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1.
Cell Death Discov ; 8(1): 318, 2022 Jul 13.
Article in English | MEDLINE | ID: mdl-35831286

ABSTRACT

To identify alternative interventions in neonatal hypoxic-ischemic encephalopathy, researchers' attention has been focused to the study of endogenous neuroprotective strategies. Based on the preconditioning concept that a subthreshold insult may protect from a subsequent harmful event, we aimed at identifying a new preconditioning protocol able to enhance Ca2+-dependent neurogenesis in a mouse model of neonatal hypoxia ischemia (HI). To this purpose, we also investigated the role of the preconditioning-linked protein controlling ionic homeostasis, Na+/Ca2+ exchanger (NCX). Hypoxic Preconditioning (HPC) was reproduced by exposing P7 mice to 20' hypoxia. HI was induced by isolating and cutting the right common carotid artery. A significant reduction in ischemic damage was observed in mice subjected to 20' hypoxia followed,3 days later, by 60' HI, thus suggesting that 20' hypoxia functions as preconditioning stimulus. HPC promoted neuroblasts proliferation in the dentate gyrus mirrored by an increase of NCX1 and NCX3-positive cells and an improvement of behavioral motor performances in HI mice. An attenuation of HPC neuroprotection as well as a reduction in the expression of neurogenesis markers, including p57 and NeuroD1, was observed in preconditioned mice lacking NCX1 or NCX3. In summary, PC in neonatal mice triggers a neurogenic process linked to ionic homeostasis maintenance, regulated by NCX1 and NCX3.

2.
Diabetes Obes Metab ; 14 Suppl 3: 136-42, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22928574

ABSTRACT

Ca(2+) extrusion from the ß-cell is mediated by two processes the Na/Ca exchanger (NCX) and the plasma membrane Ca(2+) -ATPase (PMCA). Gain of function studies show that overexpression of NCX or PMCA leads to endoplasmic reticulum (ER) Ca(2+) depletion with subsequent ER stress, decrease in ß-cell proliferation and ß-cell death by apoptosis. Interestingly, chronic exposure to cytokines or high free fatty acid concentrations also induce ER Ca(2+) depletion and ß-cell death in diabetes. Loss of function studies show, on the contrary, that heterozygous inactivation of NCX1 (Ncx1(+/-)) leads to an increase in ß-cell function (insulin production and release), and a fivefold increase in both ß-cell mass and proliferation. The mutation also increases ß-cell resistance to hypoxia, and Ncx1(+/-) islets show a two to four times higher rate of diabetes cure than Ncx1(+/+) islets when transplanted in diabetic animals. Thus, down-regulation of the Na/Ca exchanger leads to various changes in ß-cell function that are opposite to the major abnormalities seen in diabetes. This provides a unique model for the prevention and treatment of ß-cell dysfunction in diabetes and following islet transplantation.


Subject(s)
Calcium/metabolism , Diabetes Mellitus, Type 1/metabolism , Diabetes Mellitus, Type 2/metabolism , Endoplasmic Reticulum Stress/genetics , Endoplasmic Reticulum/physiology , Insulin-Secreting Cells/physiology , Regeneration , Sodium-Calcium Exchanger/genetics , Animals , Apoptosis/genetics , Cell Proliferation , Diabetes Mellitus, Experimental , Diabetes Mellitus, Type 1/genetics , Diabetes Mellitus, Type 2/genetics , Endoplasmic Reticulum/genetics , Endoplasmic Reticulum/metabolism , Homeostasis , Humans , Insulin-Secreting Cells/metabolism , Islets of Langerhans Transplantation , Mice , Plasma Membrane Calcium-Transporting ATPases/metabolism , Regeneration/genetics , Sodium-Calcium Exchanger/metabolism
3.
Diabetologia ; 53(9): 1935-46, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20499047

ABSTRACT

AIMS/HYPOTHESIS: Suppressor of cytokine signalling (SOCS) proteins are powerful inhibitors of pathways involved in survival and function of pancreatic beta cells. Whereas SOCS1 and SOCS3 have been involved in immune and inflammatory processes, respectively, in beta cells, nothing is known about SOCS2 implication in the pancreas. METHODS: Transgenic (tg) mice were generated that constitutively produced SOCS2 in beta cells (betaSOCS2) to define whether this protein is implicated in beta cell functioning and/or survival. RESULTS: Constitutive production of SOCS2 in beta cells leads to hyperglycaemia and glucose intolerance. This phenotype is not a consequence of decreased beta cell mass or inhibition of insulin synthesis. However, insulin secretion to various secretagogues is profoundly altered in intact animals and isolated islets. Interestingly, constitutive SOCS2 production dampens the rise in cytosolic free calcium concentration induced by glucose, while glucose metabolism is unchanged. Moreover, tg islets have a depletion in endoplasmic reticulum Ca(2+) stores, suggesting that SOCS2 interferes with calcium fluxes. Finally, in betaSOCS2 mice proinsulin maturation is impaired, leading to an altered structure of insulin secretory granules and augmented levels of proinsulin. The latter is likely to be due to decreased production of prohormone convertase 1 (PC1/3), which plays a key role in proinsulin cleavage. CONCLUSIONS/INTERPRETATIONS: SOCS2 was shown to be a potent regulator of proinsulin processing and insulin secretion in beta cells. While its constitutive production is insufficient to induce overt diabetes in this mouse model, it causes glucose intolerance. Thus, increased SOCS2 production could be an important event predisposing to beta cell failure.


Subject(s)
Insulin/metabolism , Islets of Langerhans/metabolism , Suppressor of Cytokine Signaling Proteins/metabolism , Animals , Blotting, Western , Body Weight/genetics , Body Weight/physiology , Electrophoresis, Polyacrylamide Gel , Endoplasmic Reticulum/metabolism , Insulin Secretion , Mice , Mice, Inbred C57BL , Phenotype , Rats , Reverse Transcriptase Polymerase Chain Reaction , Suppressor of Cytokine Signaling Proteins/genetics
4.
Am J Physiol Endocrinol Metab ; 291(3): E441-8, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16912059

ABSTRACT

Considering the insufficient supply of long-chain polyunsaturated omega-3 fatty acids often prevailing in Western populations, this report deals mainly with alterations of Ca(2+) fluxes and Ca(2+)-dependent insulin secretory events in isolated pancreatic islets from omega-3-depleted rats. In terms of (45)Ca(2+) handling, the islets from omega-3-depleted rats, compared with those from normal animals, displayed an unaltered responsiveness to an increase in extracellular K(+) concentration, a lower inflow rate and lower fractional outflow rate of the divalent cation, and higher (45)Ca(2+)-labeled cellular pool(s) at isotopic equilibrium. The latter anomaly was corrected 120 min after intravenous injection of a novel medium-chain triglyceride-fish oil (MCT:FO) emulsion, distinct from a control omega-3-poor MCT-olive oil (MCT:OO) emulsion. At 8.3 mM D-glucose, insulin release was higher in islets from omega-3-depleted rats vs. control animals, coinciding with a higher cytosolic Ca(2+) concentration. The relative magnitude of the increase in insulin output attributable to a rise in D-glucose as well as extracellular Ca(2+) or K(+) concentration, to the absence vs. presence of verapamil and to the presence vs. absence of extracellular Ca(2+), theophylline, phorbol 12-myristate 13-acetate, or Ba(2+), was always more pronounced in islets from omega-3-depleted rats injected with the MCT:OO compared with the MCT:FO emulsion. A comparable situation prevailed when comparing islets from noninjected omega-3-depleted and normal rats. In light of these and previous findings, we propose that an impairment of Na(+),K(+)-ATPase activity plays a major, although not an exclusive, role in the perturbation of Ca(2+) fluxes and Ca(2+)-dependent secretory events in the islets from omega-3-depleted rats.


Subject(s)
Calcium/metabolism , Fatty Acids, Omega-3/metabolism , Insulin/metabolism , Islets of Langerhans/metabolism , Animals , Barium/pharmacology , Cytosol/drug effects , Cytosol/metabolism , Diet , Fatty Acids, Omega-3/pharmacology , Female , Fish Oils/pharmacology , Glucose/pharmacology , In Vitro Techniques , Insulin Secretion , Islets of Langerhans/drug effects , Olive Oil , Plant Oils/pharmacology , Potassium/metabolism , Rats , Rats, Inbred Strains , Tetradecanoylphorbol Acetate/pharmacology , Theophylline/pharmacology , Verapamil/pharmacology
5.
Eur Respir J ; 19(1): 121-6, 2002 Jan.
Article in English | MEDLINE | ID: mdl-11843310

ABSTRACT

Sleep apnoea svndrome (SAS) is a largely undiagnosed and prevalent disorder. It is associated with cardiovascular morbidity as well as excessive daytime sleepiness and poor quality of life. In the present study the SleepStrip, a novel screening device is introduced, which is low cost and easy to use and is aimed for widespread use. The results of three independent validation studies, which compared the SleepStrip score (Sscore) against "gold standard" polysomnographically-determined apnoea/ hypopnoea index (AHI), are reported both separately and combined. Four hundred and two patients suspected of SAS underwent full polysomnography recordings concomitantly with the use of the SleepStrip. For all samples combined, the correlation between AHI and Sscore was r=0.73, sensitivity and specificity values ranged from 80-86% and 57-86% respectively, and the area under the curve derived from receiver-operating characteristic curves ranged from 0.81-0.92 at varying AHI thresholds. Though not intended as a substitute for polysomnography, the SleepStrip may provide initial screening information, which may be useful in both clinical and experimental settings.


Subject(s)
Sleep Apnea Syndromes/diagnosis , Adolescent , Adult , Aged , Aged, 80 and over , Equipment and Supplies , Humans , Middle Aged , Sensitivity and Specificity
6.
Diabetes Metab ; 28(6 Pt 2): 3S54-60; discussion 3S108-12, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12688634

ABSTRACT

Recent knowledge concerning the Na/Ca exchanger (NCX) in the pancreatic beta-cell is reviewed. The beta-cell expresses various NCX1 splice variants in a species specific pattern (NCX1.3 and 1.7 in the rat, NCX1.2, 1.3 and 1.7 in the mouse), in variable and different proportions. In the rat beta-cell, the exchanger displays a quite high capacity, accounts for about 70% of Ca2+ extrusion and participates to Ca2+ inflow during membrane depolarization. In the mouse, however, the contribution of the exchanger to Ca2+ extrusion is more modest, and to Ca2+ inflow less evident. The exchanger has a stoichiometry of 3 Na+ for 1 Ca2+, is electrogenic, and displays a reversal potential at -20 mV. Although being of low magnitude, the current generated by the exchanger shapes glucose-induced beta-cell electrical activity and intracellular Ca2+ oscillations. For instance, a lower Na/Ca exchange activity (and subsequent inward current) in the mouse than in the rat, explains why the mouse beta-cell displays cyclic oscillations of the membrane potential, while the rat displays a staircase increase in membrane potential without such oscillations. In addition of being of importance in cell signalling, intracellular Ca2+ may also trigger apoptosis. For instance, overexpression of the exchanger increases Ca2+-dependent and -independent beta-cell death by apoptosis, a phenomenon resulting from the depletion of ER Ca2+-stores with subsequent activation of caspase-12. Na/Ca exchange overexpression also reduces beta-cell growth. Hence, the Na/Ca exchanger is a versatile system that appears to play an important role in the function, growth and demise of the beta-cell.


Subject(s)
Adenosine Triphosphatases/metabolism , Calcium/metabolism , Islets of Langerhans/metabolism , Adenosine Triphosphatases/genetics , Alternative Splicing , Animals , Apoptosis , Genetic Variation , Homeostasis , Islets of Langerhans/enzymology , Mice , Rats
7.
Eur J Med Chem ; 36(7-8): 597-614, 2001.
Article in English | MEDLINE | ID: mdl-11600230

ABSTRACT

A series of N-guanidino substituted 2,4-diamino-5-carbonylguanidine molecules related to amiloride were synthesised and evaluated for their ability to inhibit the sodium-calcium exchanger in rat insulinoma cells (RINm5F) and human platelets. Specific chemical pathways were used to prepare the benzene derivatives designed as bioisosteric analogues of the pyrazine derivatives of amiloride. Several so-called 'simplified analogues', where some substituents of amiloride were omitted or replaced, were also prepared and included in the biological evaluation. The inhibitory potency of the sodium-calcium exchanger was screened on both cell types by measuring their effect on 45Ca(2+) uptake. Among the most active compounds, N-(2-amino-5-chloro-4-nitrobenzoyl)-N'-(1-naphtylmethyl)guanidine (IC(50)=3.4 microM) was found more active than amiloride (IC(50)=690 microM) and 3,4-dichlorobenzamil (IC(50)=15.2 microM), the reference inhibitor.


Subject(s)
Amiloride/analogs & derivatives , Amiloride/pharmacology , Benzene/chemistry , Blood Platelets/metabolism , Guanidine/pharmacology , Guanidines/chemistry , Sodium-Calcium Exchanger/antagonists & inhibitors , Amiloride/chemical synthesis , Animals , Blood Platelets/cytology , Blood Platelets/drug effects , Calcium Radioisotopes/pharmacokinetics , Diuretics/chemical synthesis , Diuretics/pharmacology , Guanidine/analogs & derivatives , Guanidine/chemical synthesis , Humans , Inhibitory Concentration 50 , Insulinoma/metabolism , Rats , Sodium-Calcium Exchanger/metabolism , Tumor Cells, Cultured/cytology , Tumor Cells, Cultured/drug effects , Tumor Cells, Cultured/metabolism
8.
Cell Calcium ; 30(3): 191-8, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11508998

ABSTRACT

The Na/Ca exchanger (NCX) is an ubiquitous transporter that plays an important role in regulating cellular Ca(2+) balance. On gel electrophoresis, the NCX1 protein migrates as two major bands of 120 and 70kDa. While the 120kDa is thought to represent the native protein, the nature of the 70kDa protein remains unclear. In this report, we describe a new NCX1 splicing pattern, identified during the cloning of NCX1 isoforms from human eye. The insertion of a newly identified sequence upstream exons B and D of the NCX1.3 isoform, generates a stop codon in frame with the NCX1 coding sequence, that should lead to a truncated Na/Ca exchanger (that we called NCX1.33) comprising only the N-terminal portion of the exchanger and a shortened intracellular loop. Insulin-secreting cells were stably transfected with NCX1.33. Overexpression was assessed at the mRNA and protein level, the truncated exchanger migrating as a70kDa band. Appropriate targeting to the plasma membrane was assessed by microfluorescence and by the increase in Na/Ca exchange activity. The results of the present study constitute a clear piece of evidence indicating that the Na/Ca exchanger 70kDa protein corresponds to the N-terminal portion of the exchanger, and is functionally active.


Subject(s)
Alternative Splicing/genetics , Sodium-Calcium Exchanger/chemistry , Sodium-Calcium Exchanger/metabolism , Amino Acid Sequence , Animals , Base Sequence , Blotting, Western , Calcium/metabolism , Cell Line , Cloning, Molecular , Exons/genetics , Eye/metabolism , Fluorescent Antibody Technique, Indirect , Humans , In Situ Hybridization , Microscopy, Fluorescence , Molecular Sequence Data , Molecular Weight , Protein Isoforms/chemistry , Protein Isoforms/genetics , Protein Isoforms/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , Rats , Reverse Transcriptase Polymerase Chain Reaction , Sodium/metabolism , Sodium-Calcium Exchanger/genetics , Transfection
9.
Biochemistry ; 40(11): 3324-32, 2001 Mar 20.
Article in English | MEDLINE | ID: mdl-11258952

ABSTRACT

The 120-kDa Na+/Ca2+ exchanger was purified and reconstituted into lipid vesicles. The secondary structure composition of the exchanger was 39% alpha-helices, 20% beta-sheets, 25% beta-turns, and 16% random coils, as analyzed by Fourier transform infrared attenuated total reflection spectroscopy. The secondary structure composition of the COOH-terminal portion of the protein was compatible with a topology model containing 4-6 transmembrane segments. Furthermore, the secondary structure of the NH2-terminal portion of the cytoplasmic loop was analyzed and found to be different from that of the COOH-terminal portion. Ca2+ and/or the exchange inhibitory peptide (XIP) failed to affect the secondary structure of the 120-kDa protein. Tertiary structure modifications induced by Ca2+ and XIP were analyzed by monitoring the hydrogen/deuterium exchange rate for the reconstituted exchanger. In the absence of ligand, 51% of the protein was accessible to solvent. Ca2+ decreased accessibility to 40%, implicating the shielding of at least 103 amino acids. When both Ca2+ and XIP were added, accessibility increased to 66%. No modification was obtained when XIP was added alone. Likewise, in the presence of Ca2+, XIP failed to modify the tertiary structure of the 70-kDa protein, suggesting that XIP acts at the level of the COOH-terminal portion of the intracellular loop. The present data describe, for the first time, conformational changes of the Na+/Ca2+ exchanger induced by Ca2+ and XIP, compatible with an interaction model where regulatory Ca2+ and inhibitory XIP bind to distinct sites, and where XIP binding requires the presence of Ca2+.


Subject(s)
Sodium-Calcium Exchanger/chemistry , Sodium-Calcium Exchanger/metabolism , Amino Acid Sequence , Animals , Cattle , Circular Dichroism , Electrophoresis, Polyacrylamide Gel , Endopeptidase K/metabolism , Hydrolysis , Immunoblotting , Ligands , Membrane Lipids/chemistry , Membrane Lipids/metabolism , Molecular Sequence Data , Molecular Weight , Myocardium/metabolism , Peptides/metabolism , Peptides/pharmacology , Protein Binding , Protein Conformation , Protein Structure, Secondary , Protein Structure, Tertiary , Sodium-Calcium Exchanger/antagonists & inhibitors , Sodium-Calcium Exchanger/isolation & purification , Spectroscopy, Fourier Transform Infrared/methods
10.
J Endocrinol ; 168(3): 517-26, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11241183

ABSTRACT

In the rat pancreatic beta-cell, Na/Ca exchange displays a quite high capacity. The cell is equipped with two alternatively spliced Na/Ca exchanger-1 (NCX1) isoforms, namely NCX1.3 and NCX1.7. To examine the existence of a possible functional difference between these splice variants, they were cloned, together with the heart variant NCX1.1, and expressed in human embryonic kidney-293 (HEK293) and Chinese hamster ovary (CHO) cells. In these two systems, the three splice variants showed a comparable level of intracellular Na+ (Na+(i))-dependent extracellular Ca2+(Ca2+(o)) uptake. Different levels of NCX1.3 and NCX1.7 transcripts were found in four rodent species, together with a marked interspecies difference in Na/Ca exchange activity. Three additional splice variants were found (NCX1.2, NCX1.9 and NCX1.13) in guinea-pigs, hamsters and mice, again in different proportions. Our data provide evidence for the activity of the three NCX1 splice variants. They also show the existence of a differential and species-specific transcription pattern of NCX1 gene products in pancreatic islet cells.


Subject(s)
Alternative Splicing , Islets of Langerhans/metabolism , Sodium-Calcium Exchanger/genetics , Amino Acid Sequence , Animals , Base Sequence , Calcium/metabolism , Cell Culture Techniques , Cricetinae , Guinea Pigs , Humans , Mice , Molecular Sequence Data , Polymerase Chain Reaction , Rats , Sodium-Calcium Exchanger/chemistry , Species Specificity , Transfection
11.
Cell Calcium ; 27(4): 231-46, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10858669

ABSTRACT

When stimulated by glucose, the pancreatic beta-cell displays large oscillations of intracellular free Ca2+ concentration ([Ca2+]i). To control [Ca2+]i, the beta-cell must be equipped with potent mechanisms for Ca2+ extrusion. We studied the expression of the plasma membrane Ca(2+)-ATPases (PMCA) in three insulin secreting preparations (a pure beta-cell preparation, RINm5F cells and pancreatic islet cells), using reverse-transcribed PCR, RNase protection assay and Western blotting. The four main isoforms, PMCA1, PMCA2, PMCA3 and PMCA4 were expressed in the three preparations. Six alternative splice mRNA variants, characterized at splice sites A, B and C were detected in the three preparations (rPMCA1xb, 2yb, 2wb, 3za, 3zc, 4xb), plus two additional variants in pancreatic islet cells (PMCA4za, 1xkb). The latter variant corresponded to a novel variant of rat PMCA1 gene lacking the exon coding for the 10th transmembrane segment, at splice site B. At the mRNA and protein level, five variants predominated (1xb, 2wb, 3za, 3zc, 4xb), whilst one additional isoform (4za), predominated at the protein level only. This provides the first evidence for the presence of PMCA2 and PMCA3 isoforms at the protein level in non-neuronal tissue. Hence, the pancreatic beta-cell is equipped with multiple PMCA isoforms with possible differential regulation, providing a full range of PMCAs for [Ca2+]i regulation.


Subject(s)
Calcium-Transporting ATPases/genetics , Calcium-Transporting ATPases/metabolism , Cell Membrane/enzymology , Islets of Langerhans/enzymology , Actins/genetics , Animals , Blotting, Western , Calcium-Transporting ATPases/immunology , Female , Gene Expression Regulation, Enzymologic , Isoenzymes/genetics , Isoenzymes/metabolism , RNA Splicing , RNA, Messenger/analysis , RNA, Messenger/genetics , Rats , Rats, Wistar , Reverse Transcriptase Polymerase Chain Reaction
12.
J Biol Chem ; 274(22): 15510-8, 1999 May 28.
Article in English | MEDLINE | ID: mdl-10336444

ABSTRACT

The secondary structure of the purified 70-kDa protein Na+/Ca2+ exchanger, functionally reconstituted into asolectin lipid vesicles, was examined by Fourier transform infrared attenuated total reflection spectroscopy. Fourier transform infrared attenuated total reflection spectroscopy provided evidence that the protein is composed of 44% alpha-helices, 25% beta-sheets, 16% beta-turns, and 15% random structures, notably the proportion of alpha-helices is greater than that corresponding to the transmembrane domains predicted by exchanger hydropathy profile. Polarized infrared spectroscopy showed that the orientation of helices is almost perpendicular to the membrane. Tertiary structure modifications, induced by addition of Ca2+, were evaluated by deuterium/hydrogen exchange kinetic measurements for the reconstituted exchanger. This approach was previously proven as a useful tool for detection of tertiary structure modifications induced by an interaction between a protein and its specific ligand. Deuterium/hydrogen exchange kinetic measurements indicated that, in the absence of Ca2+, a large fraction of the protein (40%) is inaccessible to solvent. Addition of Ca2+ increased to 55% the inaccessibility to solvent, representing a major conformational change characterized by the shielding of at least 93 amino acids.


Subject(s)
Protein Structure, Secondary , Protein Structure, Tertiary , Proteolipids/chemistry , Sodium-Calcium Exchanger/chemistry , Animals , Biological Transport , Calcium/pharmacology , Cattle , Deuterium , Heart Ventricles/metabolism , Phosphatidylcholines , Phospholipids/chemistry , Protein Conformation , Sodium-Calcium Exchanger/isolation & purification , Spectroscopy, Fourier Transform Infrared
13.
Biophys J ; 76(4): 2018-28, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10096898

ABSTRACT

We have combined the patch-clamp technique with microfluorimetry of the cytoplasmic Ca2+ concentration ([Ca2+]i) to characterize Na/Ca exchange in mouse beta-cells and to determine its importance for [Ca2+]i buffering and shaping of glucose-induced electrical activity. The exchanger contributes to Ca2+ removal at [Ca2+]i above 1 microM, where it accounts for >35% of the total removal rate. At lower [Ca2+]i, thapsigargin-sensitive Ca2+-ATPases constitute a major (70% at 0.8 microM [Ca2+]i) mechanism for Ca2+ removal. The beta-cell Na/Ca exchanger is electrogenic and has a stoichiometry of three Na+ for one Ca2+. The current arising from its operation reverses at approximately -20 mV (current inward at more negative voltages), has a conductance of 53 pS/pF (14 microM [Ca2+]i), and is abolished by removal of external Na+ or by intracellularly applied XIP (exchange inhibitory peptide). Inhibition of the exchanger results in shortening (50%) of the bursts of action potentials of glucose-stimulated beta-cells in intact islets and a slight (5 mV) hyperpolarization. Mathematical simulations suggest that the stimulatory action of glucose on beta-cell electrical activity may be accounted for in part by glucose-induced reduction of the cytoplasmic Na+ concentration with resultant activation of the exchanger.


Subject(s)
Calcium/metabolism , Islets of Langerhans/metabolism , Sodium-Calcium Exchanger/metabolism , Sodium/metabolism , Action Potentials , Adenosine Triphosphate/metabolism , Animals , Biophysical Phenomena , Biophysics , Buffers , Calcium-Transporting ATPases/antagonists & inhibitors , Enzyme Inhibitors/pharmacology , Fluorometry , In Vitro Techniques , Ion Transport/drug effects , Islets of Langerhans/drug effects , Membrane Potentials , Mice , Models, Biological , Patch-Clamp Techniques , Thapsigargin/pharmacology
14.
Biochem J ; 338 ( Pt 1): 139-45, 1999 Feb 15.
Article in English | MEDLINE | ID: mdl-9931309

ABSTRACT

The Na/Ca exchanger is associated with 160, 120 and 70 kDa polypeptides whose nature is poorly understood. We have purified and characterized the Na/Ca exchanger from bovine cardiac sarcolemmal vesicles (SLVs) by using ion-exchange and affinity chromatographies. The Na/Ca exchanger-enriched fraction was reconstituted into asolectin liposomes [lipid to protein ratio 10:1 (w/w)] that showed Na/Ca exchange activity. Under non-reducing conditions, SDS/PAGE showed a single 70 kDa polypeptide, which was further characterized by immunoblots with different antibodies: SWant, raised against the purified exchanger protein; NH2-terminus, residues 1-21; NCX1, residues 393-406; and Exon F, residues 622-644. Immunoblots under reducing conditions with SWant, NH2-terminus and NCX1 showed three bands migrating at 160, 120 and 70 kDa for SLV preparations, whereas Exon F reacted only with the 160 and 120 kDa bands. Under non-reducing conditions, immunoblots with purified reconstituted Na/Ca exchanger showed a single band at 70 kDa reacting with SWant, NH2-terminus and NCX1 but not with Exon F. We conclude that the 70 kDa protein is associated with Na/Ca exchange activity, has the same N-terminal sequence as the cloned bovine cardiac exchanger, and has its length decreased by at least 35% from its C-terminal portion as compared with that of the wild-type exchanger.


Subject(s)
Peptides/chemistry , Sodium-Calcium Exchanger/chemistry , Animals , Cattle , Endopeptidase K , Epitopes/immunology , Heart Ventricles/chemistry , Hydrolysis , Immunoblotting , Liposomes/chemistry , Molecular Weight , Peptides/immunology , Peptides/isolation & purification , Phosphatidylcholines , Phospholipids/chemistry , Sarcolemma/chemistry , Sodium-Calcium Exchanger/immunology , Sodium-Calcium Exchanger/isolation & purification
15.
Diabetes ; 47(12): 1873-80, 1998 Dec.
Article in English | MEDLINE | ID: mdl-9836518

ABSTRACT

To characterize the role played by Na/Ca exchange in the pancreatic beta-cell, phosphorothioated antisense oligonucleotides (AS-oligos) were used to knock down the exchanger in rat pancreatic beta-cells. Na/Ca exchange activity was evaluated by measuring cytosolic free Ca2+ concentration ([Ca2+]i) in single cells using fura-2. Exposure of beta-cells to 500 nmol/l of the AS-oligos for 24 h inhibited Na/Ca exchange activity by approximately 77%. In contrast, control oligonucleotides (scrambled and mismatched) did not affect Na/Ca exchange activity. In AS-oligo-treated cells, the increase in [Ca2+]i induced by membrane depolarization (K+ or the hypoglycemic sulfonylurea, tolbutamide) was reduced by 28 or 40%, respectively. Likewise, the rate of [Ca2+]i decrease after K+ or tolbutamide removal was reduced by 72 or 40%, respectively. AS-oligos treatment also abolished the nifedipine-resistant increase in [Ca2+]i induced by K+ and profoundly altered the oscillatory or sustained increases in [Ca2+]i induced by 11.1 mmol/l glucose. The present study shows that AS-oligos may specifically inhibit Na/Ca exchange in rat pancreatic beta-cells. In those cells, Na/Ca exchange appears to mediate Ca2+ entry in response to membrane depolarization and to be responsible for up to 70% of Ca2+ removal from the cytoplasm upon membrane repolarization.


Subject(s)
Calcium/metabolism , Islets of Langerhans/metabolism , Sodium/metabolism , Animals , Calcium Channel Blockers/pharmacology , Cell Adhesion/drug effects , Glucose/pharmacology , Hypoglycemic Agents/pharmacology , Ion Transport/drug effects , Islets of Langerhans/cytology , Islets of Langerhans/drug effects , Nifedipine/pharmacology , Oligonucleotides, Antisense/pharmacology , Potassium Chloride/pharmacology , RNA, Messenger/drug effects , RNA, Messenger/metabolism , Rats , Rats, Wistar , Sodium-Calcium Exchanger/antagonists & inhibitors , Sodium-Calcium Exchanger/genetics , Sodium-Calcium Exchanger/metabolism , Tolbutamide/pharmacology
16.
Am J Physiol ; 275(6): E993-E1006, 1998 12.
Article in English | MEDLINE | ID: mdl-9843742

ABSTRACT

The metabolism of beta-L-glucose pentaacetate and its interference with the catabolism of L-[U-14C]glutamine, [U-14C]palmitate, D-[U-14C]glucose, and D-[5-3H]glucose were examined in rat pancreatic islets. Likewise, attention was paid to the effects of this ester on the biosynthesis of islet peptides, the release of insulin from incubated or perifused islets, the functional behavior of individual B cells examined in a reverse hemolytic plaque assay of insulin secretion, adenylate cyclase activity in a membrane-enriched islet subcellular fraction, cAMP production by intact islets, tritiated inositol phosphate production by islets preincubated with myo-[2-3H]inositol, islet cell intracellular pH, 86Rb and 45Ca efflux from prelabeled perifused islets, and electrical activity in single isolated B cells. The results of these experiments were interpreted to indicate that the insulinotropic action of beta-L-glucose pentaacetate is not attributable to any nutritional value of the ester but, instead, appears to result from a direct effect of the ester itself on a yet unidentified receptor system, resulting in a decrease in K+ conductance, plasma membrane depolarization, and induction of electrical activity.


Subject(s)
Glucose/analogs & derivatives , Insulin/physiology , Adenylyl Cyclases/metabolism , Animals , Calcium/metabolism , Cations/metabolism , Cyclic AMP/biosynthesis , Electrophysiology , Glucose/metabolism , Glucose/pharmacokinetics , Glucose/pharmacology , Hydrogen-Ion Concentration , Hydrolysis/drug effects , Insulin/metabolism , Intracellular Membranes/metabolism , Islets of Langerhans/drug effects , Islets of Langerhans/metabolism , Islets of Langerhans/physiology , Phosphatidylinositols/metabolism , Phosphorylation/drug effects , Rats , Rats, Wistar
17.
Biochem Pharmacol ; 53(8): 1211-3, 1997 Apr 25.
Article in English | MEDLINE | ID: mdl-9175727

ABSTRACT

The nitric oxide (NO) donor SIN-1 (3-morpholinosydnonimine) induced a concentration-dependent inhibition of the secretory response to glucose. The negative insulinotropic action of SIN-1 was attenuated by the hypoglycemic sulfonylurea glibenclamide. Moreover, the NO donor enhanced 86Rb outflow from perfused islets and reduced the glucose-induced increase in 45Ca outflow. The present data provide further evidence that NO donors impair the secretory response to glucose, at least in part, by activating the ATP-sensitive K+ channels.


Subject(s)
Glyburide/pharmacology , Insulin/metabolism , Islets of Langerhans/drug effects , Molsidomine/analogs & derivatives , Animals , Calcium Channels/drug effects , Down-Regulation , Drug Interactions , Glucose , In Vitro Techniques , Insulin Secretion , Molsidomine/pharmacology , Potassium Channels/drug effects , Rats , Rats, Wistar , Secretory Rate/drug effects
18.
Cell Calcium ; 21(3): 185-93, 1997 Mar.
Article in English | MEDLINE | ID: mdl-9105728

ABSTRACT

In the pancreatic B-cell, Na/Ca exchange displays a quite high capacity and participates in the control of cytosolic free Ca2+ concentration. The Na/Ca exchanger was recently cloned in various tissues. Two genes coding for two different exchangers (NCX1 and NCX2) have been identified and evidence for several isoforms for NCX1 shown. To characterize the isoform(s) expressed in pancreatic B-cells, a RT-PCR analysis was performed on mRNA from rat pancreatic islets, purified B-cells and insulinoma B-cells (RINm5F cells). PCR amplification did not yield the expected NCX2 DNA fragment but yielded 2 NCX1 bands, corresponding to NaCa3 and NaCa7, in the three preparations. NaCa3 and NaCa7 were equally expressed in pancreatic islets and purified B-cells. In RINm5F cells, NaCa3 expression did not differ from that in islet and purified B-cells but NaCa7 was 3 times less expressed. This lower expression was accompanied by a 3 times lower Na/Ca exchange activity in RINm5F cells compared to islet cells. Our data indicate the existence of 2 NCX1 isoforms but not of NCX2 in pancreatic B-cells. The difference in both the expression patterns of NCX1 isoforms and the activity of Na/Ca exchange in islet cells and RINm5F cells is compatible with a difference in activity between NaCa3 and NaCa7.


Subject(s)
Carrier Proteins/metabolism , Islets of Langerhans/cytology , Islets of Langerhans/metabolism , Animals , Calcium/metabolism , Carrier Proteins/genetics , Cells, Cultured , Insulin/metabolism , Isoenzymes/metabolism , Polymerase Chain Reaction/methods , Rats , Rats, Inbred Strains , Sodium-Calcium Exchanger , Tissue Distribution
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