Sprouty1 Regulates Reversible Quiescence of a Self-Renewing Adult Muscle Stem Cell Pool during Regeneration

被引:256
作者
Shea, Kelly L. [1 ]
Xiang, Wanyi [1 ,2 ]
LaPorta, Vincent S. [1 ]
Licht, Jonathan D. [3 ]
Keller, Charles [4 ]
Basson, M. Albert [5 ]
Brack, Andrew S. [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Ctr Regenerat Med, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Dept Orthoped Surg, Boston, MA 02114 USA
[3] Northwestern Univ, Feinberg Sch Med, Robert H Lurie Comprehens Canc Ctr, Div Hematol Oncol, Chicago, IL 60611 USA
[4] Univ Texas Hlth Sci Ctr San Antonio, Dept Cellular & Struct Biol, San Antonio, TX 78229 USA
[5] Kings Coll London, Dept Craniofacial Dev, London SE1 9RT, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
SATELLITE CELLS; GENE-EXPRESSION; PAX7; PROLIFERATION; DISTINCT; FGF; DIFFERENTIATION; HETEROGENEITY; PROGENITORS; COMMITMENT;
D O I
10.1016/j.stem.2009.12.015
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
Satellite cells are skeletal muscle stem cells capable of self-renewal and differentiation after transplantation, but whether they contribute to endogenous muscle fiber repair has been unclear. The transcription factor Pax7 marks satellite cells and is critical for establishing the adult satellite cell pool. By using a lineage tracing approach, we show that after injury, quiescent adult Pax7(+) cells enter the cell cycle; a subpopulation returns to quiescence to replenish the satellite cell compartment, while others contribute to muscle fiber formation. We demonstrate that Sprouty1 (Spry1), a receptor tyrosine kinase signaling inhibitor, is expressed in quiescent Pax7(+) satellite cells in uninjured muscle, downregulated in proliferating myogenic cells after injury, and reinduced as Pax7(+) cells re-enter quiescence. We show that Spry1 is required for the return to quiescence and homeostasis of the satellite cell pool during repair. Our results therefore define a role for Spry1 in adult muscle stem cell biology and tissue repair.
引用
收藏
页码:117 / 129
页数:13
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