Balancing forces: architectural control of mechanotransduction

被引:733
作者
DuFort, Christopher C. [1 ,2 ]
Paszek, Matthew J. [1 ,2 ]
Weaver, Valerie M. [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif San Francisco, Dept Surg, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Ctr Bioengn & Tissue Regenerat, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Anat, UCSF Helen Diller Comprehens Canc Ctr, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, UCSF Helen Diller Comprehens Canc Ctr, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
NONENZYMATIC CROSS-LINKING; EXTRACELLULAR-MATRIX; FOCAL ADHESIONS; LIVING CELLS; STRESS FIBERS; SHEAR-STRESS; IN-VIVO; MALIGNANT PHENOTYPE; SIGNALING PATHWAYS; ENDOTHELIAL-CELLS;
D O I
10.1038/nrm3112
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
All cells exist within the context of a three-dimensional microenvironment in which they are exposed to mechanical and physical cues. These cues can be disrupted through perturbations to mechanotransduction, from the nanoscale-level to the tissue-level, which compromises tensional homeostasis to promote pathologies such as cardiovascular disease and cancer. The mechanisms of such perturbations suggest that a complex interplay exists between the extracellular microenvironment and cellular function. Furthermore, sustained disruptions in tensional homeostasis can be caused by alterations in the extracellular matrix, allowing it to serve as a mechanically based memory-storage device that can perpetuate a disease or restore normal tissue behaviour.
引用
收藏
页码:308 / 319
页数:12
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