Angiodysplasia in embryo lacking protein arginine methyltransferase 1 in vascular endothelial cells

J Biochem. 2017 Mar 1;161(3):255-258. doi: 10.1093/jb/mvw095.

Abstract

Protein arginine methyltransferase 1 (PRMT1) is involved in multiple cellular functions including proliferation and differentiation. Although PRMT1 is expressed in vascular endothelial cells (ECs), which are responsible for angiogenesis during embryonic development, its role has remained elusive. In this study, we generated endothelial-specific prmt1-knockout (Prmt1-ECKO) mice, and found that they died before embryonic day 15. The superficial temporal arteries in these embryos were poorly perfused with blood, and whole-mount 3D imaging revealed dilated and segmentalized luminal structures in Prmt1-ECKO fetuses in comparison with those of controls. Our findings provide evidence that PRMT1 is important for embryonic vascular formation.

Keywords: angiodysplasia; conditional knockout; endothellial cells; in vivo imaging; protein arginine methyltransferase 1.

MeSH terms

  • Angiodysplasia / metabolism*
  • Animals
  • Endothelial Cells / metabolism*
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Protein-Arginine N-Methyltransferases / chemistry
  • Protein-Arginine N-Methyltransferases / deficiency
  • Protein-Arginine N-Methyltransferases / metabolism*

Substances

  • Prmt1 protein, mouse
  • Protein-Arginine N-Methyltransferases