Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/54851
Title: Plasma kallikrein enhances platelet aggregation response by subthreshold doses of ADP
Authors: Ottaiano, Tatiana F. [UNIFESP]
Andrade, Sheila S. [UNIFESP]
de Oliveira, Cleide [UNIFESP]
Silva, Mariana C. C. [UNIFESP]
Buri, Marcus V. [UNIFESP]
Juliano, Maria A. [UNIFESP]
Girao, Manoel J. B. C. [UNIFESP]
Sampaio, Misako U. [UNIFESP]
Schmaier, Alvin H.
Wlodawer, Alexander
Maffei, Francisco H. A.
Oliva, Maria Luiza V. [UNIFESP]
Keywords: ADP
Integrin alphallbbeta3
Plasma kallikrein
Platelet aggregation
Issue Date: 2017
Publisher: Elsevier France-Editions Scientifiques Medicales Elsevier
Citation: Biochimie. Paris, v. 135, p. 72-81, 2017.
Abstract: Human plasma kallikrein (huPK) potentiates platelet responses to subthreshold doses of ADP, although huPK itself, does not induce platelet aggregation. In the present investigation, we observe that huPK pretreatment of platelets potentiates ADP-induced platelet activation by prior proteolysis of the G-protein -coupled receptor PAR-1. The potentiation of ADP-induced platelet activation by huPK is mediated by the integrin alpha(IIb)beta(3) through interactions with the KGD/KGE sequence motif in huPK. Integrin alpha(IIb)beta(3) is a cofactor for huPK binding to platelets to support PAR-1 hydrolysis that contributes to activation of the ADP signaling pathway. This activation pathway leads to phosphorylation of Src, AktS(473), ERK1/2, and p38 MAPK, and to Cat(2+) release. The effect of huPK is blocked by specific antagonists of PAR-1 (SCH 19197) and alpha(IIb)beta(3) (abciximab) and by synthetic peptides comprising the KGD and KGE sequence motifs of huPK. Further, recombinant plasma kallikrein inhibitor, rBbKI, also blocks this entire mechanism. These results suggest a new function for huPK. Formation of plasma kallikrein lowers the threshold for ADP-induced platelet activation. The present observations are consistent with the notion that plasma kallikrein promotes vascular disease and thrombosis in the intravascular compartment and its inhibition may ameliorate cardiovascular disease and thrombosis. (C) 2017 Elsevier B.V. and Societe Francaise de Biochimie et Biologie Moleculaire (SFBBM). All rights reserved.
URI: https://repositorio.unifesp.br/handle/11600/54851
ISSN: 0300-9084
Other Identifiers: http://dx.doi.org/10.1016/j.biochi.2017.01.010
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