Cell corpse engulfment mediated by C. elegans phosphatidylserine receptor through CED-5 and CED-12

During apoptosis, phosphatidylserine, which is normally restricted to the inner leaflet of the plasma membrane, is exposed on the surface of apoptotic cells and has been suggested to act as an "eat-me" signal to trigger phagocytosis. It is unclear how phagocytes recognize phosphatidylserin...

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Published in:Science (American Association for the Advancement of Science) Vol. 302; no. 5650; pp. 1563 - 1566
Main Authors: XIAOCHEN WANG, WU, Yi-Chun, HENSON, Peter, MITANI, Shohei, DING XUE, FADOK, Valerie A, LEE, Ming-Chia, GENGYO-ANDO, Keiko, CHENG, Li-Chun, LEDWICH, Duncan, HSU, Pei-Ken, CHEN, Jia-Yun, CHOU, Bin-Kuan
Format: Journal Article
Language:English
Published: Washington, DC American Association for the Advancement of Science 28-11-2003
The American Association for the Advancement of Science
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Summary:During apoptosis, phosphatidylserine, which is normally restricted to the inner leaflet of the plasma membrane, is exposed on the surface of apoptotic cells and has been suggested to act as an "eat-me" signal to trigger phagocytosis. It is unclear how phagocytes recognize phosphatidylserine. Recently, a putative phosphatidylserine receptor (PSR) was identified and proposed to mediate recognition of phosphatidylserine and phagocytosis. We report that psr-1, the Caenorhabditis elegans homolog of PSR, is important for cell corpse engulfment. In vitro PSR-1 binds preferentially phosphatidylserine or cells with exposed phosphatidylserine. In C. elegans, PSR-1 acts in the same cell corpse engulfment pathway mediated by intracellular signaling molecules CED-2 (homologous to the human CrkII protein), CED-5 (DOCK180), CED-10 (Rac GTPase), and CED-12 (ELMO), possibly through direct interaction with CED-5 and CED-12. Our findings suggest that PSR-1 is likely an upstream receptor for the signaling pathway containing CED-2, CED-5, CED-10, and CED-12 proteins and plays an important role in recognizing phosphatidylserine during phagocytosis.
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ISSN:0036-8075
1095-9203
DOI:10.1126/science.1087641