EFFECT OF ADENOSINE AND ADENOSINE 5'-MONOPHOSPHATE ON CELL DIVISION OF CULTURED MASTOCYTOMA P-815 CELLS
スポンサーリンク
概要
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The growth of mouse mastocytoma P-815 cells in culture (37°, 42 hr) was inhibited by exogenous adenosine (0.2 to 1.0 mM) and more effectively by AMP (0.01 to 0.1 mM), but not by adenine. The inhibited growth (a 25% inhibition by 0.5 mM adenosine and a 80% inhibition by 0.25 mM AMP) was restored to a near control level by the addition of uridine (0.5 mM) to the medium. The pretreatment (37°, 3 hr) of the cells with adenosine or AMP caused a 60% inhibition of incorporation (37°, 2 hr) of [U-^<14>C] aspartate into uracil nucleotides, accumulating ^<14>C-orotate and orotidine. Both dipyridamole, an inhibitor of adenosine uptake, and exogenous adenosine deaminase suppressed the growth inhibition induced by not only adenosine but also AMP. 2-Chloroadenosine, which is resistant to the action of adenosine deaminase, was a more potent growth inhibitor, while 3'AMP and 2'-AMP, which are not hydrolyzed to adenosine by membrane 5'-nucleotidase, were ineffective. Adenosine 5'-sulfate and other 5'-substituted adenosines were also ineffective. These observations indicate that AMP inhibits the growth of mastocytoma P-815 cells as a result of its continuous conversion to adenosine and a constant exposure of the cells to a low concentration of adenosine which readily permeates the cell membrane. In addition, adenosine, AMP and their agarose-linked forms rapidly (37°, 20 min) elevated cellular levels of cAMP. This effect was not suppressed by dipyridamole. Apparently adenosine and AMP also act extracellularly for growth inhibition by regulating cAMP levels.
- 公益社団法人日本薬学会の論文
著者
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ICHIKAWA Atsushi
Department of Hematology, Tajimi Prefectural Hospital
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Esumi Kimio
Department Of Health Chemistry Faculty Of Pharmaceutical Sciences Kyoto University
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Yatsunami Kimio
Department Of Biochemistry Faculty Of Pharmaceutical Sciences Kyoto University
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Ichikawa A
Kyoto Univ. Kyoto Jpn
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Ichikawa Atsushi
Department Of Biochemistry Faculty Of Pharmaceutical Sciences Kyoto University
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NEGISHI Manabu
Department of Biochemistry, Faculty of Pharmaceutical Sciences, Kyoto University
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TAKAGI MASAKI
Department of Health Chemistry, Faculty of Pharmaceutical Sciences, Kyoto University
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TOMITA KENKICHI
Department of Health Chemistry, Faculty of Pharmaceutical Sciences, Kyoto University
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YOKOYAMA KOHJI
Department of Health Chemistry, Faculty of Pharmaceutical Sciences, Kyoto University
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Takagi Masaki
Department Of Health Chemistry Faculty Of Pharmaceutical Sciences Kyoto University
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Yokoyama Kohji
Department Of Health Chemistry Faculty Of Pharmaceutical Sciences Kyoto University
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Negishi Manabu
Department Of Biochemistry Faculty Of Pharmaceutical Sciences Kyoto University
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Tomita Kenkichi
Department Of Health Chemistry Faculty Of Pharmaceutical Sciences Kyoto University
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