致密颗粒
分泌物
血小板
止血
颗粒(地质)
细胞生物学
溶酶体
胞吐
受体
化学
血小板活化
生物
免疫学
内科学
生物化学
医学
古生物学
酶
作者
Smita Joshi,Kanakanagavalli Shravani Prakhya,Adrienne Smith,Harry Chanzu,Ming Zhang,Sidney W. Whiteheart
出处
期刊:Platelets
[Informa]
日期:2023-08-06
卷期号:34 (1)
标识
DOI:10.1080/09537104.2023.2237114
摘要
Platelet secretion requires Soluble N-ethylmaleimide Sensitive Attachment Protein Receptors (SNAREs). Vesicle SNAREs/Vesicle-Associated Membrane Proteins (v-SNAREs/VAMPs) on granules and t-SNAREs in plasma membranes mediate granule release. Platelet VAMP heterogeneity has complicated the assessment of how/if each is used and affects hemostasis. To address the importance of VAMP-7 (V7), we analyzed mice with global deletions of V3 and V7 together or platelet-specific deletions of V2, V3, and global deletion of V7. We measured the kinetics of cargo release, and its effects on three injury models to define the context-specific roles of these VAMPs. Loss of V7 minimally affected dense and α granule release but did affect lysosomal release. V3−/−7−/− and V2Δ3Δ7−/− platelets showed partial defects in α and lysosomal release; dense granule secretion was unaffected. In vivo assays showed that loss of V2, V3, and V7 caused no bleeding or occlusive thrombosis. These data indicate a role for V7 in lysosome release that is partially compensated by V3. V7 and V3, together, contribute to α granule release, however none of these deletions affected hemostasis/thrombosis. Our results confirm the dominance of V8. When it is present, deletion of V2, V3, or V7 alone or in combination minimally affects platelet secretion and hemostasis.
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