Phosphoinositide 3-kinase and integrin signalling are involved in activation of Bruton tyrosine kinase in thrombin-stimulated platelets

FEBS Lett. 1999 Jan 22;443(1):66-70. doi: 10.1016/s0014-5793(98)01680-9.

Abstract

Bruton tyrosine kinase (Btk) plays a crucial role in the differentiation of B lymphocytes and belongs to the group of Tec kinases, which are characterised by the presence of a pleckstrin homology domain. Here we show that Btk is activated and undergoes tyrosine phosphorylation upon challenge of platelet thrombin receptor, these responses requiring engagement of alphaIIb/beta3 integrin and phosphoinositide 3-kinase activity. These data unravel a novel signalling pathway involving Btk downstream of an adhesive receptor via a complex regulation implicating the products of phosphoinositide 3-kinase, which might act to anchor Btk at the membrane.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Agammaglobulinaemia Tyrosine Kinase
  • Blood Platelets / drug effects
  • Blood Platelets / metabolism*
  • Enzyme Activation
  • Humans
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphorylation
  • Platelet Activation
  • Platelet Glycoprotein GPIIb-IIIa Complex / metabolism*
  • Protein-Tyrosine Kinases / metabolism*
  • Signal Transduction
  • Thrombin / pharmacology*

Substances

  • Platelet Glycoprotein GPIIb-IIIa Complex
  • Phosphatidylinositol 3-Kinases
  • Protein-Tyrosine Kinases
  • Agammaglobulinaemia Tyrosine Kinase
  • BTK protein, human
  • Thrombin