Differential Expression Between The Human Embryonic Stem Cell And Trypsin-selected Human Embryonic Stem Cell Subpopulation

碩士 === 國立中興大學 === 生命科學系所 === 98 === Human embryonic stem cell (HES cells) is highly sensitive to dissociation, which cause HES cells death. So far, the usual way to passage HES cells is using type IV collagenase or accutase to prevent dissociation of HES cells. Generation of homogenous and single HE...

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Main Authors: Hsiao-Chien Ting, 丁筱茜
Other Authors: Hong-Lin Su
Format: Others
Language:en_US
Published: 99
Online Access:http://ndltd.ncl.edu.tw/handle/56810926837563767468
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spelling ndltd-TW-098NCHU51050692016-08-22T04:16:42Z http://ndltd.ncl.edu.tw/handle/56810926837563767468 Differential Expression Between The Human Embryonic Stem Cell And Trypsin-selected Human Embryonic Stem Cell Subpopulation 人類胚胎幹細胞與胰蛋白&;#37238;篩選之人類胚胎幹細胞亞群間基因表現差異 Hsiao-Chien Ting 丁筱茜 碩士 國立中興大學 生命科學系所 98 Human embryonic stem cell (HES cells) is highly sensitive to dissociation, which cause HES cells death. So far, the usual way to passage HES cells is using type IV collagenase or accutase to prevent dissociation of HES cells. Generation of homogenous and single HESC is an obstacle, preventing the efficient gene transfer and clonal isolation. Previous study demonstrates Y-27632 permit survival of dissociated HES cells, but the mechanism is still unclear. In order to find out the mechanism that regulate dissociated HES cells survival, trypsin-resistant HES sublines were obtained to find out what happended in trypsin-resistant HES sublines can let it survival from trypsin-dissociation. To explore the differences in trypsin-resistant HES cells and normal HES cells, the gene expression patterns of both HES cells are analyzed at protein- and RNA-level. We have found out that cytoskeleton materials (beta-actin, alpha-tubulin and beta-tubulin) and genes that promoting cytoskeleton formation (ADD2, PAK3 and FGD1) are up-regulate in trypsin-resistant HES cells. We postulate that the polymerization and stabilization of actin-filaments and microtubules by activation of Rho/Rac/Cdc42 pathway may help trypsin-resistant HES cells overcome dissociation and survive. Moreover, we also find that the epidermal growth factor (EGF) which induces actin-filament formation also increases the survival of dissociated HES cells. However, the relationship between cytoskeletons and HES cell survival still need to be confirmed. We will further treat HES cells with microtubule regulator (Taxol and nocodazol) to confirm the relationship between microtubule and HES cell survival. Since we have find that actin-filaments and microtubules may improve survival of trypsin dissociated HES cells, the survival mechanism of dissociated HES cells may be solve. With the enhancement of cytoskeleton, it may be a simple and more efficient process to generate homogenous population of HES cells and improve gene transfer efficiency of HES cells in medical research and applications. Hong-Lin Su 蘇鴻麟 99 學位論文 ; thesis 75 en_US
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description 碩士 === 國立中興大學 === 生命科學系所 === 98 === Human embryonic stem cell (HES cells) is highly sensitive to dissociation, which cause HES cells death. So far, the usual way to passage HES cells is using type IV collagenase or accutase to prevent dissociation of HES cells. Generation of homogenous and single HESC is an obstacle, preventing the efficient gene transfer and clonal isolation. Previous study demonstrates Y-27632 permit survival of dissociated HES cells, but the mechanism is still unclear. In order to find out the mechanism that regulate dissociated HES cells survival, trypsin-resistant HES sublines were obtained to find out what happended in trypsin-resistant HES sublines can let it survival from trypsin-dissociation. To explore the differences in trypsin-resistant HES cells and normal HES cells, the gene expression patterns of both HES cells are analyzed at protein- and RNA-level. We have found out that cytoskeleton materials (beta-actin, alpha-tubulin and beta-tubulin) and genes that promoting cytoskeleton formation (ADD2, PAK3 and FGD1) are up-regulate in trypsin-resistant HES cells. We postulate that the polymerization and stabilization of actin-filaments and microtubules by activation of Rho/Rac/Cdc42 pathway may help trypsin-resistant HES cells overcome dissociation and survive. Moreover, we also find that the epidermal growth factor (EGF) which induces actin-filament formation also increases the survival of dissociated HES cells. However, the relationship between cytoskeletons and HES cell survival still need to be confirmed. We will further treat HES cells with microtubule regulator (Taxol and nocodazol) to confirm the relationship between microtubule and HES cell survival. Since we have find that actin-filaments and microtubules may improve survival of trypsin dissociated HES cells, the survival mechanism of dissociated HES cells may be solve. With the enhancement of cytoskeleton, it may be a simple and more efficient process to generate homogenous population of HES cells and improve gene transfer efficiency of HES cells in medical research and applications.
author2 Hong-Lin Su
author_facet Hong-Lin Su
Hsiao-Chien Ting
丁筱茜
author Hsiao-Chien Ting
丁筱茜
spellingShingle Hsiao-Chien Ting
丁筱茜
Differential Expression Between The Human Embryonic Stem Cell And Trypsin-selected Human Embryonic Stem Cell Subpopulation
author_sort Hsiao-Chien Ting
title Differential Expression Between The Human Embryonic Stem Cell And Trypsin-selected Human Embryonic Stem Cell Subpopulation
title_short Differential Expression Between The Human Embryonic Stem Cell And Trypsin-selected Human Embryonic Stem Cell Subpopulation
title_full Differential Expression Between The Human Embryonic Stem Cell And Trypsin-selected Human Embryonic Stem Cell Subpopulation
title_fullStr Differential Expression Between The Human Embryonic Stem Cell And Trypsin-selected Human Embryonic Stem Cell Subpopulation
title_full_unstemmed Differential Expression Between The Human Embryonic Stem Cell And Trypsin-selected Human Embryonic Stem Cell Subpopulation
title_sort differential expression between the human embryonic stem cell and trypsin-selected human embryonic stem cell subpopulation
publishDate 99
url http://ndltd.ncl.edu.tw/handle/56810926837563767468
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