Good advice for endothelial cells: Get in line, relax tension, and go with the flow.

APL Bioeng

Department of Biomedical Engineering and Department of Cellular and Molecular Medicine, Texas A&M University, College Station, Texas 77843-3120, USA.

Published: March 2020

AI Article Synopsis

  • Endothelial cells experience fluid wall shear stress and cyclic strain from blood flow and pressure, which play critical roles in vascular health and disease.
  • While ECs typically align along the direction of blood flow in healthy areas, this alignment is disrupted in regions susceptible to atherosclerosis.
  • The review emphasizes the importance of understanding the combined effects of these hemodynamic forces and their role in mechanotransduction, suggesting that integrated research could enhance our knowledge of mechanical influences on atherosclerosis development.

Article Abstract

Endothelial cells (ECs) are continuously subjected to fluid wall shear stress (WSS) and cyclic strain caused by pulsatile blood flow and pressure. It is well established that these hemodynamic forces each play important roles in vascular disease, but their combined effects are not well understood. ECs remodel in response to both WSS and cyclic strain to align along the vessel axis, but in areas prone to atherogenesis, such an alignment is absent. In this perspective, experimental and clinical findings will be reviewed, which have revealed the characteristics of WSS and cyclic strain, which are associated with atherosclerosis, spanning studies on whole blood vessels to individual cells to mechanosensing molecules. Examples are described regarding the use of computational modeling to elucidate the mechanisms by which EC alignment contributes to mechanical homeostasis. Finally, the need to move toward an integrated understanding of how hemodynamic forces influence EC mechanotransduction is presented, which holds the potential to move our currently fragmented understanding to a true appreciation of the role of mechanical stimuli in atherosclerosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044000PMC
http://dx.doi.org/10.1063/1.5129812DOI Listing

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