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前沿:通过将绿色荧光蛋白基因敲入RAG1基因座检测到腹膜B-1细胞中RAG1不表达。

Cutting edge: absence of expression of RAG1 in peritoneal B-1 cells detected by knocking into RAG1 locus with green fluorescent protein gene.

作者信息

Kuwata N, Igarashi H, Ohmura T, Aizawa S, Sakaguchi N

机构信息

Department of Immunology, Kumamoto University School of Medicine, Japan.

出版信息

J Immunol. 1999 Dec 15;163(12):6355-9.

Abstract

It has been proposed that Ig gene rearrangement in the peritoneal cavity (Pc) B-1 cells might be involved in autoantibody generation. To study possible secondary B cell maturation, we prepared mice carrying a target integration of gfp gene into a rag1 locus (rag1/gfp mice). The GFP+ cells express rag1 mRNA and are undergoing Ig gene rearrangement. RAG1 expression was studied in Pc B-1 cells to detect cells during the stage of Ig gene rearrangement. In contrast to previous reports, Pc B-1 cells did not show RAG1 expression in adolescent or elderly mice. RAG1 expression was not induced in Pc B-1 cells in vivo after stimulation by oral or i.p. administration of LPS. Our results suggest that RAG1 expression in Pc B-1 cells is inhibited for a long period under normal condition and that this suppression is an essential state which maintains allelic exclusion of Ig genes.

摘要

有人提出,腹腔(Pc)B-1细胞中的Ig基因重排可能与自身抗体的产生有关。为了研究可能的继发性B细胞成熟,我们制备了将gfp基因靶向整合到rag1基因座的小鼠(rag1/gfp小鼠)。GFP+细胞表达rag1 mRNA并正在进行Ig基因重排。研究了Pc B-1细胞中的RAG1表达,以检测Ig基因重排阶段的细胞。与先前的报道相反,Pc B-1细胞在青春期或老年小鼠中未显示RAG1表达。经口服或腹腔注射LPS刺激后,体内Pc B-1细胞中未诱导RAG1表达。我们的结果表明,在正常条件下,Pc B-1细胞中的RAG1表达长期受到抑制,并且这种抑制是维持Ig基因等位基因排斥的一种基本状态。

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