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天然人α干扰素可增强一种黏膜上皮细胞系的细胞间黏附分子-1、整合素α2和β1的表达。

Natural human interferon-alpha enhances the expression of intracellular adhesion molecule-1, integrin alpha 2 and beta 1 by a mucosal epithelial cell line.

作者信息

Dao T, Takeuchi M, Fukuda S, Kurimoto M

机构信息

Fujisaki Institute, Hayashibara Biochemical Laboratories, Inc., Okayama, Japan.

出版信息

Folia Biol (Praha). 1995;41(5):213-25.

PMID:8714771
Abstract

We have found that pretreatment of a human oral mucosal epithelial cell line KB with natural human interferon-alpha (IFN-alpha) augments the expression of intercellular adhesion molecule-1 (ICAM-1), and the complex of CD29 and CD49b, which is known as very late antigen (VLA)-2, in a dose-dependent manner, whereas the expression of other adhesion molecules such as CD44 leukocyte function associated antigen-3 (LFA-3), VLA-4 and endothelial leukocyte adhesion molecule-1 (ELAM-1) did not show any significant changes under the same conditions. The pretreatment of KB cells with IFN-alpha also induces the adhesion of these cells to the human leukemia T cell line MOLT-16 and to peripheral T lymphocytes in a dose-dependent manner. However, the adhesion of the above-mentioned T cells to KB cells was not inhibited by specific antibodies against ICAM-1, CD29, and CD49b. The results thus show that adhesion molecules other than ICAM-1, CD29, AND CD49b are responsible for the induced adhesion between T cells and IFN-alpha-pretreated KB cells.

摘要

我们发现,用人天然α干扰素(IFN-α)预处理人口腔黏膜上皮细胞系KB,可使细胞间黏附分子-1(ICAM-1)以及称为极迟抗原(VLA)-2的CD29与CD49b复合物的表达呈剂量依赖性增加,而在相同条件下,其他黏附分子如CD44白细胞功能相关抗原-3(LFA-3)、VLA-4和内皮细胞白细胞黏附分子-1(ELAM-1)的表达未显示任何显著变化。用IFN-α预处理KB细胞也可使其以剂量依赖性方式黏附于人白血病T细胞系MOLT-16和外周T淋巴细胞。然而,上述T细胞与KB细胞的黏附并不被针对ICAM-1、CD29和CD49b的特异性抗体所抑制。因此结果表明,除ICAM-1、CD29和CD49b之外的黏附分子负责T细胞与经IFN-α预处理的KB细胞之间的诱导黏附。

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