The mammalian KIR2.x inward rectifier ion channel family: Expression pattern and pathophysiology

T. P. De Boer, M. J.C. Houtman, M. Compier, M. A.G. Van Der Heyden

Research output: Contribution to journalReview articlepeer-review

52 Citations (Scopus)

Abstract

Inward rectifier currents based on KIR2.x subunits are regarded as essential components for establishing a stable and negative resting membrane potential in many excitable cell types. Pharmacological inhibition, null mutation in mice and dominant positive and negative mutations in patients reveal some of the important functions of these channels in their native tissues. Here we review the complex mammalian expression pattern of KIR2.x subunits and relate these to the outcomes of functional inhibition of the resultant channels. Correlations between expression and function in muscle and bone tissue are observed, while we recognize a discrepancy between neuronal expression and function.

Original languageEnglish
Pages (from-to)243-256
Number of pages14
JournalActa Physiologica
Volume199
Issue number3
DOIs
Publication statusPublished - Jul 2010

Keywords

  • Andersen-Tawil syndrome
  • Barium
  • Expression pattern
  • Inward rectifier current
  • K2.x
  • Thyrotoxic periodic paralysis

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