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聚肌苷酸:聚胞苷酸诱导干扰素的细胞膜受体的鉴定

Identification of a cell membrane receptor for interferon induction by poly rI:rC.

作者信息

Yoshida I, Azuma M, Kawai H, Fisher H W, Suzutani T

机构信息

Department of Microbiology, Asahikawa Medical College, Japan.

出版信息

Acta Virol. 1992 Aug;36(4):347-58.

PMID:1282777
Abstract

PR-RK, a cell line derived from rabbit kidney cells (RK-13), was insensitive to the cytotoxic effect and interferon (IFN) inducing activity of the copolymer of riboinosinic and ribocytidylic acid (poly rI:rC). However, PR-RK was sensitive to the cytotoxic effect of the copolymer of riboadenylic and ribouridylic acid (poly rA:rU). Comparison of PR-RK cells and RK-13 cells by cytofluorometric analysis revealed that the binding of poly rI:rC was considerably reduced on PR-RK cells. These results suggested that the receptor for poly rI:rC might be different from the receptor for poly rA:rU, and this difference could provide a basis for the identification of the dsRNA receptor on cell surface. Western blot analysis of the components of cell membrane fraction prepared from RK-13 cells was performed by using a monoclonal antibody, which binds to cell membrane of RK-13 cells but not to PR-RK cells, and which blocks IFN induction by poly rI:rC in RK-13 cells. The 60K protein was identified as one of the poly rI:rC receptor protein.

摘要

PR-RK是一种源自兔肾细胞(RK-13)的细胞系,对肌苷酸和胞苷酸共聚物(聚rI:rC)的细胞毒性作用和干扰素(IFN)诱导活性不敏感。然而,PR-RK对腺苷酸和尿苷酸共聚物(聚rA:rU)的细胞毒性作用敏感。通过细胞荧光分析比较PR-RK细胞和RK-13细胞发现,聚rI:rC在PR-RK细胞上的结合显著减少。这些结果表明,聚rI:rC的受体可能与聚rA:rU的受体不同,这种差异可为鉴定细胞表面的双链RNA受体提供依据。使用一种单克隆抗体对从RK-13细胞制备的细胞膜组分进行蛋白质免疫印迹分析,该抗体可与RK-13细胞的细胞膜结合,但不与PR-RK细胞结合,并且可阻断聚rI:rC在RK-13细胞中诱导IFN。60K蛋白被鉴定为聚rI:rC受体蛋白之一。

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