AIF4-induced inhibition of the ATPase activity, the Ca2+-transport activity and the phosphoprotein-intermediate formation of plasma-membrane and endo(sarco)plasmic-reticulum Ca2+-transport ATPases in different tissues. Evidence for a tissue-dependent functional difference

Biochem J. 1989 Jul 15;261(2):655-60. doi: 10.1042/bj2610655.

Abstract

AIF4- inhibits the (Ca2+ + Mg2+)-ATPase activity of the plasma-membrane and the sarcoplasmic-reticulum Ca2+-transport ATPase [Missiaen, Wuytack, De Smedt, Vrolix & Casteels (1988) Biochem. J. 253, 827-833]. The aim of the present work was to investigate this inhibition further. We now report that AIF4- inhibits not only the (Ca2+ + Mg2+)-ATPase activity, but also the ATP-dependent 45Ca2+ transport, and the formation of the phosphoprotein intermediate by these pumps. Mg2+ potentiated the effect of AIF4-, whereas K+ had no such effect. The plasma-membrane Ca2+-transport ATPase from erythrocytes was 20 times less sensitive to inhibition by AIF4- as compared with the Ca2+-transport ATPase from smooth muscle. The endoplasmic-reticulum Ca2+-transport ATPase from smooth muscle was inhibited to a greater extent than the sarcoplasmic-reticulum Ca2+-transport ATPase of slow and fast skeletal muscle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / antagonists & inhibitors*
  • Aluminum / pharmacology*
  • Aluminum Compounds*
  • Animals
  • Biological Transport, Active / drug effects
  • Calcium / pharmacokinetics*
  • Cell Membrane / enzymology*
  • Endoplasmic Reticulum / enzymology*
  • Erythrocyte Membrane / enzymology
  • Erythrocytes / enzymology
  • Fluorides / pharmacology*
  • Muscle, Smooth / enzymology
  • Muscle, Smooth / ultrastructure
  • Phosphoproteins / metabolism
  • Sarcoplasmic Reticulum / enzymology
  • Swine

Substances

  • Aluminum Compounds
  • Phosphoproteins
  • Aluminum
  • Adenosine Triphosphatases
  • Fluorides
  • Calcium
  • aluminum fluoride