A simple estimation of peroxisomal degradation with green fluorescent protein - an application for cell cycle analysis

被引:7
作者
Arai, K [1 ]
Ohkuma, S
Matsukawa, T
Kato, S
机构
[1] Kanazawa Univ, Dept Mol & Cellular Biol, Fac Pharmaceut Sci, Grad Sch Sci, Kanazawa, Ishikawa 9200946, Japan
[2] Kanazawa Univ, Dept Mol Neurobiol, Grad Sch Sci, Kanazawa, Ishikawa 9200840, Japan
关键词
autophagy; peroxisome; green fluorescein; protein; cell cycle;
D O I
10.1016/S0014-5793(01)02964-7
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
When nutrients are depleted from the environment, mammalian cells begin to degrade their own cytosol and organelles. This bulk protein degradation is mediated by autophagy. In this study, peroxisomes in living CHO-K1 cells were visualized by targeting the green fluorescent protein (GFP) tagged with a type 1 peroxisomal targeting signal. The nutrient-starved condition induced a decay of GFP fluorescence in the peroxisomes and autophagic inhibitors such as 3-methyladenine suppressed the decay of GFP fluorescence (13-60% of starvation). By double labeling the nuclear DNA and peroxisomal GFP, the autophagy specifically occurred at the G1 phase of the cell cycle and the autophagic inhibitors suppressed the G1 arrest. The vital stain technique with GFP is a very simple and useful marker to quantitatively estimate or to further study peroxisomal degradation. (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:181 / 186
页数:6
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