Apoptotic cells are rapidly phagocytosed by professional phagocytes, such as macrophages and dendritic cells. This process prevents the release of potentially noxious or immunogenic intracellular materials from dying cells, and is thought to play a critical role for the maintenance of normal functions in surrounding tissues. Milk fat globule-EGF-factor 8 (MFG-E8), secreted by activated macrophages and immature dendritic cells, links apoptotic cells and phagocytes, and promotes phagocytosis of apoptotic cells. Here, we report that an MFG-E8 mutant, designated as D89E, carrying a point mutation in an RGD motif, inhibited not only the phagocytosis of apoptotic cells by a wide variety of phagocytes, but also inhibited the enhanced production of IL-10 by thioglycollate-elicited peritoneal macrophages phagocytosing apoptotic cells. When intravenously injected into mice, the D89E protein induced the production of autoantibodies including antiphospholipids antibodies and antinuclear antibodies. The production of autoantibodies was enhanced by the coinjection of syngeneic apoptotic thymocytes. After the induction of autoantibody production by D89E, the treated mice showed a long-term elevation of the titer for autoantibodies, and developed IgG deposition in the glomeruli. These results indicated that the impairment of apoptotic cell phagocytosis led to autoantibody production.
Skip Nav Destination
Article navigation
16 August 2004
Article Contents
Article|
August 09 2004
Masking of Phosphatidylserine Inhibits Apoptotic Cell Engulfment and Induces Autoantibody Production in Mice
Kenichi Asano,
Kenichi Asano
1Department of Genetics, Osaka University Medical School,
3Laboratory for Innate Cellular Immunity, RIKEN Research Center for Allergy and Immunology, Yokohama, Kanagawa 230-0045, Japan
Search for other works by this author on:
Miyu Miwa,
Miyu Miwa
3Laboratory for Innate Cellular Immunity, RIKEN Research Center for Allergy and Immunology, Yokohama, Kanagawa 230-0045, Japan
Search for other works by this author on:
Keiko Miwa,
Keiko Miwa
4Solution Oriented Research for Science and Technology, Japan Science and Technology Corporation, Osaka 565-0871, Japan
Search for other works by this author on:
Rikinari Hanayama,
Rikinari Hanayama
1Department of Genetics, Osaka University Medical School,
Search for other works by this author on:
Hiroko Nagase,
Hiroko Nagase
1Department of Genetics, Osaka University Medical School,
Search for other works by this author on:
Shigekazu Nagata,
Shigekazu Nagata
1Department of Genetics, Osaka University Medical School,
2Laboratory of Genetics, Integrated Biology Laboratories, Graduate School of Frontier Biosciences, Osaka University, Osaka 565-0871, Japan
4Solution Oriented Research for Science and Technology, Japan Science and Technology Corporation, Osaka 565-0871, Japan
Search for other works by this author on:
Masato Tanaka
Masato Tanaka
1Department of Genetics, Osaka University Medical School,
3Laboratory for Innate Cellular Immunity, RIKEN Research Center for Allergy and Immunology, Yokohama, Kanagawa 230-0045, Japan
Search for other works by this author on:
Kenichi Asano
1Department of Genetics, Osaka University Medical School,
3Laboratory for Innate Cellular Immunity, RIKEN Research Center for Allergy and Immunology, Yokohama, Kanagawa 230-0045, Japan
Miyu Miwa
3Laboratory for Innate Cellular Immunity, RIKEN Research Center for Allergy and Immunology, Yokohama, Kanagawa 230-0045, Japan
Keiko Miwa
4Solution Oriented Research for Science and Technology, Japan Science and Technology Corporation, Osaka 565-0871, Japan
Rikinari Hanayama
1Department of Genetics, Osaka University Medical School,
Hiroko Nagase
1Department of Genetics, Osaka University Medical School,
Shigekazu Nagata
1Department of Genetics, Osaka University Medical School,
2Laboratory of Genetics, Integrated Biology Laboratories, Graduate School of Frontier Biosciences, Osaka University, Osaka 565-0871, Japan
4Solution Oriented Research for Science and Technology, Japan Science and Technology Corporation, Osaka 565-0871, Japan
Masato Tanaka
1Department of Genetics, Osaka University Medical School,
3Laboratory for Innate Cellular Immunity, RIKEN Research Center for Allergy and Immunology, Yokohama, Kanagawa 230-0045, Japan
Address correspondence to Masato Tanaka, Laboratory for Innate Cellular Immunity, RIKEN Research Center for Allergy and Immunology, 1-7-22, Suehiro, Tsurumi, Yokohama, Kanagawa 230-0045, Japan. Phone: 81-45-503-9686; Fax: 81-45-503-9685; email: [email protected]
Abbreviations used in this paper: ANA, antinuclear antibody; BMDM, bone marrow–derived macrophage; CL, cardiolipin; ds, double stranded; MFG-E8, milk fat globule-EGF-factor 8; PS, phosphatidylserine.
Received:
February 20 2004
Accepted:
July 08 2004
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2004
J Exp Med (2004) 200 (4): 459–467.
Article history
Received:
February 20 2004
Accepted:
July 08 2004
Citation
Kenichi Asano, Miyu Miwa, Keiko Miwa, Rikinari Hanayama, Hiroko Nagase, Shigekazu Nagata, Masato Tanaka; Masking of Phosphatidylserine Inhibits Apoptotic Cell Engulfment and Induces Autoantibody Production in Mice . J Exp Med 16 August 2004; 200 (4): 459–467. doi: https://doi.org/10.1084/jem.20040342
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement