Sex-Specific Platelet Activation Through Protease-Activated Receptors Reverses in Myocardial Infarction

• Published in: Arteriosclerosis, thrombosis, and vascular biology Vol. 41; no. 1; pp. 390 - 400
• Main Authors: Soo Kim, Beom, Auerbach, David A, Sadhra, Hamza, Godwin, Matthew, Bhandari, Rohan, Ling, Frederick S, Mohan, Amy, Yule, David I, Wagner, Larry, Rich, David Q, Ture, Sara, Morrell, Craig N, Timpanaro-Perrotta, Livia, Younis, Arwa, Goldenberg, Ilan, Cameron, Scott J
• Format: Journal Article
• Language: English
• Published: United States American Heart Association, Inc 01.01.2021
• Subjects: Aged; Animals; Blood Platelets - drug effects; Blood Platelets - metabolism; Case-Control Studies; Disease Models, Animal; Female; Humans; Male; Mice; Mice, Inbred C57BL; Middle Aged; Non-ST Elevated Myocardial Infarction - blood; Phenotype; Platelet Activation - drug effects; Receptor, PAR-1 - blood; Sex Factors; Signal Transduction; ST Elevation Myocardial Infarction - blood; Thrombin - pharmacology; thrombin; female; platelet activation; myocardial infarction; regression analysis
• ISSN: 1079-5642; 1524-4636
• DOI: 10.1161/ATVBAHA.120.315033

OBJECTIVE:The platelet phenotype in certain patients and clinical contexts may differ from healthy conditions. We evaluated platelet activation through specific receptors in healthy men and women, comparing this to patients presenting with ST-segment-elevation myocardial infarction and non-ST-segment-elevation myocardial infarction. APPROACH AND RESULTS:We identified independent predictors of platelet activation through certain receptors and a murine MI model further explored these findings. Platelets from healthy women and female mice are more reactive through PARs (protease-activated receptors) compared with platelets from men and male mice. Multivariate regression analyses revealed male sex and non-ST-segment-elevation myocardial infarction as independent predictors of enhanced PAR1 activation in human platelets. Platelet PAR1 signaling decreased in women and increased in men during MI which was the opposite of what was observed during healthy conditions. This trend was also observed in male and female mice in which thrombin-mediated platelet calcium mobilization was augmented coincident with platelet activation in males and attenuated in females at the time of MI. CONCLUSIONS:Sex-specific signaling in platelets seems to be a cross-species phenomenon. The divergent platelet phenotype in males and females at the time of MI suggests a sex-specific antiplatelet drug regimen should be prospectively evaluated.