혈관내피세포에서 알파시누클레인 (alpha-Synuclein)에 의한 Weibel-Palade Body의 exocytosis 조절

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dc.contributor.advisor주일로, 박상면-
dc.contributor.authorKim, Kwang-Soo-
dc.date.accessioned2019-10-21T07:17:41Z-
dc.date.available2019-10-21T07:17:41Z-
dc.date.issued2011-02-
dc.identifier.other11658-
dc.identifier.urihttps://dspace.ajou.ac.kr/handle/2018.oak/17887-
dc.description학위논문(박사)--아주대학교 일반대학원 :의생명학과,2011. 2-
dc.description.tableofcontentsⅠ. INTRODUCTION 1 Ⅱ. MATERIALS AND METHODS 5 A. MATERIALS 5 1. Reagents and Antibodies 5 2. Constructs 5 B. METHODS 6 1. Cell Culture and Transfection 6 2. RT-PCR analysis 6 3. Determination of VWF by ELISA 7 4. Leukocyte Adhesion Assay 8 5. Ral Activation Assay 8 6. Confocal Microscopy 9 7. Immuno-Electron Microscopy 9 8. Western Blot and Immunoprecipitation 10 Ⅲ. RESULTS 12 1. Three different kinds of secretagogues induce vWF secretion in HUVECs in a time dependent manners 12 2. -Syn overexpression inhibits three secretagogues-induced VWF secretion in HUVECs 14 3. WPB exocytosis is inhibited by -syn and -syn, but not by -syn overexpression 19 4. -Syn mutants (A30P, A53T and E46K) inhibit WPB exocytosis similar to that of wild-type -syn 19 5. N-terminal or NAC region of a-syn is necessary for the inhibition of PMA-induced VWF release in HUVECs 23 6. Secretagogues-induced RalA activation is suppressed by -syn overexpression 28 7. The interaction between RalGDS and -arrestin is enhanced by -syn overexpression 31 8. -Syn is localized close to WPB in HUVECs 35 9. Exogenously added recombinant -syn also inhibits VWF release in HUVECs 38 Ⅳ. DISCUSSION 41 Ⅴ. CONCLUSION 47 REFERENCES 48 국문 요약 59-
dc.language.isoeng-
dc.publisherThe Graduate School, Ajou University-
dc.rights아주대학교 논문은 저작권에 의해 보호받습니다.-
dc.title혈관내피세포에서 알파시누클레인 (alpha-Synuclein)에 의한 Weibel-Palade Body의 exocytosis 조절-
dc.typeThesis-
dc.contributor.affiliation아주대학교 일반대학원-
dc.contributor.department일반대학원 의생명과학과-
dc.date.awarded2011. 2-
dc.description.degreeMaster-
dc.identifier.localId569338-
dc.identifier.urlhttp://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000011658-
dc.subject.keywordWeibel-Palade Body Exocytosis-
dc.subject.keyword혈관내피세포-
dc.subject.keywordEndothelial Cells-
dc.subject.keyword알파시누클레인-
dc.subject.keywordalpha-Synuclein-
dc.description.alternativeAbstracta-Synuclein (a-syn) is a small presynaptic protein implicated in the pathogenesis of Parkinson’s disease. Although gathering evidence has been proposed for its physiological roles, the precise roles of a-synuclein and mechanisms remain incompletely understood. a-Synuclein is not only expressed in neuron, but also in vascular endothelium. Endothelial cells contain intracellular granules called Weibel-Palade bodies (WPBs) that contain a number of chemokines, adhesive molecules and inflammatory cytokines. This study explored whether the exocytosis of WPB is regulated by a-synuclein. Results showed that PMA-, thrombin- or forskolin-induced VWF release or translocation of P-selectin from Human Umbilical Vein Endothelial Cells (HUVECs) were inhibited by overexpression of a- and b-synuclein, but not g-synuclein. The overexpression of three point mutants (A30P, A53T and E46K) found in familial Parkinson’s disease inhibited WPB exocytosis similar to that of wild-type a-synuclein. Results also showed that the negative regulation of WPB exocytosis required the N-terminus or NAC region of a-synuclein, but not C-terminal acidic tail, and that a-synuclein affected WPB exocytosis through interference with RalA activation by enhancing the interaction of RalGDS/b-arrestin complexes. Immuno-EM analysis revealed that a-synuclein was localized close to WPB. These findings imply that a-synuclein plays as a negative regulator in WPB exocytosis in endothelial cells.-
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Graduate School of Ajou University > Department of Biomedical Sciences > 3. Theses(Master)
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