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通过双参数流式细胞术分析单纯疱疹病毒感染细胞中的DNA合成。

Analysis of DNA synthesis in herpes simplex virus infected cells by dual parameter flow cytometry.

作者信息

Lehtinen M, Kulomaa P, Kallioniemi O P, Paavonen J, Leinikki P

机构信息

Department of Biomedical Sciences, University of Tampere, Finland.

出版信息

Arch Virol. 1989;107(3-4):215-23. doi: 10.1007/BF01317918.

Abstract

The DNA incorporation of a thymidine analogue bromodeoxyuridine (BrdUrd) in herpes simplex virus type 2 (HSV-2) infected cervical cancer cell lines (CaSki and C-33 A) was studied by dual parameter flow cytometry. HSV-2 infection resulted in an exponential increase in DNA synthesis in the CaSki cells. In the less permissive C-33 A cells the proportion of DNA-synthesizing cells cycled during HSV-2 infection. The inhibition of viral DNA synthesis by phosphonoformate (PFA) was able to inhibit the virus induced changes in the CaSki but not in the C-33 A cells. In the C-33 A cells a part of the virus induced cellular DNA synthesis represents repair replication of cellular DNA.

摘要

通过双参数流式细胞术研究了胸苷类似物溴脱氧尿苷(BrdUrd)在单纯疱疹病毒2型(HSV-2)感染的宫颈癌细胞系(CaSki和C-33 A)中的DNA掺入情况。HSV-2感染导致CaSki细胞中的DNA合成呈指数增加。在较难感染的C-33 A细胞中,DNA合成细胞的比例在HSV-2感染期间循环变化。膦甲酸(PFA)对病毒DNA合成的抑制能够抑制CaSki细胞中病毒诱导的变化,但对C-33 A细胞无效。在C-33 A细胞中,病毒诱导的细胞DNA合成的一部分代表细胞DNA的修复复制。

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