Acid-base transporters modulate cell migration, growth and proliferation: Implications for structure development and remodeling of resistance arteries?

Trends Cardiovasc Med. 2013 Apr;23(3):59-65. doi: 10.1016/j.tcm.2012.09.001. Epub 2012 Dec 21.

Abstract

Disturbed acid-base transport across the plasma membrane affects intracellular pH control and has been shown--primarily based on studies with non-vascular cells--to interfere with a number of fundamental cell functions including cell migration, growth and proliferation. Here, we evaluate the effects of acid-base transport and intracellular pH on the morphology of the resistance artery wall, which is altered in a number of physiological and pathological conditions and is an independent predictor of cardiovascular risk. The current evidence supports that disturbed function and/or expression of acid-base transporters can alter resistance artery morphology--and potentially atherosclerosis-prone conduit arteries--and hence should be considered as possible mechanistic components and targets for treatment in cardiovascular disease. More experimental evidence is required, however, to evaluate the cell biological effects of acid-base transport in vascular cells, the roles of specific acid-base transporters in artery remodeling, the relative mechanistic importance of acid-base transporters in the vascular wall compared to other organs, and the therapeutic potential of modifying acid-base transport activity pharmacologically or genetically.

Publication types

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

MeSH terms

  • Acid-Base Equilibrium*
  • Animals
  • Arteries / growth & development
  • Arteries / metabolism*
  • Arteries / pathology
  • Cell Movement*
  • Cell Proliferation*
  • Cell Survival
  • Endothelial Cells / metabolism
  • Humans
  • Hydrogen-Ion Concentration
  • Hypertrophy
  • Membrane Transport Proteins / metabolism*
  • Muscle, Smooth, Vascular / metabolism
  • Myocytes, Smooth Muscle / metabolism
  • Neovascularization, Physiologic*
  • Vascular Resistance*

Substances

  • Membrane Transport Proteins