Phosphoinositide signalling in nuclei of Friend cells: DMSO-induced differentiation reduces the association of phosphatidylinositol-transfer protein with the nucleus

Biochem Biophys Res Commun. 1997 Jan 13;230(2):302-5. doi: 10.1006/bbrc.1996.5950.

Abstract

Friend erythroleukemia cells have a nuclear phosphoinositide cycle which is related to both mitogen-stimulated cell growth and erythorid differentiation. Because of the important role of the phosphatidylinositol-transfer protein (PI-TP) in phosphatidylinositol 4,5-bisphosphate (PtdInsP2) synthesis, we have analysed nuclei isolated from Friend cells for the presence of PI-TP. By Western Blotting it was demonstrated that both intact nuclei and nuclei deprived of the outer membrane contained the PI-TP alpha isoform. Upon induction of erythroid differentiation by DMSO, the amount of nuclear PI-TP alpha was greatly diminished. As shown previously, under these same conditions, nuclear phospholipase C beta1 (PLC beta1) is down-regulated as well.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carrier Proteins / metabolism*
  • Cell Differentiation
  • Cell Line
  • Cell Nucleus / drug effects
  • Cell Nucleus / physiology*
  • Cell Nucleus / ultrastructure
  • Dimethyl Sulfoxide / pharmacology*
  • Fluorescent Antibody Technique, Indirect
  • Isoenzymes / metabolism
  • Leukemia, Erythroblastic, Acute
  • Membrane Proteins*
  • Mice
  • Microscopy, Electron
  • Phosphatidylinositols / metabolism*
  • Phospholipase C beta
  • Phospholipid Transfer Proteins
  • Signal Transduction*
  • Type C Phospholipases / metabolism

Substances

  • Carrier Proteins
  • Isoenzymes
  • Membrane Proteins
  • Phosphatidylinositols
  • Phospholipid Transfer Proteins
  • Type C Phospholipases
  • Phospholipase C beta
  • Plcb1 protein, mouse
  • Dimethyl Sulfoxide