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重组γ干扰素体外诱导人子宫内膜上皮细胞HLA-DR抗原表达

Induction of HLA-DR antigen expression in human endometrial epithelial cells in vitro by recombinant gamma-interferon.

作者信息

Tabibzadeh S S, Gerber M A, Satyaswaroop P G

出版信息

Am J Pathol. 1986 Oct;125(1):90-6.

PMID:2430458
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1888430/
Abstract

Recent studies suggest that HLA-DR antigens may be inducible in some normal epithelial cells. Therefore, we studied the expression of these molecules in epithelial cell cultures derived from 9 proliferative and 7 secretory endometria with and without treatment by recombinant gamma-interferon (gamma-IFN). A panel of monoclonal antibodies to HLA-DR antigens, T cells, B cells, macrophages, endothelial cells, and cytokeratin was used to stain the cultured cells by the avidin-biotin complex method. The cultures consisted only of epithelial cells as demonstrated by expression of cytokeratin and by electron microscopy and did not contain any T or B cells, macrophages, or endothelial cells. The endometrial epithelial cells were HLA-DR-negative under routine culture conditions but expressed HLA-DR antigens after gamma-IFN treatment in a dose- and time-dependent fashion. The findings indicate that endometrial epithelium can actively synthesize HLA-DR antigens in vitro after induction by gamma-IFN.

摘要

近期研究表明,HLA - DR抗原可能在某些正常上皮细胞中被诱导产生。因此,我们研究了这些分子在来自9例增殖期和7例分泌期子宫内膜的上皮细胞培养物中的表达情况,这些培养物分别经过和未经过重组γ干扰素(γ - IFN)处理。使用一组针对HLA - DR抗原、T细胞、B细胞、巨噬细胞、内皮细胞和细胞角蛋白的单克隆抗体,通过抗生物素蛋白 - 生物素复合物法对培养细胞进行染色。如细胞角蛋白的表达及电子显微镜所示,培养物仅由上皮细胞组成,不包含任何T细胞、B细胞、巨噬细胞或内皮细胞。在常规培养条件下,子宫内膜上皮细胞HLA - DR呈阴性,但经γ - IFN处理后,以剂量和时间依赖的方式表达HLA - DR抗原。这些发现表明,子宫内膜上皮细胞在γ - IFN诱导后可在体外积极合成HLA - DR抗原。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/1888430/b33383c8678b/amjpathol00151-0100-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/1888430/c84b175b70bb/amjpathol00151-0098-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/1888430/182af281c407/amjpathol00151-0099-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/1888430/269b33adfd3e/amjpathol00151-0099-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/1888430/16a17295407d/amjpathol00151-0099-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/1888430/cc83ff4f54a9/amjpathol00151-0100-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/1888430/b33383c8678b/amjpathol00151-0100-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/1888430/c84b175b70bb/amjpathol00151-0098-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/1888430/182af281c407/amjpathol00151-0099-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/1888430/269b33adfd3e/amjpathol00151-0099-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/1888430/16a17295407d/amjpathol00151-0099-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/1888430/cc83ff4f54a9/amjpathol00151-0100-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/1888430/b33383c8678b/amjpathol00151-0100-b.jpg

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