Control of stem cell fate and function by engineering physical microenvironments

被引:180
作者
Kshitiz [1 ,2 ]
Park, JinSeok [2 ]
Kim, Peter [1 ,2 ]
Helen, Wilda [3 ]
Engler, Adam J. [3 ]
Levchenko, Andre [2 ]
Kim, Deok-Ho [1 ]
机构
[1] Univ Washington, Dept Bioengn, Seattle, WA 98195 USA
[2] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21218 USA
[3] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
关键词
SHEAR-STRESS; SMOOTH-MUSCLE; ENDOTHELIAL-CELLS; GROWTH-FACTORS; QUANTITATIVE-ANALYSIS; SIGNAL-TRANSDUCTION; MECHANICAL SIGNALS; SUBSTRATE RIGIDITY; MATRIX ADHESIONS; PROGENITOR CELLS;
D O I
10.1039/c2ib20080e
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The phenotypic expression and function of stem cells are regulated by their integrated response to variable microenvironmental cues, including growth factors and cytokines, matrix-mediated signals, and cell-cell interactions. Recently, growing evidence suggests that matrix-mediated signals include mechanical stimuli such as strain, shear stress, substrate rigidity and topography, and these stimuli have a more profound impact on stem cell phenotypes than had previously been recognized, e.g. self-renewal and differentiation through the control of gene transcription and signaling pathways. Using a variety of cell culture models enabled by micro and nanoscale technologies, we are beginning to systematically and quantitatively investigate the integrated response of cells to combinations of relevant mechanobiological stimuli. This paper reviews recent advances in engineering physical stimuli for stem cell mechanobiology and discusses how micro-and nanoscale engineered platforms can be used to control stem cell niche environments and regulate stem cell fate and function.
引用
收藏
页码:1008 / 1018
页数:11
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