Increased Wnt signaling during aging alters muscle stem cell fate and increases fibrosis

被引:1215
作者
Brack, Andrew S.
Conboy, Michael J.
Roy, Sudeep
Lee, Mark
Kuo, Calvin J.
Keller, Charles
Rando, Thomas A. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Med, Div Hematol, Stanford, CA 94305 USA
[3] Univ Texas, Hlth Sci Ctr, Dept Cellular & Struct Biol, San Antonio, TX 78229 USA
[4] VA Palo Alto Hlth Care Syst, CRECC, Stanford, CA 94305 USA
[5] VA Palo Alto Hlth Care Syst, Neurol Serv, Stanford, CA 94305 USA
关键词
D O I
10.1126/science.1144090
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
The regenerative potential of skeletal muscle declines with age, and this impairment is associated with an increase in tissue fibrosis. We show that muscle stem cells (satellite cells) from aged mice tend to convert from a myogenic to a fibrogenic lineage as they begin to proliferate and that this conversion is mediated by factors in the systemic environment of the old animals. We also show that this lineage conversion is associated with an activation of the canonical Wnt signaling pathway in aged myogenic progenitors and can be suppressed by Wnt inhibitors. Furthermore, components of serum from aged mice that bind to the Frizzled family of proteins, which are Wnt receptors, may account for the elevated Wnt signaling in aged cells. These results indicate that the Wnt signaling pathway may play a critical role in tissue-specific stem cell aging and an increase in tissue fibrosis with age.
引用
收藏
页码:807 / 810
页数:4
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