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1.
Diabetologia ; 60(10): 1999-2010, 2017 10.
Article in English | MEDLINE | ID: mdl-28721437

ABSTRACT

AIMS/HYPOTHESIS: Insufficient insulin secretion from pancreatic beta cells, which is associated with a decrease in beta cell mass, is a characteristic of type 2 diabetes. Extracellular signal-related kinase 1 and 2 (ERK1/2) inhibition in beta cells has been reported to affect insulin secretion, gene transcription and survival, although whether ERK1 and ERK2 play distinct roles is unknown. The aim of this study was to assess the individual roles of ERK1 and ERK2 in beta cells using ERK1 (also known as Mapk3)-knockout mice (Erk1 -/- mice) and pharmacological approaches. METHODS: NAD(P)H, free cytosolic Ca2+ concentration and insulin secretion were determined in islets. ERK1 and ERK2 subplasmalemmal translocation and activity was monitored using total internal reflection fluorescence microscopy. ERK1/2, mitogen and stress-activated kinase1 (MSK1) and cAMP-responsive element-binding protein (CREB) activation were evaluated by western blot and/or immunocytochemistry. The islet mass was determined from pancreatic sections. RESULTS: Glucose induced rapid subplasmalemmal recruitment of ERK1 and ERK2. When both ERK1 and ERK2 were inhibited simultaneously, the rapid transient peak of the first phase of glucose-induced insulin secretion was reduced by 40% (p < 0.01), although ERK1 did not appear to be involved in this process. By contrast, ERK1 was required for glucose-induced full activation of several targets involved in beta cell survival; MSK1 and CREB were less active in Erk1 -/- mouse beta cells (p < 0.01) compared with Erk1 +/+ mouse beta cells, and their phosphorylation could only be restored when ERK1 was re-expressed and not when ERK2 was overexpressed. Finally, the islet mass of Erk1 -/- mice was slightly increased in young animals (4-month-old mice) vs Erk1 +/+ mice (section occupied by islets [mean ± SEM]: 0.74% ± 0.03% vs 0.62% ± 0.04%; p < 0.05), while older mice (10 months old) were less prone to age-associated pancreatic peri-insulitis (infiltrated islets [mean ± SEM]: 7.51% ± 1.34% vs 2.03% ± 0.51%; p < 0.001). CONCLUSIONS/INTERPRETATION: ERK1 and ERK2 play specific roles in beta cells. ERK2 cannot always compensate for the lack of ERK1 but the absence of a clear-cut phenotype in Erk1 -/- mice shows that ERK1 is dispensable in normal conditions.


Subject(s)
Cyclic AMP Response Element-Binding Protein/metabolism , Glucose/pharmacology , Insulin-Secreting Cells/metabolism , Mitogen-Activated Protein Kinase 3/metabolism , Ribosomal Protein S6 Kinases, 90-kDa/metabolism , Animals , Calcium/metabolism , Cell Line , Cell Survival/drug effects , Cyclic AMP Response Element-Binding Protein/genetics , Insulin/metabolism , Insulin-Secreting Cells/drug effects , Islets of Langerhans/drug effects , Islets of Langerhans/metabolism , Mice , Mice, Knockout , Mitogen-Activated Protein Kinase 1/genetics , Mitogen-Activated Protein Kinase 1/metabolism , Mitogen-Activated Protein Kinase 3/genetics , Phosphorylation/drug effects , Ribosomal Protein S6 Kinases, 90-kDa/genetics
2.
EMBO Mol Med ; 7(6): 802-18, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25828351

ABSTRACT

The metabolic syndrome covers metabolic abnormalities including obesity and type 2 diabetes (T2D). T2D is characterized by insulin resistance resulting from both environmental and genetic factors. A genome-wide association study (GWAS) published in 2010 identified TP53INP1 as a new T2D susceptibility locus, but a pathological mechanism was not identified. In this work, we show that mice lacking TP53INP1 are prone to redox-driven obesity and insulin resistance. Furthermore, we demonstrate that the reactive oxygen species increase in TP53INP1-deficient cells results from accumulation of defective mitochondria associated with impaired PINK/PARKIN mitophagy. This chronic oxidative stress also favors accumulation of lipid droplets. Taken together, our data provide evidence that the GWAS-identified TP53INP1 gene prevents metabolic syndrome, through a mechanism involving prevention of oxidative stress by mitochondrial homeostasis regulation. In conclusion, this study highlights TP53INP1 as a molecular regulator of redox-driven metabolic syndrome and provides a new preclinical mouse model for metabolic syndrome clinical research.


Subject(s)
Metabolic Syndrome/physiopathology , Mitophagy , Nuclear Proteins/metabolism , Animals , Disease Models, Animal , Insulin Resistance , Mice , Nuclear Proteins/deficiency , Obesity , Oxidation-Reduction , Oxidative Stress , Reactive Oxygen Species/analysis
3.
Diabetologia ; 56(11): 2477-86, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23900510

ABSTRACT

AIMS/HYPOTHESIS: The stress-activated nuclear protein transcription regulator 1 (NUPR1) is induced in response to glucose and TNF-α, both of which are elevated in type 2 diabetes, and Nupr1 has been implicated in cell proliferation and apoptosis cascades. We used Nupr1(-/-) mice to study the role of Nupr1 in glucose homeostasis under normal conditions and following maintenance on a high-fat diet (HFD). METHODS: Glucose homeostasis in vivo was determined by measuring glucose tolerance, insulin sensitivity and insulin secretion. Islet number, morphology and beta cell area were assessed by immunofluorescence and morphometric analysis, and islet cell proliferation was quantified by analysis of BrdU incorporation. Islet gene expression was measured by gene arrays and quantitative RT-PCR, and gene promoter activities were monitored by measuring luciferase activity. RESULTS: Nupr1(-/-) mice had increased beta cell mass as a consequence of enhanced islet cell proliferation. Nupr1-dependent suppression of beta cell Ccna2 and Tcf19 promoter activities was identified as a mechanism through which Nupr1 may regulate beta cell cycle progression. Nupr1(-/-) mice maintained on a normal diet were mildly insulin resistant, but were normoglycaemic with normal glucose tolerance because of compensatory increases in basal and glucose-induced insulin secretion. Nupr1 deletion was protective against HFD-induced obesity, insulin resistance and glucose intolerance. CONCLUSIONS/INTERPRETATION: Inhibition of NUPR1 expression or activity has the potential to protect against the metabolic defects associated with obesity and type 2 diabetes.


Subject(s)
DNA-Binding Proteins/metabolism , Glucose Intolerance/metabolism , Insulin-Secreting Cells/metabolism , Neoplasm Proteins/metabolism , Animals , Blotting, Western , DNA-Binding Proteins/genetics , Female , Glucose Intolerance/genetics , Humans , Immunohistochemistry , Insulin-Secreting Cells/cytology , Male , Mice , Mice, Knockout , Neoplasm Proteins/genetics
4.
PLoS One ; 7(9): e45711, 2012.
Article in English | MEDLINE | ID: mdl-23049845

ABSTRACT

Progressive reduction in ß-cell mass is responsible for the development of type 2 diabetes mellitus, and alteration in insulin receptor substrate 2 (IRS-2) abundance plays a critical role in this process. IRS-2 expression is stimulated by the transcription factor cAMP response element-binding protein (CREB) and we recently demonstrated that Ca(2+)/calmodulin dependent kinase 4 (CaMK4) is upstream of CREB activation in ß-cells. This study investigated whether CaMK4 is also a potential target to increase ß-cell mass through CREB-mediated IRS-2 expression, by quantifying mouse MIN6 ß-cell proliferation and apoptosis following IRS-2 knockdown, CaMKs inhibition and alterations in CaMK4 and CREB expression. Expression of constitutively active CaMK4 (ΔCaMK4) and CREB (CREB(DIEDLM)) significantly stimulated ß-cell proliferation and survival. In contrast, expression of their corresponding dominant negative forms (Δ(K75E)CaMK4 and CREB(M1)) and silencing of IRS-2 increased apoptosis and reduced ß-cell division. Moreover, CREB(DIEDLM) and CREB(M1) expression completely abolished the effects of Δ(K75E)CaMK4 and of ΔCaMK4, respectively. Our results indicate that CaMK4 regulates ß-cell proliferation and apoptosis in a CREB-dependent manner and that CaMK4-induced IRS-2 expression is important in these processes.


Subject(s)
Calcium-Calmodulin-Dependent Protein Kinase Type 4/metabolism , Cyclic AMP Response Element-Binding Protein/metabolism , Gene Expression Regulation , Insulin Receptor Substrate Proteins/metabolism , Insulin-Secreting Cells/metabolism , Animals , Apoptosis , Cell Proliferation , Cell Survival , Diabetes Mellitus, Type 2/pathology , Glucose/metabolism , Humans , Insulin-Secreting Cells/pathology , Mice , Models, Biological
5.
Methods Mol Biol ; 560: 73-86, 2009.
Article in English | MEDLINE | ID: mdl-19504245

ABSTRACT

Studies of gene expression by different islet endocrine cell populations can provide useful information about signal transduction cascades regulating alpha-, beta- and delta-cell function. Experiments on expression of beta-cell gene products are relatively easy to perform in rodent islets as these islets are readily isolated at high purities from the exocrine pancreas; beta-cells are the majority cell type and their autofluorescent properties allow them to be purified from non-beta-cells by fluorescence-activated cell sorting (FACS). However, the situation is rather more complicated when investigating human islet gene expression profiles as purities of collagenase-isolated human islets are generally less than those of mouse and rat islets; beta-cells are less abundant in human islets than they are in rodent islets and conventional FACS purification of human islet beta-cells is not possible because of their high background fluorescence. In addition, FACS does not provide pure alpha- or delta-cell populations from either rodent or human islets. We have developed single-cell RT-PCR protocols to allow identification of genes expressed by human islet alpha-, beta- and delta-cells. This chapter describes these protocols and appropriate steps that should be followed to minimise generation of false-positive amplicons.


Subject(s)
Cytological Techniques , Islets of Langerhans/metabolism , Reverse Transcriptase Polymerase Chain Reaction/methods , Humans , Islets of Langerhans/cytology , Tissue Preservation
6.
Biochem Soc Trans ; 36(Pt 3): 290-3, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18481944

ABSTRACT

Studies in transgenic animals, rodent insulin-secreting cell lines and rodent islets suggest that insulin acts in an autocrine manner to regulate beta-cell mass and gene expression. Very little is known about the in vitro roles played by insulin in human islets, and the regulatory role of insulin in protecting against beta-cell apoptosis. We have identified mRNAs encoding IRs (insulin receptors) and downstream signalling elements in dissociated human islet beta-cells by single-cell RT (reverse transcription)-PCR, and perifusion studies have indicated that insulin does not have an autocrine role to regulate insulin secretion from human islets, but activation of the closely related IGF-1 (insulin-like growth factor 1) receptors is linked to inhibition of insulin secretion. Knockdown of IR mRNA by siRNAs (small interfering RNAs) decreased IR protein expression without affecting IGF-1 receptor levels, and blocked glucose stimulation of preproinsulin gene expression. Similar results were obtained when human islet IRS (IR substrate)-2 was knocked down, whereas depletion of IRS-1 caused an increase in preproinsulin mRNA levels. Studies using the mouse MIN6 beta-cell line indicated that glucose protected beta-cells from undergoing apoptosis and that this was a consequence, at least in part, of insulin release in response to elevated glucose. IGF-1 also exerted anti-apoptotic effects. These data indicate that insulin can exert autocrine effects in human islets through receptors on beta-cells. It protects beta-cells against apoptosis and increases preproinsulin mRNA synthesis, but does not affect insulin secretion.


Subject(s)
Insulin/metabolism , Islets of Langerhans/metabolism , Signal Transduction , Adaptor Proteins, Signal Transducing/genetics , Adaptor Proteins, Signal Transducing/metabolism , Animals , Apoptosis/drug effects , Autocrine Communication/drug effects , Cell Proliferation/drug effects , Gene Expression Regulation/drug effects , Humans , Insulin/pharmacology , Insulin Receptor Substrate Proteins , Islets of Langerhans/cytology , Islets of Langerhans/drug effects , Mice , RNA, Messenger/genetics , RNA, Messenger/metabolism , RNA, Small Interfering/metabolism , Receptor, Insulin/genetics , Receptor, Insulin/metabolism , Signal Transduction/drug effects
7.
J Pineal Res ; 44(3): 273-9, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18194202

ABSTRACT

Melatonin is known to inhibit insulin secretion from rodent beta-cells through interactions with cell-surface MT1 and/or MT2 receptors, but the function of this hormone in human islets of Langerhans is not known. In the current study, melatonin receptor expression by human islets was examined by reverse transcription-polymerase chain reaction (RT-PCR) and the effects of exogenous melatonin on intracellular calcium ([Ca2+]i) levels and islet hormone secretion were determined by single cell microfluorimetry and radioimmunoassay, respectively. RT-PCR amplifications indicated that human islets express mRNAs coding for MT1 and MT2 melatonin receptors, although MT2 mRNA expression was very low. Analysis of MT1 receptor mRNA expression at the single cell level indicated that it was expressed by human islet alpha-cells, but not by beta-cells. Exogenous melatonin stimulated increases in intracellular calcium ([Ca2+]i) in dissociated human islet cells, and stimulated glucagon secretion from perifused human islets. It also stimulated insulin secretion and this was most probably a consequence of glucagon acting in a paracrine fashion to stimulate beta-cells as the MT1 receptor was absent in beta-cells. Melatonin did not decrease 3', 5'-cyclic adenosine monophosphate (cyclic AMP) levels in human islets, but it inhibited cyclic AMP in the mouse insulinoma (MIN6) beta-cell line and it also inhibited glucose-stimulated insulin secretion from MIN6 cells. These data suggest that melatonin has direct stimulatory effects at human islet alpha-cells and that it stimulates insulin secretion as a consequence of elevated glucagon release. This study also indicates that the effects of melatonin are species-specific with primarily an inhibitory role in rodent beta-cells and a stimulatory effect in human islets.


Subject(s)
Islets of Langerhans/physiology , Receptors, Melatonin/physiology , Animals , Cell Line, Tumor , Colforsin/pharmacology , Cyclic AMP/metabolism , Glucagon/metabolism , Humans , Insulin/metabolism , Insulin Secretion , Islets of Langerhans/drug effects , Mice , RNA, Messenger/metabolism , Receptor, Melatonin, MT1/biosynthesis , Receptor, Melatonin, MT2/biosynthesis , Receptors, Melatonin/biosynthesis , Second Messenger Systems/physiology
8.
Toxicol Sci ; 101(2): 254-62, 2008 Feb.
Article in English | MEDLINE | ID: mdl-17998273

ABSTRACT

It has been suggested that uranium uptake and toxicity could be mediated by endocytosis and/or the type IIa sodium-dependent phosphate cotransporter (NaPi-IIa). The aim of this study was therefore to characterize in vitro the role of these two cellular mechanisms in the uptake and toxicity of low (200-3200 nM) and high (0.5 and 0.8 mM) concentrations of uranium, respectively. At low concentrations, uranium uptake in LLC-PK(1) cells was saturable (V(max) = 3.09 +/- 0.22 ng/mg protein) and characterized by a K(0.5) of 1022 +/- 63 nM and a Hill coefficient of 3.0 +/- 0.4. The potential involvement of endocytosis and NaPi-IIa in the uptake of uranium was assessed by the use of various drugs and culture conditions known to alter their relative activity, and (233)uranium uptake was monitored. Interestingly, the inhibitory effect of colchicine, cytochalasin D, phorbol 12-myristate 13-acetate, and chlorpromazine on endocytosis was highly correlated with their effect on uranium uptake, a relationship that was not true when the NaPi-IIa transport system was studied. Whereas the competitive inhibition of the NaPi-IIa by phosphonoformic acid (PFA) significantly decreased uranium uptake, this effect was not reproduced when NaPi-IIa inhibition was mediated by the replacement of extracellular Na(+) with N-methyl-D-glucamine. Uranium uptake was also not significantly altered when NaPi-IIa expression was stimulated in MDCK cells. More surprisingly, we observed by transmission electron microscopy that uranium cytotoxicity was dependent upon the extent of its intracellular precipitation, but not on its intracellular content, and was suppressed by PFA. In conclusion, our results suggest that low-dose uranium uptake is mainly mediated by absorptive endocytosis, and we propose PFA as a potential uranium chelator.


Subject(s)
Endocytosis , Sodium-Phosphate Cotransporter Proteins, Type IIa/physiology , Uranyl Nitrate , Animals , Biological Transport , Cell Survival/drug effects , Dose-Response Relationship, Drug , Endocytosis/drug effects , Foscarnet/pharmacology , Kinetics , LLC-PK1 Cells , Microscopy, Electron, Transmission , Sodium-Phosphate Cotransporter Proteins, Type IIa/antagonists & inhibitors , Sodium-Phosphate Cotransporter Proteins, Type IIa/metabolism , Swine , Uranyl Nitrate/metabolism , Uranyl Nitrate/toxicity
9.
Arch Physiol Biochem ; 113(3): 104-9, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17852048

ABSTRACT

Arachidonic acid (AA) is generated in pancreatic beta-cells through the activation of Ca2+-dependent cytosolic phospholipase A2 (cPLA2) and the consequent hydrolysis of membrane phospholipids in the sn-2 position of the glycerophospholipid backbone. AA acts as a second messenger in beta-cells to elevate cytosolic Ca2+ levels and stimulate insulin secretion, but it is not clear whether these are direct effects of AA or are dependent on its metabolism by cyclooxygenase (COX) and/or lipoxygenase (LOX) enzymes. In addition, much of the published data in this area have been generated using insulin-secreting cell lines or rodent islets, with very little information on AA generation and metabolism in human islets of Langerhans. This short review examines cPLA2, COX and LOX expression and function in insulin- secreting cell lines and rodent and human islets.


Subject(s)
Insulin/metabolism , Islets of Langerhans/enzymology , Lipoxygenase/metabolism , Prostaglandin-Endoperoxide Synthases/metabolism , Humans , Insulin Secretion
10.
Diabetes ; 56(1): 197-203, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17192482

ABSTRACT

The roles played by arachidonic acid and its cyclooxygenase (COX)-generated and lipoxygenase (LOX)-generated metabolites have been studied using rodent islets and insulin-secreting cell lines, but very little is known about COX and LOX isoform expression and the effects of modulation of arachidonic acid generation and metabolism in human islets. We have used RT-PCR to identify mRNAs for cytosolic phospholipase A(2) (cPLA(2)), COX-1, COX-2, 5-LOX, and 12-LOX in isolated human islets. COX-3 and 15-LOX were not expressed by human islets. Perifusion experiments with human islets indicated that PLA(2) inhibition inhibited glucose-stimulated insulin secretion, whereas inhibitors of COX-2 and 12-LOX enzymes enhanced basal insulin secretion and also secretory responses induced by 20 mmol/l glucose or by 50 mumol/l arachidonic acid. Inhibition of COX-1 with 100 mumol/l acetaminophen did not significantly affect glucose-stimulated insulin secretion. These data indicate that the stimulation of insulin secretion from human islets in response to arachidonic acid does not require its metabolism through COX-2 and 5-/12-LOX pathways. The products of COX-2 and LOX activities have been implicated in cytokine-mediated damage of beta-cells, so selective inhibitors of these enzymes would be expected to have a dual protective role in diabetes: they would minimize beta-cell dysfunction while maintaining insulin secretion through enhancing endogenous arachidonic acid levels.


Subject(s)
Arachidonic Acid/physiology , Insulin/metabolism , Islets of Langerhans/metabolism , Arachidonic Acid/metabolism , Base Sequence , Cadaver , Cyclooxygenase 1/genetics , Cyclooxygenase 2/genetics , DNA Primers , Humans , Insulin Secretion , Islets of Langerhans/enzymology , Lipoxygenase/genetics , Phospholipases A/genetics , RNA, Messenger/genetics , Reference Values , Reverse Transcriptase Polymerase Chain Reaction
11.
FEBS Lett ; 580(30): 6977-80, 2006 Dec 22.
Article in English | MEDLINE | ID: mdl-17161395

ABSTRACT

Insulin and glucose inhibited apoptosis in the MIN6 insulin-secreting cell line. The protective effect of 25 mM glucose was prevented by an anti-insulin antibody and this antibody-induced increase in apoptosis was reversed by the presence of excess insulin. Glucose stimulated MIN6 cell proliferation and this was inhibited by blockade of insulin secretion, by an anti-insulin antibody and by phosphatidylinositol-3 kinase (PI-3K) inhibition. Furthermore, MIN6 cell proliferation was stimulated by depolarising concentrations of KCl and by insulin itself. These data indicate that insulin secreted by beta-cells in response to elevated glucose exerts autocrine effects to protect against apoptosis and stimulate proliferation, and suggest that the insulin signalling cascade, through the PI-3K pathway, may be an effective means of maintaining beta-cell mass in diabetes.


Subject(s)
Apoptosis , Autocrine Communication , Insulin-Secreting Cells/cytology , Insulin-Secreting Cells/metabolism , Insulin/metabolism , Apoptosis/drug effects , Cell Line , Cell Proliferation/drug effects , Glucose/pharmacology , Insulin Secretion , Insulin-Secreting Cells/drug effects
12.
J Endocrinol ; 190(3): 703-10, 2006 Sep.
Article in English | MEDLINE | ID: mdl-17003271

ABSTRACT

The extracellular calcium-sensing receptor (CaR) is usually associated with systemic Ca(2+) homeostasis, but the CaR is also expressed in many other tissues, including pancreatic islets of Langerhans. In the present study, we have used human islets and an insulin-secreting cell line (MIN6) to investigate the effects of CaR activation using the calcimimetic R-568, a CaR agonist that activates the CaR at physiological concentrations of extracellular Ca(2+). CaR activation initiated a marked but transient insulin secretory response from both human islets and MIN6 cells at a sub-stimulatory concentration of glucose, and further enhanced glucose-induced insulin secretion. CaR-induced insulin secretion was reduced by inhibitors of phospholipase C or calcium-calmodulin-dependent kinases, but not by a protein kinase C inhibitor. CaR activation was also associated with an activation of p42/44 mitogen-activated protein kinases (MAPK), and CaR-induced insulin secretion was reduced by an inhibitor of p42/44 MAPK activation. We suggest that the beta-cell CaR is activated by divalent cations co-released with insulin, and that this may be an important mechanism of intra-islet communication between beta-cells.


Subject(s)
Aniline Compounds/pharmacology , Extracellular Fluid/metabolism , Insulin-Secreting Cells/metabolism , Insulin/metabolism , Protein Kinases/metabolism , Receptors, Calcium-Sensing/metabolism , Antibodies, Monoclonal/pharmacology , Benzylamines/pharmacology , Calcium/metabolism , Calcium/pharmacology , Calcium-Calmodulin-Dependent Protein Kinases/antagonists & inhibitors , Carbazoles/pharmacology , Cell Communication , Cell Line , Cells, Cultured , Estrenes/pharmacology , Flavonoids/pharmacology , Glucose/pharmacology , Humans , Immunohistochemistry , Indoles/pharmacology , Insulin Secretion , Insulin-Secreting Cells/drug effects , Mitogen-Activated Protein Kinases/antagonists & inhibitors , Mitogen-Activated Protein Kinases/immunology , Mitogen-Activated Protein Kinases/metabolism , Phenethylamines , Propylamines , Protein Kinase C/antagonists & inhibitors , Pyrrolidinones/pharmacology , RNA, Messenger/analysis , Receptors, Calcium-Sensing/antagonists & inhibitors , Receptors, Calcium-Sensing/immunology , Reverse Transcriptase Polymerase Chain Reaction , Staurosporine/pharmacology , Stimulation, Chemical , Sulfonamides/pharmacology , Type C Phospholipases/antagonists & inhibitors
13.
Diabetes ; 55(10): 2835-42, 2006 Oct.
Article in English | MEDLINE | ID: mdl-17003350

ABSTRACT

Although many studies using rodent islets and insulinoma cell lines have been performed to determine the role of insulin in the regulation of islet function, the autocrine effect of insulin on insulin gene expression is still controversial, and no consensus has yet been achieved. Because very little is known about the insulin signaling pathway in human islets, we used single-cell RT-PCR to profile the expression of genes potentially involved in the insulin signaling cascade in human beta-cells. The detection of mRNAs for insulin receptor (IR)A and IRB; insulin receptor substrate (IRS)-1 and IRS-2; phosphoinositide 3-kinase (PI3K) catalytic subunits p110alpha, p110beta, PI3KC2alpha, and PI3KC2gamma; phosphoinositide-dependent protein kinase-1; protein kinase B (PKB)alpha, PKBbeta, and PKBgamma in the beta-cell population suggests the presence of a functional insulin signaling cascade in human beta-cells. Small interfering RNA-induced reductions in IR expression in human islets completely suppressed glucose-stimulated insulin gene expression, suggesting that insulin regulates its own gene expression in human beta-cells. Defects in this regulation may accentuate the metabolic dysfunction associated with type 2 diabetes.


Subject(s)
Insulin-Secreting Cells/physiology , Insulin/physiology , 3-Phosphoinositide-Dependent Protein Kinases , Gene Expression Profiling , Humans , Insulin/genetics , Insulin Receptor Substrate Proteins , Intracellular Signaling Peptides and Proteins , Phosphatidylinositol 3-Kinases/biosynthesis , Phosphoproteins/biosynthesis , Proinsulin/biosynthesis , Protein Serine-Threonine Kinases/biosynthesis , Proto-Oncogene Proteins c-akt/biosynthesis , RNA, Small Interfering/pharmacology , Receptor, Insulin/biosynthesis , Reverse Transcriptase Polymerase Chain Reaction , Signal Transduction/genetics
14.
Am J Physiol Endocrinol Metab ; 288(3): E502-9, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15479950

ABSTRACT

Cell-to-cell interactions play an important role in the development and maintenance of the beta-cell phenotype. Here, we have investigated whether E-cadherin plays a role in regulating the growth of insulin-secreting MIN6 cells configured as three-dimensional islet-like clusters (pseudoislets). Pseudoislets form by cell aggregation rather than by proliferation from individual cells and attain the size of primary mouse islets after approximately 7 days of maintenance in culture. E-cadherin is known to mediate homotypic cell adhesion between beta-cells and has also been implicated in a number of cellular processes, including proliferation, apoptosis, and differentiation. E-cadherin and its associated intracellular elements, alpha- and beta-catenin, were upregulated in MIN6 pseudoislets. Pseudoislet formation was associated with an increased expression of cyclin-dependent kinase inhibitors and a concomitant downregulation of Ki67, suggesting an overall reduction in cellular proliferation. However, measurements of 5-bromo-2'-deoxyuridine incorporation revealed that there were no differences in the rate of MIN6 cell proliferation whether they were configured as monolayers or as pseudoislets, which is likely to be a result of their being a transformed cell line. Cells within pseudoislets were not necrotic, but apoptosis appeared to be upregulated in the islet-like structures. However, no differential expression of Fas and FasL was detected in monolayers and pseudoislets. These results suggest that cell-to-cell interactions within islet-like structures may initiate antiproliferative and proapoptotic signals.


Subject(s)
Apoptosis/physiology , Biomarkers/metabolism , Cell Communication/physiology , Islets of Langerhans/physiology , Animals , Blotting, Western , Bromodeoxyuridine/metabolism , Cadherins/metabolism , Cell Aggregation/physiology , Cell Cycle Proteins/metabolism , Cell Line, Tumor , Cell Proliferation , Cyclin-Dependent Kinase Inhibitor p21 , Cyclin-Dependent Kinase Inhibitor p27 , Cytoskeletal Proteins/metabolism , DNA/biosynthesis , Fas Ligand Protein , Histocytochemistry , In Situ Nick-End Labeling , Islets of Langerhans/cytology , Islets of Langerhans/metabolism , Ki-67 Antigen/metabolism , Membrane Glycoproteins/metabolism , Mice , Trans-Activators/metabolism , Tumor Suppressor Proteins/metabolism , alpha Catenin , beta Catenin , beta-Galactosidase/analysis , fas Receptor/metabolism
15.
Biochemistry ; 42(27): 8204-13, 2003 Jul 15.
Article in English | MEDLINE | ID: mdl-12846569

ABSTRACT

Vasopressin (VP) receptors belong to the widespread G protein-coupled receptor family. The crucial role of VP receptor intracellular loops in the coupling with the heterotrimeric G proteins was previously demonstrated by construction of a vasopressin receptor chimera. Yet, no fine structural data are available concerning the receptor molecular determinants involved in their interactions with G proteins. In this study, we synthesized both a linear and a cyclic form of the second intracellular loop (i2) of the human V(1a) vasopressin receptor isoform that is important for the interaction between the alphaq/alpha11 G protein and the receptor. These two peptides are biologically active. They specifically inhibit vasopressin binding to the V(1a) receptor, suggesting that the corresponding endogenous peptides contribute to the structure of the vasopressin binding site via intra- or intermolecular interactions with the core of the V(1a) receptor. The i2 peptide structures were determined by (1)H NMR. Both exhibit a helix and helical elements in their N- and C-terminal parts, respectively, separated by a turn imposed by a proline residue. More interestingly, the central Pro-Leu motif conserved in many GPCRs and thought to be important for coupling to G proteins can adopt different conformations. The "U" shape structure of the i2 loop is compatible with its anchoring to transmembrane domains III and IV and is very similar to the shape of bovine rhodopsin i2. Altogether, these data contribute to a better understanding of the structure of a not yet crystallized GPCR using the mimetic peptide approach.


Subject(s)
Molecular Mimicry , Receptors, Vasopressin/chemistry , Rhodopsin/chemistry , Amino Acid Sequence , Animals , CHO Cells , Cattle , Cricetinae , Models, Molecular , Molecular Sequence Data , Nuclear Magnetic Resonance, Biomolecular , Protein Conformation , Protein Folding , Protons
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