Isolation of quiescent and nonquiescent cells from yeast stationary-phase cultures

被引:246
作者
Allen, Chris
Buettner, Sabrina
Aragon, Anthony D.
Thomas, Jason A.
Meirelles, Osorio
Jaetao, Jason E.
Benn, Don
Ruby, Stephanie W.
Veenhuis, Marten
Madeo, Frank
Werner-Washburne, Margaret [1 ]
机构
[1] Univ New Mexico, Hlth Sci Ctr, Dept Biol, Albuquerque, NM 87131 USA
[2] Univ New Mexico, Hlth Sci Ctr, Dept Math & Stat, Albuquerque, NM 87131 USA
[3] Univ New Mexico, Hlth Sci Ctr, Dept Mol Genet & Microbiol, Albuquerque, NM 87131 USA
[4] Karl Franzens Univ Graz, Inst Mol Biol Biochem & Microbiol, A-8010 Graz, Austria
[5] Univ Groningen, Dept Eukaryot Microbiol, NL-9750 AA Haren, Netherlands
关键词
D O I
10.1083/jcb.200604072
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Quiescence is the most common and, arguably, most poorly understood cell cycle state. This is in part because pure populations of quiescent cells are typically difficult to isolate. We report the isolation and characterization of quiescent and nonquiescent cells from stationary-phase (SP) yeast cultures by densitygradient centrifugation. Quiescent cells are dense, unbudded daughter cells formed after glucose exhaustion. They synchronously reenter the mitotic cell cycle, suggesting that they are in a G(0) state. Nonquiescent cells are less dense, heterogeneous, and composed of replicatively older, asynchronous cells that rapidly lose the ability to reproduce. Microscopic and flow cytometric analysis revealed that nonquiescent cells accumulate more reactive oxygen species than quiescent cells, and over 21 d, about half exhibit signs of apoptosis and necrosis. The ability to isolate both quiescent and nonquiescent yeast cells from SP cultures provides a novel, tractable experimental system for studies of quiescence, chronological and replicative aging, apoptosis, and the cell cycle.
引用
收藏
页码:89 / 100
页数:12
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