Zyxin Is Involved in Fibroblast Rigidity Sensing and Durotaxis

Focal adhesions (FAs) are specialized structures that enable cells to sense their extracellular matrix rigidity and transmit these signals to the interior of the cells, bringing about actin cytoskeleton reorganization, FA maturation, and cell migration. It is known that cells migrate towards regions...

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Autores principales: Ai Kia Yip, Songjing Zhang, Lor Huai Chong, Elsie Cheruba, Jessie Yong Xing Woon, Theng Xuan Chua, Corinna Jie Hui Goh, Haibo Yang, Chor Yong Tay, Cheng-Gee Koh, Keng-Hwee Chiam
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Publicado: Frontiers Media S.A. 2021
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Acceso en línea:https://doaj.org/article/b822828024704e64a16215e1c227fbfd
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spelling oai:doaj.org-article:b822828024704e64a16215e1c227fbfd2021-11-18T09:34:20ZZyxin Is Involved in Fibroblast Rigidity Sensing and Durotaxis2296-634X10.3389/fcell.2021.735298https://doaj.org/article/b822828024704e64a16215e1c227fbfd2021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fcell.2021.735298/fullhttps://doaj.org/toc/2296-634XFocal adhesions (FAs) are specialized structures that enable cells to sense their extracellular matrix rigidity and transmit these signals to the interior of the cells, bringing about actin cytoskeleton reorganization, FA maturation, and cell migration. It is known that cells migrate towards regions of higher substrate rigidity, a phenomenon known as durotaxis. However, the underlying molecular mechanism of durotaxis and how different proteins in the FA are involved remain unclear. Zyxin is a component of the FA that has been implicated in connecting the actin cytoskeleton to the FA. We have found that knocking down zyxin impaired NIH3T3 fibroblast’s ability to sense and respond to changes in extracellular matrix in terms of their FA sizes, cell traction stress magnitudes and F-actin organization. Cell migration speed of zyxin knockdown fibroblasts was also independent of the underlying substrate rigidity, unlike wild type fibroblasts which migrated fastest at an intermediate substrate rigidity of 14 kPa. Wild type fibroblasts exhibited durotaxis by migrating toward regions of increasing substrate rigidity on polyacrylamide gels with substrate rigidity gradient, while zyxin knockdown fibroblasts did not exhibit durotaxis. Therefore, we propose zyxin as an essential protein that is required for rigidity sensing and durotaxis through modulating FA sizes, cell traction stress and F-actin organization.Ai Kia YipSongjing ZhangLor Huai ChongLor Huai ChongElsie CherubaJessie Yong Xing WoonTheng Xuan ChuaCorinna Jie Hui GohHaibo YangChor Yong TayChor Yong TayChor Yong TayChor Yong TayCheng-Gee KohKeng-Hwee ChiamFrontiers Media S.A.articlezyxinfocal adhesiondurotaxisrigidity sensingmechanotransductionBiology (General)QH301-705.5ENFrontiers in Cell and Developmental Biology, Vol 9 (2021)
institution DOAJ
collection DOAJ
language EN
topic zyxin
focal adhesion
durotaxis
rigidity sensing
mechanotransduction
Biology (General)
QH301-705.5
spellingShingle zyxin
focal adhesion
durotaxis
rigidity sensing
mechanotransduction
Biology (General)
QH301-705.5
Ai Kia Yip
Songjing Zhang
Lor Huai Chong
Lor Huai Chong
Elsie Cheruba
Jessie Yong Xing Woon
Theng Xuan Chua
Corinna Jie Hui Goh
Haibo Yang
Chor Yong Tay
Chor Yong Tay
Chor Yong Tay
Chor Yong Tay
Cheng-Gee Koh
Keng-Hwee Chiam
Zyxin Is Involved in Fibroblast Rigidity Sensing and Durotaxis
description Focal adhesions (FAs) are specialized structures that enable cells to sense their extracellular matrix rigidity and transmit these signals to the interior of the cells, bringing about actin cytoskeleton reorganization, FA maturation, and cell migration. It is known that cells migrate towards regions of higher substrate rigidity, a phenomenon known as durotaxis. However, the underlying molecular mechanism of durotaxis and how different proteins in the FA are involved remain unclear. Zyxin is a component of the FA that has been implicated in connecting the actin cytoskeleton to the FA. We have found that knocking down zyxin impaired NIH3T3 fibroblast’s ability to sense and respond to changes in extracellular matrix in terms of their FA sizes, cell traction stress magnitudes and F-actin organization. Cell migration speed of zyxin knockdown fibroblasts was also independent of the underlying substrate rigidity, unlike wild type fibroblasts which migrated fastest at an intermediate substrate rigidity of 14 kPa. Wild type fibroblasts exhibited durotaxis by migrating toward regions of increasing substrate rigidity on polyacrylamide gels with substrate rigidity gradient, while zyxin knockdown fibroblasts did not exhibit durotaxis. Therefore, we propose zyxin as an essential protein that is required for rigidity sensing and durotaxis through modulating FA sizes, cell traction stress and F-actin organization.
format article
author Ai Kia Yip
Songjing Zhang
Lor Huai Chong
Lor Huai Chong
Elsie Cheruba
Jessie Yong Xing Woon
Theng Xuan Chua
Corinna Jie Hui Goh
Haibo Yang
Chor Yong Tay
Chor Yong Tay
Chor Yong Tay
Chor Yong Tay
Cheng-Gee Koh
Keng-Hwee Chiam
author_facet Ai Kia Yip
Songjing Zhang
Lor Huai Chong
Lor Huai Chong
Elsie Cheruba
Jessie Yong Xing Woon
Theng Xuan Chua
Corinna Jie Hui Goh
Haibo Yang
Chor Yong Tay
Chor Yong Tay
Chor Yong Tay
Chor Yong Tay
Cheng-Gee Koh
Keng-Hwee Chiam
author_sort Ai Kia Yip
title Zyxin Is Involved in Fibroblast Rigidity Sensing and Durotaxis
title_short Zyxin Is Involved in Fibroblast Rigidity Sensing and Durotaxis
title_full Zyxin Is Involved in Fibroblast Rigidity Sensing and Durotaxis
title_fullStr Zyxin Is Involved in Fibroblast Rigidity Sensing and Durotaxis
title_full_unstemmed Zyxin Is Involved in Fibroblast Rigidity Sensing and Durotaxis
title_sort zyxin is involved in fibroblast rigidity sensing and durotaxis
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/b822828024704e64a16215e1c227fbfd
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