胸腺嘧啶进入扁桃体淋巴细胞的动力学及其在淋巴因子存在下的改变。

M T Szabó, A Hrabák, F Antoni
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引用次数: 0

摘要

体外研究了胸腺嘧啶对人扁桃体淋巴细胞酸溶性细胞部分的吸收。在低浓度(小于1.2微米)胸腺嘧啶下,15-20分钟呈线性摄取。摄取与时间的关系图可以外推到原点。测定KM值(0.5-0.6微米)和Vmax值。在抑制胸腺嘧啶并入DNA的淋巴因子的存在下,胸腺嘧啶进入酸溶性细胞部分的摄取也被抑制。摄取减少的特征是表观KM增加,而Vmax没有改变。抑制胸腺嘧啶结合的淋巴因子可能在体内影响和调节外源性胸腺嘧啶进入细胞。
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Kinetics of thymidine entry into tonsillar lymphocytes and its alteration in the presence of a lymphokine.

Thymidine uptake into the acid soluble cell fraction of human tonsillar lymphocytes was studied in vitro. Uptake was linear for 15-20 minutes at low concentrations (less than 1.2 microM) of thymidine. The plot of uptake versus time could be extrapolated to the origin. Value for KM (0.5-0.6 microM) and values for Vmax were determined. In the presence of a lymphokine which inhibited thymidine incorporation into DNA the uptake of thymidine into the acid soluble cell fraction was also inhibited. The decreased uptake could be characterized by an increase in the apparent KM, without the alteration of Vmax. Lymphokines which inhibit thymidine incorporation may influence and regulate in vivo the entry of the exogenous thymidine into the cells.

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