Effect of methotrexate on cells in a keratinized epithelium with an active thymidine salvage pathway assessed by autoradiography.

U Møller, N Keiding, J K Larsen
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引用次数: 4

Abstract

In the partially synchronized cell system of the hamster cheek pouch epithelium, the inhibitory effect of a bolus injection of methotrexate (Mtx) (2 g/m2, injected at 1200 hr) was analysed by means of both autoradiography and flow cytometry (FCM) in a 21-hr experiment. For autoradiography [3H]TdR and [3H]UdR were used as tracers for salvage and de novo pathways of thymidylate (TMP) synthesis, respectively. For FCM no tracers were injected. The autoradiographic studies demonstrated an active TdR salvage pathway for DNA synthesis, not affected by the impaired de novo TMP synthesis. The blocked de novo TMP synthesis was partially released 7 hr after Mtx injection, but it had not totally recovered at the end of the experiment. The decrease in the fraction of S-phase cells detected about 10 hr after Mtx injection by autoradiographic labelling with [3H]TdR and by FCM was found to be caused by a decrease in the number of cells entering S phase. However, Mtx did not influence the salvage TMP synthesis rate of cells entering S phase.

甲氨蝶呤对角化上皮细胞的影响,通过放射自显影评估胸苷残留通路。
在部分同步的仓鼠颊袋上皮细胞系统中,通过放射自显影和流式细胞术(FCM)在21小时的实验中分析了甲氨蝶呤(Mtx) (2 g/m2,在1200小时注射)的抑制作用。放射自显影用[3H]TdR和[3H]UdR分别作为胸腺苷酸(TMP)合成的恢复途径和新生途径的示踪剂。FCM未注射示踪剂。放射自显影研究表明,TdR对DNA合成有积极的挽救途径,不受TMP合成受损的影响。阻断的新生TMP合成在注射Mtx后7小时部分释放,但在实验结束时未完全恢复。注射Mtx约10小时后,[3H]TdR放射自显影标记和流式细胞仪检测到的S期细胞比例下降是由于进入S期的细胞数量减少所致。然而,Mtx不影响进入S期的细胞的补助性TMP合成率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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