Updated on 2024/07/28

Information

 

写真a

 
URUNO TAKEHITO
 
Organization
Medical Institute of Bioregulation Department of Immunobiology and Neuroscience Associate Professor
Graduate School of Medical Sciences Department of Medicine(Joint Appointment)
Graduate School of Medical Sciences Department of Medical Sciences(Joint Appointment)
Title
Associate Professor
Contact information
メールアドレス
Tel
0926426830
Homepage

Degree

  • The University of Tokyo, Ph.D.

Research History

  • 通産省工業技術院生命工学工業技術研究所(1994~1999)、アメリカ赤十字社ホランド研究所(1999~2004)、アメリカ国立衛生研究所/NIH(2004~2008)、理化学研究所CDB(2008~2009)、九州大学生体防御医学研究所免疫遺伝学分野(特任講師、2009~2013)、九州大学生体防御医学研究所免疫遺伝学分野(助教、2013~2014)、2014年2月〜現職 「細胞生理応答研究から、新しい創薬につながる研究を目指しています」 「次世代の日本の若い研究者に、世界基準の研究価値観を期待しています」

    通産省工業技術院生命工学工業技術研究所(1994~1999)、アメリカ赤十字社ホランド研究所(1999~2004)、アメリカ国立衛生研究所/NIH(2004~2008)、理化学研究所CDB(2008~2009)、九州大学生体防御医学研究所免疫遺伝学分野(特任講師、2009~2013)、九州大学生体防御医学研究所免疫遺伝学分野(助教、2013~2014)、2014年2月〜現職 「細胞生理応答研究から、新しい創薬につながる研究を目指しています」 「次世代の日本の若い研究者に、世界基準の研究価値観を期待しています」

  • なし

Research Interests・Research Keywords

  • Research theme:Immune regulation of diseases and metabolites: Structure-function analysis of the DOCK family proteins and SULTs. Development of novel molecular-targeted drugs for treating cancer, allergy, and immune diseases. Metabolite Biology

    Keyword:cancer, immune system, signal transduction, cytoskeleton, drug development

    Research period: 2009.5 - 2033.3

Awards

  • 内藤記念科学奨励金・研究助成

    2017.9   公益財団法人 内藤記念科学振興財団  

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    膵臓がんにおけるRac活性化因子DOCK1の機能解析とその選択的阻害による治療

Papers

  • Cancer-derived cholesterol sulfate is a key mediator to prevent tumor infiltration by effector T cells Invited Reviewed International journal

    Tatsuguchi T, Uruno T, Sugiura Y, Sakata D, Izumi Y, Sakurai T, Hattori Y, Oki E, Kubota N, Nishimoto K, Oyama M, Kunimura K, Ohki T, Bamba T, Tahara H, Sakamoto M, Nakamura M, Suematsu M, Fukui Y.

    INTERNATIONAL IMMUNOLOGY   34 ( 5 )   277 - 289   2022.4

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1093/intimm/dxac002

  • A conserved PI(4,5)P2–binding domain is critical for immune regulatory function of DOCK8 Reviewed International journal

    4 ( 4 )   e202000873 - e202000873   2021.2

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOCK8 is a Cdc42-specific guanine-nucleotide exchange factor that is essential for development and functions of various subsets of leukocytes in innate and acquired immune responses. Although DOCK8 plays a critical role in spatial control of Cdc42 activity during interstitial leukocyte migration, the mechanism remains unclear. We show that the DOCK homology region (DHR)-1 domain of DOCK8 binds specifically to phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2) and is required for its recruitment to the plasma membrane. Structural and biochemical analyses reveal that DOCK8 DHR-1 domain consists of a C2 domain-like core with loops creating the upper surface pocket, where three basic residues are located for stereospecific recognition of phosphoinositides. Substitution of the two basic residues, K576 and R581, with alanine abolished PI(4,5)P2 binding in vitro, ablated the ability of DOCK8 to activate Cdc42 and support leukocyte migration in three-dimensional collagen gels. Dendritic cells carrying the mutation exhibited defective interstitial migration in vivo. Thus, our study uncovers a critical role of DOCK8 in coupling PI(4,5)P2 signaling with Cdc42 activation for immune regulation.

    DOI: 10.26508/lsa.202000873

  • Targeting Ras-Driven Cancer Cell Survival and Invasion through Selective Inhibition of DOCK1.

    Takehito Uruno

    Cell reports   2017.5

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.celrep.2017.04.016

  • The transcription factor EPAS1 links DOCK8 deficiency to atopic skin inflammation via IL-31 induction.

    Takehito Uruno

    Nature communications   2017.1

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1038/ncomms13946

  • DOCK2 regulates MRGPRX2/B2-mediated mast cell degranulation and drug-induced anaphylaxis

    Kazufumi Kunimura, Sayaka Akiyoshi, Takehito Uruno, Keisuke Matsubara, Daiji Sakata, Kenji Morino, Kenichiro Hirotani, Yoshinori Fukui

    Journal of Allergy and Clinical Immunology   151 ( 6 )   1585 - 1594.e9   2023.6

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.jaci.2023.01.029

  • Cholesterol sulfate limits neutrophil recruitment and gut inflammation during mucosal injury. International journal

    Kenji Morino, Kazufumi Kunimura, Yuki Sugiura, Yoshihiro Izumi, Keisuke Matsubara, Sayaka Akiyoshi, Rae Maeda, Kenichiro Hirotani, Daiji Sakata, Seiya Mizuno, Satoru Takahashi, Takeshi Bamba, Takehito Uruno, Yoshinori Fukui

    Frontiers in immunology   14   1131146 - 1131146   2023.3

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.3389/fimmu.2023.1131146

  • Identification of a functional DOCK8 gene polymorphism associated with atopic dermatitis Reviewed

    Kazufumi Kunimura, Kazuhiko Yamamura, Takeshi Nakahara, Makiko Kido-Nakahara, Takehito Uruno, Yoshinori Fukui

    Allergy   77 ( 12 )   3670 - 3672   2022.7

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1111/all.15429

  • Pharmacological intervention of cholesterol sulfate-mediated T cell exclusion promotes antitumor immunity Reviewed International journal

    Takaaki Tatsuguchi, Takehito Uruno, Yuki Sugiura, Kounosuke Oisaki, Daisuke Takaya, Daiji Sakata, Yoshihiro Izumi, Takaya Togo, Yuko Hattori, Kazufumi Kunimura, Testuya Sakurai, Teruki Honma, Takeshi Bamba, Masafumi Nakamura, Motomu Kanai, Makoto Suematsu, Yoshinori Fukui

    Biochemical and Biophysical Research Communications   2022.4

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.bbrc.2022.04.035

  • DOCK8 deficiency causes a skewing to type 2 immunity in the gut with expansion of group 2 innate lymphoid cells Reviewed International journal

    Matsubara K, Kunimura K, Yamane N, Aihara R, Sakurai T, Sakata D, Uruno T, Fukui Y.

    Biochem Biophys Res Commun.   559   135 - 140   2021.6

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    Language:English  

    DOI: 10.1016/j.bbrc.2021.04.094.

  • Targeted inhibition of EPAS1–driven IL-31 production by a small-molecule compound

    2021.4

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.jaci.2021.03.029

  • DOCK8 controls survival of group 3 innate lymphoid cells in the gut through Cdc42 activation International journal

    Ryosuke Aihara, Kazufumi Kunimura, Mayuki Watanabe, Takehito Uruno, Nana Yamane, Tetsuya Sakurai, Daiji Sakata, Fusanori Nishimura, Yoshinori Fukui

    International Immunology   2020.9

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1093/intimm/dxaa066

  • S100A4 Protein Is Essential for the Development of Mature Microfold Cells in Peyer’s Patches International journal

    29 ( 9 )   2823 - 2834   2019.11

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    Language:English   Publishing type:Research paper (scientific journal)  

    Intestinal microfold cells (M cells) in Peyer's patches are a special subset of epithelial cells that initiate mucosal immune responses through uptake of luminal antigens. Although the cytokine receptor activator of nuclear factor-κB ligand (RANKL) expressed on mesenchymal cells triggers differentiation into M cells, other environmental cues remain unknown. Here, we show that the metastasis-promoting protein S100A4 is required for development of mature M cells. S100A4-producing cells are a heterogenous cell population including lysozyme-expressing dendritic cells and group 3 innate lymphoid cells. We found that in the absence of DOCK8, a Cdc42 activator critical for interstitial leukocyte migration, S100A4-producing cells are reduced in the subepithelial dome, resulting in a maturation defect of M cells. While S100A4 promotes differentiation into mature M cells in organoid culture, genetic inactivation of S100a4 prevents the development of mature M cells in mice. Thus, S100A4 is a key environmental cue that regulates M cell differentiation in collaboration with RANKL.

    DOI: 10.1016/j.celrep.2019.10.091

  • Selective role of neurokinin B in IL-31-induced itch response in mice.

    Takehito Uruno

    The Journal of allergy and clinical immunology   144 ( 4 )   1130 - 1133.e8   2019.8

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.jaci.2019.06.031

  • Cholesterol sulfate is a DOCK2 inhibitor that mediates tissue-specific immune evasion in the eye International journal

    Tetsuya Sakurai, Takehito Uruno, Yuki Sugiura, Takaaki Tatsuguchi, Kazuhiko Yamamura, Miho Ushijima, Yuko Hattori, Mutsuko Kukimoto-Niino, Chiemi Mishima-Tsumagari, Mayuki Watanabe, Makoto Suematsu, Yoshinori Fukui

    Science Signaling   11 ( 541 )   2018.7

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1126/scisignal.aao4874

  • The Rac Activator DOCK2 Mediates Plasma Cell Differentiation and IgG Antibody Production. International journal

    Takehito Uruno

    Frontiers in immunology   9   243 - 243   2018.2

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.3389/fimmu.2018.00243

  • DOCK1 inhibition suppresses cancer cell invasion and macropinocytosis induced by self-activating Rac1P29S mutation.

    Takehito Uruno

    Biochemical and biophysical research communications   2018.2

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.bbrc.2018.02.073

  • Thymic epithelial cell-specific deletion of Jmjd6 reduces Aire protein expression and exacerbates disease development in a mouse model of autoimmune diabetes.

    Takehito Uruno

    Biochemical and biophysical research communications   2017.5

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.bbrc.2017.05.113

  • DOCK8 Protein Regulates Macrophage Migration through Cdc42 Protein Activation and LRAP35a Protein Interaction.

    Takehito Uruno

    The Journal of biological chemistry   2016.12

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1074/jbc.M116.736306

  • Intronic regulation of Aire expression by Jmjd6 for self-tolerance induction in the thymus.

    Takehito Uruno

    Nature communications   2015.11

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1038/ncomms9820

  • DOCK2 and DOCK5 Act Additively in Neutrophils To Regulate Chemotaxis, Superoxide Production, and Extracellular Trap Formation Reviewed International journal

    Mayuki Watanabe, Masao Terasawa, Kei Miyano, Toyoshi Yanagihara, Takehito Uruno, Fumiyuki Sanematsu, Akihiko Nishikimi, Jean Francois Cote, Hideki Sumimoto, Yoshinori Fukui

    JOURNAL OF IMMUNOLOGY   193 ( 11 )   2014.12

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.4049/jimmunol.1400885

  • DOCK2 and DOCK5 act additively in neutrophils to regulate chemotaxis, superoxide production, and extracellular trap formation.

    Takehito Uruno

    Journal of immunology (Baltimore, Md. : 1950)   2014.10

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.4049/jimmunol.1400885

  • DOCK5 functions as a key signaling adaptor that links Fc epsilon RI signals to microtubule dynamics during mast cell degranulation Reviewed International journal

    Kana Ogawa, Yoshihiko Tanaka, Takehito Uruno, Duan Xuefeng, Yosuke Harada, Fumiki Sanematsu, Kazuhiko Yamamura, Masao Terasawa, Akihiko Nishikimi, Jena Francois Cote, Yoshinori Fukui

    JOURNAL OF EXPERIMENTAL MEDICINE   211 ( 7 )   2014.6

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1084/jem.20131926

  • DOCK5 functions as a key signaling adaptor that links FcεRI signals to microtubule dynamics during mast cell degranulation.

    2014.6

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    Mast cells play a key role in the induction of anaphylaxis, a life-threatening IgE-dependent allergic reaction, by secreting chemical mediators that are stored in secretory granules. Degranulation of mast cells is triggered by aggregation of the high-affinity IgE receptor, FcεRI, and involves dynamic rearrangement of microtubules. Although much is known about proximal signals downstream of FcεRI, the distal signaling events controlling microtubule dynamics remain elusive. Here we report that DOCK5, an atypical guanine nucleotide exchange factor (GEF) for Rac, is essential for mast cell degranulation. As such, we found that DOCK5-deficient mice exhibit resistance to systemic and cutaneous anaphylaxis. The Rac GEF activity of DOCK5 is surprisingly not required for mast cell degranulation. Instead, DOCK5 associated with Nck2 and Akt to regulate microtubule dynamics through phosphorylation and inactivation of GSK3β. When DOCK5-Nck2-Akt interactions were disrupted, microtubule formation and degranulation response were severely impaired. Our results thus identify DOCK5 as a key signaling adaptor that orchestrates remodeling of the microtubule network essential for mast cell degranulation.

    DOI: 10.1084/jem.20131926

  • Dimerization of DOCK2 is essential for DOCK2-mediated Rac activation and lymphocyte migration.

    Takehito Uruno

    PloS one   2012.9

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1371/journal.pone.0046277

  • Blockade of inflammatory responses by a small-molecule inhibitor of the Rac activator DOCK2. International journal

    Takehito Uruno

    Chemistry & biology   19 ( 4 )   488 - 97   2012.4

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.chembiol.2012.03.008

  • DOCK8は免疫反応時の間質樹状細胞遊走に重要なCdc42アクチベータである

    日本免疫学会総会・学術集会記録   41   2012.3

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1182/blood-2012-01-407098

  • Racグアニンヌクレオチド交換因子DOCK2及びそのパートナーELMO1のそれらの自己阻害化形からの相互排除のための構造的基盤

    109 ( 9 )   2012.2

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1073/pnas.1113512109

  • Molecular basis for barbed end uncapping by CARMIL homology domain 3 of mouse CARMIL-1.

    Takehito Uruno

    The Journal of biological chemistry   2010.7

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1074/jbc.M110.134221

  • Selective control of type I IFN induction by the Rac activator DOCK2 during TLR-mediated plasmacytoid dendritic cell activation. International journal

    Takehito Uruno

    The Journal of experimental medicine   207 ( 4 )   721 - 30   2010.3

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1084/jem.20091776

  • Purification of capping protein using the capping protein binding site of CARMIL as an affinity matrix.

    Takehito Uruno

    Protein expression and purification   2009.5

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.pep.2009.05.002

  • CARMIL is a potent capping protein antagonist: identification of a conserved CARMIL domain that inhibits the activity of capping protein and uncaps capped actin filaments.

    Takehito Uruno

    The Journal of biological chemistry   2006.1

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1074/jbc.m513186200, 10.1074/jbc.M513186200

  • Interaction of cortactin and Arp2/3 complex is required for sphingosine-1-phosphate-induced endothelial cell remodeling.

    Takehito Uruno

    Experimental cell research   2004.8

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.yexcr.2004.03.023

  • Sequential interaction of actin-related proteins 2 and 3 (Arp2/3) complex with neural Wiscott-Aldrich syndrome protein (N-WASP) and cortactin during branched actin filament network formation.

    Takehito Uruno

    The Journal of biological chemistry   2003.5

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1074/jbc.m301997200, 10.1074/jbc.M301997200

  • Haematopoietic lineage cell-specific protein 1 (HS1) promotes actin-related protein (Arp) 2/3 complex-mediated actin polymerization.

    Takehito Uruno

    The Biochemical journal   2003.4

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1042/BJ20021791

  • Osmotic stress-induced remodeling of the cortical cytoskeleton.

    Takehito Uruno

    American journal of physiology. Cell physiology   2002.9

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    DOI: 10.1152/ajpcell.00018.2002

  • Activation of Arp2/3 complex-mediated actin polymerization by cortactin

    URUNO T

    Nat. Cell Biol.   3   259 - 266   2001.3

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    Activation of Arp2/3 complex-mediated actin polymerization by cortactin.
    Cortactin, a filamentous actin (F-actin)-associated protein and prominent substrate of Src, is implicated in progression of breast tumours through gene amplification at chromosome 11q13. However, the function of cortactin remains obscure. Here we show that cortactin co-localizes with the Arp2/3 complex, a de novo actin nucleator, at dynamic particulate structures enriched with actin filaments. Cortactin binds directly to the Arp2/3 complex and activates it to promote nucleation of actin filaments. The interaction of cortactin with the Arp2/3 complex occurs at an amino-terminal domain that is rich in acidic amino acids. Mutations in a conserved amino-acid sequence of DDW abolish both the interaction with the Arp2/3 complex and complex activation. The N-terminal domain is not only essential but also sufficient to target cortactin to actin-enriched patches within cells. Interestingly, the ability of cortactin to activate the Arp2/3 complex depends on an activity for F-actin binding, which is almost 20-fold higher than that of the Arp2/3 complex. Our data indicate a new mechanism for activation of actin polymerization involving an enhanced interaction between the Arp2/3 complex and actin filaments.

    DOI: 10.1038/35060051

  • Fibroblast growth factor-1 interacts with the glucose-regulated protein GRP75/mortalin.

    Takehito Uruno

    The Biochemical journal   1999.10

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1042/bj3430461

  • Distinct regulation of myoblast differentiation by intracellular and extracellular fibroblast growth factor-1.

    Takehito Uruno

    Growth factors (Chur, Switzerland)   1999.1

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.3109/08977199909103519

  • The C-terminal region of fibroblast growth factor-1 is crucial for its biological activity and high level protein expression in mammalian cells.

    Takehito Uruno

    Growth factors (Chur, Switzerland)   1999.1

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.3109/08977199909002129

  • Expression of the fibroblast growth factor family and their receptor family genes during mouse brain development.

    Takehito Uruno

    Brain research. Molecular brain research   1996.9

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/0169-328x(96)00108-8, 10.1016/0169-328X(96)00108-8

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Presentations

  • A tumor metabolite impacting immunotherapy efficacy: Cholesterol sulfate regulates tumor-immune interactions Invited International conference

    Takehito Uruo, Takaaki Tatsuguchi, Yuki Sugiura, Yoshinori Fukui

    Keystone Symposia on "Cancer Immunotherapy: Mechanisms of Response versus Resistance"  2023.3 

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    Event date: 2023.3

    Language:English   Presentation type:Symposium, workshop panel (public)  

    Country:Japan  

  • コレステロール代謝と疾患制御の新たな展開

    宇留野武人(オーガナイザー)、大石由美子(オーガナイザー) 講演者リスト: 佐藤 隆一郎(東京大学大学院 農学生命科学研究科) Esperanza Perucha(Centre for Inflammation Biology and Cancer Immunology;Centre for Rheumatic Diseases, King’s College London) 高橋 勇人(慶應義塾大学医学部) 大石 由美子(日本医科大学 大学院医学研究科) 小黒 秀行(University of Connecticut Health Center) 國村 和史(九州大学 生体防御医学研究所) 宇留野 武人(九州大学 生体防御医学研究所)

    第95回日本生化学大会  2022.11 

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    Event date: 2022.11

    Language:Japanese   Presentation type:Symposium, workshop panel (public)  

    Venue:名古屋国際会議場   Country:Japan  

    コレステロールは、細胞膜の主要構成成分の一つであると共に、各種ステロイドホルモン生合成の起点となり、生命活動の維持に不可欠の役割を果たす。社会の長寿高齢化が進む中で、コレステロールと生活習慣病や慢性疾患の関係に大きな関心が寄せられているが、依然として不明な点が多く残されている。最近、その代謝過程で生じる様々なコレステロール代謝産物が、免疫応答やがん、炎症制御において重要な役割を担うことが次々と明らかにされ、トランスレーショナル・リサーチの観点からも大きな注目を集めている。そこで、本シンポジウムでは、これら最新の知見を紹介し、コレステロール代謝と生体機能・疾患制御の関係性を新たな視点から俯瞰することで、コレステロール・バイオロジーの更なる進化と発展を促す機会としたい。

  • ホスファチジン酸産生酵素PLD1は好中球細胞外トラップの形成に必須である

    @宇留野 武人、@相原 良亮

    第101回日本生理学会大会  2024.3 

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    Event date: 2024.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:福岡県北九州市小倉   Country:Japan  

  • がん免疫療法に対する抵抗性を付与する腫瘍メタボライト

    @宇留野 武人、#竜口 崇明、@杉浦 悠毅、@福井 宣規

    第27回日本がん免疫学会総会  2023.7 

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    Event date: 2023.7

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:三重県津市   Country:Japan  

  • マウスハーダー腺の加齢に伴うトランスクリプトーム・リピドーム変化

    宇留野武人、高橋政友

    日本生理学会 第100回記念大会  2023.3 

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    Event date: 2023.3

    Language:Japanese  

    Venue:国立京都国際会館   Country:Japan  

  • A tumor metabolite impacting immunotherapy efficacy: Cholesterol sulfate regulates tumor-immune interactions Invited

    Takehito Uruno, Takaaki Tatsuguchi, Yuki Sugiura, Yoshinori Fukui

    Keystone Symposia "Cancer Immunotherapy: Mechanisms of Response versus Resistance"  2023.3 

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    Event date: 2023.3

    Language:Others  

    Country:Other  

  • RAS変異を有する難治性がんの新規分子標的治療薬の開発

    宇留野武人、坂田大治、福井宣規、生長幸之助

    第94回日本生化学会大会  2021.11 

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    Event date: 2021.11 - 2022.6

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:京都   Country:Japan  

  • DOCK1 as a novel molecular target for controlling cancer cell survival and invasion International conference

    Tatsuguchi T, Uruno T, Fukui Y

    25th Biennial Congress on the European Association for Cancer Research  2018.7 

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    Event date: 2018.7

    Language:English  

    Country:Netherlands  

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MISC

  • DOCK-family proteins: key players in immune surveillance mechanisms

    Takehito Uruno

    International Immunology   2019.10

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    Language:English  

    DOI: 10.1093/intimm/dxz067

Professional Memberships

  • The Japanese Biochemical Society

  • 日本生理学会

  • 日本がん免疫学会

  • 日本がん免疫学会

Academic Activities

  • Screening of academic papers

    Role(s): Peer review

    2023

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    Type:Peer review 

    Number of peer-reviewed articles in foreign language journals:2

  • 事前準備、運営全般 International contribution

    ( 九州大学病院キャンパス ) 2014.11

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    Type:Competition, symposium, etc. 

    Number of participants:300

Research Projects

  • 令和5年度 鈴木謙三記念医科学応用研究財団 研究助成

    2024

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    Grant type:Donation

  • 基盤研究(B) 腫瘍の免疫特権環境形成における硫酸化コレステロールの役割と創薬応用

    2021.4 - 2024.3

    九州大学(日本) 

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    Authorship:Principal investigator 

    腫瘍の免疫特権環境形成における硫酸化コレステロールの役割と創薬応用、機能生物化学関連分野

  • AMED革新的がん医療実用化研究事業、「RAS変異を有する難治性がんの新規分子標的治療薬の非臨床評価」

    2019.7 - 2022.3

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    Authorship:Principal investigator 

  • RAS変異を有する難治性がんの新規分子標的治療薬の非臨床評価

    2019 - 2021

    AMED 革新的がん医療実用化研究事業

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    Authorship:Principal investigator  Grant type:Contract research

  • 基盤研究(B) 腫瘍の免疫回避機構におけるRac活性化因子DOCK1の機能

    2018.4 - 2021.3

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    Authorship:Principal investigator 

  • リジン水酸化酵素Jmjd6を介したAire発現制御の分子基盤とその進化学的考察

    2016.4 - 2019.3

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    Authorship:Coinvestigator(s) 

  • 革新的先端研究開発支援事業インキュベートタイプ(LEAP) DOCKファミリー分子の生体機能と動作原理の理解に基づく革新的医薬品の創出

    2015.11 - 2020.3

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    Authorship:Coinvestigator(s) 

  • 基盤研究(C) ヒト変異型Racによる細胞癌化におけるDOCKファミリー分子の役割

    2014.4 - 2017.3

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    Authorship:Principal investigator 

  • 創薬等支援技術基盤プラットフォーム事業「大型創薬研究基盤を活用した創薬オープンイノベーションの推進(九州大学拠点推進事業)」

    2014.4 - 2016.3

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    Authorship:Coinvestigator(s) 

  • 次世代がん研究戦略推進プロジェクト

    2014.4 - 2015.3

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    Authorship:Coinvestigator(s) 

  • 橋渡し研究・新規開発シーズA

    2014.4 - 2015.3

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    Authorship:Collaborating Investigator(s) (not designated on Grant-in-Aid) 

  • 基盤研究(A) DOCKファミリー分子の生体機能と動作原理の統合的理解

    2014.1 - 2016.3

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    Authorship:Coinvestigator(s) 

▼display all

Class subject

  • 免疫学

    2023.4 - 2023.9   First semester

  • 医学研究特論 I

    2023.4 - 2023.9   First semester

  • 医学研究特論 I

    2021.10 - 2022.3   Second semester

FD Participation

  • 2019.10   Role:Panelist   Title:馬出地区4部局合同男女共同参画FD

    Organizer:[Undergraduate school/graduate school/graduate faculty]

  • 2017.10   Role:Participation   Title:「無意識のバイアスからの開放:ダイバーシティのススメ」

    Organizer:University-wide

  • 2016.10   Role:Participation   Title:「なぜ今『女性活躍推進法』か?    —男女共同参画の必要性と九州大学における取組み—」

    Organizer:University-wide

Other educational activity and Special note

  • 2023  Class Teacher 

  • 2021  Special Affairs 

  • 2017  Special Affairs 

Media Coverage

  • がん抑える新化合物 九大など、副作用少ない薬開発に期待 TV or radio program

    2017.5

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    がん抑える新化合物 九大など、副作用少ない薬開発に期待

  • 九州大・研究グループ がん抑える新たな化合物を開発 Newspaper, magazine

    2017.5

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    九州大・研究グループ がん抑える新たな化合物を開発