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Identification of the antigen molecule that is recognized by a human brown adipocyte-specific monoclonal antibody

Research Project

Project/Area Number 18K08533
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 54040:Metabolism and endocrinology-related
Research InstitutionTokyo Medical and Dental University (2020-2021)
National Center for Global Health and Medicine (2018-2019)

Principal Investigator

Saeki Kumiko  東京医科歯科大学, 大学院医歯学総合研究科, 非常勤講師 (80322717)

Project Period (FY) 2018-04-01 – 2022-03-31
Project Status Completed (Fiscal Year 2021)
Budget Amount *help
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2020: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2019: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2018: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywords褐色脂肪細胞 / 肥満 / 糖尿病 / 代謝 / ヒト胚性幹細胞 / モノクローナル抗体 / 免疫沈降 / 血清マーカー / ヒト褐色脂肪細胞 / 血清診断マーカー / 高感度検出系
Outline of Final Research Achievements

Brown adipose tissue (BAT) enhances energy expenditure via heat production. It also secrets various metabolism-improving factors, thus contributing to obesity prevention. Since the amounts of BAs decrease with age, obesity and diabetes in humans, it has been suggested that there is a subgroup of "BAT failure" in metabolic syndrome. To advance our understanding of human BATs, a feasible technique to measure BAT amounts in a living body is required. To overcome labor, cost and safety issues that the current technique has, we tried to obtain a serum marker for human BAT by identifying the antigen molecule that is recognized by “BA-specific
monoclonal antibody raised against human embryonic stem cell-derived brown adipocytes (hBA)", which dose not cross-react with other human tissues. By purifying the target molecule from hBA lysates, we obtained information regarding the candidate for the antigen molecule. We are currently investigating the "hBA-specific modification" of this molecule.

Academic Significance and Societal Importance of the Research Achievements

世界的に肥満者が増加しているが、コロナ禍では運動不足やストレスにより肥満者の増加は加速している。健康寿命延伸と医療費削減のために肥満予防は重要課題である。エネルギー消費型脂肪である褐色脂肪組織(BAT)は、食事に起因する肥満や中年太りへの抑制効果を発揮ことが知られており、肥満・代謝症候群にはBAT不全症が相当数含まれていると想定される。本研究により採血検査で簡便にヒト生体BAT量が測定できるようになれば健康診断でのBAT評価が可能となり、BAT不全症に対してより早く介入することできる。また採血検査という簡便性から肥満者が多い途上国への技術移転も容易であり、世界の肥満対策にも大きく貢献できる。

Report

(5 results)
  • 2021 Annual Research Report   Final Research Report ( PDF )
  • 2020 Research-status Report
  • 2019 Research-status Report
  • 2018 Research-status Report
  • Research Products

    (9 results)

All 2021 2020 2019 2018

All Journal Article (5 results) (of which Peer Reviewed: 5 results,  Open Access: 5 results) Presentation (3 results) (of which Invited: 1 results) Patent(Industrial Property Rights) (1 results) (of which Overseas: 1 results)

  • [Journal Article] Cold-induced Conversion of Connective Tissue Skeleton in Brown Adipose Tissues2021

    • Author(s)
      Yudasaka M, Okamatsu-Ogura Y, Tanaka T, Saeki K, Kataura H.
    • Journal Title

      ACTA HISTOCHEMICA ET CYTOCHEMICA

      Volume: 54 Issue: 5 Pages: 131-141

    • DOI

      10.1267/ahc.21-00030

    • NAID

      130008112278

    • ISSN
      0044-5991, 1347-5800
    • Year and Date
      2021-10-29
    • Related Report
      2021 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] New Role for Growth/Differentiation Factor 15 in the Survival of Transplanted Brown Adipose Tissues in Cooperation with Interleukin-62020

    • Author(s)
      Oka Masako、Kobayashi Norihiko、Matsumura Kazunori、Nishio Miwako、Nakano Kenta、Okamura Tadashi、Okochi Hitoshi、Minamisawa Tamiko、Shiba Kiyotaka、Saeki Kumiko
    • Journal Title

      Cells

      Volume: 9 Issue: 6 Pages: 1365-1365

    • DOI

      10.3390/cells9061365

    • Related Report
      2020 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] The Remaining Mysteries about Brown Adipose Tissues2020

    • Author(s)
      Nishio Miwako、Saeki Kumiko
    • Journal Title

      Cells

      Volume: 9 Issue: 11 Pages: 2449-2449

    • DOI

      10.3390/cells9112449

    • Related Report
      2020 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Exogenous Cytokine-Free Differentiation of Human Pluripotent Stem Cells into Classical Brown Adipocytes.2019

    • Author(s)
      Oka M, Kobayashi N, Matsumura K, Nishio M, Saeki K.
    • Journal Title

      Cells

      Volume: 8 Issue: 4 Pages: 373-373

    • DOI

      10.3390/cells8040373

    • Related Report
      2018 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Fasting-dependent Vascular Permeability Enhancement in Brown Adipose Tissues Evidenced by Using Carbon Nanotubes as Fluorescent Probes.2018

    • Author(s)
      Yudasaka M, Yomogida Y, Zhang M, Nakahara M, Kobayashi N, Tanaka T, Okamatsu-Ogura Y, Saeki K, Kataura H.
    • Journal Title

      Sci Rep

      Volume: 8 Issue: 1 Pages: 14446-14446

    • DOI

      10.1038/s41598-018-32758-8

    • Related Report
      2018 Research-status Report
    • Peer Reviewed / Open Access
  • [Presentation] 1型糖尿病モデルマウスを用いたタークペプチドの前臨床試験2020

    • Author(s)
      佐伯 久美子
    • Organizer
      サイエンスフォーラム2020オンライン -根治に向けてのカウントダウン 6 ―
    • Related Report
      2020 Research-status Report
    • Invited
  • [Presentation] A human brown adipocyte-specific monoclonal antibody for an evaluation of brown adipose tissue mass in humans2019

    • Author(s)
      Masako Oka, Kazunori Matsumura, Kumiko Saeki
    • Organizer
      第42回 日本分子生物学会年会
    • Related Report
      2019 Research-status Report
  • [Presentation] ES細胞由来褐色脂肪細胞特異的モノクローナル抗体の作製と抗原分子の同定2018

    • Author(s)
      岡雅子
    • Organizer
      第77回日本癌学会学術総会
    • Related Report
      2018 Research-status Report
  • [Patent(Industrial Property Rights)] PLURIPOTENT STEM CELL-DERIVED BROWN ADIPOCYTES, PLURIPOTENT STEM CELL-DERIVED CELL AGGREGATE, METHOD FOR PRODUCING SAME, AND CELL THERAPY AND MEDICAL THERAPY THEREFOR2018

    • Inventor(s)
      佐伯久美子、湯尾明、西尾美和子、川崎正子、佐伯晃一、長谷川護
    • Industrial Property Rights Holder
      国立研究開発法人国立国際医療研究センター、株式会社IDファーマ
    • Industrial Property Rights Type
      特許
    • Filing Date
      2018
    • Acquisition Date
      2018
    • Related Report
      2018 Research-status Report
    • Overseas

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Published: 2018-04-23   Modified: 2023-01-30  

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