Generation of cell lines with tetracycline-regulated autophagy and a role for autophagy in controlling cell size

被引:0
作者
Hosokawa, Nao
Hara, Yukichi
Mizushima, Noboru
机构
[1] Tokyo Metropolitan Inst Med Sci, Dept Bioregulat & Metab, Bunkyo Ku, Tokyo 1138613, Japan
[2] Tokyo Med & Dent Univ, Sch Hlth Sci, Dept Biochem & Biophys, Bunkyo Ku, Tokyo 1138519, Japan
[3] Japan Sci & Technol Agcy, PRESTO, Kawaguchi 3320012, Japan
关键词
autophagy; cell size; starvation; atrophy;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Autophagy is an intracellular bulk degradation system. We established mouse fibroblast lines coupling the Tet-off system with an Atg5(-1-) mouse embryonic fibroblast line to artificially regulate autophagic ability. In the presence of doxycycline (Dox), Atg5 expression was completely suppressed and these cells were autophagy-defective. After removal of Dox, autophagic ability was restored within 6 h. Very low levels of Atg5 could induce an autophagy competent state. We applied this novel system to examine the contribution of autophagy to controlling cell size. Cell size reduction in response to starvation was significantly inhibited in cells unable to undergo autophagy. The generated cell lines will be useful reagents for future mechanistic studies into the regulation and physiologic significance of autophagy. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2623 / 2629
页数:7
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