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通过位点特异性细胞毒性T淋巴细胞克隆对SV40 T抗原表位缺失变体进行体外筛选。

In vitro selection of SV40 T antigen epitope loss variants by site-specific cytotoxic T lymphocyte clones.

作者信息

Tanaka Y, Tevethia S S

机构信息

Department of Microbiology, Penn State University College of Medicine, Hershey 17033.

出版信息

J Immunol. 1988 Jun 15;140(12):4348-54.

PMID:2453578
Abstract

SV40-transformed cells of C57BL/6 (B6) mouse origin (H-2b) express four distinct predominant antigenic sites, I, II, III, and IV, on SV40 large tumor (T) Ag that are recognized by SV40 T Ag-specific CTL clones. In this study, we selected SV40 T Ag-positive cell lines which had lost one or more of the antigenic sites, by in vitro cocultivation of a SV40-transformed B6 mouse kidney cell line (K-0) with SV40 T Ag site-specific CTL clones, Y-1 (site I specific), Y-2 (site II specific), Y-3 (site III specific), and Y-4 (site IV specific). All of the CTL-resistant cell lines expressed large quantities of cell surface H-2 class I Ag. K-1 cells selected by CTL clone Y-1 lost the expression of antigenic sites I, II, and III, but not site IV. K-2 and K-3 cells selected by CTL clones Y-2 and Y-3, respectively, were found to be negative for sites II and III but expressed sites I and IV. K-4 cells selected by CTL clone Y-4 lost the expression of only site IV. K-1,4 cells (sites I-, II-, III-, IV-) were selected from K-1 cells by cocultivation with CTL clone Y-4, K-2,4 cells (sites I+, II-, III-, IV-) were selected from K-2 cells by CTL clone Y-4. K-3,1 cells (sites I-, II-, III-, IV+) were selected from K-3 cells by CTL clone Y-1, and K-3,1,4 cells (sites I-, II-, III-, IV-) were selected from K-3,1 cells by CTL clone Y-4. From K-4 cells, K-4,1 cells (sites I-, II-, III-, IV-) and K-4,3 cells (sites I+, II-, III-, IV-) were selected by CTL clone Y-1 and Y-3, respectively. The antigenic site loss variant cell lines K-1, K-1,4, K-3,1 K-3,1,4, K-4,1, and K-4,3 synthesized SV40 T Ag molecules of 75, 75, 78, 78, 81, and 88 kDa, respectively. Expression of wild-type SV40 T Ag in the antigenic site loss variants by infection with SV40 or transfection with cloned SV40 DNA restored the CTL recognition sites on the variant cells.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

源自C57BL/6(B6)小鼠(H-2b)的SV40转化细胞在SV40大肿瘤(T)抗原上表达四个不同的主要抗原位点,即I、II、III和IV,这些位点可被SV40 T抗原特异性CTL克隆识别。在本研究中,我们通过将SV40转化的B6小鼠肾细胞系(K-0)与SV40 T抗原位点特异性CTL克隆Y-1(位点I特异性)、Y-2(位点II特异性)、Y-3(位点III特异性)和Y-4(位点IV特异性)进行体外共培养,筛选出失去一个或多个抗原位点的SV40 T抗原阳性细胞系。所有抗CTL细胞系均大量表达细胞表面H-2 I类抗原。经CTL克隆Y-1筛选的K-1细胞失去了抗原位点I、II和III的表达,但未失去位点IV的表达。分别经CTL克隆Y-2和Y-3筛选的K-2和K-3细胞被发现位点II和III呈阴性,但表达位点I和IV。经CTL克隆Y-4筛选的K-4细胞仅失去位点IV的表达。通过与CTL克隆Y-4共培养从K-1细胞中筛选出K-1,4细胞(位点I-、II-、III-、IV-),通过CTL克隆Y-4从K-2细胞中筛选出K-2,4细胞(位点I+、II-、III-、IV-)。通过CTL克隆Y-1从K-3细胞中筛选出K-3,1细胞(位点I-、II-、III-、IV+),通过CTL克隆Y-4从K-3,1细胞中筛选出K-3,1,4细胞(位点I-、II-、III-、IV-)。分别通过CTL克隆Y-1和Y-3从K-4细胞中筛选出K-4,1细胞(位点I-、II-、III-、IV-)和K-4,3细胞(位点I+、II-、III-、IV-)。抗原位点缺失变异细胞系K-1、K-1,4、K-3,1、K-3,1,4、K-4,1和K-4,3分别合成了75、75、78、78、81和88 kDa的SV40 T抗原分子。通过用SV40感染或用克隆的SV40 DNA转染在抗原位点缺失变异体中表达野生型SV40 T抗原,可恢复变异细胞上的CTL识别位点。(摘要截断于250字)

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