Hennighausen G, Hehl E M, Rychly J
Arch Toxicol Suppl. 1985;8:500-3. doi: 10.1007/978-3-642-69928-3_119.
Ecto-ATPase was present in thymocytes of mice and rats with higher activity in rat thymocytes. In rat but not in mouse thymocytes the ecto-ATPase was inhibited in vitro by HgCl2, tricyclohexyltin chloride, di-n-butyltin dichloride, DDT, gamma HCH and desipramine. The EC50 values ranged from 8 X 10(-7) mol/l for HgCl2 to 4 X 10(-4) mol/l for desipramine. Ecto-ATPase activity in thymocytes was not a valuable indicator of the cytotoxic effects of chemicals in vitro. Inhibition of the enzyme was not accompanied by changes of the electrophoretic mobility of thymocytes. A decrease of the spontaneous mitotic activity of thymocytes in vitro is a very sensitive parameter of cytotoxic and cytostatic drug effects.
胞外ATP酶存在于小鼠和大鼠的胸腺细胞中,在大鼠胸腺细胞中的活性更高。在大鼠而非小鼠的胸腺细胞中,胞外ATP酶在体外会受到氯化汞、三环己基氯化锡、二正丁基二氯化锡、滴滴涕、γ-六氯环己烷和地昔帕明的抑制。半数有效浓度(EC50)值范围从氯化汞的8×10⁻⁷摩尔/升到地昔帕明的4×10⁻⁴摩尔/升。胸腺细胞中的胞外ATP酶活性不是化学物质体外细胞毒性作用的一个有价值指标。该酶的抑制并未伴随胸腺细胞电泳迁移率的变化。体外胸腺细胞自发有丝分裂活性的降低是细胞毒性和细胞抑制药物作用的一个非常敏感的参数。