Molecular physiology of platelet ADP receptors

Authors
Citation
Sp. Kunapuli, Molecular physiology of platelet ADP receptors, DRUG DEV R, 45(3-4), 1998, pp. 135-139
Citations number
46
Categorie Soggetti
Pharmacology & Toxicology
Journal title
DRUG DEVELOPMENT RESEARCH
ISSN journal
02724391 → ACNP
Volume
45
Issue
3-4
Year of publication
1998
Pages
135 - 139
Database
ISI
SICI code
0272-4391(199811/12)45:3-4<135:MPOPAR>2.0.ZU;2-7
Abstract
Extracellular nucleotides have been implicated in a number of physiologic f unctions. Nucleotides act on cell surface receptors known as P2 receptors o f which several subtypes have been cloned. Both ATP and ADP are stored in p latelets and are released upon platelet activation. During vascular injury, nucleotides play an important role in hemostasis by activating platelets. Classic pharmacologic studies have identified ADP receptors on platelets, d esignated P2T receptor. The P2T receptor is now resolved into three P2 rece ptor subtypes, the P2Y(1), the P2X(1), and the P2T(AC) receptor, which rema ins to be cloned. Although the P2Y(1) receptor solely mediates ADP-induced platelet shape change, both the P2Y1 and P2T(AC) receptors are essential fo r ADP-induced fibrinogen receptor activation on platelets. The function of the P2X(1) receptor remains to be elucidated. Thus the complexities in the functional characterization of platelet ADP receptors now appear to be reso lved. Drug Dev. Res. 45:135-139, 1998. (C) 1998 Wiley-Liss, Inc.