[Role and function of voltage-gated chloride channels of the CIC family and their defects leading to genetic diseases]

Postepy Hig Med Dosw. 2002;56(3):307-13.
[Article in Polish]

Abstract

There are 9 channels of the ClC family in mammals and few others in fishes, plants, yeast and bacteria. The ClC channels are present in different tissues and play a role in transmembrane potential stabilization, transepithelial transport, cell volume regulation, acidification of intracellular organelles. The genetic defects of ClC-1 chloride channel lead to myotonias, the defect in ClC-5 channel to the formation of stones in kidney, while the defect in ClC-Kb channel leads to the Bartter's syndrome.

Publication types

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

MeSH terms

  • Acid-Base Equilibrium / physiology
  • Animals
  • Bartter Syndrome / genetics*
  • Chloride Channels / genetics*
  • Chloride Channels / metabolism*
  • Electrochemistry
  • Humans
  • Ion Transport / physiology
  • Kidney Calculi / genetics*
  • Membrane Potentials / physiology
  • Mutation
  • Myotonia Congenita / genetics*
  • Organelles / metabolism

Substances

  • CLC-1 channel
  • Chloride Channels