Nuclear mechanotransduction on skin stem cell fate regulation

被引:1
|
作者
Biggs, Leah C. [1 ]
Miroshnikova, Yekaterina A. [2 ]
机构
[1] Max Planck Inst Mol Biomed, Dept Cell & Tissue Dynam, D-48149 Munster, Germany
[2] NIDDKD, Lab Mol Biol, NIH, Bethesda, MD 20892 USA
关键词
PROLIFERATION; KERATINOCYTE; EXPRESSION; DIFFERENTIATION; ORGANIZATION; ADHESION; BETA-1-INTEGRIN; LINEAGES; ABSENCE; GENOME;
D O I
10.1016/j.ceb.2024.102328
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mammalian skin is a highly dynamic and regenerative organ that has long been recognized as a mechanically active composite of tissues withstanding daily compressive and tensile forces that arise from body movement. Importantly, cell- and tissue-scale mechanical signals are critical regulators of skin morphogenesis and homeostasis. These signals are sensed at the cellular periphery and transduced by mechanosensitive proteins within the plasma membrane to the cytoskeletal networks, and eventually into the nucleus to regulate chromatin organization and gene expression. The role of each of these nodes in producing a coherent mechanoresponse at both celland tissue-scales is emerging. Here we focus on the key cytoplasmic and nuclear mechanosensitive structures that are critical for the mammalian skin development and homeostatic maintenance. We propose that the mechanical state of the skin, in particular of its nuclear compartment, is a critical rheostat that fine-tunes developmental and homeostatic processes essential for the proper function of the organ.
引用
收藏
页数:9
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