A home away from home: Challenges and opportunities in engineering in vitro muscle satellite cell niches

被引:93
作者
Cosgrove, Benjamin D. [1 ,2 ,3 ,4 ]
Sacco, Alessandra [1 ,2 ,4 ]
Gilbert, Penney M. [1 ,2 ,4 ]
Blau, Helen M. [1 ,2 ,3 ,4 ]
机构
[1] Stanford Univ, Sch Med, Baxter lab Genet Pharmacol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Mol Imaging Program Stanford, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Stem Cell Biol & Regenerat Med Inst, Stanford, CA 94305 USA
关键词
Skeletal muscle stem cell; Self-renewal; Hydrogel; Tethered ligand; Matrix stiffness; Biomaterials; Niche microenvironment; HEMATOPOIETIC STEM-CELLS; ADULT SKELETAL-MUSCLE; SELF-RENEWAL; GROWTH-FACTOR; MOLECULAR REGULATION; PROGENITOR CELLS; BONE-MARROW; EXPRESSION; DIFFERENTIATION; ACTIVATION;
D O I
10.1016/j.diff.2009.08.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Satellite cells are skeletal muscle stem cells with a principal role in postnatal skeletal muscle regeneration. Satellite cells, like many tissue-specific adult stem cells, reside in a quiescent state in an instructive, anatomically defined niche. The satellite cell niche constitutes a distinct membrane-enclosed compartment within the muscle fiber, containing a diversity of biochemical and biophysical signals that influence satellite cell function. A major limitation to the study and clinical utility of satellite cells is that upon removal from the muscle fiber and plating in traditional plastic tissue culture platforms, their muscle stem cell properties are rapidly lost. Clearly, the maintenance of stem cell function is critically dependent on in vivo niche signals, highlighting the need to create novel in vitro microenvironments that allow for the maintenance and propagation of satellite cells while retaining their potential to function as muscle stem cells. Here, we discuss how emerging biomaterials technologies offer great promise for engineering in vitro microenvironments to meet these challenges. In engineered biomaterials, signaling molecules can be presented in a manner that more closely mimics cell-cell and cell-matrix interactions, and matrices can be fabricated with diverse rigidities that approximate in vivo tissues. The development of in vitro microenvironments in which niche features can be systematically modulated will be instrumental not only to future insights into muscle stem cell biology and therapeutic approaches to muscle diseases and muscle wasting with aging, but also will provide a paradigm for the analysis of numerous adult tissue-specific stem cells. (C) 2009 International Society of Differentiation. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:185 / 194
页数:10
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