Thromb Haemost 1998; 79(06): 1184-1190
DOI: 10.1055/s-0037-1615038
Rapid Communication
Schattauer GmbH

Difference of [Ca2+]i Movements in Platelets Stimulated by Thrombin and TRAP: the Involvement of αIIbβ3-Mediated TXA2 Synthesis

Toshiaki Aoki
1   From the Department of Pharmacology, Medicinal Biology Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., Japan
,
Yoshiaki Tomiyama
2   Second Department of Internal Medicine, Osaka University Medical School, Japan
,
Shigenori Honda
2   Second Department of Internal Medicine, Osaka University Medical School, Japan
,
Kayoko Senzaki
1   From the Department of Pharmacology, Medicinal Biology Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., Japan
,
Akito Tanaka
1   From the Department of Pharmacology, Medicinal Biology Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., Japan
,
Mitsuru Okubo
1   From the Department of Pharmacology, Medicinal Biology Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., Japan
,
Fumie Takahashi
1   From the Department of Pharmacology, Medicinal Biology Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., Japan
,
Hisashi Takasugi
1   From the Department of Pharmacology, Medicinal Biology Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., Japan
,
Jiro Seki
1   From the Department of Pharmacology, Medicinal Biology Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., Japan
› Author Affiliations
Further Information

Publication History

Received 02 June 1997

Accepted after resubmission 25 February 1998

Publication Date:
07 December 2017 (online)

Preview

Summary

This study investigated the difference of [Ca2+]i movement in platelets in response to thrombin and TRAP. The involvement of αIIbβ3 in this signaling was also studied. Stimulation of platelets with thrombin at 0.03 U/ml caused platelet aggregation and a two-peak increase in [Ca2+]i. The second peak of [Ca2+]i, but not the first peak was abolished by the inhibition of platelet aggregation with αIIbβ3 antagonists or by scavenging endogenous ADP with apyrase. A cyclooxygenase inhibitor, aspirin, and a TXA2 receptor antagonist, BM13505, also abolished the second peak of [Ca2+]i but not the first peak, although these regents did not inhibit aggregation. Under the same assay conditions, measurement of TXB2 demonstrated that αIIbβ3 antagonists and aspirin almost completely inhibited the production of TXB2. In contrast to thrombin-stimulation, TRAP caused only a single peak of [Ca2+]i even in the presence of platelet aggregation, and a high level of [Ca2+]i increase was needed for the induction of platelet aggregation. The inhibition of aggregation with αIIbβ3 antagonists had no effect on [Ca2+]i change and TXB2 production induced by TRAP. Inhibition studies using anti-GPIb antibodies suggested that GPIb may be involved in the thrombin response, but not in the TRAP. Our findings suggest that low dose thrombin causes a different [Ca2+]i response and TXA2 producing signal from TRAP. Endogenous ADP release and fibrinogen binding to αIIbβ3 are responsible for the synthesis of TXA2 which results in the induction of the second peak of [Ca2+]i in low thrombin- but not TRAP-stimulated platelets.