The VE-cadherin/AmotL2 mechanosensory pathway suppresses aortic inflammation and the formation of abdominal aortic aneurysms

Nat Cardiovasc Res. 2023 Jul;2(7):629-644. doi: 10.1038/s44161-023-00298-8. Epub 2023 Jun 29.

Abstract

Endothelial cells respond to mechanical forces exerted by blood flow. Endothelial cell-cell junctions and the sites of endothelial adhesion to the matrix sense and transmit mechanical forces to the cellular cytoskeleton. Here we show that the scaffold protein AmotL2 connects junctional VE-cadherin and actin filaments to the nuclear lamina. AmotL2 is essential for the formation of radial actin filaments and the alignment of endothelial cells, and, in its absence, nuclear integrity and positioning are altered. Molecular analysis demonstrated that VE-cadherin binds to AmotL2 and actin, resulting in a cascade that transmits extracellular mechanical signals to the nuclear membrane. Furthermore, the endothelial deficit of AmotL2 in mice fed normal diet provoked a pro-inflammatory response and abdominal aortic aneurysms (AAAs). Transcriptome analysis of human AAA samples revealed a negative correlation between AmotL2 and inflammation of the aortic intima. These findings offer insight into the link between junctional mechanotransduction and vascular disease.

MeSH terms

  • Actin Cytoskeleton / metabolism
  • Actins / genetics
  • Actins / metabolism
  • Angiomotins
  • Animals
  • Antigens, CD* / genetics
  • Antigens, CD* / metabolism
  • Aorta, Abdominal / metabolism
  • Aorta, Abdominal / pathology
  • Aortic Aneurysm, Abdominal* / metabolism
  • Aortic Aneurysm, Abdominal* / pathology
  • Aortitis / metabolism
  • Aortitis / pathology
  • Cadherins* / genetics
  • Cadherins* / metabolism
  • Disease Models, Animal
  • Endothelial Cells / metabolism
  • Endothelial Cells / pathology
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Humans
  • Male
  • Mechanotransduction, Cellular*
  • Mice
  • Mice, Inbred C57BL

Substances

  • Cadherins
  • Antigens, CD
  • cadherin 5
  • AMOTL2 protein, human
  • Angiomotins
  • Actins