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作 者:易富贤[1] 孙平[1] 黄韶玲[1] 刘文兰[1] 郭兆贵[1]
机构地区:[1]湖南医科大学分子药理研究室,长沙410078
出 处:《生理学报》1999年第4期425-429,共5页Acta Physiologica Sinica
摘 要:包括血管内皮细胞在内的多种细胞和组织存在腺苷三磷酸双磷酸酶(apyrase) , 但心内膜内皮细胞是否含有apyrase 尚无报道。本文旨在研究牛心内膜内皮细胞apyrase 的特性。以无机磷释放法检测培养牛心内膜内皮细胞(BEEC) apyrase 的活性。公认的apyrase 抑制剂叠氮钠呈浓度依赖性地抑制apyrase 活性; 另一种apyrase 抑制剂氟化钠(20 mmol/L) 也明显抑制apyrase 活性。而Na+ /K+ATPase 的抑制剂哇巴因(3 mmol/L) 却不能抑制该酶活性。BEECapyrase 活性依赖于钙或镁等二价阳离子以及pH 的改变, EDTA 或EGTA (1mmol/L) 均能完全抑制其活性, 在pH 值为8-5 时活性最高。由此可见, 牛心内膜内皮细胞存在叠氮钠敏感的、依赖于二价阳离子和pH 值的腺苷三磷酸双磷酸酶活性。Apyrase activities in some tissues and cells, such as peripheral vascular endothelial cells, have been reported, but these in endocardium endothelial cells have not been reported. The present study was to characterise the properties of bovine endocardium endothelial cells (BEEC) associated apyrase. Apyrase activity was assayed by inorganic phosphate release, which could be inhibited concentration dependently by NaN 3, an apyrase inhibitor. NaF (20 mmol/L), another inhibitor of apyrase, also markedly inhibited the activity. EDTA or EGTA (1 mmol/L) could also inhibit the activity completely. However, the inhibitor for Na +/K + ATPase, ouabain (3 mmol/L) did not affect the enzyme activity. BEEC apyrase activity was dependent on divalent cations (Ca 2+ or Mg 2+ ) and pH value.
分 类 号:Q556[生物学—生物化学] R331.31[医药卫生—人体生理学]
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