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Genetical, morphological, and functional analysis of CHMP2B in a patient of familial FTD

Research Project

Project/Area Number 23590390
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Human pathology
Research InstitutionNiigata University

Principal Investigator

TOYOSHIMA Yasuko  新潟大学, 脳研究所, 准教授 (20334675)

Co-Investigator(Kenkyū-buntansha) IKEUCHI Takeshi  新潟大学, 脳研究所, 教授 (20372469)
TAKAHASHI Hitoshi  新潟大学, 脳研究所, 教授 (90206839)
Project Period (FY) 2011 – 2013
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2013: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2012: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
Fiscal Year 2011: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Keywords前頭側頭葉型認知症 / CHMP2B / オートファジー / ユビキチン陽性封入体 / ALS / エンドソーム / 前頭側頭型認知症
Research Abstract

The charged multivesicular body protein 2B gene (CHMP2B) was recently associated with frontotemporal lobar degeneration (FTLD) associated to chromosome 3 in a Danish FTLD family (FTD-3). We report a Japanese family of FTD-3 that developed FTLD in 6members of 3 successive generations. Interestingly, 4 members of 2 successive generations had gastric cancer, and FTLD and gastric cancer cosegregated in the two family members. CHMP2B encode a component of the heteromeric ESCRT-III complex (endosomal sorting complex required for transport III). Dysfunction of the endosomal systems may lead FTLD and cancer.We observed ubiquitin-positive and TDP-43-negative neuronal intracytoplasmic inclusions as previously reported. We could not find any mutation in the CHMP2B gene, however, we observed shorten splicing variant of the m-RNA. The variant showed modified amino acid sequence in the C-terminal.

Report

(4 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • 2012 Research-status Report
  • 2011 Research-status Report
  • Research Products

    (9 results)

All 2014 2013 2012

All Journal Article (8 results) (of which Peer Reviewed: 8 results) Presentation (1 results)

  • [Journal Article] TDP-43 pathology in polyglutamine diseases : with reference to amyotrphic lateral sclerosis2014

    • Author(s)
      Toyoshima Y, Takahashi H
    • Journal Title

      Neuropathology

      Volume: 34(1) Pages: 77-82

    • Related Report
      2013 Final Research Report
    • Peer Reviewed
  • [Journal Article] Transportin 1 accumulates in FUS inclusions in adult-onset ALS without FUS mutation2013

    • Author(s)
      Takeuchi R, Toyoshima Y, Tada M, Shiga A, Tanaka H, Shimohata M, Kimura K, Morita T, Kakita A, Nishizawa M, Takahashi H
    • Journal Title

      Neuropathol Appl Neurobiol

      Volume: 39(5) Pages: 580-4

    • Related Report
      2013 Final Research Report
    • Peer Reviewed
  • [Journal Article] Sporadic ALS with compound heterozygous mutations in the SQSTM1 gene2013

    • Author(s)
      Shimizu H, Toyoshima Y, Shiga A, Yokoseki A, Arakawa K, Sekine Y, Shimohata T, Ikeuchi T, Nishizawa M, Kakita A, Onodera O, Takahashi H
    • Journal Title

      Acta Neuropathol

      Volume: 126(3) Pages: 453-9

    • Related Report
      2013 Final Research Report
    • Peer Reviewed
  • [Journal Article] Transportin 1accumulates in FUS inclusions inadult-onset ALS without FUS mutation2013

    • Author(s)
      Takeuchi R, Toyoshima Y, Tada M, ShigaA, Tanaka H, Shimohata M, Kimura K,Morita T, Kakita A, Nishizawa M,Takahashi H
    • Journal Title

      Neuropathol Appl Neurobiol

      Volume: Epub Issue: 5 Pages: 580-584

    • DOI

      10.1111/nan.12022

    • Related Report
      2013 Annual Research Report 2012 Research-status Report
    • Peer Reviewed
  • [Journal Article] Sporadic ALS with compound heterozygous mutation in the SQSTM1 gene.2013

    • Author(s)
      Shimizu H, Toyoshima Y, Shiga A, Yokoseki A, Arakawa K, Sekine Y, Shimohata T, Ikeuchi T, Nishizawa M, Kakita A, Onodera O, Takahashi H
    • Journal Title

      Acta Neuropathol

      Volume: 126 Issue: 3 Pages: 453-459

    • DOI

      10.1007/s00401-013-1150-5

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Journal Article] TDP-43 pathology in polyglutamine diseases: with reference to amyotrphic lateral sclerosis2013

    • Author(s)
      YasukoToyoshima and Hitoshi Takahashi
    • Journal Title

      Neuropathology

      Volume: 34 Issue: 1 Pages: 77-82

    • DOI

      10.1111/neup.12053

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Autophagy-related proteins (p62, NBR1 and LC3) in intranuclear inclusions in neurodegenerative diseases2012

    • Author(s)
      Mori F, Tanji K, Odagiri S, Toyoshima Y, Yoshida M, Kakita A, Takahashi H, Wakabayashi K
    • Journal Title

      Neurosci Lett.

      Volume: 522(2) Pages: 134-8

    • Related Report
      2013 Final Research Report
    • Peer Reviewed
  • [Journal Article] Ubiquilin immunoreactivity in cytoplasmic and nuclear inclusions in synucleinopathies, polyglutamine diseases and intranuclear inclusion body disease2012

    • Author(s)
      Mori F, Tanji K, Odagiri S, Toyoshima Y, Yoshida M, Ikeda T, Sasaki H, Kakita A, Takahashi H, Wakabayashi K
    • Journal Title

      Acta Neuropathol

      Volume: 124(1) Pages: 149-51

    • Related Report
      2013 Final Research Report
    • Peer Reviewed
  • [Presentation] シンポジウム「ALS: TDP-43 の発見とその後」 ALS以外の疾患におけるTDP-43 proteinopathy2012

    • Author(s)
      豊島靖子
    • Organizer
      第53回日本神経病理学会総会学術研究会
    • Place of Presentation
      新潟
    • Related Report
      2012 Research-status Report

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Published: 2011-08-05   Modified: 2019-07-29  

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