Dissecting Receptor-Mediated Ca〔2+〕 Influx Pathways: TRP Channels and Their Native Counterparts

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  • Mori Yasuo
    Center for Integrative Bioscience, Okazaki National Research Institutes Departmet of Cell Physiology, National Institute for Physiological Sciences, Okazaki National Research Institutes School of Life Science, The Graduate University for Advanced Studies
  • Inoue Ryuji
    Department of Pharmacology, Faculty of Medicine, Kyushu University
  • Ishii Masakazu
    Center for Integrative Bioscience, Okazaki National Research Institutes Departmet of Cell Physiology, National Institute for Physiological Sciences, Okazaki National Research Institutes
  • Hara Yuji
    Center for Integrative Bioscience, Okazaki National Research Institutes Department of Information Physiology, National Institute for Physiological Sciences, Okazaki National Research Institutes School of Life Science, The Graduate University for Advanced Studies
  • Imoto Keiji
    Department of Information Physiology, National Institute for Physiological Sciences, Okazaki National Research Institutes School of Life Science, The Graduate University for Advanced Studies

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タイトル別名
  • Dissecting Receptor-Mediated Ca2+ Influx Pathways: TRP Channels and Their Native Counterparts.

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抄録

Cellular stimulation from the surrounding extracellular environment via receptors and other pathways evoke activation of Ca2+-permeable cation channels that form essential signaling pathways in controlling biological responses. An important clue to understand the molecular mechanisms underlying these cation channels (tentatively termed as receptor-mediated cation channels (RMCC)) was first provided through molecular studies of the transient receptor potential (trp) protein (TRP), which controls light-induced depolarization in Drosophila photoreceptor cells. Use of the genetic information and recombinant expression technique lead to the discovery of numerous mammalian TRP homologues revealing novel RMCCs. In this review, we focus on the dramatic progress in the molecular investigation of RMCC in mammalian systems. The recent findings should provide powerful tools for the development of novel pharmaceutical targets.

収録刊行物

  • Jpn.J.Pharmacol.

    Jpn.J.Pharmacol. 87 (4), 245-252, 2001

    公益社団法人 日本薬理学会

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