4.2 Article

Global architecture of the F-actin cytoskeleton regulates cell shape-dependent endothelial mechanotransduction

Journal

INTEGRATIVE BIOLOGY
Volume 6, Issue 3, Pages 300-311

Publisher

OXFORD UNIV PRESS
DOI: 10.1039/c3ib40223a

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Funding

  1. National Science Foundation [CMMI 1129611, CBET 1149401]
  2. National Institute of Health [1R21HL114011]
  3. American Heart Association [12SDG12180025]
  4. Department of Mechanical Engineering at the University of Michigan, Ann Arbor
  5. Directorate For Engineering [1129611] Funding Source: National Science Foundation
  6. Directorate For Engineering
  7. Div Of Chem, Bioeng, Env, & Transp Sys [1149401] Funding Source: National Science Foundation
  8. Div Of Civil, Mechanical, & Manufact Inn [1129611] Funding Source: National Science Foundation

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Uniaxial stretch is an important biophysical regulator of cell morphology (or shape) and functions of vascular endothelial cells (ECs). However, it is unclear whether and how cell shape can independently regulate EC mechanotransductive properties under uniaxial stretch. Herein, utilizing a novel uniaxial cell-stretching device integrated with micropost force sensors, we reported the first experimental evidence showing cell shape-dependent EC mechanotransduction via cytoskeleton (CSK) contractile forces in response to uniaxial stretch. Combining experiments and theoretical modeling from first principles, we showed that it was the global architecture of the F-actin CSK that instructed the cell shape-dependent EC mechanotransductive process. Furthermore, a cell shape-dependent nature was relayed in EC mechanotransduction via dynamic focal adhesion (FA) assembly. Our results suggested a novel mechanotransductive process in ECs wherein the global architecture of the F-actin CSK, governed by cell shape, controls mechanotransduction via CSK contractile forces and force-dependent FA assembly under uniaxial stretch.

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