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鼻上皮细胞在分化和激活过程中B7-H3及其他T细胞配体基因的表达。

Expression of genes for B7-H3 and other T cell ligands by nasal epithelial cells during differentiation and activation.

作者信息

Saatian Bahman, Yu Xiao-Ying, Lane Andrew P, Doyle Thanh, Casolaro Vincenzo, Spannhake Ernst Wm

机构信息

Department of Environmental Health Sciences, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.

出版信息

Am J Physiol Lung Cell Mol Physiol. 2004 Jul;287(1):L217-25. doi: 10.1152/ajplung.00132.2003. Epub 2004 Mar 26.

Abstract

Epithelial cells of the human respiratory tract express human leukocyte antigen (HLA) and the costimulatory molecules B7-1 and B7-2. Little is known, however, about the constitutive expression of genes encoding for the more recently identified members of the B7 homolog family of costimulatory molecules or about the influence of cellular differentiation and cytokines on their activity or on that of HLA or B7-1 and B7-2. Human nasal epithelial (HNE) cells were grown at the air-liquid interface (ALI) for 2 or 21 days to model in vivo conditions. Expression of genes for HLA-B and HLA-DR1 increased during mucociliary differentiation during this period and became more similar to HNE cells obtained fresh by brush biopsy from nasal turbinates. Gene transcripts for B7-H3 and B7-H2 were abundantly expressed in cells cultured at the ALI, but neither their activities nor that of B7-2 was significantly altered during differentiation. IFN-gamma and TNF-alpha upregulated mRNA encoding for both HLA molecules, but not for the B7 molecules. This study describes, for the first time, the expression of B7-H3 and B7-H2 by HNE cells and thus expands the range of potential costimulatory signals through which these cells may interact with activated mucosal T lymphocytes. In addition, the results suggest that the extent of mucociliary differentiation of cultured cells may influence this capability.

摘要

人类呼吸道的上皮细胞表达人类白细胞抗原(HLA)以及共刺激分子B7-1和B7-2。然而,对于共刺激分子B7同源家族中最近发现的成员的编码基因的组成性表达,或者细胞分化和细胞因子对其活性以及对HLA或B7-1和B7-2活性的影响,人们所知甚少。人鼻上皮(HNE)细胞在气液界面(ALI)培养2天或21天以模拟体内条件。在此期间,HLA-B和HLA-DR1的基因表达在黏液纤毛分化过程中增加,并且变得更类似于通过从鼻甲刷检新鲜获得的HNE细胞。B7-H3和B7-H2的基因转录本在ALI培养的细胞中大量表达,但在分化过程中它们的活性以及B7-2的活性均未发生显著改变。干扰素-γ和肿瘤坏死因子-α上调了两种HLA分子的编码mRNA,但未上调B7分子的编码mRNA。本研究首次描述了HNE细胞对B7-H3和B7-H2的表达,从而扩展了这些细胞可能与活化的黏膜T淋巴细胞相互作用的潜在共刺激信号范围。此外,结果表明培养细胞的黏液纤毛分化程度可能会影响这种能力。

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