TY - JOUR
T1 - Interrelation of platelet aggregation, release reaction and thromboxane A2 production
AU - Balduini, Carlo L.
AU - Bertolino, Giampiera
AU - Noris, Patrizia
AU - Sinigaglia, Fabiola
AU - Bisio, Antonella
AU - Torti, Mauro
N1 - Funding Information:
ACKNOWLEDGMENTS: This work was supported by grants from MPl and CNR, Italy. We thank prof. Damiani (Institute of Biochemistry, Genova, Italy) for the gift of the monoclonal antibody PBM 6.4.
PY - 1988/10/31
Y1 - 1988/10/31
N2 - Aggregation of platelets, stimulated by different agonists, was inhibited by omitting sample stirring or by preincubation of platelets with a monoclonal antibody against glycoproteins IIb-IIIa or with a pentapeptide containing the sequence Arg-Gly-Asp-Ser. In platelets stimulated by collagen, ADP and epinephrine, the inhibition of aggregation paralleled a reduction of both release reaction and thromboxane A2 formation. When thrombin was the stimulus, ATP release and thromboxane A2 production were unaffected (or only slightly modified) by the inhibition of platelet aggregation. These data add further evidence to the hypothesis that aggregation supports the activation of platelets stimulated by weak agonists.
AB - Aggregation of platelets, stimulated by different agonists, was inhibited by omitting sample stirring or by preincubation of platelets with a monoclonal antibody against glycoproteins IIb-IIIa or with a pentapeptide containing the sequence Arg-Gly-Asp-Ser. In platelets stimulated by collagen, ADP and epinephrine, the inhibition of aggregation paralleled a reduction of both release reaction and thromboxane A2 formation. When thrombin was the stimulus, ATP release and thromboxane A2 production were unaffected (or only slightly modified) by the inhibition of platelet aggregation. These data add further evidence to the hypothesis that aggregation supports the activation of platelets stimulated by weak agonists.
UR - http://www.scopus.com/inward/record.url?scp=0023812362&partnerID=8YFLogxK
U2 - 10.1016/S0006-291X(88)80918-5
DO - 10.1016/S0006-291X(88)80918-5
M3 - Article
SN - 0006-291X
VL - 156
SP - 822
EP - 829
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -