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Elucidation of Fibrosis Regulation Mechanisms by Damage-Associated Molecular Patterns

Research Project

Project/Area Number 21K15465
Research Category

Grant-in-Aid for Early-Career Scientists

Allocation TypeMulti-year Fund
Review Section Basic Section 49070:Immunology-related
Research InstitutionThe University of Tokyo

Principal Investigator

Hangai Sho  東京大学, 先端科学技術研究センター, 客員研究員 (50785350)

Project Period (FY) 2021-04-01 – 2023-03-31
Project Status Completed (Fiscal Year 2022)
Budget Amount *help
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2022: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2021: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
Keywordsダメージ関連分子パターン / 造血幹細胞 / HMGB1 / 炎症 / 線維化 / ダメージ関連分子
Outline of Research at the Start

組織の線維化は自己免疫疾患やがんなど様々な疾患で見られる難治性病態である。線維化の発症には上皮細胞に対する傷害・細胞死と、それに引き続いて起こる炎症・免疫応答が重要であるが、どのような分子がこうした応答を惹起するかは不明である。ダメージ関連分子(以下DAMPs)は死細胞から放出され、自然免疫受容体を介して炎症・免疫応答を惹起する分子として近年注目を集めている。本研究では申請者が独自に開発したマウスモデルを用いて、代表的なDAMPであるHMGB1を中心にDAMPsによる線維化制御機構の解明を行う。さらに申請者らが開発したDAMPsの阻害剤を用いてDAMPsを標的とした抗線維化療法の開発を目指す。

Outline of Final Research Achievements

HMGB1 is known to be an important gene in ontogeny process and has been suggested to play a role in tissue stem cell homeostasis. However, its detailed function has not been elucidated yet. In this study, we show that HMGB1 contributes to hematopoietic stem cell (HSC) homeostasis. Mechanistically, we propose that HMGB1 contributes to HSC homeostasis by regulating the expression of stemness- and cell cycle-related genes in addition to regulating DNA repair response pathway. Furthermore, HMGB1 was found to play an important role in the proliferation of leukemic stem cells in a mouse model of chronic myelogenous leukemia.

Academic Significance and Societal Importance of the Research Achievements

HMGB1は細胞がダメージを受けた際に放出され炎症・免疫応答を惹起するdamage-associated molecular patternsの一つとして近年研究が進んでいたが、個体発生においても重要な役割を果たすことが示唆されていた。しかしながら詳細は機能は不明であり、特に組織幹細胞における役割については個体レベルでの解析は全くなされていなかった。本研究はHMGB1の造血幹細胞の恒常性維持における役割を初めて明らかにした点で画期的である。さらにHMGB1が慢性骨髄性白血病の病態形成において重要でありかつ治療標的となりうることを示した点で意義のあるものと言える。

Report

(3 results)
  • 2022 Annual Research Report   Final Research Report ( PDF )
  • 2021 Research-status Report
  • Research Products

    (9 results)

All 2023 2022 2021 Other

All Journal Article (6 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 6 results,  Open Access: 3 results) Presentation (2 results) Remarks (1 results)

  • [Journal Article] Tumor cell-derived spermidine is an oncometabolite that suppress TCR clustering for intratumoral CD8+ T cell activation2023

    • Author(s)
      Sana Hibino, Shotaro Eto, Sho Hangai, Keiko Endo, Sanae Ashitani, Maki Sugaya, Tsuyoshi Osawa, Tomoyoshi Soga, Tadatsugu Taniguchi, Hideyuki Yanai
    • Journal Title

      Proceedings of the National Academy of Sciences

      Volume: -

    • Related Report
      2022 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Signal transducing innate receptors in tumor immunity2021

    • Author(s)
      Hangai Sho、Kimura Yoshitaka、Taniguchi Tadatsugu、Yanai Hideyuki
    • Journal Title

      Cancer Science

      Volume: - Issue: 7 Pages: 2578-2591

    • DOI

      10.1111/cas.14848

    • Related Report
      2021 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] The impact of damage-associated molecules released from canine tumor cells on gene expression in macrophages2021

    • Author(s)
      Eto Shotaro、Yanai Hideyuki、Hangai Sho、Kato Daiki、Nishimura Ryohei、Nakagawa Takayuki
    • Journal Title

      Scientific Reports

      Volume: 11 Issue: 1 Pages: 8525-8525

    • DOI

      10.1038/s41598-021-87979-1

    • Related Report
      2021 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Orchestration of myeloid-derived suppressor cells in the tumor microenvironment by ubiquitous cellular protein TCTP released by tumor cells2021

    • Author(s)
      Hangai Sho、Kawamura Takeshi、Kimura Yoshitaka、Chang Ching-Yun、Hibino Sana、Yamamoto Daisuke、Nakai Yousuke、Tateishi Ryosuke、Oshima Masanobu、Oshima Hiroko、Kodama Tatsuhiko、Moriya Kyoji、Koike Kazuhiko、Yanai Hideyuki、Taniguchi Tadatsugu
    • Journal Title

      Nature Immunology

      Volume: 22 Issue: 8 Pages: 947-957

    • DOI

      10.1038/s41590-021-00967-5

    • Related Report
      2021 Research-status Report
    • Peer Reviewed
  • [Journal Article] Damage-associated molecular patterns and Toll-like receptors in the tumor immune microenvironment2021

    • Author(s)
      Yanai Hideyuki、Hangai Sho、Taniguchi Tadatsugu
    • Journal Title

      International Immunology

      Volume: 33 Issue: 12 Pages: 841-846

    • DOI

      10.1093/intimm/dxab050

    • Related Report
      2021 Research-status Report
    • Peer Reviewed
  • [Journal Article] Identification and characterization of a novel Enterococcus bacteriophage with potential to ameliorate murine colitis2021

    • Author(s)
      Nishio Junko、Negishi Hideo、Yasui-Kato Mika、Miki Shoji、Miyanaga Kazuhiko、Aoki Kotaro、Mizusawa Takuma、Ueno Masami、Ainai Akira、Muratani Masafumi、Hangai Sho、Yanai Hideyuki、Hasegawa Hideki、Ishii Yoshikazu、Tanji Yasunori、Taniguchi Tadatsugu
    • Journal Title

      Scientific Reports

      Volume: 11 Issue: 1 Pages: 20231-20231

    • DOI

      10.1038/s41598-021-99602-4

    • Related Report
      2021 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Presentation] TCTP released by tumor cells orchestrates dynamics of myeloid-derived suppressor cells in the tumor microenvironmt2022

    • Author(s)
      Sho Hangai, Hideyuki Yanai, Tadatsugu Taniguchi
    • Organizer
      第81回 日本癌学会学術総会
    • Related Report
      2022 Annual Research Report
  • [Presentation] Translationally-controlled tumor protein (TCTP) released by tumor cells orchestrates dynamics of myeloid-derived suppressor cells in the tumor microenvironment2021

    • Author(s)
      半谷 匠
    • Organizer
      第50回日本免疫学会学術集会
    • Related Report
      2021 Research-status Report
  • [Remarks] ダメージを受けたがん細胞由来分子が 免疫応答の抑制により がんの増殖に寄与していることを発見

    • URL

      https://www.rcast.u-tokyo.ac.jp/ja/news/release/20210709.html

    • Related Report
      2021 Research-status Report

URL: 

Published: 2021-04-28   Modified: 2024-01-30  

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