Rapid cell corpse clearance by stabilin-2, a membrane phosphatidylserine receptor

被引:360
作者
Park, S-Y [1 ,2 ]
Jung, M-Y [1 ]
Kim, H-J [1 ]
Lee, S-J [1 ]
Kim, S-Y [1 ]
Lee, B-H [1 ]
Kwon, T-H [1 ]
Park, R-W [1 ]
Kim, I-S [1 ]
机构
[1] Kyungpook Natl Univ, Sch Med, Cell & Matrix Res Inst, Dept Biochem & Cell Biol, Taegu 700422, South Korea
[2] Dongguk Univ, Sch Med, Dept Biochem, Kyungju, South Korea
关键词
phagocytosis; phosphatidylserine; macrophages; stabilin-2; FEEL-2; HARE;
D O I
10.1038/sj.cdd.4402242
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Rapid phagocytic clearance of apoptotic cells is crucial for the prevention of both inflammation and autoimmune responses. Phosphatidylserine (PS) at the external surface of the plasma membrane has been proposed to function as a general 'eat me' signal for apoptotic cells. Although several soluble bridging molecules have been suggested for the recognition of PS, the PS-specific membrane receptor that binds directly to the exposed PS and provides a tickling signal has yet to be definitively identified. In this study, we provide evidence that stabilin-2 is a novel PS receptor, which performs a key function in the rapid clearance of cell corpses. It recognizes PS on aged red blood cells and apoptotic cells, and mediates their engulfment. The downregulation of stabilin-2 expression in macrophages significantly inhibits phagocytosis, and anti-stabilin-2 monoclonal antibody provokes the release of the anti-inflammatory cytokine, transforming growth factor-ss. Furthermore, the results of time-lapse video analyses indicate that stabilin-2 performs a crucial function in the rapid clearance of aged and apoptotic cells. These data indicate that stabilin-2 is the first of the membrane PS receptors to provide tethering and tickling signals, and may also be involved in the resolution of inflammation and the prevention of autoimmunity.
引用
收藏
页码:192 / 201
页数:10
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