EFFECT OF P-AMINOBENZOIC ACID N-XYLOSIDE SODIUM SALT (K-247) ON METABOLISM AND FUNCTIONS OF NORMAL LYMPHOCYTES AND LEUKEMIC CELLS
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概要
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An N-xyloside derivative of p-aminobenzoic acid, K-247,was investigated for the ability to induce changes of Phospholipid metabolism and membrane transport in murine splenic lymphocytes and leukemic cells. K-247 induced an increase of [^3H] methyl group incorporation into phospholipid in both normal lymphocytes and leukemic cells (L-1210 and M1 cells). However, K-247 accelerated the turnover of phosphatidylinositol (PI) measured by [^<32>P] incorporation into PI in L-1210 cells and M1 cells but not in normal lymphocytes ^<45>Ca^<2+> influx into normal lymphocytes and leukemic cells was also increased by K-247. A methyltransferase inhibitor, 5'-deoxy-5'-S-isobutyl adenosine (SIBA), suppressed both the increase of phospholipid methylation and that of Ca^<2+> influx. It seemed that Ca^<2+> transport might be regulated by membrane phospholipid methylation. On the other hand, K-247 was found to suppress [^3H] aminoisobutylic acid (AIB) uptake into L-1210 cells and M1 cells. Protein synthesis in L-1210 cells and M1 cells slightly decreased but RNA and DNA syntheses in both normal and leukemic cells were not affected by K-247. These results suggest that K-247 mainly acts on cell membranes, which are more sensitive to K-247 in leukemic cells than in normal lymphocytes. K-247 also induced differentiation of M1 cells into macrophages and granulocytes with phagocytic activity and morphological characteristics. Moreover, K-247 elevated the Con A response of murine thymocytes, most of which were immature T cells and had low reactivity to Con A, and caused a decrease of Thy 1.2 antigen on thymocytes. It seemed that K-247 also affected maturation of thymocytes.
- 公益社団法人日本薬学会の論文
著者
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Nakajima Shinji
Division Of Chemical Toxicology And Immunochemistry Faculty Of Pharmaceutical Sciences University Of
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Toyoshima Satoshi
Division Of Chemical Toxicology And Immunochemistry Faculty Of Pharmaceutical Sciences The Universit
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Toyoshima Satoshi
Division Of Chemical Toxicology And Immunochemistry Faculty Of Pharmaceutical Sciences University Of
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OSAWA TOSHIAKI
Division of Chemical Toxicology and Immunochemistry, Faculty of Pharmaceutical Sciences, University
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OGUCHI YOSHIHARU
Division of Chemical Toxicology and Immunochemistry, Faculty of Pharmaceutical Sciences, University
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Osawa Toshiaki
Division Of Chemical Toxicology And Immunochemistry Faculty Of Pharmaceutical Sciences University Of
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Oguchi Yoshiharu
Division Of Chemical Toxicology And Immunochemistry Faculty Of Pharmaceutical Sciences University Of
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Osawa Toshiaki
Division Of Chemical Toxicology And Immunochemistry Faculty Of Pharmaceutical Sciences University Of
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Osawa Toshiaki
Division Of Chemical Toxicology And Immunochemistry Faculty Of Pharmaceutical Science University Of
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