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Molecular mechanism for phagocytosis of apoptotic cells

Research Project

Project/Area Number 12670115
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field General medical chemistry
Research InstitutionOsaka University

Principal Investigator

TANAKA Masato  Medical School, Osaka University, Associate Professor, 医学系研究科, 助教授 (00294059)

Co-Investigator(Kenkyū-buntansha) NAGATA Shigekazu  Medical School, Osaka University, Professor, 医学系研究科, 教授 (70114428)
Project Period (FY) 2000 – 2001
Project Status Completed (Fiscal Year 2001)
Budget Amount *help
¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 2001: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 2000: ¥2,200,000 (Direct Cost: ¥2,200,000)
KeywordsApoptosis / Macrophage / Phagocytosis / MFG-E8
Research Abstract

To elucidate the molecular mechanism for phagocytosis of apoptotic cells by macrophages, we have established an assay to detect phagocytosis of apoptotic cells. We have shown that the apoptotic cells expressing ICAD mutant undergo DNA fragmentation only after they are phagocytosed by macrophages, and we took advantage of the findings for the assay. That is, macrophages were cultured with apoptotic thymocytes expressing the ICAD mutant, and were stained with anti-Mac 1 antibody and TUNEL. The macrophages with apoptotic cells showed Mac-1 and TUNEL double positive. Using the assay, we could quantitate the percentage of macrophages that phagocytose apoptotic cells. We next screened the series of monoclonal antibodies raised against mouse peritoneal macrophages with the assay, and found that an antibody (designated 2422 Ab) increased the percentage of macrophages that engulfed the apoptotic cells. A molecule recognized by 2422 Ab was purified by affinity chromatography, and a mass spectrometry analysis of the protein identified them as mouse milk fat globule-EGF-factor 8 (MFG-E8), a secreted protein. MFG-E8 specifically bound to apoptotic cells by recognizing phosphatidylserine exposed on outer cell membrane. MFG-E8 engaged by phospholipid bound to cells, in particular to avb3-integrin-expressing cells via its RGD motif. The addition of MFG-E8 rendered NIH3T3 cells to engulf apoptotic cells. MFG-E8 carrying a point mutation in the RGB motif behaved as a dominant negative form, and inhibited the phagocytosis of apoptotic cells by peritoneal macrophages in vitro and in vivo. These results indicated that MFG-E8 secreted from activated macrophages binds to apoptotic cells, and brings them to phagocytes for engulfment.

Report

(3 results)
  • 2001 Annual Research Report   Final Research Report Summary
  • 2000 Annual Research Report
  • Research Products

    (12 results)

All Other

All Publications (12 results)

  • [Publications] D.Mcllroy et al.: "An auxiliary mode of apoptotic DNA fragmentation provided by phagocytes"Genes Dev. 14. 549-558 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] K.Shudo et al.: "The membrane-bound but not the soluble form of human Fas ligand is responsible for its inflammatory activity"Eur J Immunol. 31. 2504-2511 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] T.Itai et al.: "Processing of tumor necrosis factor by the membrane-bound TNF-α-converting enzyme, but not its truncated soluble form"Eur J Biochem. 268. 2074-2082 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] R.Hanayama et al.: "Identification of a factor that links apoptotic cell to phagocytes"Nature. (in press). (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] McIlroy, D. et al.: "An auxiliary mode of apoptotic DNA fragmentation provided by phagocytes"Genes and Development. 14. 49-58 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] Shudo, K. et al.: "The membrane-bound but not the soluble form of human Fas ligand is responsible for its inflammatory activity"Eur J Immunol. 31. 2504-11 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] Itai, T. et al: "Processing of tumor necrosis factor by the membrane-bound TNF-α- converting enzyme, but not its truncated soluble form"Eur J Biochem. 268. 2074-82 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] Hanayama R. et al.: "Identification of a factor that links apoptotic cells to phagocytes."Nature. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] K.Shudo et al.: "The membrane-bound but not the soluble form of human Fas ligand is responsible for its inflammatory activity"Eur J Immunol. 31. 2504-2511 (2001)

    • Related Report
      2001 Annual Research Report
  • [Publications] T.Itai et al.: "Processing of tumor necrosis factor by the membrane-bound TNF-α-converting enzyme, but not its truncated soluble form"Eur J Biochem. 268. 2074-2082 (2001)

    • Related Report
      2001 Annual Research Report
  • [Publications] R.Hanayama et al.: "Identification of a factor that links apoptotic cells to phagocytes"Nature. (in press). (2002)

    • Related Report
      2001 Annual Research Report
  • [Publications] McIlroy,D. et al.: "An auxiliary mode of apoptotic DNA fragmentation provided by phagocytes"GENES & DEVELOPMENT. 14. 549-558 (2000)

    • Related Report
      2000 Annual Research Report

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Published: 2000-04-01   Modified: 2016-04-21  

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