Møller U, Keiding N, Larsen J K
Cell Tissue Kinet. 1984 Sep;17(5):497-507. doi: 10.1111/j.1365-2184.1984.tb00608.x.
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.
在仓鼠颊囊上皮细胞部分同步化的细胞系统中,于21小时的实验里,通过放射自显影术和流式细胞术(FCM)分析了大剂量注射甲氨蝶呤(Mtx)(2 g/m²,于1200时注射)的抑制作用。对于放射自显影术,[³H]TdR和[³H]UdR分别用作胸苷酸(TMP)合成的补救途径和从头合成途径的示踪剂。对于流式细胞术,未注射示踪剂。放射自显影研究表明,存在用于DNA合成的活跃TdR补救途径,且不受受损的TMP从头合成的影响。Mtx注射7小时后,受阻的TMP从头合成部分得到缓解,但在实验结束时仍未完全恢复。通过用[³H]TdR进行放射自显影标记以及流式细胞术检测发现,Mtx注射后约10小时检测到的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并不影响进入S期细胞的补救性TMP合成速率。