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小鼠巨噬细胞杂交体中II类抗原表达的重新激活。

Reactivation of class II antigen expression in murine macrophage hybrids.

作者信息

Zuckerman S H, Schreiber R D, Marder P

机构信息

Department of Immunology, Lilly Research Labs, Indianapolis, IN 46285.

出版信息

J Immunol. 1988 Feb 1;140(3):978-83.

PMID:2963070
Abstract

The induction of class II antigen on primary macrophages and on several macrophage cell lines has been demonstrated after exposure to IFN-gamma. The murine macrophage cell line PU5 (H-2d haplotype) does not express class II antigen constitutively and only trace levels are detected after induction with IFN-gamma. In an attempt to understand the nature of the defect in PU5, stable macrophage hybrids were derived by fusing a thymidine kinase-negative variant of PU5 with thioglycollate elicited peritoneal macrophages from CBA/J mice (H-2k haplotype). Hybrid clones isolated after HAT selection had approximately 35% more DNA than the PU5 parent suggesting that chromosomal loss had occurred post-fusion. While none of the hybrids expressed class II antigens of the k haplotype, constitutive expression of class II antigens of the d haplotype was detected by both micro-ELISA and by flow cytometry. Incubation of these hybrids with IFN-gamma resulted in a further increase in class II expression. Co-ordinate reactivation of both I-A and I-E antigens was observed in the PU5-macrophage hybrids. In contrast, although the IFN-gamma receptor on PU5 and the macrophage hybrids was indistinguishable by Scatchard analysis, neither intracellular class II antigen nor transcription of class II mRNA was detected in IFN-gamma-treated PU5. Reactivation was dependent on the PU5 fusion partner and was not related to a general post-fusion event as hybrids formed between PU5 and the murine fibroblast line A9 did not express class II antigen constitutively or after IFN-gamma induction.

摘要

在暴露于γ干扰素后,已证实原代巨噬细胞和几种巨噬细胞系上会诱导II类抗原。小鼠巨噬细胞系PU5(H-2d单倍型)组成性不表达II类抗原,用γ干扰素诱导后仅检测到微量水平。为了了解PU5中缺陷的本质,通过将PU5的胸苷激酶阴性变体与来自CBA/J小鼠(H-2k单倍型)的巯基乙酸盐诱导的腹腔巨噬细胞融合,获得了稳定的巨噬细胞杂种。在HAT选择后分离的杂种克隆的DNA比PU5亲本大约多35%,这表明融合后发生了染色体丢失。虽然没有一个杂种表达k单倍型的II类抗原,但通过微量ELISA和流式细胞术都检测到了d单倍型II类抗原的组成性表达。用γ干扰素孵育这些杂种导致II类表达进一步增加。在PU5-巨噬细胞杂种中观察到I-A和I-E抗原的协同重新激活。相比之下,尽管通过Scatchard分析PU5和巨噬细胞杂种上的γ干扰素受体无法区分,但在经γ干扰素处理的PU5中未检测到细胞内II类抗原或II类mRNA的转录。重新激活取决于PU5融合伙伴,并且与一般的融合后事件无关,因为PU5与小鼠成纤维细胞系A9之间形成的杂种在组成性或γ干扰素诱导后都不表达II类抗原。

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