Autophagic regulation of platelet biology

被引:11
作者
Luo, Xu-ling [1 ]
Jiang, Jin-yong [1 ]
Huang, Zhen [1 ]
Chen, Lin-xi [1 ]
机构
[1] Univ South China, Hunan Prov Cooperat Innovat Ctr Mol Target New Dr, Learning Key Lab Pharmacoprote, Inst Pharm & Pharmacol, Hengyang, Peoples R China
基金
中国国家自然科学基金;
关键词
autophagy; megakaryocytes; mitophagy; platelets; MITOCHONDRIAL DYSFUNCTION; DC-SIGN; ACTIVATION; APOPTOSIS; MEGAKARYOCYTES; PROTECTS; THROMBOPOIESIS; HEMOSTASIS; EXPRESSION; THROMBOSIS;
D O I
10.1002/jcp.28243
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Platelets, developed from megakaryocytes, are characterized by anucleate and short-life span hemocyte in mammal vessel. Platelets are very important in the cardiovascular system. Studies indicate the occurrence of autophagy platelets and megakaryocytes. Moreover, abnormal autophagy decreases the number of platelets and suppresses platelet aggregation. In addition, mitophagy, as a kind of selective autophagy, could inhibit platelet aggregation under oxidative stress or hypoxic, whereas promote platelet aggregation after reperfusion. Finally, autophagy regulates hemorrhagic and thrombosis diseases by influencing the number and function of platelets. In this paper, the role of autophagy in platelets and megakaryocytes, as well as coupled with the promotive or inhibitory role of hemorrhagic and thrombosis diseases are elucidated. Therefore, autophagy may be a potentially therapeutic target in modulating the platelet-related diseases.
引用
收藏
页码:14483 / 14488
页数:6
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