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ABSTRACT: Background
Previously, several studies have shown that Tyro3, Axl, and Mertk (TAM) receptors participate in platelet activation and thrombosis. However, the role of individual receptors is not fully understood.Methods
Using single receptor-deficient platelets from TAM knockout mice in the C57BL/6 J strain, we performed a knockout study using single TAM-deficient mice. We treated platelets isolated from TAM knockout mice with the Glycoprotein VI (GPVI) agonists convulxin, poly(PHG), and collagen-related triple-helical peptide (CRP), as well as thrombin for in-vitro experiments. We used a laser-induced cremaster arterial injury model for thrombosis experiments in vivo.Results
Deficiency of the tyrosine kinase receptors, Axl or Tyro3, but not Mertk, inhibited aggregati
SUBMITTER: Zhou J
PROVIDER: S-EPMC6291976 | biostudies-literature | 2018 Dec
REPOSITORIES: biostudies-literature