Tyrosine 537 within the Na+,K+-ATPase alpha-subunit is essential for AP-2 binding and clathrin-dependent endocytosis

J Biol Chem. 2002 May 10;277(19):17108-11. doi: 10.1074/jbc.M201326200. Epub 2002 Feb 21.

Abstract

In renal epithelial cells endocytosis of Na(+),K(+)-ATPase molecules is initiated by phosphorylation of its alpha(1)-subunit, leading to activation of phosphoinositide 3-kinase and adaptor protein-2 (AP-2)/clathrin recruitment. The present study was performed to establish the identity of the AP-2 recognition domain(s) within the Na(+),K(+)-ATPase alpha(1)-subunit. We identified a conserved sequence (Y(537)LEL) within the alpha(1)-subunit that represents an AP-2 binding site. Binding of AP-2 to the Na(+),K(+)-ATPase alpha(1)-subunit in response to dopamine (DA) was increased in OK cells stably expressing the wild type rodent alpha-subunit (OK-WT), but not in cells expressing the Y537A mutant (OK-Y537A). DA treatment was associated with increased alpha(1)-subunit abundance in clathrin vesicles from OK-WT but not from OK-Y537A cells. In addition, this mutation also impaired the ability of DA to inhibit Na(+),K(+)-ATPase activity. Because phorbol esters increase Na(+),K(+)-ATPase activity in OK cells, and this effect was not affected by the Y537A mutation, the present results suggest that the identified motif is specifically required for DA-induced AP-2 binding and Na(+),K(+)-ATPase endocytosis.

Publication types

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

MeSH terms

  • Adaptor Proteins, Vesicular Transport
  • Animals
  • Carrier Proteins / metabolism*
  • Cell Line
  • Clathrin / metabolism*
  • Dopamine / pharmacology
  • Endocytosis*
  • Membrane Proteins / metabolism*
  • Microscopy, Confocal
  • Models, Chemical
  • Mutation
  • Opossums
  • Phorbol Esters / pharmacology
  • Plasmids / metabolism
  • Precipitin Tests
  • Protein Binding
  • Protein Structure, Tertiary
  • Sodium-Potassium-Exchanging ATPase / chemistry*
  • Sodium-Potassium-Exchanging ATPase / genetics
  • Sodium-Potassium-Exchanging ATPase / metabolism
  • Transfection
  • Tyrosine / chemistry*
  • Tyrosine / metabolism

Substances

  • Adaptor Proteins, Vesicular Transport
  • Carrier Proteins
  • Clathrin
  • Membrane Proteins
  • Phorbol Esters
  • Tyrosine
  • Sodium-Potassium-Exchanging ATPase
  • Dopamine