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Cytoskeletons and cell death-associated proteins expressed in neuronal cells in the neurofilament gene-manipulated mice

Research Project

Project/Area Number 14570030
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field General anatomy (including Histology/Embryology)
Research InstitutionKoshien University

Principal Investigator

GOTOW Takahiro  Koshien University, College of Nutrition, Professor, 栄養学部, 教授 (20135693)

Co-Investigator(Kenkyū-buntansha) UCHIYAMA Yasuo  Osaka University, Graduate School of Medicine, Department of Cell Biology and Neuroscience, Professor, 大学院・医学系研究科, 教授 (10049091)
Project Period (FY) 2002 – 2003
Project Status Completed (Fiscal Year 2003)
Budget Amount *help
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2003: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 2002: ¥2,500,000 (Direct Cost: ¥2,500,000)
KeywordsNeurofilament / Gene-manipulated mice / NFsubunit-deficient mice / NF-M or / and NF-H tail-less mice / Organization of axoplasm / Microtubule / Mitochondria / Neuronal cell death / 神経軸索 / NF-H C末端除去マウス / NF-M C末端除去マウス / NF-H及びNF-M C末端同時除去マウス / ウエスタンブロット法 / 急速連結ディープエッチ法 / NF-H欠損マウス / NF-HのC末端除去マウス / リン酸化 / 軸索細胞の構築 / 軸索輸送 / NF-Mの発現
Research Abstract

Neurofilaments (NFs) are composed of three proteins, NF-L,NF-M and NP-H, and NF-M and NP-H are provided with uniquely extended and phosphorylated carboxyl-terminal tail domains that do not appear in other intermediate filament proteins. In collaboration with American researchers at California (UCSD) and New York Universities we generated knockout mice that do not express each of these subunit proteins as well as knockin mice that lack only the carboxyl-terminal tail of NF-M or/and NF-H, to know how the deletions of each NF subunit protein and of the extended carboxy-terminal tails of NF-M or/and NF-H are related with NF organization in the neuron, axonal structure, axonal transport of NFs, organizations of other cytoskeletons and membrane-bound organelles, and expression of other NF subunit proteins. When NF-L was deleted, NFs were not assembled in neurons. Such axons were much thinner but provided with many more microtubules and mitochondria. Compared with NF-H, the deletion of NF-M had more effective influence on axonal calibers and NF organization, suggesting that NF-M is more essential for the NF function. Since the carboxyl-terminal tail of NF-M appears to be more important for NF organization and function, we deleted only this tail domain of NF-M or/and NF-H, and found as expected that NF-M tail was more necessary for the NF organization. However, more drastic changes in axoplasmic organizations, such as irregularity of NF alignment, Increase in density of microtubules as well as mitochondria, were obtained when both NF-M and NF-H tails were simultaneously deleted. These results suggest that both NF-M and NP-H tails, which form crossbridges between NFs, are necessary for NF organization and axonal functions, and are also associated with regulation of neuronal cell death through the change in function of mitochondria.

Report

(3 results)
  • 2003 Annual Research Report   Final Research Report Summary
  • 2002 Annual Research Report
  • Research Products

    (15 results)

All Other

All Publications (15 results)

  • [Publications] Rao, M.V.: "Gene replacement in mice reveals that the heavily phosphorylated tail of neurofilament heavy subunit does not affect axonal caliber or the transit of cargoes in slow axonal transport."Journal of Cell Biology. 158. 681-693 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Yoshida, S.: "PDX-1 induces differentiation of intestinal epithelioid IEC-6 into insulin-producing cells."Diabetes. 51. 2505-2513 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Yabuta, N.: "Mammalian Mcm2/4/6/7 complex forms a toroidal structure."Genes to Cells. 8. 413-421 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Garcia, M.L.: "MF-M is an essential target for the myelin-directed "outside-in" signaling cascade that mediates radial axonal growth."Journal of Cell Biology. 163. 1011-1020 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Rao, M.V.: "The neurofilament middle molecular mass subunit carboxyl-terminal tail domains is essential for the radial growth and cytoskeletal architecture of axons but not for regulating neurofilament transport rate."Journal of Cell Biology. 163. 1021-1031 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Rao, M.V., et al.: "Gene replacement in mice reveals that the heavilyphosphorylated tail of neurofilament heavy subunit does not affect axonal caliber or the transit of cargoes in slow axonal transport"Journal of Cell Biology. 158. 681-693 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Yoshida, S., et al.: "PDX-1 induces differentiation of intestinal epithelioid IEC-6 into insulin-producing cells"Diabetes. 51. 2505-2513 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Yabuta N., et al.: "Mammalian Mcm2/4/6/7 complex forms a toroidal structure"Genes to Cells. 413-421 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Garcia, M.L., et al.: "MF-M is an essential target for the myelin-directed "outside-in" signaling cascade that mediates radial axonal growth"Journal of Cell Biology. 163. 1011-1020 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Rao, M.V., et al.: "The neurofilament middle molecular mass subunit carboxylterminal tail domains is essential for the radial growth and cytoskeletal architecture of axons but not for regulating neurofilament transport rate"Journal of Cell Biology. 163. 1021-1031 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Yabuta, N.: "Mammalian Mcm2/4/6/7 complex forms a toroidal structure"Genes to Cells. 8. 413-421 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Garcia, M.L.: "MF-M is an essential target for the myelin-directed "outside-in"signaling cascade that mediates radial axonal growth"J.Cell Biol.. 163. 1011-1020 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Rao, M.V.: "The neurofilament middle molecular mass subunit carboxyl-terminal tail domains is essential for the radial growth and cytoskeletal architecture of axons but not for regulating neurofilament transport rate"J.Cell Biol.. 163. 1021-1031 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Rao, M.V.: "Gene replacement in mice reveals that the heavily phosphorylated tail of neurofilament heavy subunit does not affect axonal caliber or the transit of cargoes in slow axonal transport"Journal of Cell Biology. 158. 681-693 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Yoshida, S.: "PDX-1 induces differentiation of intestinal epithelioid IEC-6 into insulin-producing cells"Diabetes. 51. 2505-2513 (2002)

    • Related Report
      2002 Annual Research Report

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Published: 2002-04-01   Modified: 2016-04-21  

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