Cx43 Facilitates Mesenchymal Transition of Endothelial Cells Induced by Shear Stress

J Vasc Res. 2023;60(4):204-212. doi: 10.1159/000533320. Epub 2023 Sep 6.

Abstract

Objectives: This study aimed to determine the function of Cx43 in the endothelial-to-mesenchymal transition (EndMT) process of endothelial cells (ECs) and to explore the potential signaling pathways underlying these functions.

Methods: ECs were extracted from rat aorta. ECs were transfected with Cx43 cDNA and Cx43 siRNA and then exposed to 5 or 12 dyne/cm2. Immunofluorescence staining was used to detect the expression of SM22α, Cx43, and acetylated α-tubulin in ECs. Western blotting was used to detect the protein expression of α-SMA, CD31, Cx43, H1-calponin, Ift88, and p-smad3 in ECs.

Results: The expression of αSMA, SM22α, and Cx43 was significantly increased, and CD31 was markedly decreased in ECs treated with laminar shear stress at 5 dyn/cm2. The Cx43 cDNA transfection could induce the expression of SM22α or H1-calponin and attenuate CD31 expression in ECs. Also, Cx43 overexpression harms cilia formation in ECs exposed to 5 dyn/cm2, accompanied with the regulated Ift88 and smad signaling.

Conclusions: This study found that laminar shear stress at 5 dyn/cm2 would increase the expression of Cx43 to facilitate the EndMT process of ECs, associated with morphological changes in primary cilia and the decreased expression of Ift88 in ECs.

Keywords: Cilia; Cx43; Endothelial-to-mesenchymal transition; Shear stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Connexin 43* / genetics
  • DNA, Complementary
  • Endothelial Cells*
  • Rats
  • Signal Transduction
  • Stress, Mechanical

Substances

  • Connexin 43
  • DNA, Complementary
  • Gja1 protein, rat

Grants and funding

This work was supported by the National Natural Science Foundation of China (81200206 to Zongqi Zhang).