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Molecular mechanism of porphyrin synthesis in the skin

Research Project

Project/Area Number 18K08261
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 53050:Dermatology-related
Research InstitutionHirosaki University

Principal Investigator

Nakano Hajime  弘前大学, 医学研究科, 准教授 (90281922)

Co-Investigator(Kenkyū-buntansha) 澤村 大輔  弘前大学, 医学研究科, 教授 (60196334)
Project Period (FY) 2018-04-01 – 2021-03-31
Project Status Completed (Fiscal Year 2020)
Budget Amount *help
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2020: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2019: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2018: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Keywordsポルフィリン症 / 遺伝性ポルフィリン症 / ヘム生合成 / ポルフィリン / 表皮角化細胞 / 真皮線維芽細胞 / メラノサイト / 皮膚線維芽細胞 / 線維芽細胞 / 毛細血管内皮細胞 / ポルフィリン代謝
Outline of Final Research Achievements

We investigated the expression of nine enzymes involved in the hem biosynthesis pathway in epidermal keratinized cells (KC), dermal fibroblasts (FB), and melanocytes (MC), which are the three major cells that make up human skin. Total RNA was extracted from each cultured cell and the gene expression of heme biosynthesis-related enzymes was examined by RT-PCR. The expression of all genes encoding eight enzymes other than ALAS2 was confirmed. Cytoplasmic proteins were extracted from KC, FB, and MC and Western blotting was performed. Protein expression of eight heme biosynthesis-related enzymes other than ALAS2 was confirmed, and ALAD, UROS, CPOX, and PPOX in MC, FECH protein expression level was found to be significantly higher than in other cells.

Academic Significance and Societal Importance of the Research Achievements

ヒトの皮膚構成細胞における、ヘム生合成経路で働く9つの酵素の遺伝子およびタンパク発現レベルを世界で最初に解析した。メラノサイトでの高い発現が証明され、この事実がメラノサイトのどのような生理的活動と関連するのかを明らかにするために、更なる研究が必要となり、学術的発展が期待される。

Report

(4 results)
  • 2020 Annual Research Report   Final Research Report ( PDF )
  • 2019 Research-status Report
  • 2018 Research-status Report
  • Research Products

    (14 results)

All 2020 2019 2018

All Journal Article (8 results) (of which Peer Reviewed: 4 results,  Open Access: 2 results) Presentation (5 results) (of which Invited: 5 results) Book (1 results)

  • [Journal Article] Analysis of the mechanism underlying a mild phenotype of hereditary coproporphyria due to a homozygous missense mutation in the transcription initiation codon of the coproporphyrinogen III oxidase gene2020

    • Author(s)
      Fukui Tomohisa、Akasaka Eijiro、Rokunohe Daiki、Matsuzaki Yasushi、Sawamura Daisuke、Kabashima Kenji、Nakano Hajime
    • Journal Title

      Journal of Dermatological Science

      Volume: 100 Issue: 2 Pages: 156-159

    • DOI

      10.1016/j.jdermsci.2020.06.006

    • Related Report
      2020 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Novel mutation of the ferrochelatase gene in a Japanese family with erythropoietic protoporphyria.2020

    • Author(s)
      Saito A, Okiyama N, Inoue S, Kubota N, Nakamura Y, Ishitsuka Y, Watanabe R, Nakano H, Fujisawa Y.
    • Journal Title

      J Dermatol.

      Volume: 47 Issue: 4

    • DOI

      10.1111/1346-8138.15258

    • Related Report
      2019 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] 成人期に確定診断に至った骨髄性プロトポルフィリン症.2019

    • Author(s)
      木岡茉奈, 兪 明寿, 谷崎英昭, 黒川晃夫, 森脇真一, 中野  創.
    • Journal Title

      皮膚病診療

      Volume: 41 Pages: 657-660

    • Related Report
      2019 Research-status Report
    • Peer Reviewed
  • [Journal Article] The first Japanese case of familial porphyria cutanea tarda diagnosed by a UROD mutation2019

    • Author(s)
      Matsui Akinobu、Akasaka Eijiro、Rokunohe Daiki、Matsuzaki Yasushi、Sawamura Daisuke、Nakano Hajime
    • Journal Title

      Journal of Dermatological Science

      Volume: 93 Issue: 1 Pages: 65-67

    • DOI

      10.1016/j.jdermsci.2018.11.004

    • Related Report
      2018 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] 骨髄性プロトポルフィリン症の家族例.2019

    • Author(s)
      丸田 志野, 宮下 梓, 中野 創, 尹 浩信.
    • Journal Title

      皮膚病診療

      Volume: 41 Pages: 17-20

    • Related Report
      2018 Research-status Report
  • [Journal Article] ポルフィリン症2019

    • Author(s)
      中野 創
    • Journal Title

      診断と治療

      Volume: 107s Pages: 67-67

    • Related Report
      2018 Research-status Report
  • [Journal Article] 遺伝子解析により診断した多様性ポルフィリン症の1例.2018

    • Author(s)
      浦野 聖子, 宇佐神 治子, 中野 創, 戸倉 新樹.
    • Journal Title

      皮膚科の臨床

      Volume: 60 Pages: 1345-1348

    • Related Report
      2018 Research-status Report
  • [Journal Article] 遺伝性皮膚疾患.2018

    • Author(s)
      中野 創
    • Journal Title

      MB Derma

      Volume: 268 Pages: 295-302

    • Related Report
      2018 Research-status Report
  • [Presentation] わかりやすい遺伝性皮膚疾患2018

    • Author(s)
      中野 創
    • Organizer
      第34回日本臨床皮膚科医会総会・臨床学術大会
    • Related Report
      2018 Research-status Report
    • Invited
  • [Presentation] 遺伝性皮膚ポリフィリン症の診断スキル2018

    • Author(s)
      中野 創
    • Organizer
      第117回日本皮膚科学会総会
    • Related Report
      2018 Research-status Report
    • Invited
  • [Presentation] 遺伝性皮膚ポルフィリン症の遺伝子診断2018

    • Author(s)
      中野 創
    • Organizer
      第40回日本光医学・光生物学会
    • Related Report
      2018 Research-status Report
    • Invited
  • [Presentation] 皮膚ポリフィリン症2018

    • Author(s)
      中野 創
    • Organizer
      第69回日本皮膚科学会中部支部学術大会
    • Related Report
      2018 Research-status Report
    • Invited
  • [Presentation] ファブリー病の遺伝子解析2018

    • Author(s)
      中野 創
    • Organizer
      Fabry next generation meeting in Tohoku
    • Related Report
      2018 Research-status Report
    • Invited
  • [Book] 皮膚疾患の最新の治療2019-2020.2019

    • Author(s)
      中野 創
    • Total Pages
      310
    • Publisher
      南江堂
    • ISBN
      9784524245482
    • Related Report
      2018 Research-status Report

URL: 

Published: 2018-04-23   Modified: 2022-01-27  

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