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单纯疱疹病毒诱导小鼠p30所需的条件。

Conditions required for induction of murine p30 by herpes simplex virus.

作者信息

Isom H, Colberg A, Reed C, Rapp F

出版信息

Int J Cancer. 1978 Jul 15;22(1):22-7. doi: 10.1002/ijc.2910220106.

Abstract

Mouse cells (line N cIA cl10) contain 1.2-2.5 ng murine leukaemia virus (MuLV) p30 antigen/mg of protein; this amount of antigen is measurable by competition radioimmunoassay (RIA) but is not detectable by indirect immunofluorescence (IF). Infection of N cIA cl10 cells with herpes simplex virus type 2 (HSV-2) induces expression of MuLV p30. Induction by HSV-2 does not require either cell or virus DNA synthesis and is optimal 8 h post infection when cells at 50-70% confluence are infected at a multiplicity of infection (MOI) of 5-8 PFU/cell. At an MOI of 2.5, 70-80% of the cells express HSV antigens while none of the cells express p30; at an MOI of 5.0, 70-80% of the cells express HSV antigens but 55% of the cells express p30. Using the conditions reported in this paper for preparation of competing antigen, induction of p30 by HSV-2 (strain 333) infection is not measurable by competition RIA.

摘要

小鼠细胞(N cIA cl10系)每毫克蛋白质含有1.2 - 2.5纳克鼠白血病病毒(MuLV)p30抗原;该抗原量可用竞争放射免疫测定法(RIA)检测到,但用间接免疫荧光法(IF)检测不到。用2型单纯疱疹病毒(HSV - 2)感染N cIA cl10细胞可诱导MuLV p30的表达。HSV - 2诱导不需要细胞或病毒DNA合成,当处于50 - 70%汇合度的细胞以5 - 8个空斑形成单位(PFU)/细胞的感染复数(MOI)进行感染时,感染后8小时诱导效果最佳。在MOI为2.5时,70 - 80%的细胞表达HSV抗原,但没有细胞表达p30;在MOI为5.0时,70 - 80%的细胞表达HSV抗原,但55%的细胞表达p30。按照本文报道的制备竞争抗原的条件,HSV - 2(333株)感染诱导的p30用竞争RIA检测不到。

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