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Publication : Kinesin-1 Is a New Actor Involved in Platelet Secretion and Thrombus Stability.

First Author  Adam F Year  2018
Journal  Arterioscler Thromb Vasc Biol Volume  38
Issue  5 Pages  1037-1051
PubMed ID  29519941 Mgi Jnum  J:285152
Mgi Id  MGI:6385464 Doi  10.1161/ATVBAHA.117.310373
Citation  Adam F, et al. (2018) Kinesin-1 Is a New Actor Involved in Platelet Secretion and Thrombus Stability. Arterioscler Thromb Vasc Biol 38(5):1037-1051
abstractText  OBJECTIVE: Platelet secretion is crucial for many physiological platelet responses. Even though several regulators of the fusion machinery for secretory granule exocytosis have been identified in platelets, the underlying mechanisms are not yet fully characterized. APPROACH AND RESULTS: By studying a mouse model (cKO [conditional knockout](Kif5b)) lacking Kif5b (kinesin-1 heavy chain) in its megakaryocytes and platelets, we evidenced unstable hemostasis characterized by an increase of blood loss associated to a marked tendency to rebleed in a tail-clip assay and thrombus instability in an in vivo thrombosis model. This instability was confirmed in vitro in a whole-blood perfusion assay under blood flow conditions. Aggregations induced by thrombin and collagen were also impaired in cKO(Kif5b) platelets. Furthermore, P-selectin exposure, PF4 (platelet factor 4) secretion, and ATP release after thrombin stimulation were impaired in cKO(Kif5b) platelets, highlighting the role of kinesin-1 in alpha-granule and dense granule secretion. Importantly, exogenous ADP rescued normal thrombin induced-aggregation in cKO(Kif5b) platelets, which indicates that impaired aggregation was because of defective release of ADP and dense granules. Last, we demonstrated that kinesin-1 interacts with the molecular machinery comprising the granule-associated Rab27 (Ras-related protein Rab-27) protein and the Slp4 (synaptotagmin-like protein 4/SYTL4) adaptor protein. CONCLUSIONS: Our results indicate that a kinesin-1-dependent process plays a role for platelet function by acting into the mechanism underlying alpha-granule and dense granule secretion.
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