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Receptor-mediated cell mechanosensing.

作者信息

Chen Yunfeng, Ju Lining, Rushdi Muaz, Ge Chenghao, Zhu Cheng

机构信息

Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA 30332.

Parker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA 30332.

出版信息

Mol Biol Cell. 2017 Nov 7;28(23):3134-3155. doi: 10.1091/mbc.E17-04-0228. Epub 2017 Sep 27.


DOI:10.1091/mbc.E17-04-0228
PMID:28954860
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5687017/
Abstract

Mechanosensing describes the ability of a cell to sense mechanical cues of its microenvironment, including not only all components of force, stress, and strain but also substrate rigidity, topology, and adhesiveness. This ability is crucial for the cell to respond to the surrounding mechanical cues and adapt to the changing environment. Examples of responses and adaptation include (de)activation, proliferation/apoptosis, and (de)differentiation. Receptor-mediated cell mechanosensing is a multistep process that is initiated by binding of cell surface receptors to their ligands on the extracellular matrix or the surface of adjacent cells. Mechanical cues are presented by the ligand and received by the receptor at the binding interface; but their transmission over space and time and their conversion into biochemical signals may involve other domains and additional molecules. In this review, a four-step model is described for the receptor-mediated cell mechanosensing process. Platelet glycoprotein Ib, T-cell receptor, and integrins are used as examples to illustrate the key concepts and players in this process.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d62/5687017/059f48515a52/3134fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d62/5687017/fb1f4726a458/3134fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d62/5687017/64aaf5474416/3134fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d62/5687017/48fb035fccac/3134fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d62/5687017/7efb30d6dcf1/3134fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d62/5687017/bf52914b43e6/3134fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d62/5687017/059f48515a52/3134fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d62/5687017/fb1f4726a458/3134fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d62/5687017/64aaf5474416/3134fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d62/5687017/48fb035fccac/3134fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d62/5687017/7efb30d6dcf1/3134fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d62/5687017/bf52914b43e6/3134fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d62/5687017/059f48515a52/3134fig6.jpg

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[10]
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本文引用的文献

[1]
Dual Biomembrane Force Probe enables single-cell mechanical analysis of signal crosstalk between multiple molecular species.

Sci Rep. 2017-10-27

[2]
Flow-induced elongation of von Willebrand factor precedes tension-dependent activation.

Nat Commun. 2017-8-23

[3]
Mechanosensing in the immune response.

Semin Cell Dev Biol. 2017-8-19

[4]
Contractile actomyosin arcs promote the activation of primary mouse T cells in a ligand-dependent manner.

PLoS One. 2017-8-17

[5]
Mechanosensing drives acuity of T-cell recognition.

Proc Natl Acad Sci U S A. 2017-8-15

[6]
Mechanotransduction at the cell-matrix interface.

Semin Cell Dev Biol. 2017-7-25

[7]
A discontinuous autoinhibitory module masks the A1 domain of von Willebrand factor.

J Thromb Haemost. 2017-8-9

[8]
Interfacing 3D magnetic twisting cytometry with confocal fluorescence microscopy to image force responses in living cells.

Nat Protoc. 2017-7

[9]
Ionic CD3-Lck interaction regulates the initiation of T-cell receptor signaling.

Proc Natl Acad Sci U S A. 2017-6-28

[10]
Quantifying forces in cell biology.

Nat Cell Biol. 2017-6-19

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