Connexins in epidermal homeostasis and skin disease

Biochim Biophys Acta. 2012 Aug;1818(8):1952-61. doi: 10.1016/j.bbamem.2011.09.004. Epub 2011 Sep 10.

Abstract

The expression of multiple connexin (Cx) types in the epidermis, their differential expression during wound closure and the association of skin pathology with specific Cx gene mutations, are indicative of important functions for Cxs in the skin. In this review, we focus on the role of Cx proteins in the epidermis and during wound healing and discuss mutations in Cx genes which cause skin disease. This article is part of a Special Issue entitled: The Communicating junctions, composition, structure and characteristics.

Publication types

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

MeSH terms

  • Animals
  • Connexin 26
  • Connexin 30
  • Connexin 43 / metabolism
  • Connexins / metabolism*
  • Craniofacial Abnormalities / genetics
  • Ectodermal Dysplasia / genetics
  • Epidermis / metabolism*
  • Erythrokeratodermia Variabilis / genetics
  • Eye Abnormalities / genetics
  • Foot Deformities, Congenital / genetics
  • Homeostasis
  • Humans
  • Keratinocytes / cytology
  • Models, Biological
  • Mutation
  • Skin Diseases / metabolism*
  • Syndactyly / genetics
  • Tooth Abnormalities / genetics
  • Wound Healing
  • Xenopus

Substances

  • Connexin 30
  • Connexin 43
  • Connexins
  • GJB6 protein, human
  • Connexin 26

Supplementary concepts

  • Oculodentodigital Dysplasia