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Role of Li+-permeable Na+/Ca2+ exchanger, NCLX, in the regulation of cytosolic Ca2+ and exocytosis in pancreatic β-cell
췌장 베타세포의 세포내 칼슘과 인슐린 분비 조절에 대한 리튬 투과성 소디움/칼슘 교환 기전의 역할

DC Field Value Language
dc.contributor.advisor호원경-
dc.contributor.author한영은-
dc.date.accessioned2017-07-14T01:43:59Z-
dc.date.available2017-07-14T01:43:59Z-
dc.date.issued2015-08-
dc.identifier.other000000067214-
dc.identifier.urihttps://hdl.handle.net/10371/122293-
dc.description학위논문 (박사)-- 서울대학교 대학원 : 의과학과 생리학전공, 2015. 8. 호원경.-
dc.description.abstractNa+/Ca2+ exchangers are key players for Ca2+ clearance in pancreatic β-cells, but their molecular determinants and exact roles in insulin secretion are not fully understood. In the present study, I investigated the role of Na+/Ca2+ exchangers on cytosolic Ca2+ dynamics and exocytosis in rat INS-1 insulinoma cells. I newly discovered that the Li+-permeable Na+/Ca2+ exchanger (NCLX), which was known as mitochondrial Na+/Ca2+ exchanger, contributed to the Na+-dependent Ca2+ movement across the plasma membrane in INS-1 cells. Na+/Ca2+ exchange activity by NCLX was comparable to that by the Na+/Ca2+ exchanger, NCX. I also confirmed the presence of NCLX proteins on the plasma membrane using immunocytochemistry and cell surface biotinylation experiments. I further investigated the role of NCLX on exocytosis function by measuring the capacitance increase in response to repetitive depolarization in small interfering (si)NCLX-transfected INS-1 cells. siRNA-mediated downregulation of NCLX did not affect the initial exocytosis, but significantly suppressed sustained exocytosis and recovery of exocytosis. XIP (NCX inhibitory peptide) or Na+ replacement for inhibiting Na+-dependent Ca2+ clearance also selectively suppressed sustained exocytosis. Consistent with the idea that sustained exocytosis requires ATP dependent-vesicle recruitment, mitochondrial function, assessed by mitochondrial membrane potential (ΔΨ), was impaired by siNCLX or XIP. However, depolarization-induced exocytosis was hardly affected by changes in intracellular Na+ concentration, suggesting a negligible contribution of mitochondrial Na+/Ca2+ exchanger. In addition, I discovered that oligomycin inhibited sustained exocytosis in the presence of intracellular ATP, suggesting that local metabolic control by mitochondria is critical for this phase. Taken together, my data indicate that Na+/Ca2+ exchanger-mediated Ca2+ clearance mediated by NCLX and NCX is crucial for optimizing mitochondrial function, which in turn contributes to vesicle recruitment for sustained exocytosis in pancreatic β-cells.-
dc.description.tableofcontentsCONTENTS
ABSTRACT.......................................................................................................i
CONTENTS.................................................................................................... iii
LIST OF FIGURES...........................................................................................v
LIST OF ABBREVIATIONS......................................................................... vii
INTRODUCTION.............................................................................................1
1. General description of insulin secretion mechanism in pancreatic β-cells ..............................................................................................................1
2. Regulation of intracellular Ca2+ in pancreatic β-cells............................2
3. Na+/Ca2+ exchangers at the plasmalemma and mitochondria and their roles in regulating insulin secretion ......................................................3
4. Aim of the present study........................................................................5
MATERIALS AND METHODS.....................................................................10
1. Cell Culture .........................................................................................10
2. Preparation of Mouse Pancreatic Tissue Section.................................10
3. Ca2+ Measurements..............................................................................11
4. Immunofluorescence Staining.............................................................12
5. Western Blot Analysis and Biotinylation Experiment .........................14
6. NCLX Knockdown..............................................................................15
7. Capacitance Measurement...................................................................15
8. Measurement of Mitochondrial Membrane Potential (ΔΨm)...............16
9. Statistical Analysis...............................................................................17
RESULTS........................................................................................................18
1. Role of plasma membrane NCLX in cytosolic Ca2+ dynamics............18
2. Immunodetection of NCLX on the plasma membrane in pancreatic β-cells .....................................................................................................20
3. Role of NCLX on the Exocytosis Function.........................................22
4. Downregulation of NCLX induces mitochondrial dysfunction to suppress sustained exocytosis.............................................................26
DISCUSSION .................................................................................................48
REFERENCES................................................................................................56
ABSTRACT in KOREAN..............................................................................65
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dc.formatapplication/pdf-
dc.format.extent2310154 bytes-
dc.format.mediumapplication/pdf-
dc.language.isoen-
dc.publisher서울대학교 대학원-
dc.subjectPancreatic β-cell-
dc.subjectCa2+ transport-
dc.subjectNa+/Ca2+ exchanger-
dc.subjectExocytosis-
dc.subjectCapacitance-
dc.subject.ddc610-
dc.titleRole of Li+-permeable Na+/Ca2+ exchanger, NCLX, in the regulation of cytosolic Ca2+ and exocytosis in pancreatic β-cell-
dc.title.alternative췌장 베타세포의 세포내 칼슘과 인슐린 분비 조절에 대한 리튬 투과성 소디움/칼슘 교환 기전의 역할-
dc.typeThesis-
dc.contributor.AlternativeAuthorYoung Eun Han-
dc.description.degreeDoctor-
dc.citation.pagesviii, 67-
dc.contributor.affiliation의과대학 의과학과-
dc.date.awarded2015-08-
Appears in Collections:
College of Medicine/School of Medicine (의과대학/대학원)Dept. of Biomedical Sciences (대학원 의과학과)Theses (Ph.D. / Sc.D._의과학과)
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