Clathrin-mediated integrin αIIbβ3 trafficking controls platelet spreading

Abstract

Dynamic endocytic and exocytic trafficking of integrins is an important mechanism for cell migration, invasion, and cytokinesis. Endocytosis of integrin can be classified as clathrin dependent and clathrin independent manners. And rapid delivery of endocytic integrins back to the plasma membrane is key intracellular signals and is indispensable for cell movement. Integrin αIIbβ3 plays a critical role in thrombosis and hemostasis. Although previous studies have demonstrated that internalization of fibrinogen-bound αIIbβ3 may regulate platelet activation, the roles of endocytic and exocytic trafficking of integrin αIIbβ3 in platelet activation are unclear. In this study, we found that a selective inhibitor of clathrin-mediated endocytosis pitstop 2 inhibited human platelet spreading on immobilized fibrinogen (Fg). Mechanism studies revealed that pitstop 2 did not block the endocytosis of αIIbβ3 and Fg uptake, but inhibit the recycling of αIIbβ3 to plasma membrane during platelet or CHO cells bearing αIIbβ3 spreading on immobilized Fg. And pitstop 2 enhanced the association of αIIbβ3 with clathrin, and AP2 indicated that pitstop 2 inhibit platelet activation is probably due to disturbance of the dynamic dissociation of αIIbβ3 from clathrin and AP2. Further study demonstrated that Src/PLC/PKC was the key pathway to trigger the endocytosis of αIIbβ3 during platelet activation. Pitstop 2 also inhibited platelet aggregation and secretion. Our findings suggest integrin αIIbβ3 trafficking is clathrin dependent and plays a critical role in platelet spreading, and pitstop 2 may serve as an effective tool to address clathrin-mediated trafficking in platelets.

Keywords:

• Blood platelets
• clathrin-coated vesicles
• endocytosis
• integrin αIIbβ3
• pitstop 2

Funding

This work was supported in part by the Program of the National Natural Science Foundation of China (81270278 to X.L., 81600104 to X.F.), China Postdoctoral Science Foundation (2015M580336, 2016T90374) to X.F. and Shanghai Health Bureau Research Projects (201540094).

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Additional information

Funding

This work was supported in part by the Program of the National Natural Science Foundation of China (81270278 to X.L., 81600104 to X.F.), China Postdoctoral Science Foundation (2015M580336, 2016T90374) to X.F. and Shanghai Health Bureau Research Projects (201540094).