF: MIN6 were treated with 250 nM LUXendin645 before live imaging, or fixation and mounting on slides using Vectashield Hardset containing DAPI. Imaging was performed using a Crest X-Light spinning disk system in bypass (widefield) mode. Excitation was delivered at λ = 640/30 nm through a ×60/1.4 NA objective using a Lumencor SPECTRA X light engine. Emission was collected at λ = 700/75 nm using a Photometrics Delta Evolve EMCDD. A 250–500 frame raw image sequence was captured (~2 min) before offline super resolution radial fluctuation (SRRF) analysis to generate a single super-resolution snapshot using the NanoJ plugin for ImageJ (NIH)38.
STED microscopy: MIN6 cells were treated with 100, 200, and 400 nM LUXendin651 before fixation (4% paraformaldehyde, 20 min). Cells were mounted in Mowiol supplemented with DABCO and imaged on an Abberior STED 775/595/RESOLFT QUAD scanning microscope (Abberior Instruments GmbH, Germany) equipped with STED lines at λ = 595 and λ = 775 nm, excitation lines at λ = 355, 405, 485, 561, and 640 nm, spectral detection, and a UPlanSApo ×100/1.4 oil immersion objective lens. Following excitation at λ = 640 nm, fluorescence was acquired in the spectral window λ = 650–800 nm. For live-imaging, MIN6 cells were seeded on 18 mm coverslips 24–48 h prior to treatment with 400 nM LUXendin651 for 30–45 min before washing once in full medium. Coverslips were transferred into a magnetic chamber (Chamlide CMB, Live Cell Instrument) and washed once with HBSS buffer (Lonza, with additional 5 mM HEPES bubbled with carbogen for 5 min and pH adjusted to 7.4 with NaOH), which was also used as imaging buffer at 24 °C. Live imaging was performed within 45 min after mounting.
Deconvolution was performed with Richardson–Lucy algorithm on Imspector software. FWHM was measured on raw data and calculated using OriginPro 2017 software with Gaussian fitting (n = 15 profiles). Minimum and maximum intensity values refer to intensities after deconvolution for STED images and smoothing with a 1-pixel lowpass Gaussian filter for confocal images. Spatial GLP1R expression patterns were analyzed using the F- and G-functions, where F = distance between an object of interest and its nearest neighbor, and G = distance from a given position to the nearest object of interest (FIJI Spatial Statistic 2D/3D plugin)57. Both measures were compared to a random distribution of the same measured objects, with a shift away from the mean ± 95% confidence intervals indicating a non-random or more clustered organization (i.e. more space or smaller distance between objects). Cells possessing highly concentrated GLP1R clusters were identified based upon their fluorescence above a threshold of the population mean fluorescence +1 s.d.
Single-molecule microscopy: For single-molecule experiments, CHO-K1-SNAP_GLP1R cells were seeded onto 25 mm clean glass coverslips at a density of 3 × 105 per well. On the following day, cells were labeled in culture medium with 100 pM LUXendin645 or LUXendin651 for 20 min; this concentration avoids labeling all GLP1R, which would otherwise preclude single-molecule analysis in a stable cell line. At the end of the incubation, cells were washed 3 × 5 min in culture medium. Cells were then imaged at 37 °C in phenol-red free Hank’s balanced salt solution, using a custom built TIRF microscope (Cairn Research) based on an Eclipse Ti2 (Nikon, Japan) equipped with an EMCCD camera (iXon Ultra, Andor), 637 nm diode laser, and a ×100 oil-immersion objective (NA 1.49, Nikon). Image sequences were acquired with an exposure time of 60 ms.
Image sequences were analyzed with an automated particle detection software (utrack) in the MATLAB environment40,58. To analyze the motion of receptors, the time-averaged mean-squared displacement (TA-MSD)59 of individual trajectories from TIRF image sequences was computed40. To calculate the diffusion coefficient (D), the TA-MSD data were fitted with the following equation:
where t indicates time, α is the anomalous diffusion exponent and σerr is a constant offset for localization error. Only trajectories lasting at least 50 frames were analyzed (ntraj = 5057 for Cy5 and 8612 for SiR). Trajectories were then categorized according to the diffusion parameters D and α. Particles with D < 0.01 μm2 s−α were considered to be immobile. Normal diffusion was assigned to particles that had D ≥ 0.01 μm2 s−α and 0.75 ≤ α ≤ 1.25. Sub-diffusion and super-diffusion were assigned to particles with D ≥ 0.01 μm2 s−α and α < 0.75 or α > 1.25, respectively.
Mice were injected subcutaneously with 100 pmol/g of LUXendin645 and left for two hours before terminal anaesthesia and transcardial perfuse fixation with 4% fresh formalin. Brains were serially sectioned at 30 µm and mounted on slides before imaging, as above. Super-resolution snapshots (~140 nm lateral resolution) were acquired using a Zeiss LSM880 equipped with an Airyscan module and a ×63/1.2W objective. Brain clearing was carried out using the 3DISCO protocol60. Samples were suspended on a needle, before imaging using a custom-built optical projection tomography (OPT) platform, with images collected after excitation at λ = 470 and 660 nm. Images were reconstructed using custom-written MATLAB scripts and visualized in Volocity (Perkin-Elmer).
Two-photon in vivo imaging
Female and male C57BL/6J mice 7–12 weeks of age were used. Each mouse was anesthetized with isoflurane and a small, 1 cm vertical incision was made at the level of the pancreas. The exposed organ was orientated underneath the animal and pressed against a 50 mm glass-bottom dish for imaging on an inverted microscope. Body temperature was maintained using heat pads and heating elements on the objective. The mouse received Hoechst 33342 (1 mg/kg in PBS) to label nuclei, a 150 kDa fluorescein-conjugated dextran (1 mg/kg in PBS) to label vasculature, and 75 μL of 30 µM LUXendin555 via retro-orbital IV injection. Images were collected using a Leica SP8 microscope, equipped with a ×25/0.95 NA objective and Spectra Physics MaiTai DeepSee mulitphoton laser. Excitation was delivered at λ = 850 nm, with signals collected with a HyD detector at λ = 460/50, λ = 525/50, λ = 624/40 nm for Hoechst, FITC, and LUXendin555, respectively. Blood was collected from the tail vein prior to and 30 min after LUXendin555 injection, and glucose was measured using an AlphaTrak2 glucometer. All in vivo imaging experiments were performed with approval and oversight from the Indiana University Institutional Animal Care and Use Committee (IACUC).
Stem cell differentiation and gene expression analyses
WA01/H1 hESCs were differentiated using the protocol published by Nair et al.61. Briefly, dissociated H1 hESCs were plated on six-well plates at a density of 5.5 million cells in 5.5 mL media per well. The plates were incubated at 37 °C and 5% CO2 on an orbital shaker at 100 rpm to induce spheroid formation. After 24 h, six-step differentiation was induced. Differentiation was stopped at day 21 and spheroids labelled with LUXendin645, fixed in 4% formaldehyde and co-stained with insulin and glucagon. To confirm differentiation, a subset of spheroids was paraffin-embedded, sectioned at 5 µm and stained for insulin and NKX6-1. Primary antibodies were guinea pig anti-insulin 1:500 (Dako Cytomation, #A0564), mouse monoclonal anti-glucagon 1:2000 (Sigma-Aldrich, #G2654), and rabbit monoclonal anti-NKX6-1 (D8O4R) 1:400 (Cell Signaling, #54551). Secondary antibodies were donkey anti-guinea pig FITC, donkey anti-mouse FITC, and donkey anti-rabbit Cy3 1:200 (Jackson Immuno Research Laboratories, #706-096-148, #715-096-150, #711-166-152). The spheroids and sections were imaged using a Leica SP8 confocal microscope with a ×20/0.75 IMM objective. Manders’ co-efficient (Coloc 2 plugin for FIJI) was used to quantify the extent of overlap of LUXendin645 signal with the insulin or glucagon channels (M1).
nCounter gene expression assay (Nanostring, WA) was used to assess GLP1R gene expression in hESCs, differentiated β-like cells, and human islets. The values are normalized to six different housekeeping genes (B2M, GAPDH, GUSB, HPRT1, POLR2A, and TBP). Human islets were obtained from Alberta Islet Distribution Program. Sex, age, and BMI of each islet sample were: #1: Male, 53 y.o., 33.7 kg/m2, #2: Female, 17 y.o., 22.7 kg/m2, #3: Male, 18 y.o., 22.9 kg/m2. WA01/H1 hESCs were obtained under MTA from WiCell (Madison WI) and institutional use was approved by the BCCHR/UBC Human Research Ethics Board (Approval # H09-00676).
For FACS analysis, LUXendin-labelled spheroids were collected, incubated with Accumax at 37 °C for 10 min and dissociated into single cells. CMRL with 1% BSA was added, followed by filtering through a 40-mm nylon filter. Cells were centrifuged for 5 min at 200×g, washed with PBS, and resuspended in 500 µL of PBS. LUXendin+ and LUXendin− cells were sorted into TRIzol for further qPCR using a BD FACSAria IIu. RNA was isolated with TRIzol, DNase-treated with Turbo DNAse Free, and reverse transcribed with Superscript III. TaqMan qPCR was performed and data were normalized by TBP. Primers used were: GLP1R (forward [F], 5′-GTGCTATACATCCACTTCAGGG-3′; reverse [R], 5′-GCTCTGGTTATCGCCTCTG-3′; and probe 5-TCCACCTGAACCTGTTTGCATCCT-3′), NKX6-1 (F, 5′-TCGTTTGGCCTATTCGTTGG-3′; R, 5′-TGTCTCCGAGTCCTGCTTC-3′; and probe 5-TGCTTCTTCCTCCACTTGGTCCG-3′), INS (F, 5′-CTAGTGTGCGGGGAACG-3′; R, 5′-CACGCTTCTGCAGGGAC-3′; and probe 5-CGGCGGGTCTTGGGTGTGTA-3′), GCG (F, 5′-GTCCAGATACTTGCTGTAGTCAC-3′; R, 5′-ACGTTCCCTTCAAGACACAG-3′; and probe 5-ATGGCGCTTGTCCTCGTTCATCT-3′), and TBP (F, 5′-GAGAGTTCTGGGATTGTACCG-3′; R, 5′-ATCCTCATGATTACCGCAGC-3′; and probe 5-TGGGATTATATTCGGCGTTTCGGGC-3′).
Measurements were performed on discrete samples unless otherwise stated. All analyses were conducted using GraphPad Prism software. Unpaired or paired Student's t-test was used for pairwise comparisons. Multiple interactions were determined using one-way or two-way ANOVA followed by Bonferonni’s, Dunn’s, or Sidak’s posthoc tests (accounting for degrees of freedom).
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
LUXendins are freely available for academic use. Glp1r(GE)−/−, GLU-YFP, and GLP1RCre animals are subject to a Material Transfer Agreement. The source data underlying Figs. 2a–c, g, k, 3b–f, 4f and h, 5e–g, 6c, 8b and d, and 9c–f and Supplementary Figs. 12, 15, and 16 are provided as a Source Data file. Raw image files are available upon reasonable request.
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We thank Bettina Mathes and Alexandra Teslenko for excellent synthetic support. D.J.H. was supported by a Diabetes UK R.D. Lawrence (12/0004431) Fellowship, a Wellcome Trust Institutional Support Award, MRC Confidence in Concept, MRC (MR/N00275X/1 and MR/S025618/1) Project and Diabetes UK (17/0005681) Project Grants. A.T. and B.J.J. were funded by an MRC Project Grant (MR/R010676/1). G.D. was supported by an MRC CDA Fellowship (MR/P009824/1). A.K.L. was supported by R03 DK115990 and Human Islet Research Network UC4 DK104162 (to A.K.L.; RRID:SCR_014393). Intravital microscopy core services were supported by NIH NIDDK Grant P30 DK097512 to the Indiana University School of Medicine. F.C.L. received operating support from CIHR PJT 156377. Fellowship support was provided by the Juvenile Diabetes Research Foundation (S.S.), and the Michael Smith Foundation for Health Research (S.S.), and the Manpei Suzuki Diabetes Foundation (S.S.). S.T. was supported by grants from the MRC (MR/N02589X/1) and NIH (R01 DK095757). B.H. was supported by the Wellcome Trust (095101, 200837 and 106130). D.C. was funded by the Deutsche Forschungsgemeinschaft (SFB/Transregio 166-Project C1) and a Wellcome Trust Senior Research Fellowship (212313/Z/18/Z). This project has received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme (Starting Grant 715884 to D.J.H.). We thank Prof. Anna Gloyn (University of Oxford) for provision of reagents, Dr. Birgit Koch (MPI, Heidelberg) for helpful discussions on Glp1r(GE)−/− mice and Dr. Jacqueline Naylor (MedImmune) for generation of parental SNAP_GLP1R-INS1GLP1R−/− cells. Lastly, we thank Dr. Jocelyn E. Manning Fox and Prof. Patrick E. MacDonald for provision of human islets via the Alberta Diabetes Institute IsletCore at the University of Alberta in Edmonton with the assistance of the Human Organ Procurement and Exchange (HOPE) program, Trillium Gift of Life Network (TGLN) and other Canadian organ procurement organizations.
The authors declare no competing interests.
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Ast, J., Arvaniti, A., Fine, N.H.F. et al. Super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics. Nat Commun 11, 467 (2020). https://doi.org/10.1038/s41467-020-14309-w