Substrate rigidity regulates the formation and maintenance of tissues

被引:334
作者
Guo, WH
Frey, MT
Burnham, NA
Wang, YL
机构
[1] Univ Massachusetts, Sch Med, Dept Physiol, Worcester, MA 01605 USA
[2] Worcester Polytech Inst, Dept Biomed Engn, Worcester, MA 01609 USA
[3] Worcester Polytech Inst, Dept Phys, Worcester, MA 01609 USA
关键词
D O I
10.1529/biophysj.105.070144
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The ability of cells to form tissues represents one of the most fundamental issues in biology. However, it is unclear what triggers cells to adhere to one another in tissues and to migrate once a piece of tissue is planted on culture surfaces. Using substrates of identical chemical composition but different flexibility, we show that this process is controlled by substrate rigidity: on stiff substrates, cells migrate away from one another and spread on surfaces, whereas on soft substrates they merge to form tissue-like structures. Similar behavior was observed not only with fibroblastic and epithelial cell lines but also explants from neonatal rat hearts. Cell compaction on soft substrates involves a combination of weakened adhesions to the substrate and myosin II-dependent contractile forces that drive cells toward one another. Our results suggest that tissue formation and maintenance is regulated by differential mechanical signals between cell-cell and cell-substrate interactions, which in turn elicit differential contractile forces and adhesions to determine the preferred direction of cell migration and association.
引用
收藏
页码:2213 / 2220
页数:8
相关论文
共 44 条
[1]   Nascent focal adhesions are responsible for the generation of strong propulsive forces in migrating fibroblasts [J].
Beningo, KA ;
Dembo, M ;
Kaverina, I ;
Small, JV ;
Wang, YL .
JOURNAL OF CELL BIOLOGY, 2001, 153 (04) :881-887
[2]  
Bernstein Lori R., 1994, Current Opinion in Oncology, V6, P106, DOI 10.1097/00001622-199401000-00015
[3]   Comparison of calibration methods for atomic-force microscopy cantilevers [J].
Burnham, NA ;
Chen, X ;
Hodges, CS ;
Matei, GA ;
Thoreson, EJ ;
Roberts, CJ ;
Davies, MC ;
Tendler, SJB .
NANOTECHNOLOGY, 2003, 14 (01) :1-6
[4]   MEASURING THE NANOMECHANICAL PROPERTIES AND SURFACE FORCES OF MATERIALS USING AN ATOMIC FORCE MICROSCOPE [J].
BURNHAM, NA ;
COLTON, RJ .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS, 1989, 7 (04) :2906-2913
[5]   HAPTOTAXIS AND MECHANISM OF CELL MOTILITY [J].
CARTER, SB .
NATURE, 1967, 213 (5073) :256-&
[6]   Extracellular matrix rigidity causes strengthening of integrin-cytoskeleton linkages [J].
Choquet, D ;
Felsenfeld, DP ;
Sheetz, MP .
CELL, 1997, 88 (01) :39-48
[7]   Signaling pathways controlling cell polarity and chemotaxis [J].
Chung, CY ;
Funamoto, S ;
Firtel, RA .
TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (09) :557-566
[8]   Defects in cell adhesion and the visceral endoderm following ablation of nonmuscle myosin heavy chain II-A in mice [J].
Conti, MA ;
Even-Ram, S ;
Liu, CY ;
Yamada, KM ;
Adelstein, RS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (40) :41263-41266
[9]   Stresses at the cell-to-substrate interface during locomotion of fibroblasts [J].
Dembo, M ;
Wang, YL .
BIOPHYSICAL JOURNAL, 1999, 76 (04) :2307-2316
[10]   Substrate compliance versus ligand density in cell on gel responses [J].
Engler, A ;
Bacakova, L ;
Newman, C ;
Hategan, A ;
Griffin, M ;
Discher, D .
BIOPHYSICAL JOURNAL, 2004, 86 (01) :617-628