Over-expressing ES cell-specific transcription factors suppresses the differentiation of myoblasts
碩士 === 國立中央大學 === 生命科學研究所 === 94 === The potential of cell mediated tissue regeneration is hampered by both immune rejections of engrafted allogenic ES cells and the difficulties of isolating and propagating autologous stem cells. However, if the somatic cells can be induced to transdifferentiate in...
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ndltd-TW-094NCU051050142019-05-15T20:21:54Z http://ndltd.ncl.edu.tw/handle/xbaj2w Over-expressing ES cell-specific transcription factors suppresses the differentiation of myoblasts 大量表現幹細胞專有轉錄因子抑制肌肉細胞走向分化 Yu-Jung Chang 張毓容 碩士 國立中央大學 生命科學研究所 94 The potential of cell mediated tissue regeneration is hampered by both immune rejections of engrafted allogenic ES cells and the difficulties of isolating and propagating autologous stem cells. However, if the somatic cells can be induced to transdifferentiate into precursors of target cell types in vitro, cell mediated tissue regeneration will be more applicable. In this study, we introduced two ES cell-specific transcription factors, Nanog and Oct3, into sol8 myoblast using retrovirus system and examined the effects on differentiation stage of the stable clones. Over expressing Nanog and Oct3 simultaneously, but not independently, impaired the terminal differentiation of Sol8 myoblasts. Furthermore, the expression of myogenic regulator factors (MRFs), MyoD and Myogenin, is abolished in Sol8-Nanog/Oct3 cells. In addition, the slightly repression of Myf5 expression could be further diminished after β-mercaptoethanol treatment. Our data suggest that although over expressing Nanog and Oct3 in myoblasts can surpress myogenic differentiation, whether those cells acquired pluripotency still needs to be further investigated. Shen-Liang Chen 陳盛良 2006 學位論文 ; thesis 67 zh-TW |
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碩士 === 國立中央大學 === 生命科學研究所 === 94 === The potential of cell mediated tissue regeneration is hampered by both immune
rejections of engrafted allogenic ES cells and the difficulties of isolating and
propagating autologous stem cells. However, if the somatic cells can be induced to
transdifferentiate into precursors of target cell types in vitro, cell mediated tissue
regeneration will be more applicable. In this study, we introduced two ES cell-specific
transcription factors, Nanog and Oct3, into sol8 myoblast using retrovirus system and
examined the effects on differentiation stage of the stable clones. Over expressing
Nanog and Oct3 simultaneously, but not independently, impaired the terminal
differentiation of Sol8 myoblasts. Furthermore, the expression of myogenic regulator
factors (MRFs), MyoD and Myogenin, is abolished in Sol8-Nanog/Oct3 cells. In addition, the slightly repression of Myf5 expression could be further diminished after β-mercaptoethanol treatment. Our data suggest that although over expressing Nanog and Oct3 in myoblasts can surpress myogenic differentiation, whether those cells acquired pluripotency still needs to be further investigated.
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author2 |
Shen-Liang Chen |
author_facet |
Shen-Liang Chen Yu-Jung Chang 張毓容 |
author |
Yu-Jung Chang 張毓容 |
spellingShingle |
Yu-Jung Chang 張毓容 Over-expressing ES cell-specific transcription factors suppresses the differentiation of myoblasts |
author_sort |
Yu-Jung Chang |
title |
Over-expressing ES cell-specific transcription factors suppresses the differentiation of myoblasts |
title_short |
Over-expressing ES cell-specific transcription factors suppresses the differentiation of myoblasts |
title_full |
Over-expressing ES cell-specific transcription factors suppresses the differentiation of myoblasts |
title_fullStr |
Over-expressing ES cell-specific transcription factors suppresses the differentiation of myoblasts |
title_full_unstemmed |
Over-expressing ES cell-specific transcription factors suppresses the differentiation of myoblasts |
title_sort |
over-expressing es cell-specific transcription factors suppresses the differentiation of myoblasts |
publishDate |
2006 |
url |
http://ndltd.ncl.edu.tw/handle/xbaj2w |
work_keys_str_mv |
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