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大鼠淋巴因子激活的杀伤细胞上选择性诱导的一种细胞表面分子的鉴定与特性分析。

Identification and characterization of a cell-surface molecule that is selectively induced on rat lymphokine-activated killer cells.

作者信息

Imboden J B, Eriksson E C, McCutcheon M, Reynolds C W, Seaman W E

机构信息

Department of Medicine, University of California, San Francisco.

出版信息

J Immunol. 1989 Nov 1;143(9):3100-3.

PMID:2809220
Abstract

We have identified a 40- to 45-kDa cell-surface molecule designated gp42, that is expressed in high levels by rat lymphokine-activated killer (LAK) cells of NK cell origin. gp42 cannot be detected on the precursors of LAK cells and is not present on resting or activated T cells. Rather, expression of gp42 is selectively induced on NK cells by the high concentrations of rIL-2 that are required for the induction of LAK activity. Although the function of gp42 is not known, the selective nature of its expression suggests a role for this molecule in regulating responses that are unique to IL-2-activated NK cells.

摘要

我们已经鉴定出一种分子量为40至45 kDa的细胞表面分子,命名为gp42,它在源自NK细胞的大鼠淋巴因子激活的杀伤(LAK)细胞中高水平表达。在LAK细胞的前体细胞上检测不到gp42,静止或活化的T细胞上也不存在。相反,高浓度的rIL-2可选择性诱导NK细胞上gp42的表达,而rIL-2是诱导LAK活性所必需的。尽管gp42的功能尚不清楚,但其表达的选择性表明该分子在调节IL-2激活的NK细胞特有的反应中起作用。

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