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Apoptosis in human thymocytes after treatment with glucocorticoids.

机译:糖皮质激素治疗后人胸腺细胞凋亡。

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摘要

Treatment of unfractionated human thymocytes in culture with the synthetic glucocorticoid dexamethasone induced cell death, as measured by trypan blue exclusion, after several hours of incubation. In purified subsets of human cortical and medullary thymocytes dexamethasone caused cell lysis with similar kinetics in both populations; 50% of thymocytes were killed after 20-24 h of incubation with the steroid. The mechanism of dexamethasone-induced cell death seems to correspond to apoptosis since degradation of DNA into oligonucleosome-sized fragments could be observed in the cultures treated with the steroid. A certain degree of DNA fragmentation and cell death could also be observed in control cultures of thymocytes. In contrast, peripheral T lymphocytes were resistant to the cytolytic effect of glucocorticoid hormone. The killing of human thymocytes by dexamethasone was inhibited by cycloheximide, suggesting that this cell death program requires a fully operating protein synthesis machinery and perhaps the induction of new proteins.
机译:孵育数小时后,用台盼蓝排除法测量合成的糖皮质激素地塞米松对培养物中未分离的人类胸腺细胞的诱导的细胞死亡。在人类皮层和髓样胸腺细胞的纯化子集中,地塞米松引起的细胞裂解在两个群体中具有相似的动力学。与类固醇孵育20-24小时后,杀死了50%的胸腺细胞。地塞米松诱导的细胞死亡机制似乎与细胞凋亡相对应,因为在用类固醇处理的培养物中可以观察到DNA降解为寡核小体大小的片段。在胸腺细胞的对照培养物中也可以观察到一定程度的DNA断裂和细胞死亡。相反,外周T淋巴细胞对糖皮质激素的细胞溶解作用有抗性。地塞米松对人胸腺细胞的杀灭作用被环己酰亚胺抑制,这表明该细胞死亡程序需要一个完全运转的蛋白质合成机制,也可能需要诱导新蛋白质。

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