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酒精摄入对小鼠自然杀伤(NK)细胞、白细胞介素2刺激的NK细胞以及淋巴因子激活的杀伤细胞中穿孔素、颗粒酶A和颗粒酶B的调节作用。

Modulation of perforin, granzyme A, and granzyme B in murine natural killer (NK), IL2 stimulated NK, and lymphokine-activated killer cells by alcohol consumption.

作者信息

Spitzer J H, Meadows G G

机构信息

Cancer Prevention and Research Center, Washington State University, Pullman, Washington, 99164-6510, USA.

出版信息

Cell Immunol. 1999 Jun 15;194(2):205-12. doi: 10.1006/cimm.1999.1511.

Abstract

Alcohol consumption in mice suppresses the cytolytic activity of natural killer (NK) and lymphokine-activated killer (LAK) cells through unknown mechanisms. Herein, we found that alcohol consumption decreased target cell-induced release of granzyme A activity in freshly isolated splenic NK cells, in NK cells stimulated for 18 h with 1000 IU/ml of interleukin 2, and in LAK cells. The total activity and protein expression of granzymes A and B also were lower in these cells than in cells isolated from water-drinking mice. Interleukin 2 increased granzyme A protein expression independent of alcohol consumption; however, this increase was associated with decreased enzyme activity. In contrast, granzyme B protein expression and enzymatic activity increased in response to interleukin 2. Perforin activity and protein expression were reduced in LAK cells generated from alcohol-consuming mice. We conclude that the mechanism underlying the suppression of NK and LAK cytolytic activity by alcohol consumption involves the collective reduction of target-induced release, activity, and expression of perforin and granular proteases.

摘要

小鼠摄入酒精会通过未知机制抑制自然杀伤(NK)细胞和淋巴因子激活的杀伤(LAK)细胞的细胞溶解活性。在此,我们发现,摄入酒精会降低新鲜分离的脾NK细胞、用1000 IU/ml白细胞介素2刺激18小时的NK细胞以及LAK细胞中靶细胞诱导的颗粒酶A活性释放。这些细胞中颗粒酶A和B的总活性及蛋白表达也低于从饮水小鼠分离的细胞。白细胞介素2可增加颗粒酶A蛋白表达,且与酒精摄入无关;然而,这种增加与酶活性降低有关。相反,颗粒酶B蛋白表达和酶活性会因白细胞介素2而增加。从摄入酒精的小鼠产生的LAK细胞中穿孔素活性和蛋白表达降低。我们得出结论,摄入酒精抑制NK和LAK细胞溶解活性的机制涉及靶细胞诱导的穿孔素和颗粒蛋白酶释放、活性及表达的共同降低。

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