Suppr超能文献

补体C4A和C4B基因在类风湿性滑膜细胞、人单核细胞样细胞及肝癌衍生细胞系中的表达差异

Unequal expression of complement C4A and C4B genes in rheumatoid synovial cells, human monocytoid and hepatoma-derived cell lines.

作者信息

Falus A, Kramer J, Walcz E, Varga Z, Setalo J, Jobst K, Lakatos T, Merétey K

机构信息

Department of Immunology, National Institute of Rheumatology and Physiotherapy, Budapest, Hungary.

出版信息

Immunology. 1989 Sep;68(1):133-6.

Abstract

C4A and C4B are closely related homologous complement proteins encoded in the class III region of major histocompatibility complex (MHC). The regulation of their expression is under genetic and hormonal control. In this study we investigated the synovial fluid plasma ratio of C4A and C4B of rheumatoid (RA) and osteoarthritis (OA) patients, and a predominance of the C4B gene expression by the synovial macrophages of RA patients was demonstrated. To clarify the tissue specificity of the expression of C4A and C4B genes, human monocytoid cell line U937 and hepatoma-derived HepG2 cells were studied. The gene expression of C4A and C4B were markedly different in these cells since a relative predominance of C4B mRNA in U937 cells and excess of that of C4A in HepG2 cells were detected. Recombinant interferon-gamma (IFN-gamma) up-regulated the expression of C4A gene in both cells, but had apparently no effect on the C4B gene. Our results demonstrate dissimilar expression patterns for the two human C4 genes, suggesting different tissue specific regulation of human C4A and C4B.

摘要

C4A和C4B是紧密相关的同源补体蛋白,由主要组织相容性复合体(MHC)III类区域编码。它们的表达受遗传和激素控制。在本研究中,我们调查了类风湿性关节炎(RA)和骨关节炎(OA)患者的C4A和C4B的滑液血浆比率,并证实RA患者的滑膜巨噬细胞中C4B基因表达占优势。为了阐明C4A和C4B基因表达的组织特异性,我们研究了人单核细胞系U937和肝癌衍生的HepG2细胞。在这些细胞中,C4A和C4B的基因表达明显不同,因为在U937细胞中检测到C4B mRNA相对占优势,而在HepG2细胞中C4A的mRNA过量。重组干扰素-γ(IFN-γ)上调了两种细胞中C4A基因的表达,但对C4B基因显然没有影响。我们的结果表明两种人类C4基因的表达模式不同,提示人类C4A和C4B存在不同的组织特异性调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e60d/1385517/4b97f0c844b6/immunology00136-0137-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验