4.8 Article

Zyxin and actin structure confer anisotropic YAP mechanotransduction

Journal

ACTA BIOMATERIALIA
Volume 152, Issue -, Pages 313-320

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2022.08.079

Keywords

YAP; Mechanotransduction; Focal adhesion; Anisotropy; Actin repair; Cytoskeleton

Funding

  1. National Taiwan University [NTU-JP110L7214]
  2. Ministry of Science and Technology [MOST 1082321-B-002-061-MY2, 110-2221-E-002-011-MY2]
  3. National Health Research Institute [NHRI-EX111-10910EI]

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Cells respond differently to anisotropic loading, with parallel stretch activating YAP nuclear translocation and inducing actin cytoskeleton damage and repair mediated by focal adhesion kinase (FAK) and zyxin.
Tissues and the embedded cells experience anisotropic deformations due to their functions and anatomi-cal locations. The resident cells, such as tenocytes and muscle cells, are often restricted by their extracel-lular matrix and organize parallel to their major loading direction, yet most studies on cellular responses to strains use isotropic substrates without predetermined organizations. To understand how confined cells sense and respond to anisotropic loading, we combine cell patterning and uniaxial stretch to have precise geometric control. Dynamic stretch parallel to the long axis of the cell activates YAP nuclear transloca-tion, but not when stretched in the perpendicular direction. Looking at the initial cytoskeleton response, parallel stretch leads to actin breakage and repair within the first minute, mediated by zyxin, the focal adhesion protein. In addition, this zyxin-mediated repair response is controlled by focal adhesion kinase (FAK) and leads to YAP signaling. As these factors are intimately involved in a wide range of mechanical regulation, our findings point to new roles of zyxin and YAP in anisotropic mechanotransduction, and may provide additional perspectives in cellular adaptive responses and tissue homeostasis.Statement of significanceStructure and deformation of tissues control gene expression, migration, and proliferation of the resident cells. In an effort to understand the underlying mechanisms, we find that the transcription cofactor YAP respond to mechanical stretch in a direction-dependent manner. We demonstrate that parallel stretch induces actin cytoskeleton damage, focal adhesion kinase (FAK) activation, and zyxin relocation, which are involved in the anisotropic YAP signaling. Our findings provide additional perspectives in the interactions of tissue structure and cell mechanotransduction.(c) 2022 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

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