血小板
细胞凋亡
骨髓
程序性细胞死亡
离体
生物
癌症研究
免疫学
癌症
体内
医学
细胞生物学
遗传学
作者
Marion Lebois,Emma C. Josefsson
出处
期刊:Platelets
[Informa]
日期:2016-04-21
卷期号:27 (6): 497-504
被引量:89
标识
DOI:10.3109/09537104.2016.1161739
摘要
The lifespan of platelets in circulation is brief, close to 10 days in humans and 5 days in mice. Bone marrow residing megakaryocytes produce around 100 billion platelets per day. In a healthy individual, the majority of platelets are not consumed by hemostatic processes, but rather their lifespan is controlled by programmed cell death, a canonical intrinsic apoptosis program. In the last decade, insights from genetically manipulated mouse models and pharmacological developments have helped to define the components of the intrinsic, or mitochondrial, apoptosis pathway that controls platelet lifespan. This review focuses on the molecular regulation of apoptosis in platelet survival, reviews thrombocytopenic conditions linked to enhanced platelet death, examines implications of chemotherapy-induced thrombocytopenia through apoptosis-inducing drugs in cancer therapy as well as discusses ex vivo aging of platelets.
科研通智能强力驱动
Strongly Powered by AbleSci AI