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2001 Fiscal Year Final Research Report Summary

Identification of novel cytochrome c releasing factor and analysis of its molecular function on apoptosis

Research Project

Project/Area Number 12680695
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Cell biology
Research InstitutionOsaka University

Principal Investigator

SHIMIZU Shigeomi  Osaka University, Graduate School of Medicine, Associate Professor Medical School, 医学系研究科, 助教授 (70271020)

Project Period (FY) 2000 – 2001
Keywordsapoptosis / mitochondria / Bax / cytochrome c
Research Abstract

Mitochondria play an essential role in apoptosis by releasing apoptogenic factors including cytochrome c into the cytoplasm. To explore its molecular mechanisms, I planned two studies ; (1) Analysis of Bax translocation mechanisms, and (2) Identification of novel cytochrome c releasing factor.
(1)Analysis of Bax translocation mechanisms- Bax, one of crucial proapoptotic Bcl2 family protein, is normally localized in the cytoplasm, and translocate to the mitochondria during apoptosis. To investigate the mechanisms of this translocation, we found that cytoplasmic protein 14-3-36 is normally bound to Bax in the cytoplasm, and that Bax dissociates from 14-3-36 during apoptosis to induce apoptotic changes in the mitochondria. In isolated mitochondria, immunodepletion of 14-3-36 from cell lysates enhanced integration of recombinant Bax into the mitochondrial membrane, and 14-3-36 inhibited Bax integration. These findings indicate that 14-3-39 plays a crucial role in negatively regulating Bax activity in living cells.
(2) Identification of novel cytochrome c releasing factor- To identify the novel cytochrome c releasing factor, we purified this factor from irradiated thymus in mice. Addition gf irradiated, but not normal, thymus cytosol to mitochondria significantly induced cytochrome c release. Using FPLC column following amino acid. sequencing, we purified and identified this factor from apoptotic thymus cytosol. This recombinant protein actually induced cytochrome c release when added into mitochondria. These findings might imply that this factor is a novel cytochrome c releasing factor exerting on radiation-induced apoptosis.

  • Research Products

    (13 results)

All Other

All Publications (13 results)

  • [Publications] S.Shimizu, et al.: "Pro-apoptotic BH3-only Bcl-2 family members induce cytochrome c release, but not mitochondrial membrane potential loss, and do not directly modulate VDAC acivity"Proc. Natl. Acad. Sci. USA. 97. 577-582 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Y.Tsujimoto, et al.: "Bcl-2 family : Life-or death switch"FEBS lett.. 466. 6-10 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] S.Shimizu et al.: "BH4 domain of anti-apoptotic Bcl-2 family members closes VDAC, and inhibits apoptotic mitocliondrial changes and cell death"Proc. Natl. Acad. Sci. USA. 97. 3100-3105 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] S.Shimizu, et al.: "Electrophysiological study of a novel large pore formed by Bax and VDAC, which is permeable to cytochrome c"J. Biol. Chem.. 275. 12321-12325 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] S.Shimizu, et al.: "Bax and Bcl-xL independently regulate apoptotic changes of yeast mitochondria that require VDAC but not adenine nucleotide translocator"Oncogene. 19. 4309-4318 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] S.Shimizu, et al.: "Essential role of voltage-dependent anion channel in various forms of apoptosis in mammalian cells"J. Cell Biol.. 152. 237-250 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 清水重臣, 他: "新ミトコンドリア学"共立出版. 434 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] S. Himizu, et al.: "Pro-apoptotic BH3-only Bcl-2 family members induce cytochrome c release, but not mitochondrial membrane potential loss, and do not directly modulate VDAC activity"Proc. Natl. Acad. Sci USA. 97. 577-582 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Y. Tsujimoto, et al.: "Bcl-2 family : Ofe-or-death switch"FEBS lett.. 466. 6-10 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] S. Shimizu, et al.: "BH4 domain of anti-apoptotic Bcl-2 family members closes VDAC, and inhibits apoptotic mitochondrial changes and cell death"Proc. Natl. Acad. Sci. USA. 97. 3100-3105 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] S. Shimizu, et al.: "Eelectrophysiological study of a novel large pore formed by Bax and VDAC, which is permeable to cytochrome c"J. Biol, Chem. 275. 12321-12325 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] S. Shimizu, et al.: "Bax and Bcl-xL independently regulate apoptotic changes of yeast mitochondria that require VDAC but not adenine nucleotide translocator"Oncogene. 19. 4309-4318 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] S. Shiniizu, et al.: "Essential role of voltage-dependent anion channel in various forms of apoptosis in mammalian cells"J. Cell Biol.. 152. 237-250 (2001)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 2003-09-17  

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