Claudin-5 levels are reduced in human end-stage cardiomyopathy

J Mol Cell Cardiol. 2008 Jul;45(1):81-7. doi: 10.1016/j.yjmcc.2008.04.005. Epub 2008 Apr 25.

Abstract

Claudin-5 is a transmembrane cell junction protein that is a component of tight junctions in endothelial cell layers. We have previously shown that claudin-5 also localizes to lateral membranes of murine cardiomyocytes at their junction with the extracellular matrix. Claudin-5 levels are specifically reduced in myocytes from a mouse model of muscular dystrophy with cardiomyopathy. To establish whether claudin-5 is similarly specifically reduced in human cardiomyopathy, we compared the levels of claudin-5 with other cell junction proteins in 62 cardiomyopathic end-stage explant samples. We show that claudin-5 levels are reduced in at least 60% of patient samples compared with non-failing controls. Importantly, claudin-5 reductions can be independent of connexin-43, a gap junction protein previously reported to be reduced in failing heart samples. Other cell junction proteins including alpha-catenin, beta-catenin, gamma-catenin, desmoplakin, and N-cadherin are reduced in only a small number of failing samples and only in combination with reduced claudin-5 or connexin-43 levels. We also show that reduced claudin-5 levels can be present independently from dystrophin alterations, which are known to be capable of causing and resulting from cardiomyopathy. These data are the first to show alterations of a tight junction protein in human cardiomyopathy samples and suggest that claudin-5 may participate in novel mechanisms in the pathway to end-stage heart failure.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / metabolism
  • Cadherins / metabolism
  • Cardiomyopathies / metabolism*
  • Cardiomyopathies / pathology
  • Catenins / metabolism
  • Claudin-5
  • Connexin 43
  • Desmoplakins / metabolism
  • Female
  • Gap Junctions / metabolism*
  • Gap Junctions / pathology
  • Humans
  • Male
  • Membrane Proteins / metabolism*
  • Mice
  • Muscle Proteins / metabolism*
  • Myocytes, Cardiac / metabolism*
  • Myocytes, Cardiac / pathology
  • Tight Junctions / metabolism*
  • Tight Junctions / pathology

Substances

  • Antigens, CD
  • CDH2 protein, human
  • CLDN5 protein, human
  • Cadherins
  • Catenins
  • Claudin-5
  • Connexin 43
  • Desmoplakins
  • GJA1 protein, human
  • Membrane Proteins
  • Muscle Proteins