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Hideki Sumimoto

Hideki Sumimoto

D-Index & Metrics

Biology and Biochemistry

D-Index
79
Citations
18859
World Ranking
4392
National Ranking
288

Overview

Hideki Sumimoto is affiliated with Kyushu University in Japan and conducts research primarily in the fields of biochemistry, genetics and molecular biology, neuroscience, and medicine. Their work encompasses various subfields including immunology, molecular biology, cell biology, sensory systems, and physiology.

Their research covers several main topics such as neutrophil, myeloperoxidase and oxidative mechanisms, hearing and cochlea-related genetics, nitric oxide and endothelin effects, cancer-related molecular mechanisms, receptor mechanisms and signaling pathways, pancreatic function and diabetes, and renin-angiotensin system studies.

Sumimoto has authored notable recent papers including:

  • "GPR125 (ADGRA3) is an autocleavable adhesion GPCR that traffics with Dlg1 to the basolateral membrane and regulates epithelial apicobasal polarity" (2022, Journal of Biological Chemistry)
  • "Hepatocyte polarity establishment and apical lumen formation are organized by Par3, Cdc42, and aPKC in conjunction with Lgl" (2021, Journal of Biological Chemistry)
  • "Altered Fhod3 Expression Involved in Progressive High-Frequency Hearing Loss via Dysregulation of Actin Polymerization Stoichiometry in The Cuticular Plate" (2023, bioRxiv - Cold Spring Harbor Laboratory)
  • "The NADPH oxidases DUOX1 and DUOX2 are sorted to the apical plasma membrane in epithelial cells via their respective maturation factors DUOXA1 and DUOXA2" (2024, Genes to Cells)
  • "Fhod3 Controls the Dendritic Spine Morphology of Specific Subpopulations of Pyramidal Neurons in the Mouse Cerebral Cortex" (2020, Cerebral Cortex)

Their frequent collaborators include:

  • Sachiko Kamakura
  • Junya Hayase
  • Akira Kohda
  • Ryu Takeya
  • Masafumi Nakamura

Sumimoto has published repeatedly in several scientific venues, most extensively in Genes to Cells and the Journal of Biological Chemistry, with additional publications in bioRxiv (Cold Spring Harbor Laboratory), Cerebral Cortex, and EMBO Reports.

Best Publications

  • Structure, regulation and evolution of Nox‐family NADPH oxidases that produce reactive oxygen species

    Hideki Sumimoto

  • A Novel Superoxide-producing NAD(P)H Oxidase in Kidney

    Akira Shiose;Junya Kuroda;Kazuhiko Tsuruya;Momoki Hirai

  • Protein Kinase C–Dependent Increase in Reactive Oxygen Species (ROS) Production in Vascular Tissues of Diabetes: Role of Vascular NAD(P)H Oxidase

    Toyoshi Inoguchi;Toshiyo Sonta;Hirotaka Tsubouchi;Takashi Etoh

  • Novel Human Homologues of p47phox and p67phox Participate in Activation of Superoxide-producing NADPH Oxidases

    Ryu Takeya;Noriko Ueno;Keiichiro Kami;Masahiko Taura

  • TRPC3 and TRPC6 are essential for angiotensin II-induced cardiac hypertrophy.

    Naoya Onohara;Motohiro Nishida;Ryuji Inoue;Hiroyuki Kobayashi

  • Molecular composition and regulation of the Nox family NAD(P)H oxidases.

    Hideki Sumimoto;Kei Miyano;Ryu Takeya

  • Role of Src homology 3 domains in assembly and activation of the phagocyte NADPH oxidase

    Hideki Sumimoto;Youhko Kage;Hiroyuki Nunoi;Hiroyuki Sasaki

  • Increased expression of NAD(P)H oxidase subunits, NOX4 and p22phox, in the kidney of streptozotocin-induced diabetic rats and its reversibity by interventive insulin treatment

    T. Etoh;T. Inoguchi;M. Kakimoto;N. Sonoda

  • Tetratricopeptide repeat (TPR) motifs of p67(phox) participate in interaction with the small GTPase Rac and activation of the phagocyte NADPH oxidase

    Hirofumi Koga;Hiroaki Terasawa;Hiroyuki Nunoi;Koichiro Takeshige

  • Arachidonic acid and phosphorylation synergistically induce a conformational change of p47phox to activate the phagocyte NADPH oxidase.

    Akira Shiose;Hideki Sumimoto

  • The superoxide-producing NAD(P)H oxidase Nox4 in the nucleus of human vascular endothelial cells

    Junya Kuroda;Kazunori Nakagawa;Tomoko Yamasaki;Kei Ichiro Nakamura

  • Mechanism for phosphorylation-induced activation of the phagocyte NADPH oxidase protein p47(phox). Triple replacement of serines 303, 304, and 328 with aspartates disrupts the SH3 domain-mediated intramolecular interaction in p47(phox), thereby activating the oxidase.

    Tetsuro Ago;Hiroyuki Nunoi;Takashi Ito;Hideki Sumimoto

  • Phosphorylation of p47phox directs phox homology domain from SH3 domain toward phosphoinositides, leading to phagocyte NADPH oxidase activation.

    Tetsuro Ago;Futoshi Kuribayashi;Hidekazu Hiroaki;Ryu Takeya

  • HIV-1 Tat acts as a processivity factor in vitro in conjunction with cellular elongation factors.

    Hiroyuki Kato;Hideki Sumimoto;Philippe Pognonec;Chein Hwa Chen

  • Involvement of TRPM7 in cell growth as a spontaneously activated Ca2+ entry pathway in human retinoblastoma cells.

    Toyohisa Hanano;Yuji Hara;Juan Shi;Hiromitsu Morita

  • Assembly and Activation of the Phagocyte NADPH Oxidase SPECIFIC INTERACTION OF THE N-TERMINAL Src HOMOLOGY 3 DOMAIN OF p47phox WITH p22phox IS REQUIRED FOR ACTIVATION OF THE NADPH OXIDASE

    Hideki Sumimoto;Kenichiro Hata;Kazuhito Mizuki;Takashi Ito

  • Novel modular domain PB1 recognizes PC motif to mediate functional protein–protein interactions

    Takashi Ito;Yasushi Matsui;Tetsuro Ago;Kazuhisa Ota

  • Phosphoinositide 3-kinase-dependent and -independent activation of the small GTPase Rac2 in human neutrophils.

    Takashi Akasaki;Hirofumi Koga;Hideki Sumimoto

  • Diverse recognition of non-PxxP peptide ligands by the SH3 domains from p67phox, Grb2 and Pex13p

    Keiichiro Kami;Ryu Takeya;Hideki Sumimoto;Daisuke Kohda

  • Tetratricopeptide Repeat (TPR) Motifs of p67 phox Participate in Interaction with the Small GTPase Rac and Activation of the

    Hirofumi Koga;Koichiro Takeshige;Hideki Sumimoto

Frequent Co-Authors

Koichiro Takeshige
Koichiro Takeshige Kyushu University
Takashi Ito
Takashi Ito Kyushu University
Fuyuhiko Inagaki
Fuyuhiko Inagaki Hokkaido University
Daisuke Kohda
Daisuke Kohda Kyushu University
Motohiro Nishida
Motohiro Nishida Kyushu University
Robert G. Roeder
Robert G. Roeder Rockefeller University
Yasuo Mori
Yasuo Mori Kyoto University
Yoshiyuki Sakaki
Yoshiyuki Sakaki Toyohashi University of Technology
Yasuyuki Fukumaki
Yasuyuki Fukumaki Kyushu University
Masami Horikoshi
Masami Horikoshi University of Tokyo

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