Visualizing mechanical modulation of nanoscale organization of cell-matrix adhesions

被引:11
|
作者
Ou, Guanqing [1 ,2 ,3 ]
Thakar, Dhruv [3 ]
Tung, Jason C. [3 ]
Miroshnikova, Yekaterina A. [1 ,2 ,3 ]
Dufort, Christopher C. [3 ]
Gutierrez, Edgar [4 ]
Groisman, Alex [4 ]
Weaver, Valerie M. [3 ,5 ,6 ,7 ,8 ]
机构
[1] Univ Calif Berkeley, Berkeley, CA 94720 USA
[2] Univ Calif San Francisco, San Francisco Joint Grad Grp Bioengn, San Francisco, CA 94143 USA
[3] UCSF, Dept Surg, Ctr Bioengn & Tissue Regenerat, San Francisco, CA 94143 USA
[4] Univ Calif San Diego, Dept Phys, San Diego, CA USA
[5] UCSF, Dept Anat, San Francisco, CA 94143 USA
[6] UCSF, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
[7] UCSF, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA
[8] UCSF, UCSF Helen Diller Comprehens Canc Ctr, San Francisco, CA 94143 USA
关键词
INTERFERENCE-CONTRAST MICROSCOPY; DYNAMICS;
D O I
10.1039/c6ib00031b
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mechanical properties of the extracellular matrix influence cell signaling to regulate key cellular processes, including differentiation, apoptosis, and transformation. Understanding the molecular mechanisms underlying mechanotransduction is contingent upon our ability to visualize the effect of altered matrix properties on the nanoscale organization of proteins involved in this signalling. The development of super-resolution imaging techniques has afforded researchers unprecedented ability to probe the organization and localization of proteins within the cell. However, most of these methods require use of substrates like glass or silicon wafers, which are artificially rigid. In light of a growing body of literature demonstrating the importance of mechanical properties of the extracellular matrix in regulating many aspects of cellular behavior and signaling, we have developed a system that allows scanning angle interference microscopy on a mechanically tunable substrate. We describe its implementation in detail and provide examples of how it may be used to aide investigations into the effect of substrate rigidity on intracellular signaling.
引用
收藏
页码:795 / 804
页数:10
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