Ca2+-activated Cl-channels

Loretta Ferrera, Olga Zegarra-Moran, Luis L J V Galietta

Research output: Contribution to journalArticlepeer-review

Abstract

Ca2+-activated Cl-channels (CaCCs) are plasma membrane proteins involved in various important physiological processes. In epithelial cells, CaCC activity mediates the secretion of Cl-and of other anions, such as bicarbonate and thiocyanate. In smooth muscle and excitable cells of the nervous system, CaCCs have an excitatory role coupling intracellular Ca2+ elevation to membrane depolarization. Recent studies indicate that TMEM16A (transmembrane protein 16 A or anoctamin 1) and TMEM16B (transmembrane protein 16 B or anoctamin 2) are CaCCforming proteins. Induced expression of TMEM16A and B in null cells by transfection causes the appearance of Ca2+-activated Cl-currents similar to those described in native tissues. Furthermore, silencing of TMEM16A by RNAi causes disappearance of CaCC activity in cells from airway epithelium, biliary ducts, salivary glands, and blood vessel smooth muscle. Mice devoid of TMEM16A expression have impaired Ca2+-dependent Cl-secretion in the epithelial cells of the airways, intestine, and salivary glands. These animals also show a loss of gastrointestinal motility, a finding consistent with an important function of TMEM16A in the electrical activity of gut pacemaker cells, that is, the interstitial cells of Cajal. Identification of TMEM16 proteins will help to elucidate the molecular basis of Cl-transport.

Original languageEnglish
Pages (from-to)2155-2174
Number of pages20
JournalComprehensive Physiology
Volume1
Issue number4
DOIs
Publication statusPublished - Oct 2011

ASJC Scopus subject areas

  • Physiology
  • Physiology (medical)
  • Medicine(all)

Fingerprint Dive into the research topics of 'Ca2+-activated Cl-channels'. Together they form a unique fingerprint.

Cite this