Impaired vascular contractility and blood pressure homeostasis in the smooth muscle alpha-actin null mouse

FASEB J. 2000 Nov;14(14):2213-20. doi: 10.1096/fj.99-0927com.

Abstract

The smooth muscle (SM) alpha-actin gene activated during the early stages of embryonic cardiovascular development is switched off in late stage heart tissue and replaced by cardiac and skeletal alpha-actins. SM alpha-actin also appears during vascular development, but becomes the single most abundant protein in adult vascular smooth muscle cells. Tissue-specific expression of SM alpha-actin is thought to be required for the principal force-generating capacity of the vascular smooth muscle cell. We wanted to determine whether SM alpha-actin gene expression actually relates to an actin isoform's function. Analysis of SM alpha-actin null mice indicated that SM alpha-actin is not required for the formation of the cardiovascular system. Also, SM alpha-actin null mice appeared to have no difficulty feeding or reproducing. Survival in the absence of SM alpha-actin may result from other actin isoforms partially substituting for this isoform. In fact, skeletal alpha-actin gene, an actin isoform not usually expressed in vascular smooth muscle, was activated in the aortas of these SM alpha-actin null mice. However, even with a modest increase in skeletal alpha-actin activity, highly compromised vascular contractility, tone, and blood flow were detected in SM alpha-actin-defective mice. This study supports the concept that SM alpha-actin has a central role in regulating vascular contractility and blood pressure homeostasis, but is not required for the formation of the cardiovascular system.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actins / genetics*
  • Actins / metabolism
  • Animals
  • Blood Flow Velocity / physiology
  • Blood Pressure / physiology*
  • Blotting, Northern
  • Female
  • Gene Expression Regulation, Developmental
  • Homeostasis
  • Immunohistochemistry
  • In Vitro Techniques
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred Strains
  • Mice, Knockout
  • Muscle Contraction / physiology*
  • Muscle, Skeletal / metabolism
  • Muscle, Smooth, Vascular / blood supply
  • Muscle, Smooth, Vascular / metabolism
  • Muscle, Smooth, Vascular / physiopathology*
  • Mutation
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Tissue Distribution

Substances

  • Actins
  • RNA, Messenger