Autoimmune disease and impaired uptake of apoptotic cells in MFG-E8-deficient mice.

نویسندگان

  • Rikinari Hanayama
  • Masato Tanaka
  • Kay Miyasaka
  • Katsuyuki Aozasa
  • Masato Koike
  • Yasuo Uchiyama
  • Shigekazu Nagata
چکیده

Apoptotic cells expose phosphatidylserine and are swiftly engulfed by macrophages. Milk fat globule epidermal growth factor (EGF) factor 8 (MFG-E8) is a protein that binds to apoptotic cells by recognizing phosphatidylserine and that enhances the engulfment of apoptotic cells by macrophages. We report that tingible body macrophages in the germinal centers of the spleen and lymph nodes strongly express MFG-E8. Many apoptotic lymphocytes were found on the MFG-E8-/- tingible body macrophages, but they were not efficiently engulfed. The MFG-E8-/- mice developed splenomegaly, with the formation of numerous germinal centers, and suffered from glomerulonephritis as a result of autoantibody production. These data demonstrate that MFG-E8 has a critical role in removing apoptotic B cells in the germinal centers and that its failure can lead to autoimmune diseases.

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Autoimmune Disease and Impaired Uptake of Apoptotic Cells in Germinal Centers of MFG-E8–Deficient Mice

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An Apoptosis-Associated Mammary Protein Deficiency Leads to Enhanced Production of IgM Antibodies against Multiple Damage-Associated Molecules

Milk fat globule epidermal growth factor 8 (MFG-E8) is a protein that binds to apoptotic cells by recognizing phosphatidylserine and enhances the engulfment of apoptotic cells by macrophages. Many apoptotic cells are left unengulfed in the germinal centers of the spleen in the MFG-E8-deficient (MFG-E8(-/-)) mice, and these mice develop an autoimmune disease resembling human systemic lupus eryth...

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عنوان ژورنال:
  • Science

دوره 304 5674  شماره 

صفحات  -

تاریخ انتشار 2004