Piwi Is Required to Limit Exhaustion of Aging Somatic Stem Cells

被引:65
作者
Sousa-Victor, Pedro [1 ]
Ayyaz, Arshad [1 ]
Hayashi, Rippei [2 ]
Qi, Yanyan [1 ]
Madden, David T. [1 ,3 ]
Lunyak, Victoria V. [4 ]
Jasper, Heinrich [1 ,5 ]
机构
[1] Buck Inst Res Aging, 8001 Redwood Blvd, Novato, CA 94945 USA
[2] IMBA, Dr Bohrgasse 3, A-1030 Vienna, Austria
[3] Touro Univ Calif, Coll Pharm, 1310 Club Dr, Vallejo, CA 94592 USA
[4] Aelan Cell Technol, 665-280 Third St, San Francisco, CA 94107 USA
[5] Genentech Inc, Immunol Discovery, 1 DNA Way, San Francisco, CA 94080 USA
关键词
TRANSPOSABLE ELEMENTS; CHROMATIN STATE; PIRNA PATHWAY; SELF-RENEWAL; DROSOPHILA; GERMLINE; HOMEOSTASIS; EXPRESSION; ACTIVATION; APOPTOSIS;
D O I
10.1016/j.celrep.2017.08.059
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sophisticated mechanisms that preserve genome integrity are critical to ensure the maintenance of regenerative capacity while preventing transformation of somatic stem cells (SCs), yet little is known about mechanisms regulating genome maintenance in these cells. Here, we show that intestinal stem cells (ISCs) induce the Argonaute family protein Piwi in response to JAK/STAT signaling during acute proliferative episodes. Piwi function is critical to ensure heterochromatin maintenance, suppress retrotransposon activation, and prevent DNA damage in homeostasis and under regenerative pressure. Accordingly, loss of Piwi results in the loss of actively dividing ISCs and their progenies by apoptosis. We further show that Piwi expression is sufficient to allay age-related retrotransposon expression, DNA damage, apoptosis, and mis-differentiation phenotypes in the ISC lineage, improving epithelial homeostasis. Our data identify a role for Piwi in the regulation of somatic SC function, and they highlight the importance of retrotransposon control in somatic SC maintenance.
引用
收藏
页码:2527 / 2537
页数:11
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