传出细胞增多
气体6
吞噬作用
生物
细胞凋亡
梅尔特克
巨噬细胞
细胞生物学
磷脂酰丝氨酸
免疫学
受体酪氨酸激酶
激酶
体外
生物化学
膜
磷脂
作者
Bernadette Anne Chua,Jamie Ann Ngo,Kathy Situ,Christina M. Ramirez,Haruko Nakano,Kouki Morizono
出处
期刊:Virology
[Elsevier BV]
日期:2018-01-02
卷期号:515: 176-190
被引量:22
标识
DOI:10.1016/j.virol.2017.12.025
摘要
Efferocytosis, the phagocytic clearance of apoptotic cells, can provide host protection against certain types of viruses by mediating phagocytic clearance of infected cells undergoing apoptosis. It is known that HIV-1 induces apoptosis and HIV-1-infected cells are efferocytosed by macrophages, although its molecular mechanisms are unknown. To elucidate the roles that efferocytosis of HIV-1-infected cells play in clearance of infected cells, we sought to identify molecules that mediate these processes. We found that protein S, present in human serum, and its homologue, Gas6, can mediate phagocytosis of HIV-1-infected cells by bridging receptor tyrosine kinase Mer, expressed on macrophages, to phosphatidylserine exposed on infected cells. Efferocytosis of live infected cells was less efficient than dead infected cells; however, a significant fraction of live infected cells were phagocytosed over 12h. Our results suggest that efferocytosis not only removes dead cells, but may also contribute to macrophage removal of live virus producing cells.
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