首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Relatively low-dose cyclophosphamide is likely to induce apoptotic cell death in rat thymus through Fas/Fas ligand pathway.
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Relatively low-dose cyclophosphamide is likely to induce apoptotic cell death in rat thymus through Fas/Fas ligand pathway.

机译:相对低剂量的环磷酰胺很可能通过Fas / Fas配体途径诱导大鼠胸腺凋亡。

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摘要

Cyclophosphamide (CPA) is widely used as an efficiently antineoplastic drug, but also causes immunosuppression as its adverse-side effect. To understand the effect of low- or relative low-dose CPA on the immune system, apoptotic cell death in rat thymus, either exposed to different doses of CPA (0, 2, 7, 20 and 70 mg/kg) for 12 h or exposed to 70 mg/kg for different times (4-48 h), was investigated by DNA fragmentation (DNA ladder) detection and in situ morphological examination using hematoxylin and eosin (H and E) staining. Immunohistochemical staining for Fas protein expression in the thymus of rats exposed to CPA was performed. Results showed that exposure of rats to CPA 0-70 mg/kg for 12 h did not cause significant decrease in the ratio of thymus weight to body weight. However, the ratio of thymus weight to body weight was decreased significantly at 48 h after exposure to 70 mg/kg CPA. Exposure to 20 and 70 mg/kg CPA for 12 h caused a visible DNA ladder in gel electrophoresis. DNA ladder formation was increased progressively in the groups from 8 h to optimal magnitude at 12-24 h and then disappeared at 48 h after 70 mg/kg CPA. This pattern was confirmed by a quantitative evaluation of the apoptotic cells using H and E staining. Expression of Fas protein was enhanced in the thymus of rats exposed to 70 mg/kg CPA for 4-8 h as compared to control rats. These results are different from previous studies on high dose CPA and the induction of the apoptotic cell death in thymus by low or relative low doses of CPA might be a result of Fas/Fas-ligand interactions. Copyright 1999 Elsevier Science B.V.
机译:环磷酰胺(CPA)被广泛用作有效的抗肿瘤药,但由于其副作用也引起免疫抑制。要了解低剂量或相对低剂量CPA对免疫系统的影响,可将大鼠胸腺的凋亡细胞死亡,暴露于不同剂量的CPA(0、2、7、20和70 mg / kg)12小时或通过苏木精和曙红(H和E)染色的DNA片段检测(DNA阶梯)和原位形态学检查,研究了暴露于70 mg / kg不同时间(4-48小时)的样品。对暴露于CPA的大鼠胸腺中Fas蛋白表达进行了免疫组织化学染色。结果表明,大鼠在0-70 mg / kg的CPA中暴露12 h不会导致胸腺重量与体重的比率显着降低。然而,在暴露于70 mg / kg CPA后48小时,胸腺重量与体重的比例显着降低。暴露于20和70 mg / kg CPA持续12 h在凝胶电泳中引起可见的DNA阶梯。组中的DNA梯形形成从8小时逐渐增加到12-24小时的最佳幅度,然后在70 mg / kg CPA后48小时消失。通过使用H和E染色对凋亡细胞进行定量评估,证实了这种模式。与对照大鼠相比,暴露于70 mg / kg CPA 4-8 h的大鼠胸腺中Fas蛋白的表达增强。这些结果与以前关于高剂量CPA的研究不同,低或相对低剂量的CPA诱导胸腺凋亡细胞死亡可能是Fas / Fas-配体相互作用的结果。版权所有1999 Elsevier Science B.V.

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