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Immunocyte Ca2+ influx system mediated by LTRPC2.
Sano, Y; Inamura, K; Miyake, A; Mochizuki, S; Yokoi, H; Matsushime, H; Furuichi, K.
Afiliación
  • Sano Y; Molecular Medicine Laboratories, Institute for Drug Discovery Research, Yamanouchi Pharmaceutical Co., Ltd., 21 Miyukigaoka, Tsukuba, Ibaraki 305-8585, Japan. sano.yorikata@yamanouchi.co.jp
Science ; 293(5533): 1327-30, 2001 Aug 17.
Article en En | MEDLINE | ID: mdl-11509734
We characterized an activation mechanism of the human LTRPC2 protein, a member of the transient receptor potential family of ion channels, and demonstrated that LTRPC2 mediates Ca2+ influx into immunocytes. Intracellular pyrimidine nucleotides, adenosine 5'-diphosphoribose (ADPR), and nicotinamide adenine dinucleotide (NAD), directly activated LTRPC2, which functioned as a Ca2+-permeable nonselective cation channel and enabled Ca2+ influx into cells. This activation was suppressed by intracellular adenosine triphosphate. These results reveal that ADPR and NAD act as intracellular messengers and may have an important role in Ca2+ influx by activating LTRPC2 in immunocytes.
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Bases de datos: MEDLINE Asunto principal: Monocitos / Linfocitos T / Canales de Calcio / Antígenos CD / Calcio / Eosinófilos / Canales Iónicos / Proteínas de la Membrana Límite: Humans Idioma: En Revista: Science Año: 2001 Tipo del documento: Article País de afiliación: Japón
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Bases de datos: MEDLINE Asunto principal: Monocitos / Linfocitos T / Canales de Calcio / Antígenos CD / Calcio / Eosinófilos / Canales Iónicos / Proteínas de la Membrana Límite: Humans Idioma: En Revista: Science Año: 2001 Tipo del documento: Article País de afiliación: Japón