Dissecting cellular mechanics: Implications for aging, cancer, and immunity

被引:20
作者
Harris, Michael J. [1 ,2 ]
Wirtz, Denis [1 ,2 ,3 ,4 ]
Wu, Pei-Hsun [1 ,2 ]
机构
[1] Johns Hopkins Univ, Johns Hopkins Phys Sci Oncol Ctr, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21231 USA
[4] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21231 USA
关键词
Cellular viscoelasticity; Cell mechanics; Cancer; Immunology; Cell microenvironment; SINGLE-PARTICLE TRACKING; BREAST-CANCER; NUCLEAR MECHANICS; MATRIX STIFFNESS; DENDRITIC CELLS; IN-VITRO; F-ACTIN; MIGRATION; FORCE; MICROSCOPY;
D O I
10.1016/j.semcdb.2018.10.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cells are dynamic structures that must respond to complex physical and chemical signals from their surrounding environment. The cytoskeleton is a key mediator of a cell's response to the signals of both the extracellular matrix and other cells present in the local microenvironment and allows it to tune its own mechanical properties in response to these cues. A growing body of evidence suggests that altered cellular viscoelasticity is a strong indicator of disease state; including cancer, laminopathy (genetic disorders of the nuclear lamina), infection, and aging. Here, we review recent work on the characterization of cell mechanics in disease and discuss the implications of altered viscoelasticity in regulation of immune responses. Finally, we provide an overview of techniques for measuring the mechanical properties of cells deeply embedded within tissues.
引用
收藏
页码:16 / 25
页数:10
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