Regulation of the ROMK channel: interaction of the ROMK with associate proteins

Am J Physiol. 1999 Dec;277(6):F826-31. doi: 10.1152/ajprenal.1999.277.6.F826.

Abstract

The ROMK channel plays an important role in K recycling in the thick ascending limb (TAL) and K secretion in the cortical collecting duct (CCD). A large body of evidence indicates that the ROMK channel is a key component of the native K secretory channel identified in the apical membrane of the TAL and the CCD. Although the ROMK channel shares several key regulatory mechanisms with the native K secretory channel in a variety of respects, differences in the channel modulatory mechanism are clearly present between the ROMK channel and the native K secretory channel. Therefore, it is possible that additional associate proteins are required to interact with the ROMK channel to assemble the native K secretory channel. This notion is supported by recent reports showing that cystic fibrosis transmembrane conductance regulator (CFTR) and A kinase anchoring proteins (AKAP) interact with the ROMK channels to restore the response to ATP sensitivity and protein kinase A stimulation. This review is an attempt to summarize the up-to-date progress regarding the interaction between the ROMK channel and the associate proteins in forming the native K secretory channel.

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Carrier Proteins / physiology
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Cystic Fibrosis Transmembrane Conductance Regulator / physiology*
  • Humans
  • Kidney Cortex / physiology*
  • Kidney Tubules, Collecting / physiology*
  • Potassium Channels / physiology*
  • Potassium Channels, Inwardly Rectifying*
  • Protein Kinases / metabolism

Substances

  • CFTR protein, human
  • Carrier Proteins
  • KCNJ1 protein, human
  • Potassium Channels
  • Potassium Channels, Inwardly Rectifying
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Adenosine Triphosphate
  • Protein Kinases
  • Cyclic AMP-Dependent Protein Kinases