Sca-1 expression is required for efficient remodeling of the extracellular matrix during skeletal muscle regeneration

被引:50
作者
Kafadar, Kimberly A. [1 ]
Yi, Lin [2 ]
Ahmad, Yusra [1 ]
So, Leslie [2 ]
Rossi, Fabio [2 ]
Pavlath, Grace K. [1 ]
机构
[1] Emory Univ, Dept Pharmacol, Atlanta, GA 30322 USA
[2] Univ British Columbia, Biomed Res Ctr, Vancouver, BC V6T 1Z3, Canada
基金
加拿大自然科学与工程研究理事会; 美国国家卫生研究院;
关键词
Skeletal muscle; Sca-1; Regeneration; Satellite cell; MMP; Extracellular matrix; Fibrosis; Stem cells; STEM-CELL ANTIGEN-1; HEPATOCYTE GROWTH-FACTOR; COX-2; PATHWAY; T-CELLS; GENE; METALLOPROTEINASES; DIFFERENTIATION; ACTIVATION; MIGRATION; PROTEIN;
D O I
10.1016/j.ydbio.2008.10.036
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sca-1 (Stem Cell Antigen-1) is a member of the Ly-6 family proteins that functions in cell growth, differentiation, and self-renewal in multiple tissues. In skeletal muscle Sca-1 negatively regulates myoblast proliferation and differentiation, and may function in the maintenance of progenitor cells. We investigated the role of Sca-1 in skeletal muscle regeneration and show here that Sca-1 expression is upregulated in a subset of myogenic cells upon muscle injury. We demonstrate that extract from crushed muscle upregulates Sca-1 expression in myoblasts in vitro, and that this effect is reversible and independent of cell proliferation. Sca-1(-/-) mice exhibit defects in muscle regeneration, with the development of fibrosis following injury. Sca-1(-1-) muscle displays reduced activity of matrix metalloproteinases, critical regulators of extracellular matrix remodeling. interestingly, we show that the number of satellite cells is similar in wild-type and Sca-1(-/-) muscle, suggesting that in sat satellite cells Sca-1 does not play a role in self-renewal. We hypothesize that Sca-1 upregulates, directly or indirectly, the activity of matrix metalloproteinases, leading to matrix breakdown and efficient muscle regeneration. Further elucidation of the role of Sca-1 in matrix remodeling may aid in the development of novel therapeutic strategies for the treatment of fibrotic diseases. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:47 / 59
页数:13
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