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Biophysical and Biochemical Roles of Shear Stress on Endothelium: A Revisit and New Insights

  • Chak Kwong Cheng
  • , Nanping Wang
  • , Li Wang*
  • , Yu Huang*
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

Hemodynamic shear stress, the frictional force exerted by blood flow on the endothelium, mediates vascular homeostasis. This review examines the biophysical nature and biochemical effects of shear stress on endothelial cells, with a particular focus on its impact on cardiovascular pathophysiology. Atherosclerosis develops preferentially at arterial branches and curvatures, where disturbed flow patterns are most prevalent. The review also highlights the range of shear stress across diverse human arteries and its temporal variations, including aging-related alterations. This review presents a summary of the critical mechanosensors and flow-sensitive effectors that respond to shear stress, along with the downstream cellular events that they regulate. The review evaluates experimental models for studying shear stress in vitro and in vivo, as well as their potential limitations. The review discusses strategies targeting shear stress, including pharmacological approaches, physiological means, surgical interventions, and gene therapies. Furthermore, the review addresses emerging perspectives in hemodynamic research, including single-cell sequencing, spatial omics, metabolomics, and multiomics technologies. By integrating the biophysical and biochemical aspects of shear stress, this review offers insights into the complex interplay between hemodynamics and endothelial homeostasis at the preclinical and clinical levels. © 2025 The Authors.
Original languageEnglish
Pages (from-to)752-772
JournalCirculation Research
Volume136
Issue number7
Online published27 Mar 2025
DOIs
Publication statusPublished - 28 Mar 2025

Funding

This work was supported by the Hong Kong Research Grants Council (T12-101/23-N, SRFS2021-4S04, 11103222, and 14109720), the Natural Science Foundation of China (No. 82230012), and the City University of Hong Kong Start-Up Fund . This work was also substantially supported by a fellowship award from the Research Grants Council of the Hong Kong Special Administrative Region, China (project No. CityU PDFS2223-1S01).

Research Keywords

  • atherosclerosis
  • endothelial cells
  • exercise
  • hemodynamics
  • multiomics

RGC Funding Information

  • RGC-funded

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