Phosphatidylinositol 3,4,5-trisphosphate regulates Ca(2+) entry via btk in platelets and megakaryocytes without increasing phospholipase C activity

EMBO J. 2000 Jun 15;19(12):2793-802. doi: 10.1093/emboj/19.12.2793.

Abstract

The role of phosphatidylinositol 3,4,5-trisphosphate (PI3,4,5P(3)) and Btk in signalling by the collagen receptor glycoprotein VI was investigated. PI3,4,5P(3) was increased in platelets from mice deficient in the SH2 domain-containing inositol 5-phosphatase (SHIP), in response to collagen related peptide (CRP). Tyrosine phosphorylation and activation of phospholipase Cgamma2 (PLCgamma2) were unaltered in SHIP(-/-) platelets, whereas Btk was heavily tyrosine phosphorylated under basal conditions and maximally phosphorylated by low concentrations of CRP. There was an increase in basal Ca(2+), maximal expression of P-selectin, and potentiation of Ca(2+) and aminophospholipid exposure to CRP in SHIP(-/-) platelets in the presence of Ca(2+) (1 mM). Microinjection of PI3,4, 5P(3) into megakaryocytes caused a 3-fold increase in Ca(2+) in response to CRP, which was absent in X-linked immunodeficiency (Xid) mice, which have a mutation in the PH domain of Btk. There was a corresponding partial reduction in the sustained level of intracellular Ca(2+) in response to CRP in Xid mice but no change in PLC activity. These results demonstrate a novel pathway of Ca(2+) entry that involves PI3,4,5P(3) and Btk, and which is independent of increased PLC activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Agammaglobulinaemia Tyrosine Kinase
  • Animals
  • Biological Transport
  • Blood Platelets / metabolism*
  • Calcium / metabolism*
  • Coagulants / analysis
  • Genetic Linkage
  • Humans
  • Immunologic Deficiency Syndromes / genetics
  • Megakaryocytes / metabolism*
  • Mice
  • P-Selectin
  • Phosphatidylinositol Phosphates / metabolism*
  • Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases
  • Phosphoric Monoester Hydrolases / genetics
  • Phosphorylation
  • Platelet Membrane Glycoproteins / agonists
  • Protein Precursors / analysis
  • Protein-Tyrosine Kinases / metabolism*
  • Severe Combined Immunodeficiency
  • Type C Phospholipases / metabolism*
  • X Chromosome / genetics

Substances

  • Coagulants
  • P-Selectin
  • Phosphatidylinositol Phosphates
  • Platelet Membrane Glycoproteins
  • Protein Precursors
  • phosphatidylinositol 3,4,5-triphosphate
  • platelet membrane glycoprotein VI
  • Protein-Tyrosine Kinases
  • Agammaglobulinaemia Tyrosine Kinase
  • BTK protein, human
  • Btk protein, mouse
  • Phosphoric Monoester Hydrolases
  • INPPL1 protein, human
  • Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases
  • Type C Phospholipases
  • Calcium