Regulation of erythrocyte lifespan: do reactive oxygen species set the clock?

被引:41
作者
Hattangadi, Shilpa M.
Lodish, Harvey F.
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] Childrens Hosp Boston, Boston, MA USA
关键词
D O I
10.1172/JCI32559
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The forkhead box O (Foxo) subfamily of transcription factors regulates expression of genes important for many cellular processes, ranging from initiation of cell cycle arrest and apoptosis to induction of DNA damage repair. Invertebrate Foxo orthologs such as DAF-16 also regulate longevity. Cellular responses inducing resistance to ROS are important for cellular survival and organism lifespan, but until recently, mammalian factors regulating resistance to oxidative stress have not been well characterized. Marinkovic and colleagues demonstrate in this issue of the JCI that Foxo3 is specifically required for induction of proteins that regulate the in vivo oxidative stress response in murine erythrocytes (see the related article beginning on page 2133). Their work offers the interesting hypothesis that in so doing, Foxo3 may regulate the lifespan of red blood cells, and underlies the importance of understanding the direct targets of this transcription factor and its regulation.
引用
收藏
页码:2075 / 2077
页数:3
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