D-Galactose-Specific Sea Urchin Lectin Sugar-Specifically Inhibited Histamine Release Induced by Datura stramonium Agglutinin : Differences Between Sugar-Specific Effects of Sea Urchin Lectin and Those of D-Galactose- or L-Fucose-Specific Plant Lectins
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概要
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A new sea urchin lectin from Toxopneustes pileolus, is D(+)galactose (Gal)-, D(+)fucose (Fuc)-specific. Incubation of rat peritoneal mast cells with the lectin in the presence of 0.3 mM CaCl2 for 10 min significantly and dose-dependently inhibited the histamine release induced by N-acetyl glucosamine (GlcNAc)-specific Datura stramonium agglutinin (DSA), an activator of the Gi-protein-dependent pathway in mast cells. This inhibition by the sea urchin lectin was sugar-specifically reversed in the presence of D(+)Gal or D(+)Fuc but not L(−)Fuc. The sea urchin lectin had no effect on the histamine release induced by compound 48/80, slightly inhibited the histamine release induced by substance P and mastoparan, and slightly enhanced the histamine release induced by melittin, but these effects were not dose-dependent. Compound 48/80, substance P, mastoparan and melittin are mast cell activators without sugar residues. It is suggested that the lectin binds to D(+)Gal residues of DSA to interfere with mast cell activation induced by DSA, a glycoprotein with arabinose and Gal residues. The effects of plant lectins with affinity to D(+)Gal, N-acetyl galactosamine and/or sialic acid and L(−)Fuc on the histamine release induced by DSA, compound 48/80 and substance P were also examined.
- 社団法人 日本薬理学会の論文
- 2001-04-01
著者
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Uchida Masaatsu
Department Of Molecular Pharmacology Meiji College Of Pharmacy
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Uchida Masaatsu
Department Of Pharmacology Meiji Pharmaceutical University
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Suzuki-nishimura Tamiko
Department Of Pharmacology Meiji Pharmaceutical University
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Nakagawa Hideyuki
Department Of Anesthesiology Saitama International Medical Center Saitama Medical University
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Nakagawa Hideyuki
Department Of Life Science University Of Tokushima
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UCHIDA Masaatsu
Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, University of Tokyo
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SUZUKI-NISHIMURA Tamiko
Department of Molecular Pharmacology, Meiji College of Pharmacy
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