γ-Aminobutyric acid (GABA) has been shown to inhibit apoptosis of rodent β-cells in vitro. In this study, we show that activation of GABAA receptors (GABAA-Rs) or GABAB-Rs significantly inhibits oxidative stress–related β-cell apoptosis and preserves pancreatic β-cells in streptozotocin-rendered hyperglycemic mice. Moreover, treatment with GABA, or a GABAA-R– or GABAB-R–specific agonist, inhibited human β-cell apoptosis following islet transplantation into NOD/scid mice. Accordingly, activation of GABAA-Rs and/or GABAB-Rs may be a useful adjunct therapy for human islet transplantation. GABA-R agonists also promoted β-cell replication in hyperglycemic mice. While a number of agents can promote rodent β-cell replication, most fail to provide similar activities with human β-cells. In this study, we show that GABA administration promotes β-cell replication and functional recovery in human islets following implantation into NOD/scid mice. Human β-cell replication was induced by both GABAA-R and GABAB-R activation. Hence, GABA regulates both the survival and replication of human β-cells. These actions, together with the anti-inflammatory properties of GABA, suggest that modulation of peripheral GABA-Rs may represent a promising new therapeutic strategy for improving β-cell survival following human islet transplantation and increasing β-cells in patients with diabetes.
A central focus of research in the type 1 diabetes (T1D) field is to develop ways to safely improve β-cell survival and function and promote their replication. The addition of γ-aminobutyric acid (GABA) or the GABAB receptor (GABAB-R)–specific agonist baclofen to culture media has been shown to inhibit β-cell apoptosis in cultured rodent cell lines and islets (1,2). It remains to be determined whether GABA treatment can inhibit mouse β-cell apoptosis in vivo or, more importantly, whether it can protect human β-cells from stress-induced apoptosis. If GABA can inhibit human β-cell apoptosis, elucidating whether this effect is mediated through the G-protein–coupled GABAB-Rs, and/or the chloride channel GABAA-Rs will enable more specific drug targeting.
GABA can promote neurogenesis and neuronal proliferation and is a neuronal survival factor (3–8). GABA has also been shown to promote rodent β-cell replication (1,2). Those studies, however, differentially pointed to GABAA-Rs or GABAB-Rs as modulators of GABA’s effects, making it important to clarify whether one or both types of GABA receptors modulate rodent β-cell replication. While a number of mitogens and growth factors can promote rodent β-cell replication, most fail to promote human β-cell replication (reviewed in refs. 9,10). Therefore, a key question is whether GABA can promote human β-cell replication. Even a small amount of GABA-induced human β-cell replication may be clinically useful by lowering insulin requirements and reducing the risk for long-term complications in T1D patients (11).
RESEARCH DESIGN AND METHODS
Analysis of mouse and human β-cell apoptosis.
All experiments were approved by University of California Los Angeles’ Animal Research Committee. Male C57BL/6 mice (10 weeks old) received streptozotocin (STZ) (Sigma-Aldrich; 80 mg/kg/day for 2 days) intraperitoneally. Mildly hyperglycemic mice (blood glucose levels of 250–300 mg/dL) were given plain water or water containing GABA (2 or 6 mg/mL; Sigma-Aldrich), the GABAB-R–specific agonist baclofen (0.25 mg/mL; Sigma-Aldrich), or the GABAA-R–specific agonist muscimol (4.5 mg/mL; Bachem Bioscience). Forty-eight hours later, their pancreatic sections (4 μm) were subjected to TUNEL using a POD cell death detection kit (Boehringer Ingelheim). After development with diaminobenzidine, the sections were stained with guinea pig anti-insulin (Zymed Laboratories) at 4°C overnight and alkaline phosphatase–conjugated anti-guinea pig IgG (Piece) and visualized using the Valcan Fact Red Chromogen Kit 2 (Biocare Medical). The percentages of insulin+ β-cells or TUNEL+ apoptotic islet cells in total islet cells of at least 25 islets from individual mice were calculated in a blinded manner.
To study apoptosis in human islets, freshly isolated human islets from the Integrated Islet Distribution Program were implanted under the kidney capsule (2,000 islets/mouse) of STZ-induced diabetic NOD/scid mice. The recipients were treated as described above. Their kidney sections (4 μm) were stained by TUNEL using a click-iT TUNEL Alexa Fluor 488 (Invitrogen) and costained with guinea pig anti-insulin. Subsequently, the sections were incubated with phycoerythrin (PE)–anti-guinea pig IgG and counterstained with DAPI. At least 2,500 human islet cells in 10 fields (original magnification ×400) from individual grafts were counted. The percentages of insulin+ β-cells or TUNEL+ apoptotic β-cells in total islet cells within the grafts of individual recipients were determined in a blinded manner.
Analysis of mouse β-cell replication.
C57BL/6 mice were STZ-rendered mildly hyperglycemic and randomly provided with water containing: 1) BrdU (0.8 mg/mL; Sigma-Aldrich), 2) BrdU plus GABA (2 or 6 mg/mL), or 3) BrdU plus baclofen (0.25 mg/mL) for 14 days. Other mice received a 14-day micro-osmotic pump (Alzet) subcutaneously containing 2 mg muscimol in 100 μL of PBS or vehicle alone and water containing BrdU. At the end of treatment, their pancreatic sections (5 μm) were stained with guinea pig anti-insulin and biotinylated anti-BrdU (AbD Serotec) followed by fluorescein isothiocyanate–anti-guinea pig IgG and PE-streptavidin and counterstaining with 4′,6-diamidino-2-phenylindole (DAPI). The percentages of BrdU+insulin+ β-cells in DAPI+ islet cells of 25 islets from individual mice were determined in a blinded manner.
Analysis of human β-cell replication.
Mildly hyperglycemic NOD/scid mice were implanted with adult human islets (2,000 islets/mouse) under the kidney capsule. The mice were treated for 14 days, as described above. At the end of treatment, the kidney tissue sections (5 μm) were subjected to immunofluorescent analysis of BrdU+insulin+ human β-cells, as described above. In another set of experiments, kidney tissue sections were subjected to immunofluorescent analysis of BrdU+insulin+ and Ki67+insulin+ human β-cells using PE–anti-human Ki67 (eBioscience). The percentages of BrdU+insulin+ or Ki67+insulin+ β-cells in 2,500 islet cells of 10 fields (original magnification ×400) of each islet graft were determined in a blinded manner.
Data are expressed as the mean ± SEM of individual groups (N = 4–9/group) from two separate experiments. The difference between groups was determined by Student t test. A P value of <0.05 was considered statistically significant.
We treated C57BL/6 mice with STZ to induce β-cell oxidative stress and mild hyperglycemia and then randomized them into groups that received plain water, water containing GABA (2 or 6 mg/mL), the GABAB-R–specific agonist baclofen, or the GABAA-R–specific agonist muscimol for 48 h. The percentages of apoptotic islet cells and insulin+ β-cells in individual mice were characterized by TUNEL and immunohistochemistry assays (Fig. 1A and 2). The frequency of apoptotic islet cells in mice treated with GABA at 2 mg/mL was significantly reduced compared with that in control mice (Fig. 2A). The percentage of apoptotic islet cells in mice treated with GABA at 6 mg/mL was even lower (Fig. 2A). Thus, GABA treatment inhibited oxidative stress–related β-cell apoptosis, and its affects tended to be dose-dependent. Similarly, treatment with baclofen or muscimol decreased the frequency of apoptotic islet cells (Fig. 2A). Additionally, the percentages of insulin+ β-cells in the mice treated with GABA, baclofen, or muscimol were significantly higher than that in the control mice (Fig. 2B). Thus, activation of either GABAA-Rs or GABAB-Rs preserved β-cells from STZ-induced apoptosis.
We next examined the ability of GABA administration to limit β-cell apoptosis after human islet implantation. Transplanted islets undergo immediate hypoxic stress due to lack of vascularization, and a large percentage of β-cell mass is lost due to apoptosis within the first 3 days after implantation (12–14). Hyperglycemic NOD/scid mice received human islets under their kidney capsule and plain water or water containing GABA (6 mg/mL), baclofen, or muscimol. Two days later, their kidney sections were stained by TUNEL and anti-insulin antibodies (Fig. 1B). In comparison with the control group, there were significantly reduced percentages of apoptotic cells and increased frequencies of insulin+ β-cells in human islets that were implanted into mice that were treated with GABA, baclofen, or muscimol (Fig. 2C and D). Thus, activation of either GABAA-R or GABAB-R limits β-cell apoptosis in transplanted human islets. Accordingly, the inclusion of GABA in the treatment regimen following clinical human islet transplantation may reduce the number of islets required to achieve insulin independence.
To assess whether oral GABA promotes mouse β-cell replication in vivo, we STZ-rendered C57BL/6 mice mildly hyperglycemic (∼250–300 mg/dL) and provided them with water containing BrdU with, or without, GABA (2 or 6 mg/mL) for 14 days. Since: 1) low levels of β-cell replication would be difficult to detect as a change in β-cell mass and 2) GABA treatment can promote functional recovery of degranulated β-cells, leading to an increase in insulin+ islet cells and an apparent increase in β-cell mass, we first assessed β-cell replication using anti-insulin and anti-BrdU staining (Fig. 1C). While BrdU+insulin+ β-cells accounted for ∼1% of the islet cells in control mice, newly replicated β-cells reached ∼2.2 and 3.1% of the islets cells in mice that had been treated with 2 and 6 mg/mL of GABA, respectively (Fig. 3A). Since anti-BrdU staining can reflect DNA repair within damaged β-cells, we examined the frequency of BrdU+insulin+ cells that had a punctated BrdU+ staining pattern. There was no significant difference in the frequency of punctated BrdU+ islet cells among these groups of mice (data not shown), indicating that DNA repair in β-cells was similar in all groups. Additionally, we observed that the percentages of insulin+ cells in pancreatic islets significantly increased in both GABA-treated groups, relative to that in the control mice (Fig. 3B). Thus, oral GABA treatment promoted β-cell replication and functional recovery in hyperglycemic mice.
To assess whether GABAA-R and/or GABAB-R activation mediated GABA’s effect on β-cell replication, in another set of experiments, we treated hyperglycemic C57BL/6 mice with baclofen or muscimol together with BrdU for 14 days. We observed that treatment with either muscimol or baclofen elevated the percentages of BrdU+insulin+ β-cells in the pancreatic islets by more than twofold, as compared with that in the control group (Fig. 3C). Thus, activation of either GABAA-Rs or GABAB-Rs promotes mouse β-cell replication. We also observed a greater number of insulin+ cells in pancreatic islets from muscimol- or baclofen-treated mice, relative to that in the control mice (Fig. 3D). Collectively, our data indicate that GABA, through GABAA-Rs and GABAB-Rs, enhanced β-cell replication and functional recovery in hyperglycemic mice.
We next examined whether oral GABA promotes human β-cell replication in mice following islet transplantation. Adult human islets were implanted under the kidney capsule of hyperglycemic NOD/scid mice. These mice were randomized and provided with water containing BrdU with, or without, GABA or baclofen for 14 days. Other groups of mice received PBS or PBS plus muscimol via an osmotic mini-pump for 14 days, along with water containing BrdU. At the end of treatment, kidneys containing the islet grafts were removed, and the percentages of BrdU+insulin+ β-cells in total islet cells within the islet grafts of individual recipients were determined by immunofluorescent assays (Fig. 1D). We observed that while ∼0.8% of human islet cells were BrdU+insulin+ in the control group, ∼2% of islet cells were BrdU+insulin+ in mice that had been treated with GABA, baclofen, or muscimol (Fig. 4A). Additionally, we observed that GABA, baclofen, and muscimol treatment significantly increased the percentages of total insulin+ cells within the islet grafts, as compared with that in the control grafts (Fig. 4B). In an additional set of human islet transplantation studies, we again observed that GABA treatment increased the frequency of BrdU+insulin+ β-cells (data not shown), as well as Ki67+insulin+ β-cells, compared with the control group (0.89 vs. 0.4%; P < 0.02; [Figs. 1E and 4C]). Thus, both anti-BrdU and anti-Ki67 staining demonstrate that GABA treatment enhanced human β-cell replication. Conceivably, GABA-R promoted β-cell replication may reduce exogenous insulin requirements and limit the development of hyperglycemia-related complications in T1D patients.
In summary, we observed that activation of GABAA-R or GABAB-R inhibited oxidative stress–related β-cell apoptosis and preserved pancreatic β-cells in hyperglycemic mice. Similarly, treatment with either a GABAA-R– or GABAB-R–specific agonist inhibited human islet cell apoptosis in mice following islet transplantation. Furthermore, treatment with either a GABAA-R– or GABAB-R–specific agonist promoted mouse and human β-cell replication in mice. Hence, GABA acts as a growth factor that regulates the survival and replication of islet β-cells.
GABA can inhibit autoreactive Th1 cell responses directly ex vivo (15–17), increase regulatory T cells (2,18), inhibit antigen-presenting cell function (2,19), and inhibit inflammation in mouse models of T1D (2,16,20), rheumatoid arthritis (17), multiple sclerosis (19), and type 2 diabetes (18). Twenty-six weeks of GABA treatment did not significantly alter the numbers or percentages of splenic CD4+, CD8+, T, and B lymphocytes (16), nor did long-term GABA treatment desensitize T cells to GABA-mediated inhibition (16,17). Several studies have suggested that local inflammation helps promote β-cell replication (21 and references therein). Accordingly, although inflammation should be very limited in the C57Bl/6 and NOD/scid mouse models that we have studied, GABA’s anti-inflammatory activity may have partially counteracted its pro–β-cell replication activity.
GABA’s anti-inflammatory properties, together with its ability to promote β-cell replication and functional recovery, suggest that modulation of peripheral GABA-Rs may be a promising strategy for preserving and increasing islet β-cells. GABA has little capacity to pass through the blood–brain barrier and is safe for human consumption (22–25). Therefore, our findings may provide a basis for the design of new therapies for patients with type I and II diabetes.
See accompanying commentary, p. 3674.
This work was supported by grants from JDRF (40-2009-710 and 17-2012-30) and the National Institutes of Health (DK-092480 to D.L.K.). J.T. and D.L.K. are inventors of GABA-related patents. D.L.K. serves on the Scientific Advisory Board of Diamyd Medical. No other potential conflicts of interest relevant to this article were reported.
J.T. conceived, designed, and performed the experiments; analyzed the data; and wrote the manuscript. H.D. performed the experiments and analyzed the data. Z.C., A.G., Y.J., and M.A.A. performed the experiments. D.L.K. conceived and designed the experiments and wrote the manuscript. J.T. and D.L.K. are the guarantors of this work and, as such, had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
The authors regret that space limitations preclude referencing many previous studies that provided important contributions to the field. The authors thank Peter Butler for comments on the manuscript and the Integrated Islet Distribution Program for providing isolated human islets.