The platelet cytoskeleton regulates the aggregation-dependent synthesis of phosphatidylinositol 3,4-bisphosphate induced by thrombin

FEBS Lett. 2000 Jan 28;466(2-3):355-8. doi: 10.1016/s0014-5793(00)01100-5.

Abstract

Pretreatment of intact platelets with cytochalasin D prevented actin polymerization and cytoskeleton reorganization induced by thrombin, but did not affect platelet aggregation. Under these conditions, synthesis of phosphatidylinositol 3,4-bisphosphate (PtdIns(3,4)P2) stimulated by thrombin was strongly inhibited, while production of phosphatidic acid was unaffected. The inhibitory effect of cytochalasin D was not observed when platelet aggregation was prevented by the RGDS peptide. We also found that cytochalasin D did not affect PtdIns(3,4)P2 synthesis induced by concanavalin A (ConA), which is known to occur through an aggregation-independent mechanism. Moreover, thrombin, but not ConA, induced the translocation of phosphatidylinositol 3-kinase to the cytoskeleton. This process was equally inhibited by both the RGDS peptide and cytochalasin D. These results demonstrate that the cytoskeleton represents a functional link between thrombin-induced aggregation and synthesis of PtdIns(3,4)P2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blood Platelets / drug effects*
  • Blood Platelets / physiology
  • Cytochalasin D / pharmacology
  • Cytoskeleton / drug effects*
  • Cytoskeleton / physiology
  • Humans
  • In Vitro Techniques
  • Phosphatidylinositol Phosphates / chemical synthesis*
  • Platelet Aggregation*
  • Thrombin / pharmacology*

Substances

  • Phosphatidylinositol Phosphates
  • phosphatidylinositol 3,4-diphosphate
  • Cytochalasin D
  • Thrombin