Identification of a factor that links apoptotic cells to phagocytes

Rikinari Hanayama, Masato Tanaka, Keiko Miwa, Azusa Shinohara, Akihiro Iwamatsu and Shigekazu Nagata ()
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Rikinari Hanayama: Osaka University Medical School
Masato Tanaka: Osaka University Medical School
Keiko Miwa: Osaka University Medical School
Azusa Shinohara: Central Laboratories for Key Technology, Kirin Brewery Co., Ltd
Akihiro Iwamatsu: Central Laboratories for Key Technology, Kirin Brewery Co., Ltd
Shigekazu Nagata: Osaka University Medical School

Nature, 2002, vol. 417, issue 6885, 182-187

Abstract: Abstract Apoptotic cells are rapidly engulfed by phagocytes to prevent the release of potentially noxious or immunogenic intracellular materials from the dying cells, thereby preserving the integrity and function of the surrounding tissue1. Phagocytes engulf apoptotic but not healthy cells, indicating that the apoptotic cells present a signal to the phagocytes, and the phagocytes recognize the signal using a specific receptor2. Here, we report a factor that links apoptotic cells to phagocytes. We found that milk fat globule-EGF-factor 8 (MFG-E8)3,4, a secreted glycoprotein, was produced by thioglycollate-elicited macrophages. MFG-E8 specifically bound to apoptotic cells by recognizing aminophospholipids such as phosphatidylserine. MFG-E8, when engaged by phospholipids, bound to cells via its RGD (arginine-glycine-aspartate) motif—it bound particularly strongly to cells expressing αvβ3 integrin. The NIH3T3 cell transformants that expressed a high level of αvβ3 integrin were found to engulf apoptotic cells when MFG-E8 was added. MFG-E8 carrying a point mutation in the RGD motif behaved as a dominant-negative form, and inhibited the phagocytosis of apoptotic cells by peritoneal macrophages in vitro and in vivo. These results indicate that MFG-E8 secreted from activated macrophages binds to apoptotic cells, and brings them to phagocytes for engulfment.

Date: 2002
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DOI: 10.1038/417182a

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