ABCC8 and ABCC9: ABC transporters that regulate K+ channels

Joseph Bryan, Alvaro Munoz, Xinna Zhang, Martina Düfer, Gisela Drews, Peter Krippeit-Drews, Lydia Aguilar-Bryan

Research output: Contribution to journalReview article

114 Scopus citations

Abstract

The sulfonylurea receptors (SURs) ABCC8/SUR1 and ABCC9/SUR2 are members of the C-branch of the transport adenosine triphosphatase superfamily. Unlike their brethren, the SURs have no identified transport function; instead, evolution has matched these molecules with K+ selective pores, either K IR6.1/KCNJ8 or KIR6.2/KCNJ11, to assemble adenosine triphosphate (ATP)-sensitive K+ channels found in endocrine cells, neurons, and both smooth and striated muscle. Adenine nucleotides, the major regulators of ATP-sensitive K+ (KATP) channel activity, exert a dual action. Nucleotide binding to the pore reduces the activity or channel open probability, whereas Mg-nucleotide binding and/or hydrolysis in the nucleotide-binding domains of SUR antagonize this inhibitory action to stimulate channel openings. Mutations in either subunit can alter this balance and, in the case of the SUR1/KIR6.2 channels found in neurons and insulin-secreting pancreatic β cells, are the cause of monogenic forms of hyperinsulinemic hypoglycemia and neonatal diabetes. Additionally, the subtle dysregulation of KATP channel activity by a KIR6.2 polymorphism has been suggested as a predisposing factor in type 2 diabetes mellitus. Studies on KATP channel null mice are clarifying the roles of these metabolically sensitive channels in a variety of tissues.

Original languageEnglish (US)
Pages (from-to)703-718
Number of pages16
JournalPflugers Archiv European Journal of Physiology
Volume453
Issue number5
DOIs
StatePublished - Feb 2007

Keywords

  • ABCC8
  • ABCC9
  • Diabetes
  • Hypoglycemia
  • K channels
  • KCNJ11
  • KCNJ8

ASJC Scopus subject areas

  • Physiology

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