Regulation of glycogen synthase kinase 3 in human platelets: a possible role in platelet function?

Full text not archived in this repository.

Please see our End User Agreement.

It is advisable to refer to the publisher's version if you intend to cite from this work. See Guidance on citing.

Add to AnyAdd to TwitterAdd to FacebookAdd to LinkedinAdd to PinterestAdd to Email

Barry, F. A., Graham, G. J., Fry, M. J. and Gibbins, J. M. orcid id iconORCID: https://orcid.org/0000-0002-0372-5352 (2003) Regulation of glycogen synthase kinase 3 in human platelets: a possible role in platelet function? FEBS Letters, 553 (1-2). pp. 173-178. ISSN 0014-5793 doi: 10.1016/s0014-5793(03)01015-9

Abstract/Summary

In this study we show that both glycogen synthase kinase 3 (GSK3) isoforms, GSK3alpha and GSK3beta, are present in human platelets and are phosphorylated on Ser(21) and Ser(9), respectively, in platelets stimulated with collagen, convulxin and thrombin. Phosphorylation of GSK3alpha/beta was dependent on phosphoinositide 3-kinase (PI3K) activity and independent of platelet aggregation, and correlated with a decrease in GSK3 activity that was preserved by pre-incubating platelets with PI3K inhibitor LY294002. Three structurally distinct GSK3 inhibitors, lithium, SB415286 and TDZD-8, were found to inhibit platelet aggregation. This implicates GSK3 as a potential regulator of platelet function. (C) 2003 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

Altmetric Badge

Item Type Article
URI https://reading-clone.eprints-hosting.org/id/eprint/10665
Identification Number/DOI 10.1016/s0014-5793(03)01015-9
Refereed Yes
Divisions Life Sciences > School of Biological Sciences
Interdisciplinary centres and themes > Institute for Cardiovascular and Metabolic Research (ICMR)
Uncontrolled Keywords platelet, platelet activation, platelet aggregation, glycogen synthase, kinase 3, phosphoinositide 3-kinase, protein kinase B, RECEPTOR GAMMA-CHAIN, GLYCOPROTEIN-VI, COLLAGEN RECEPTOR, INTEGRIN, ALPHA(2)BETA(1), TYROSINE PHOSPHORYLATION, ALZHEIMERS-DISEASE, INTACT-CELLS, INHIBITORS, ACTIVATION, 3-KINASE
Publisher Elsevier
Download/View statistics View download statistics for this item

University Staff: Request a correction | Centaur Editors: Update this record

Search Google Scholar