A Novel Gene Rogdi Regulates Proliferation, Migration and Activation of Rat Hepatic Stellate Cells

碩士 === 國立中山大學 === 生物科學系研究所 === 97 === Rogdi was a novel gene with unknown function. According to GeneBank database, the gene is located on chromsome 10q12 and the length of coding regeion is 864 bp that encods 287 animo acids. Earlier studies in our laboratory showed that human ROGDI influenced rate...

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Main Authors: Ren-Chao Liu, 劉仁超
Other Authors: Chung-Lung Cho
Format: Others
Language:zh-TW
Published: 2009
Online Access:http://ndltd.ncl.edu.tw/handle/4v23be
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spelling ndltd-TW-097NSYS51120282019-05-15T19:28:01Z http://ndltd.ncl.edu.tw/handle/4v23be A Novel Gene Rogdi Regulates Proliferation, Migration and Activation of Rat Hepatic Stellate Cells 一個調控大鼠肝星狀細胞增生、移動與活化的新基因Rogdi Ren-Chao Liu 劉仁超 碩士 國立中山大學 生物科學系研究所 97 Rogdi was a novel gene with unknown function. According to GeneBank database, the gene is located on chromsome 10q12 and the length of coding regeion is 864 bp that encods 287 animo acids. Earlier studies in our laboratory showed that human ROGDI influenced rate of cell proliferaion in HeLa, Hep3B and NIH3T3 cells. In addition, we found Rogdi protien was up-regulated in fibrotic livers. Following various types of injury to liver, quiescent hepatic stellate cells (HSCs) transform to activated phenotype, leading to exprssion of α-SMA, increasing rate of cell proliferation and depositing of extracellular matrix. In this study, we found that Rogdi protein was up-regulated in activated HSCs isolated and cultured from rat livers. By either overexpression or RNA interference of Rogdi, we found that Rogdi affected rate of HSCs proliferation, and expressions of α-SMA and collagen type I. Expression of Rogdi protein was induced after PDGF treatment of rat HSCs. Additionally, we found that Rogdi was involved in MAPK and PI3K/Akt pathways. Furthermore, using wound healing assay and migration assay, Rogdi was found to regulate migration of activated HSCs. Chung-Lung Cho 卓忠隆 2009 學位論文 ; thesis 87 zh-TW
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description 碩士 === 國立中山大學 === 生物科學系研究所 === 97 === Rogdi was a novel gene with unknown function. According to GeneBank database, the gene is located on chromsome 10q12 and the length of coding regeion is 864 bp that encods 287 animo acids. Earlier studies in our laboratory showed that human ROGDI influenced rate of cell proliferaion in HeLa, Hep3B and NIH3T3 cells. In addition, we found Rogdi protien was up-regulated in fibrotic livers. Following various types of injury to liver, quiescent hepatic stellate cells (HSCs) transform to activated phenotype, leading to exprssion of α-SMA, increasing rate of cell proliferation and depositing of extracellular matrix. In this study, we found that Rogdi protein was up-regulated in activated HSCs isolated and cultured from rat livers. By either overexpression or RNA interference of Rogdi, we found that Rogdi affected rate of HSCs proliferation, and expressions of α-SMA and collagen type I. Expression of Rogdi protein was induced after PDGF treatment of rat HSCs. Additionally, we found that Rogdi was involved in MAPK and PI3K/Akt pathways. Furthermore, using wound healing assay and migration assay, Rogdi was found to regulate migration of activated HSCs.
author2 Chung-Lung Cho
author_facet Chung-Lung Cho
Ren-Chao Liu
劉仁超
author Ren-Chao Liu
劉仁超
spellingShingle Ren-Chao Liu
劉仁超
A Novel Gene Rogdi Regulates Proliferation, Migration and Activation of Rat Hepatic Stellate Cells
author_sort Ren-Chao Liu
title A Novel Gene Rogdi Regulates Proliferation, Migration and Activation of Rat Hepatic Stellate Cells
title_short A Novel Gene Rogdi Regulates Proliferation, Migration and Activation of Rat Hepatic Stellate Cells
title_full A Novel Gene Rogdi Regulates Proliferation, Migration and Activation of Rat Hepatic Stellate Cells
title_fullStr A Novel Gene Rogdi Regulates Proliferation, Migration and Activation of Rat Hepatic Stellate Cells
title_full_unstemmed A Novel Gene Rogdi Regulates Proliferation, Migration and Activation of Rat Hepatic Stellate Cells
title_sort novel gene rogdi regulates proliferation, migration and activation of rat hepatic stellate cells
publishDate 2009
url http://ndltd.ncl.edu.tw/handle/4v23be
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