首页> 美国卫生研究院文献>Journal of Virology >Effect of actinomycin D on the expression of herpes simplex virus-common surface antigen in cells transformed by herpes simplex virus type 2.
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Effect of actinomycin D on the expression of herpes simplex virus-common surface antigen in cells transformed by herpes simplex virus type 2.

机译:放线菌素D对2型单纯疱疹病毒转化细胞中单纯疱疹病毒共有表面抗原表达的影响。

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摘要

Using rabbit antiserum hyperimmune to herpes simplex virus (HSV) type 1, the expression of HSV-common surface antigen(s) was studied by indirect immunofluorescence tests in cells transformed by HSV type 2 and in derived tumor cells. The following results were obtained. (i) Antiserum to HSV type 1 reacted specifically with surface antigen present on the plasma membrane of both HSV type 2-infected and HSV type 2-transformed hamster cells. (ii) The expression of this antigen was enhanced in the absence of active protein synthesis in transformed cells, but not in tumor cells, after culture for 3 to 5 h at 37 degrees C. (iii) This enhancement of expression was maintained for 20 h in the presence of actinomycin D, but this prolonged expression required active protein synthesis. (iv) The enhancing effect observed in the presence of actinomycin D continued for some time after removal of the drug, for example, for 20 h after 5 h of treatment with 2 microgram/ml of actinomycin D per ml. Actinomycin D had no detectable effect on antigen expression in tumor cells. (v) The protease inhibitor antipain inhibited the actinomycin D-enhanced expression without causing significant cell damage but did not modify the transient enhanced expression of antigen when cells were seeded in the absence of actinomycin D. These results indicate that in transformed cells antigen expression can be enhanced in at least two ways.
机译:使用对1型单纯疱疹病毒(HSV)的兔抗血清超免疫,通过间接免疫荧光测试在2型HSV转化的细胞和衍生的肿瘤细胞中研究了HSV常见表面抗原的表达。获得了以下结果。 (i)针对HSV 1型的抗血清与存在于被HSV 2型感染和HSV 2型转化的仓鼠细胞的质膜上的表面抗原特异性反应。 (ii)在37摄氏度下培养3至5小时后,在转化细胞中没有活性蛋白合成的情况下,该抗原的表达得以增强,而在肿瘤细胞中则没有。(iii)这种表达增强保持20%。 h在放线菌素D存在下,但是这种延长的表达需要活性蛋白合成。 (iv)在放线菌素D存在下观察到的增强作用在除去药物后持续了一段时间,例如,在用每毫升2微克/毫升放线菌素D处理5小时后持续了20小时。放线菌素D对肿瘤细胞中的抗原表达没有可检测的作用。 (v)当在没有放线菌素D的情况下接种细胞时,蛋白酶抑制剂antipain抑制放线菌素D增强的表达而不会引起明显的细胞损伤,但没有改变抗原的瞬时增强表达。这些结果表明,在转化细胞中,抗​​原表达可以至少可以通过两种方式进行增强。

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