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免疫干扰素可激活人类内皮细胞和真皮成纤维细胞中的多个II类主要组织相容性复合体基因以及相关的恒定链基因。

Immune interferon activates multiple class II major histocompatibility complex genes and the associated invariant chain gene in human endothelial cells and dermal fibroblasts.

作者信息

Collins T, Korman A J, Wake C T, Boss J M, Kappes D J, Fiers W, Ault K A, Gimbrone M A, Strominger J L, Pober J S

出版信息

Proc Natl Acad Sci U S A. 1984 Aug;81(15):4917-21. doi: 10.1073/pnas.81.15.4917.

DOI:10.1073/pnas.81.15.4917
PMID:6431411
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC391603/
Abstract

Immune interferon (IFN-gamma) increases the surface expression of HLA-A,B antigens and induces the surface expression of HLA-DR antigens on vascular endothelial cells and dermal fibroblasts. Here we report that IFN-gamma induces parallel expression of two other class II major histocompatibility complex (MHC) antigens, SB and DC. Maximal surface expression of all three antigens is reached in 4-6 days, and HLA-DR and -SB are induced to a higher level of expression than HLA-DC. For all three class II antigens, induction is marked by the de novo appearance of detectable transcripts of class II heavy and light chains and of the non-MHC-encoded invariant chain, suggestive of the transcription of multiple previously silent genes. Class I message levels and antigen expression are also increased by IFN-gamma at similar rates but from initial levels that are 50% of maximal. After removal of IFN-gamma, class II antigen expression persists for at least 4 days, while mRNA levels decrease rapidly. The parallel induction and persistence of the several class II MHC antigens may be important in conferring immune accessory function on vascular and stromal cells.

摘要

免疫干扰素(IFN-γ)可增加HLA-A、B抗原的表面表达,并诱导血管内皮细胞和真皮成纤维细胞表面HLA-DR抗原的表达。在此我们报告,IFN-γ可诱导另外两种Ⅱ类主要组织相容性复合体(MHC)抗原SB和DC的平行表达。所有三种抗原在4-6天达到最大表面表达,且HLA-DR和-SB的诱导表达水平高于HLA-DC。对于所有三种Ⅱ类抗原,诱导的标志是Ⅱ类重链和轻链以及非MHC编码的恒定链可检测转录本的从头出现,提示多个先前沉默基因的转录。Ⅰ类信息水平和抗原表达也以相似的速率被IFN-γ增加,但起始水平为最大值的50%。去除IFN-γ后,Ⅱ类抗原表达持续至少4天,而mRNA水平迅速下降。几种Ⅱ类MHC抗原的平行诱导和持续存在可能在赋予血管和基质细胞免疫辅助功能方面很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8501/391603/589303bcc07c/pnas00616-0311-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8501/391603/9ba2b63e8f59/pnas00616-0309-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8501/391603/35cfc3346649/pnas00616-0310-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8501/391603/589303bcc07c/pnas00616-0311-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8501/391603/9ba2b63e8f59/pnas00616-0309-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8501/391603/35cfc3346649/pnas00616-0310-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8501/391603/589303bcc07c/pnas00616-0311-a.jpg

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