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氯化汞可诱导兔肺泡巨噬细胞产生白三烯B4。

Mercuric chloride induces the production of leukotriene B4 by rabbit alveolar macrophages.

作者信息

Kudo N, Waku K

机构信息

Faculty of Pharmaceutical Sciences, Teikyo University, Kanagawa, Japan.

出版信息

Arch Toxicol. 1994;68(3):179-86. doi: 10.1007/s002040050052.

Abstract

The effects of HgCl2 on the production of leukotriene B4 (LTB4) by rabbit alveolar macrophages were investigated. Alveolar macrophages synthesized only a small amount of LTB4 when incubated in Hanks' balanced salt solution (HBSS) in the absence of stimuli or chemical reagents (0.2 +/- 0.1 ng/10(6) cells). The amount of LTB4 synthesized was greatly enhanced when macrophages were incubated with 5 x 10(-6) M HgCl2 (5.3 +/- 0.2 ng/10(6) cells). Increases in levels of free arachidonic acid (20:4), a precursor of eicosanoids, were also observed on treatment of [3H]20:4-labeled cells with HgCl2 in a concentration-dependent manner. We confirmed that [3H]20:4 was mainly liberated from the alkenyl subclass of ethanolamine glycerophospholipids (EGP). Degradation of alkenyl-EGP was also observed when HgCl2 and [3H]20:4-labeled lipids were incubated in HBSS, resulting in an increase in the level of [3H]20:4-labeled lysoEGP. When a microsomal fraction prepared from macrophages was added to the same mixture, [3H]20:4 was liberated from [3H]20:4-containing lysoEGP. These results suggest that the alkenyl linkage of EGP was degraded in the presence of HgCl2 with resultant formation of lysoEGP which was subsequently hydrolyzed by lysophospholipase. As a consequence, the level of free 20:4 in and the rate of production of LTB4 by alveolar macrophages were elevated.

摘要

研究了氯化汞(HgCl2)对兔肺泡巨噬细胞白三烯B4(LTB4)产生的影响。在无刺激物或化学试剂的情况下,将肺泡巨噬细胞置于汉克斯平衡盐溶液(HBSS)中孵育时,仅合成少量LTB4(0.2±0.1 ng/10(6)个细胞)。当巨噬细胞与5×10(-6) M HgCl2一起孵育时,LTB4的合成量大大增加(5.3±0.2 ng/10(6)个细胞)。在用HgCl2处理[3H]20:4标记的细胞时,还观察到二十碳烯酸(20:4)(类花生酸的前体)水平以浓度依赖性方式增加。我们证实[3H]20:4主要从乙醇胺甘油磷脂(EGP)的烯基亚类中释放出来。当HgCl2和[3H]20:4标记的脂质在HBSS中孵育时,也观察到烯基-EGP的降解,导致[3H]20:4标记的溶血EGP水平增加。当将从巨噬细胞制备的微粒体部分添加到相同混合物中时,[3H]20:4从含[3H]20:4的溶血EGP中释放出来。这些结果表明,在HgCl2存在下,EGP的烯基连接被降解,导致溶血EGP的形成,随后溶血EGP被溶血磷脂酶水解。因此,肺泡巨噬细胞中游离20:4的水平和LTB4的产生速率升高。

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