Annexin I is an endogenous ligand that mediates apoptotic cell engulfment

被引:349
作者
Arur, S
Uche, UE
Rezaul, K
Fong, M
Scranton, V
Cowan, AE
Mohler, W
Han, DK
机构
[1] Univ Connecticut, Sch Med, Ctr Vasc Biol, Dept Physiol, Farmington, CT 06030 USA
[2] Univ Connecticut, Sch Med, Ctr Biomed Imaging Technol, Farmington, CT 06030 USA
[3] Univ Connecticut, Sch Med, Dept Genet & Dev Biol, Farmington, CT 06030 USA
关键词
D O I
10.1016/S1534-5807(03)00090-X
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Engulfment of apoptotic cells requires presentation of new cell surface ligands by the dying cells. Using a differential proteomics technology, we identify that annexin I is a caspase-dependent engulfment ligand; it is recruited from the cytosol and exported to the outer plasma membrane leaflet, colocalizes with phosphatidylserine, and is required for efficient clearance of apoptotic cells. Furthermore, phosphatidylserine receptor (PSR) clustering around apoptotic cells indicates a requirement for annexin I. In the nematode Caenorhabditis elegans, downregulation of the annexin homolog prevents efficient engulfment of pharyngeal cell corpses. These results provide novel mechanistic insights into how apoptotic cells are removed and may explain a pathogenic mechanism of chronic inflammatory diseases where annexin I autoantibodies have been described.
引用
收藏
页码:587 / 598
页数:12
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