Matrix elasticity directs stem cell lineage specification

被引:10652
作者
Engler, Adam J.
Sen, Shamik
Sweeney, H. Lee
Discher, Dennis E. [1 ]
机构
[1] Univ Penn, Muscle Inst, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Engn & Appl Sci, Philadelphia, PA 19104 USA
[3] Univ Penn, Cell & Mol Biol Grad Grp, Philadelphia, PA 19104 USA
[4] Univ Penn, Phys Grad Grp, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/j.cell.2006.06.044
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microenvironments appear important in stem cell lineage specification but can be difficult to adequately characterize or control with soft tissues. Naive mesenchymal stem cells (MSCs) are shown hereto specify lineage and commit to phenotypes with extreme sensitivity to tissue-level elasticity. Soft matrices that mimic brain are neurogenic, stiffer matrices that mimic muscle are myogenic, and comparatively rigid matrices that mimic collagenous bone prove osteogenic. During the initial week in culture, reprogramming of these lineages is possible with addition of soluble induction factors, but after several weeks in culture, the cells commit to the lineage specified by matrix elasticity, consistent with the elasticity-insensitive commitment of differentiated cell types. Inhibition of nonmuscle myosin II blocks all elasticity-directed lineage specification-without strongly perturbing many other aspects of cell function and shape. The results have significant implications for understanding physical effects of the in vivo microenvironment and also for therapeutic uses of stem cells.
引用
收藏
页码:677 / 689
页数:13
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