Deletion of Glutamate Dehydrogenase in ß-Cells Abolishes Part of the Insulin Secretory Response Not Required for Glucose Homeostasis
2008; Elsevier BV; Volume: 284; Issue: 2 Linguagem: Inglês
10.1074/jbc.m806295200
ISSN1083-351X
AutoresStefania Carobbio, Francesca Frigerio, Blanca Rubı́, Laurène Vetterli, Maria Bloksgaard, Asllan Gjinovci, Shirin Pournourmohammadi, Pedro L. Herrera, Walter Reith, Susanne Mandrup, Pierre Maechler,
Tópico(s)Sirtuins and Resveratrol in Medicine
ResumoInsulin exocytosis is regulated in pancreatic ß-cells by a cascade of intracellular signals translating glucose levels into corresponding secretory responses. The mitochondrial enzyme glutamate dehydrogenase (GDH) is regarded as a major player in this process, although its abrogation has not been tested yet in animal models. Here, we generated transgenic mice, named ßGlud1–/–, with ß-cell-specific GDH deletion. Our results show that GDH plays an essential role in the full development of the insulin secretory response. In situ pancreatic perfusion revealed that glucose-stimulated insulin secretion was reduced by 37% in ßGlud1–/–. Furthermore, isolated islets with either constitutive or acute adenovirus-mediated knock-out of GDH showed a 49 and 38% reduction in glucose-induced insulin release, respectively. Adenovirus-mediated re-expression of GDH in ßGlud1–/– islets fully restored glucose-induced insulin release. Thus, GDH appears to account for about 40% of glucose-stimulated insulin secretion and to lack redundant mechanisms. In ßGlud1–/– mice, the reduced secretory capacity resulted in lower plasma insulin levels in response to both feeding and glucose load, while body weight gain was preserved. The results demonstrate that GDH is essential for the full development of the secretory response in ß-cells. However, maximal secretory capacity is not required for maintenance of glucose homeostasis in normo-caloric conditions. Insulin exocytosis is regulated in pancreatic ß-cells by a cascade of intracellular signals translating glucose levels into corresponding secretory responses. The mitochondrial enzyme glutamate dehydrogenase (GDH) is regarded as a major player in this process, although its abrogation has not been tested yet in animal models. Here, we generated transgenic mice, named ßGlud1–/–, with ß-cell-specific GDH deletion. Our results show that GDH plays an essential role in the full development of the insulin secretory response. In situ pancreatic perfusion revealed that glucose-stimulated insulin secretion was reduced by 37% in ßGlud1–/–. Furthermore, isolated islets with either constitutive or acute adenovirus-mediated knock-out of GDH showed a 49 and 38% reduction in glucose-induced insulin release, respectively. Adenovirus-mediated re-expression of GDH in ßGlud1–/– islets fully restored glucose-induced insulin release. Thus, GDH appears to account for about 40% of glucose-stimulated insulin secretion and to lack redundant mechanisms. In ßGlud1–/– mice, the reduced secretory capacity resulted in lower plasma insulin levels in response to both feeding and glucose load, while body weight gain was preserved. The results demonstrate that GDH is essential for the full development of the secretory response in ß-cells. However, maximal secretory capacity is not required for maintenance of glucose homeostasis in normo-caloric conditions. Pancreatic ß-cells produce the hormone insulin that is essential for glucose homeostasis. Upon nutrient stimulation, elevation of cytosolic calcium in the ß-cell is the primary and necessary signal for insulin exocytosis (1Henquin J.C. Diabetes. 2000; 49: 1751-1760Crossref PubMed Scopus (946) Google Scholar). Then, increasing the magnitude of the secretory response requires amplification of the calcium signal supported by metabolism-derived additive factors (2Maechler P. Carobbio S. Rubi B. Int. J. Biochem. Cell Biol. 2006; 38: 696-709Crossref PubMed Scopus (106) Google Scholar). The enzyme glutamate dehydrogenase (GDH, 2The abbreviations used are: GDH, glutamate dehydrogenase; BCH, 2-aminobicyclo-[2,2,1]heptane-2-carboxylic acid; ITT, insulin tolerance test. EC 1.4.1.3) has been proposed to participate to the development of the secretory response. GDH is a homohexamer located in the mitochondrial matrix that catalyzes the reversible reaction: α-ketoglutarate + NH3 + NAD(P)H ⇆ glutamate + NAD(P)+; inhibited by GTP and activated by ADP (3Hudson R.C. Daniel R.M. Comp. Biochem. Physiol. B. 1993; 106: 767-792Crossref PubMed Scopus (228) Google Scholar, 4Frigerio F. Casimir M. Carobbio S. Maechler P. Biochim. Biophys. Acta. 2008; 1777: 965-972Crossref PubMed Scopus (70) Google Scholar). Regarding ß-cell, allosteric activation of GDH by l-leucine or its non-metabolized analogue BCH has triggered most of the attention over the last three decades (5Sener A. Malaisse W.J. Nature. 1980; 288: 187-189Crossref PubMed Scopus (283) Google Scholar). To date, the role of GDH in ß-cell function remains unclear and debated. Specifically, GDH might play a role in glucose-induced amplifying pathway through generation of glutamate (6Maechler P. Wollheim C.B. Nature. 1999; 402: 685-689Crossref PubMed Scopus (440) Google Scholar, 7Hoy M. Maechler P. Efanov A.M. Wollheim C.B. Berggren P.O. Gromada J. FEBS Lett. 2002; 531: 199-203Crossref PubMed Scopus (69) Google Scholar). GDH is also an amino acid sensor triggering insulin release upon glutamine stimulation in conditions of GDH allosteric activation (8Sener A. Malaisse-Lagae F. Malaisse W.J. Proc. Natl. Acad. Sci. U. S. A. 1981; 78: 5460-5464Crossref PubMed Scopus (109) Google Scholar, 9Fahien L.A. MacDonald M.J. Kmiotek E.H. Mertz R.J. Fahien C.M. J. Biol. Chem. 1988; 263: 13610-13614Abstract Full Text PDF PubMed Google Scholar, 10Li C. Matter A. Kelly A. Petty T.J. Najafi H. MacMullen C. Daikhin Y. Nissim I. Lazarow A. Kwagh J. Collins H.W. Hsu B.Y. Yudkoff M. Matschinsky F.M. Stanley C.A. J. Biol. Chem. 2006; 281: 15064-15072Abstract Full Text Full Text PDF PubMed Scopus (60) Google Scholar). Recently, the importance of GDH has been further highlighted by studies showing that SIRT4, a mitochondrial ADP-ribosyltransferase, down-regulates GDH activity and thereby modulates insulin secretion (11Haigis M.C. Mostoslavsky R. Haigis K.M. Fahie K. Christodoulou D.C. Murphy A.J. Valenzuela D.M. Yancopoulos G.D. Karow M. Blander G. Wolberger C. Prolla T.A. Weindruch R. Alt F.W. Guarente L. Cell. 2006; 126: 941-954Abstract Full Text Full Text PDF PubMed Scopus (956) Google Scholar, 12Ahuja N. Schwer B. Carobbio S. Waltregny D. North B.J. Castronovo V. Maechler P. Verdin E. J. Biol. Chem. 2007; 282: 33583-33592Abstract Full Text Full Text PDF PubMed Scopus (329) Google Scholar). GDH is encoded by a well-conserved 45-kb gene named GLUD1, which is organized into 13 exons (13Michaelidis T.M. Tzimagiorgis G. Moschonas N.K. Papamatheakis J. Genomics. 1993; 16: 150-160Crossref PubMed Scopus (70) Google Scholar). A decade ago, clinical data and associated genetic studies revealed GDH as a key enzyme for the control of insulin secretion. Indeed, mutations rendering GDH more active are responsible for a hyperinsulinism syndrome (14Stanley C.A. Lieu Y.K. Hsu B.Y. Burlina A.B. Greenberg C.R. Hopwood N.J. Perlman K. Rich B.H. Zammarchi E. Poncz M. N. Engl. J. Med. 1998; 338: 1352-1357Crossref PubMed Scopus (620) Google Scholar). Mutations producing a less active, or even nonactive, GDH enzyme have not been reported, leaving open the question if such mutations would be either lethal or asymptomatic. Despite these numerous reports on GDH and insulin secretion, abrogation of GDH in ß-cells has not been tested in animal models until now. As a consequence, it is not yet established if GDH is in fact required for normal ß-cell function and glucose homeostasis. Here, we generated transgenic mice lacking GDH specifically in ß-cells and questioned the putative requirement of GDH for ß-cell function as well as the consequences of GDH abrogation on glucose homeostasis. Transgene Cloning—By screening a RPCI-22 mouse 129 BAC library (MRC Genome Resource Facility, The Hospital of Sick Children, Toronto, Canada) with a cDNA probe corresponding to human GLUD1 exons 6–8, we obtained two fragments, respectively, of 6 and 10 kb comprising the sequence of Glud1 exon 7. Successively, three DNA fragments of the 129 SvJ Glud1 locus were inserted into the cloning sites of the targeting vector. They comprised 3 kb of the region upstream Glud1 exon 7 (short arm), 0.6 kb of the region containing Glud1 exon 7, and 5.6 kb of the region downstream Glud1 exon 7 (long arm). The three fragments were obtained by PCR using a RPCI-22 129 BAC clone as template and ligated into the KSloxPfrtNeoBS (3′-5′) vector (15Bonnafe E. Touka M. AitLounis A. Baas D. Barras E. Ucla C. Moreau A. Flamant F. Dubruille R. Couble P. Collignon J. Durand B. Reith W. Mol. Cell. Biol. 2004; 24: 4417-4427Crossref PubMed Scopus (159) Google Scholar). The resulting targeting construct contained two loxP sites flanking Glud1 exon 7, one frt-flanked neomycin resistance cassette, and two homology arms. Generation of Glud1lox/lox Mouse—The targeting vector (15 μg) was linearized at the single SacII site and electroporated into three batches of 1.7 × 107 R1 ES cells, a cell line derived from (129/Sv × 129/Sv-CP)F1 3.5-day blastocysts (16Nagy A. Rossant J. Nagy R. Abramow-Newerly W. Roder J.C. Proc. Natl. Acad. Sci. U. S. A. 1993; 90: 8424-8428Crossref PubMed Scopus (1987) Google Scholar). Cells were then cultured in the presence of G418 (0.7 mg/ml) for 6 days. Homologous recombination events were identified by PCR and Southern blot analyses, see supporting information. Correctly targeted ES cell clones were injected into C57BL/6J blastocysts and implanted into recipient females (Karolinska Institutet, Stockholm, Sweden). Resulting chimeric mice (F0) were backcrossed to C57BL/6J mice and germline transmission into F1 was assessed by PCR and Southern blot analyses. The Glud1lox/lox mouse line was obtained following deletion of the frt-flanked neomycin resistance cassette by crossing heterozygous with Flpe deleter mice (17Rodriguez C.I. Buchholz F. Galloway J. Sequerra R. Kasper J. Ayala R. Stewart A.F. Dymecki S.M. Nat. Genet. 2000; 25: 139-140Crossref PubMed Scopus (897) Google Scholar). Generation ßGlud1–/– Mouse—Glud1 floxed animals were crossed with mice expressing the Cre recombinase under a rat insulin promoter (18Herrera P.L. Development. 2000; 127: 2317-2322Crossref PubMed Google Scholar). Heterozygous ßGlud1–/+ were then bred with homozygous Glud1lox/lox to obtain homozygous ßGlud1–/– mice. Mice were maintained on a mixed (C57BL/6J × 129/Sv) genetic background. Mouse breeding and handling was carried out in our local certified animal facility according to procedures that were approved by the Animal Care and Experimentation authorities of the Canton of Geneva. Genotyping and Immunoblotting—Transgenic animals were identified by PCR on genomic DNA extracted from tail biopsies (Genelute Mammalian Genomic DNA kit, Sigma, Buchs, Switzerland). Primers (purchased from Microsynth GmbH, Baglach, Switzerland) used to genotype floxed mice were: 5′-TGTAATGTGTCTGTGTGTCAC and 5′-CTAAGGACCCAGACAGTGG (86-bp fragment). Primers to genotype RIP-Cre mice were: 5′-TAAGGCTAAGTAGAGGTGT and 5′-TCCATGGTGATACAAGGGAC (350-bp fragment). GDH protein was analyzed by immunoblotting as described (19Carobbio S. Ishihara H. Fernandez-Pascual S. Bartley C. Martin-Del-Rio R. Maechler P. Diabetologia. 2004; 47: 266-276Crossref PubMed Scopus (78) Google Scholar) on 13% SDS-PAGE that was run using 10 μg of proteins from pancreatic islet extract or standards of purified bovine GDH (Roche Applied Science, Rotkreuz, Switzerland). Immunohistochemistry—Adult mouse pancreata were harvested in cold phosphate-buffered saline and treated overnight at 4 °C in 4% paraformaldehyde before embedding in paraffin and 5-μm thick tissue sections were mounted on adhesive-coated slides. Pancreata sections were incubated with a diluted primary antibody for 2 h at room temperature, and with an appropriate Cy3-(Jackson ImmunoResearch Laboratories, Inc, WestGrove, PA) or ALEXA-conjugated (Molecular Probes, Inc., Eugene, OR) anti-IgG serum for 1 h. The antibodies and their dilution used in the present analysis were as follows: guinea pig anti-insulin (Dako, Carpinteria, CA, dilution 1/400), rabbit anti-glucagon (Dako, Carpinteria, CA; dilution 1/100). Sections were analyzed on a Zeiss Axiophot microscope equipped with an Axiocam color CCD camera (Carl Zeiss, Feldbach, Switzerland). Islet morphology was analyzed to discriminate between organized versus disorganized islets. As a criterion, islets with more than 10% α-cells present in the core of the islets were considered as disorganized. Pancreatic Islets Isolation and Adenoviral Treatment—Mouse pancreatic islets were isolated by collagenase digestion as described previously (19Carobbio S. Ishihara H. Fernandez-Pascual S. Bartley C. Martin-Del-Rio R. Maechler P. Diabetologia. 2004; 47: 266-276Crossref PubMed Scopus (78) Google Scholar) and cultured free-floating in RPMI 1640 medium before use. For rescue experiments, ectopic expression of hGLUD1 was achieved by transducing islets isolated from ßGlud1–/– with the recombinant adenovirus Ad-GDH over a 90-min period as detailed previously (19Carobbio S. Ishihara H. Fernandez-Pascual S. Bartley C. Martin-Del-Rio R. Maechler P. Diabetologia. 2004; 47: 266-276Crossref PubMed Scopus (78) Google Scholar) and islets were used the next day for secretion assays and control immunoblotting. For acute in vitro GDH knock-out, islets isolated from control and transgenic Glud1lox/lox mice were subjected to adenoviral treatment for 90 min with 0.4 μl/ml of the recombinant adenovirus rAdInsPNCre, thereby enabling expression of nuclear-localized Cre recombinase specifically in ß-cells (20Ishihara H. Maechler P. Gjinovci A. Herrera P.L. Wollheim C.B. Nat. Cell Biol. 2003; 5: 330-335Crossref PubMed Scopus (335) Google Scholar). Islets transduced with rAdInsPNCre were kept in culture for 3 days before insulin secretion assays. Insulin Secretion and Measurements—Prior to the experiments, islets were maintained for 2 h in glucose-free culture medium. For static incubations, islets were then washed and preincubated further in glucose-free Krebs-Ringer bicarbonate HEPES buffer (KRBH, containing in mm: 135 NaCl, 3.6 KCl, 10 HEPES (pH 7.4), 5 NaHCO3, 0.5 NaH2PO4, 0.5 MgCl2, 1.5 CaCl2, 0.1% bovine serum albumin). Then, batches of 10 islets were hand-picked and incubated as described (21Rubi B. del Arco A. Bartley C. Satrustegui J. Maechler P. J. Biol. Chem. 2004; 279: 55659-55666Abstract Full Text Full Text PDF PubMed Scopus (98) Google Scholar) for 30 min at 37 °C at basal (2.8 mm) glucose and stimulated with 22.8 mm glucose or 5 mm glutamine plus 10 mm BCH (2-aminobicyclo-[2,2,1]heptane-2-carboxylic acid). At the end of the assay period, islets were resuspended in acid-EtOH to determine their insulin contents. For islets perifusions (19Carobbio S. Ishihara H. Fernandez-Pascual S. Bartley C. Martin-Del-Rio R. Maechler P. Diabetologia. 2004; 47: 266-276Crossref PubMed Scopus (78) Google Scholar), 10 hand-picked islets were put per chamber of 250 μl volume, thermostatted at 37 °C (Brandel, Gaithersburg, MD). The flux was set at 0.5 ml/min, and fractions were collected every minute after a 20-min washing period at basal 2.8 mm glucose. In situ pancreatic perfusion was performed in anesthetized mice as described (22Maechler P. Gjinovci A. Wollheim C.B. Diabetes. 2002; 51: S99-S102Crossref PubMed Google Scholar) with a 1.5 ml/min perfusion rate. Pancreatic insulin content was determined in mouse pancreata that were first frozen in liquid nitrogen, then homogenized, resuspended in cold acid ethanol, and left at 4 °C for 48 h with sonication after 24 h. Insulin concentration in these different collected samples was measured by radioimmunoassay (Linco Research Inc., St. Charles, MO). A bioluminescent assay kit (Roche Applied Science) was used to measure ATP levels in batches of 10 isolated islets following a 30-min incubation period at 37 °C in the presence of 2.8 and 22.8 mm glucose. The enzymatic activity of GDH in isolated islets was measured as described (19Carobbio S. Ishihara H. Fernandez-Pascual S. Bartley C. Martin-Del-Rio R. Maechler P. Diabetologia. 2004; 47: 266-276Crossref PubMed Scopus (78) Google Scholar) under the oxidative deamination direction as NADH fluorescence excited at 340 nm and measured at 460 nm in a fluorescence plate reader (Fluostar Optima, BMG Labtechnologies, Offenburg, Germany). Glucose Tolerance and Insulin Release Tests—Overnight (15 h) fasted mice were injected intraperitoneally with glucose (3 g/kg body weight). Whole blood was collected from tail vein at times 0, 15, 30, 60, 120 min for glucose level measurements using a glucometer (Glucotrend, Roche Applied Science). Additionally, plasma insulin levels were determined from time 0 and 15-min blood sampling using an ultrasensitive mouse insulin ELISA (Mercodia AB, Uppsala, Sweden). For the insulin tolerance test, overnight fasted mice were injected intraperitoneally with human recombinant insulin (0.75 units/kg body weight, Novo Nordisk Pharma AG, Küsnacht, Switzerland) and glucose levels determined (Glucotrend) in blood collected from the tail vein at the indicated time intervals. Insulin resistance was estimated using the homeostasis model assessment index (HOMA-IR) calculated as follows: fasting glucose (mm) × fasting insulin (milliunits/ml)/22.5 (23Matthews D.R. Hosker J.P. Rudenski A.S. Naylor B.A. Treacher D.F. Turner R.C. Diabetologia. 1985; 28: 412-419Crossref PubMed Scopus (25651) Google Scholar, 24Konrad D. Rudich A. Schoenle E.J. Diabetologia. 2007; 50: 833-839Crossref PubMed Scopus (88) Google Scholar, 25Xia Z. Sniderman A.D. Cianflone K. J. Biol. Chem. 2002; 277: 45874-45879Abstract Full Text Full Text PDF PubMed Scopus (86) Google Scholar). Circulating glucagon and insulin levels from fed and fasted mice were determined on multiplex suspension array system (Bio-Plex, Bio-Rad Laboratories, Reinach, Switzerland) using LincoPlex kits for mouse hormones (Linco Research Inc.). Statistical Analysis—Data are presented as mean ± S.D. Differences between the ßGlud1–/– and the control group were analyzed by two-tailed Student's t test for unpaired data. A p value lower than 0.05 was considered statistically significant. Generation of Transgenic Mice—We generated transgenic mice with ß-cell-specific conditional abrogation of GDH using the loxP-flp-recombinase strategy. The targeting vector carried Glud1 (NCBI Access No. P26443) exon 7, comprising the NADH binding site essential for GDH activity (13Michaelidis T.M. Tzimagiorgis G. Moschonas N.K. Papamatheakis J. Genomics. 1993; 16: 150-160Crossref PubMed Scopus (70) Google Scholar), flanked by two loxP sites (Fig. 1A). We cloned 5′ and 3′ regions flanking exon 7 as 3-kb and 5.6-kb fragments, respectively. The targeting vector also contained a neor-cassette (positive marker) flanked by two Flp/frt sites. The resulting founder mice were crossed to obtain F1 mice carrying a mutant Glud1 genomic locus containing the exon 7 flanked by loxP sites and the neor-cassette (Glud1-neor-lox). Next, excision of the neor-cassette by crossing F1 with Flp deleter mice gave rise to mice carrying intact Glud1 exon 7 flanked by loxP sites only (Glud1lox/lox). Constitutive ß-Cell-specific GDH Knock-out—Glud1lox/lox mice were crossed with mice expressing the Cre recombinase under the control of an insulin promoter (RIP), generating mice with ß-cell-specific GDH knock-out (ßGlud1–/–). Allele analysis in different tissues revealed that the 278-bp knock-out allele was detected in pancreas and not in other tissues (Fig. 1B). In particular, we did not detect homologous recombination in the brain following a cross with the RIP-Cre transgenic line used in our study (18Herrera P.L. Development. 2000; 127: 2317-2322Crossref PubMed Google Scholar), unlike what was reported using another RIP-Cre mouse line (26Ristow M. Mulder H. Pomplun D. Schulz T.J. Muller-Schmehl K. Krause A. Fex M. Puccio H. Muller J. Isken F. Spranger J. Muller-Wieland D. Magnuson M.A. Mohlig M. Koenig M. Pfeiffer A.F. J. Clin. Investig. 2003; 112: 527-534Crossref PubMed Scopus (126) Google Scholar). At the protein level, immunoblotting following SDS-PAGE on isolated islets (Fig. 1C) showed efficient targeted GDH knock-out, although the lowest unspecific band was unchanged. Some residual expression could be contributed by the non-ß-cells. GDH enzymatic activity was reduced by 60% (p < 0.05) in islets isolated from ßGlud1–/– mice compared with controls (Fig. 1D). The remaining activity corresponds approximately to the proportion of non-ß-cells composing the islets. As control mice, we used Glud1lox/lox animals obtained from the same litters as ßGlud1–/– mice to optimize standardization of the genetic background between the two groups. Phenotype and Pancreatic Secretory Responses of ß-Cell GDH Knockout Mice—Surprisingly, ß-cell-specific GDH knock-out mice were not diabetic, no glucosuria was detected, and the growth and organ weights were normal compared with control mice (Fig. 2, A and B). Based on the unexpected normal development of the animals, despite deletion of GDH in ß-cells, we measured insulin secretion in the in situ pancreatic perfusion preparation (Fig. 2C), a model that integrates paracrine and neuronal effectors of the ß-cell. This physiological model demonstrated clear reduction of the secretory response evoked by 22.8 mm glucose in ßGlud1–/– mice versus controls; both during the first (–48%, p < 0.01) and the second (–37%, p < 0.05) phases (Fig. 2D). The data show that abrogation of the mitochondrial enzyme GDH in ß-cells limits both the phase of secretion commonly associated with the amplifying pathway (second phase) as well as the triggering pathway (first phase). In good agreement with basal versus stimulated insulin secretion measured in the perfused pancreas (Fig. 2C), circulating insulin concentrations were not significantly different in the fasted state, but the increase associated with the fed state was reduced by 55% (p < 0.05) in ßGlud1–/– mice (Table 1).TABLE 1Plasma analysis in control and ßGlud1–/– miceControlaMice of 5-7 months of age.βGlud1-/-aMice of 5-7 months of age.Glucagon (pmol/l) Fast26.3 ± 10.127.8 ± 9.9Insulin (pmol/l) Fed143.3 ± 27.4bp < 0.05 versus fasted mice of corresponding genotype; n = 4-7.65.2 ± 10.5bp < 0.05 versus fasted mice of corresponding genotype; n = 4-7.,cp < 0.05 versus control. Fast29.3 ± 6.224.7 ± 5.0a Mice of 5-7 months of age.b p < 0.05 versus fasted mice of corresponding genotype; n = 4-7.c p < 0.05 versus control. Open table in a new tab Islet Phenotype of Constitutive ß-Cell-specific GDH Knockout—Insulin secretory defects have been associated with modified islet organization in general and infiltration of α-cells within the core of the islet in particular (27Gorogawa S. Fujitani Y. Kaneto H. Hazama Y. Watada H. Miyamoto Y. Takeda K. Akira S. Magnuson M.A. Yamasaki Y. Kajimoto Y. Hori M. Biochem. Biophys. Res. Commun. 2004; 319: 1159-1170Crossref PubMed Scopus (67) Google Scholar). Accordingly, we analyzed islet cell distribution by immunostaining on pancreatic sections (Fig. 3, A and B). Most of the control islets (70%) exhibited the expected α- and ß-cell distribution, i.e. insulin ß-cells in the core of the islet and glucagon α-cells forming its periphery. In ßGlud1–/– animals, the percentage of disorganized islets was as high as 67%, revealing α-cells mixed with ß-cells in the core of the islet (Fig. 3C). It should be noted that RIP-Cre transgene does not by itself promote changes in islet morphology (18Herrera P.L. Development. 2000; 127: 2317-2322Crossref PubMed Google Scholar). Pancreatic insulin contents were not affected in ßGlud1–/– animals compared with controls (124.1 ± 24.9 and 125.7 ± 9.1 ng/g pancreas of wet mass, respectively), and islets were similarly distributed in the whole pancreas. Functions of the α-cells were apparently not affected by GDH knockout in ß-cells, as revealed by similar plasma glucagon levels between the two groups under fasting (stimulatory) conditions (Table 1). A primary function of mitochondrial metabolism is to produce ATP that is necessary in ß-cells for triggering (first phase) and maintaining (second phase) the secretory response. At this point, it could be hypothesized that ß-cell GDH knock-out would impair the primary function of mitochondrial activation that is to generate ATP and thereby inhibit glucose-stimulated insulin secretion. ATP levels were slightly lower under basal glucose concentrations (2.8 mm) in islets of ßGlud1–/– mice. However, upon glucose stimulation (22.8 mm), islet ATP concentrations increased similarly between the two groups (Fig. 3D). GDH knock-out did not affect glucose-induced ATP generation. Interestingly, data suggest that maintenance of basal housekeeping ATP levels under low glucose conditions might be normally contributed by GDH-dependent metabolism. Secretory Responses of Isolated Islets with Constitutive ß-Cell GDH Knock-out—Kinetics of secretory responses were analyzed in perifusion experiments on islets isolated from ßGlud1–/– compared with controls. Basal insulin release measured at 2.8 mm glucose was not affected by the absence of GDH. When stimulated with 22.8 mm glucose, control and ßGlud1–/– islets exhibited glucose-stimulated insulin release (Fig. 4A). However, constitutive abrogation of GDH in ß-cells resulted in markedly reduced secretory responses, both during first phase (–68%, p < 0.01) and second sustained phase (–49%, p < 0.05). These data demonstrate that GDH is essential for the full development of the secretory response. To test if the reduced glucose-evoked insulin release observed in ßGlud1–/– islets was a direct consequence of the absence of GDH, we reintroduced GDH by means of adenoviral transduction (Fig. 4B). Insulin secretion stimulated with 22.8 mm glucose was increased 5.7-fold in control islets (p < 0.01) and only 2.0-fold in ßGlud1–/– islets (p < 0.05). Following ectopic re-expression of GDH in ßGlud1–/– islets, amplitude of the secretory response was rescued to similar levels compared with controls (4.9-fold, p < 0.05). As expected from a previous study (19Carobbio S. Ishihara H. Fernandez-Pascual S. Bartley C. Martin-Del-Rio R. Maechler P. Diabetologia. 2004; 47: 266-276Crossref PubMed Scopus (78) Google Scholar), overexpression of GDH did not significantly modify glucose-induced insulin release compared with control islets (Fig. 4B). Secretory Responses of Isolated Islets with Acute in Vitro ß-Cell GDH Knock-out—To investigate whether abrogation of GDH could induce compensatory pathways in the ß-cells, we also performed acute in vitro knock-out in islets of transgenic floxed mice. Islets isolated from Glud1lox/lox mice were transduced with a recombinant adenovirus (rAdInsPNCre) expressing the Cre recombinase specifically in ß-cells (20Ishihara H. Maechler P. Gjinovci A. Herrera P.L. Wollheim C.B. Nat. Cell Biol. 2003; 5: 330-335Crossref PubMed Scopus (335) Google Scholar). PCR analysis demonstrated in vitro homologous recombination resulting in the knock-out of GDH in ß-cells of islets isolated from transgenic Glud1lox/lox mice but not in islets from wild-type animals (Fig. 5A). In control islets, stimulatory glucose concentration (22.8 mm) induced a 4.9-fold (p < 0.05) increase in insulin secretion compared with basal release (Fig. 5B). The secretory response evoked by 22.8 mm glucose was reduced by 38% (p < 0.02) in islets with acute abrogation of GDH. These results are in accordance with knockdown of GDH by antisense approach in insulinoma INS-1E cells (2Maechler P. Carobbio S. Rubi B. Int. J. Biochem. Cell Biol. 2006; 38: 696-709Crossref PubMed Scopus (106) Google Scholar). Insulin release was also stimulated by a mixture commonly used to specifically induce GDH-dependent insulin secretion (5Sener A. Malaisse W.J. Nature. 1980; 288: 187-189Crossref PubMed Scopus (283) Google Scholar), i.e. 5 mm glutamine plus the l-leucine analogue BCH (10 mm) serving as an allosteric activator of GDH. The resulting amino acid dependent secretory response had a magnitude of 3.2-fold (p < 0.005) in control islets, that was inhibited by 47% (p < 0.03) in knock-out islets. As both acute (Fig. 5) and constitutive (Fig. 4) knock-outs exhibited similar secretion impairments, we can conclude that redundant mechanisms do not exist at the cellular level. Glucose Homeostasis in ß-Cell GDH Knock-out—Parameters related to the control of glucose homeostasis were measured at 2, 5, and 12 months of age. After a 15-h fasting period, glycemia were similar to controls in ßGlud1–/– mice of all tested ages. Intraperitoneal glucose tolerance tests (ipGTT) were performed on 2- and 5-month-old mice. Despite the severe reduction in glucose-stimulated insulin secretion in ßGlud1–/– animals (Fig. 2, C and D), blood glucose excursions were similar to controls (Fig. 6, A and E). At 2 months of age, plasma insulin levels measured 15 min following intraperitoneal glucose injection were reduced by 38% (p < 0.001) in ßGlud1–/– mice (Fig. 6C). When performing an insulin tolerance test (ITT) in 2-month-old mice, blood glucose lowering was faster in ßGlud1–/– mice compared with controls (Fig. 6B). Low circulating insulin concentrations associated with accelerated glucose clearance suggested higher sensitivity of peripheral tissues. However, ITT performed in 5-month-old mice did not show significant differences between knock-outs and controls (Fig. 6F). To further investigate insulin sensitivity in 2- and 5-month-old mice, we calculated the HOMA index as a surrogate of euglycemic clamp test (28Ye F. Tao R. Cong W. Tian J. Liu Q. J. Biochem. Biophys. Methods. 2008; 70: 978-984Crossref PubMed Scopus (17) Google Scholar). As expected, insulin resistance increased with age in both groups (Fig. 6D) and ßGlud1–/– mice exhibited similar HOMA-IR compared with controls. It should be noticed that RIP-Cre transgenic mice used in the present study (18Herrera P.L. Development. 2000; 127: 2317-2322Crossref PubMed Google Scholar) exhibit normal glucose homeostasis (see Fig. 6, A and E and Refs. 29Pro
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