Anisotropic Effects of Mechanical Strain on Neural Crest Stem Cells

被引:9
作者
Li, Xian [1 ,2 ]
Chu, Julia S. [2 ]
Yang, Li [1 ]
Li, Song [2 ]
机构
[1] Chongqing Univ, Bioengn Coll, Project Lab Biomech & Tissue Repair 111, Chongqing 400044, Peoples R China
[2] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
Neural crest stem cells; Cyclic uniaxial strain; Micropatterning; Anisotropic; SMOOTH-MUSCLE-CELLS; TGF-BETA; PROGENITOR CELLS; CYCLIC STRAIN; IN-VITRO; TISSUE; PROLIFERATION; DIFFERENTIATION; DEACETYLASES; EXPRESSION;
D O I
10.1007/s10439-011-0403-5
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Neural crest stem cells (NCSCs) are multipotent and play an important role during the development and tissue regeneration. However, the anisotropic effects of mechanical strain on NCSCs are not known. To investigate the anisotropic mechanosensing by NCSCs, NCSCs derived from induced pluripotent stem cells were cultured on micropatterned membranes, and subjected to cyclic uniaxial strain in the direction parallel or perpendicular to the microgrooves. Cell and nuclear shape were both regulated by micropatterning and mechanical strain. Among the unpatterned, parallel-patterned and perpendicular-patterned groups, mechanical strain caused an increase in histone deacetylase activity in the parallel-patterned group, accompanied by the increase of cell proliferation. In addition, mechanical strain increased the expression of contractile marker calponin-1 but not other differentiation markers in the unpatterned and parallel-patterned groups. These results demonstrated that NCSCs responded differently to the anisotropic mechanical environment. Understanding the mechanical regulation of NCSCs will reveal the role of mechanical factors in NCSC differentiation during development, and provide a basis for using NCSCs for tissue engineering.
引用
收藏
页码:598 / 605
页数:8
相关论文
共 31 条
[11]   Anisotropic mechanosensing by mesenchymal stem cells [J].
Kurpinski, Kyle ;
Chu, Julia ;
Hashi, Craig ;
Li, Song .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (44) :16095-16100
[12]   Isolation and directed differentiation of neural crest stem cells derived from human embryonic stem cells [J].
Lee, Gabsang ;
Kim, Hyesoo ;
Elkabetz, Yechiel ;
Al Shamy, George ;
Panagiotakos, Georgia ;
Barberi, Tiziano ;
Tabar, Viviane ;
Studer, Lorenz .
NATURE BIOTECHNOLOGY, 2007, 25 (12) :1468-1475
[13]   Histone acetyltransferases and deacetylases in the control of cell proliferation and differentiation [J].
Lehrmann, H ;
Pritchard, LL ;
Harel-Bellan, A .
ADVANCES IN CANCER RESEARCH, VOL 86, 2002, 86 :41-65
[14]   Mechanical stress-initiated signal transductions in vascular smooth muscle cells [J].
Li, CH ;
Xu, QB .
CELLULAR SIGNALLING, 2000, 12 (07) :435-445
[15]   Innate diversity of adult human arterial smooth muscle cells - Cloning of distinct subtypes from the internal thoracic artery [J].
Li, SH ;
Fan, YS ;
Chow, LH ;
Van Den Diepstraten, C ;
van der Veer, E ;
Sims, SM ;
Pickering, JG .
CIRCULATION RESEARCH, 2001, 89 (06) :517-525
[16]   Biophysical Regulation of Histone Acetylation in Mesenchymal Stem Cells [J].
Li, Yuan ;
Chu, Julia S. ;
Kurpinski, Kyle ;
Li, Xian ;
Bautista, Diana M. ;
Yang, Li ;
Sung, K. -L. Paul ;
Li, Song .
BIOPHYSICAL JOURNAL, 2011, 100 (08) :1902-1909
[17]   Developmental basis of vascular smooth muscle diversity [J].
Majesky, Mark W. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2007, 27 (06) :1248-1258
[18]  
Moustakas A, 2001, J CELL SCI, V114, P4359
[19]   Functional arteries grown in vitro [J].
Niklason, LE ;
Gao, J ;
Abbott, WM ;
Hirschi, KK ;
Houser, S ;
Marini, R ;
Langer, R .
SCIENCE, 1999, 284 (5413) :489-493
[20]  
Park IH, 2008, NATURE, V451, P141, DOI [10.1038/nature06534, 10.1038/natureO6534]