https://scholars.lib.ntu.edu.tw/handle/123456789/159993
標題: | TGF-Β對於肝癌細胞死亡的調控與機制之研究(4/5) | 作者: | 陳瑞華 Chen, Ruey-Hwa |
公開日期: | 26-五月-2003 | 出版社: | 臺北市:國立臺灣大學醫學院分子醫學研究所 | 摘要: | Death associated protein kinase (DAP-kinase) is a calcium/calmodulin-dependent serine/threonine kinase, and participates in various apoptosis systems. However, its apoptosis-promoting mechanism is poorly understood. Here, we demonstrate that DAP-kinase suppresses integrin-mediated cell adhesion and signal transduction, whereas dominant-negative interference of this kinase promotes adhesion. This effect of DAP-kinase is neither a consequence of apoptosis, nor a result of decreased expression of integrins. Rather, DAP-kinase downregulates integrin activity through an inside-out mechanism. We present evidence indicating that this adhesion-inhibitory effect accounts for a major mechanism of the apoptosis induced by DAP-kinase. First, in growth-arrested fibroblasts, DAP-kinase triggers apoptosis in cells plated on fibronectin, but does not affect the death of cells on poly-L-lysine. Second, in epithelial cells, DAP-kinase induces apoptosis in the anoikis-sensitive MCF10A cells, but not in the anoikis-resistant BT474 cells. Most importantly, the apoptosis-promoting effect of DAP-kinase is completely abolished by enforced activation of integrin-mediated signaling pathways from either integrin itself or its downstream effector FAK. Finally, we show integrin or FAK activation blocks the ability of DAP-kinase to upregulate p53. Our results indicate that DAP-kinase exerts apoptotic effect by suppressing integrin functions and integrin-mediated survival signals, thereby activating a p53-dependent apoptotic pathway. |
URI: | http://ntur.lib.ntu.edu.tw//handle/246246/23776 | 其他識別: | 912321B002001 | Rights: | 國立臺灣大學醫學院分子醫學研究所 |
顯示於: | 分子醫學研究所 |
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912321B002001.pdf | 2.38 MB | Adobe PDF | 檢視/開啟 |
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