Not Ca2+ but CAMP is the second messenger for morphological changes in rat megakaryocyte

Biochem Biophys Res Commun. 1995 Jun 6;211(1):282-8. doi: 10.1006/bbrc.1995.1808.

Abstract

ATP and thrombin both induced Ca2+ mobilization from intracellular Ca2+ store site of megakaryocyte, the progenitor cell of platelet (Uneyama C., Uneyama H. and Akaike N. (1993) J. Physiol. (Lond.), 470, 73-749). Since in platelet, thrombin is known as a strong agonist and ADP is known as a weak agonist, we further investigated the effect of these agonists on megakaryocyte. Thrombin induced Ca2+ mobilization, 5-hydroxy tryptamine (5-HT) release and aggregatory morphological changes in megakaryocyte, but ATP induced only Ca2+ mobilization. Thrombin-induced 5-HT release was inhibited by adenylate cyclase-activating drugs, and the morphological changes could be induced by H-8, an inhibitor of cAMP-dependent protein kinase. These results suggest that the Ca2+ mobilization is not sufficient to induce morphological changes, and the signal to cause morphological changes in megakaryocyte may be cAMP.

MeSH terms

  • Adenosine Diphosphate / pharmacology
  • Adenosine Triphosphate / pharmacology
  • Animals
  • Bone Marrow Cells
  • Calcium / metabolism*
  • Cells, Cultured
  • Cyclic AMP / metabolism*
  • Female
  • Male
  • Megakaryocytes / drug effects
  • Megakaryocytes / physiology*
  • Megakaryocytes / ultrastructure*
  • Membrane Potentials / drug effects
  • Microscopy, Electron, Scanning
  • Potassium Channels / physiology
  • Rats
  • Rats, Wistar
  • Second Messenger Systems*
  • Serotonin / metabolism
  • Thrombin / pharmacology

Substances

  • Potassium Channels
  • Serotonin
  • Adenosine Diphosphate
  • Adenosine Triphosphate
  • Cyclic AMP
  • Thrombin
  • Calcium