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大肠杆菌内毒素对不同类型大鼠肝细胞培养物中细胞骨架的影响。

Alterations induced on cytoskeleton by Escherichia coli endotoxin in different types of rat liver cell cultures.

作者信息

Pagani R, Portolés M T, De La Viña S, Melzner I, Vergani G

机构信息

Department of Biochemistry and Molecular Biology I, Universidad Complutense, Madrid, Spain.

出版信息

Histol Histopathol. 2003 Jul;18(3):837-48. doi: 10.14670/HH-18.837.

Abstract

Endotoxins (lipopolysaccharide, LPS) from Gram-negative bacteria are considered as the agents responsible for the induction of endotoxic shock, producing severe cellular metabolic dishomeostasis. Cytotoxic lesions, as well as functional and metabolic disturbances, occur mainly in the liver, which is one of the target organs and exerts an LPS clearance function. In an attempt to approach the molecular basis of endotoxic shock, and to propose an experimental model, we have focused this study on cytoskeleton (microtubules and microfilaments) alterations induced by different doses of endotoxin in different target liver cells. Microfilaments and microtubules were studied by immunofluorescence and different microscopy techniques (optic fluorescence microscopy and confocal laser scanning microscopy) in order to improve the cytoskeleton study resolution. Parenchymal and sinusoidal cell morphology, severely damaged by the LPS action, is related to a disturbance on the cytoskeletal organisation, even more evident in a particular proliferating rat liver cell culture. The most relevant changes are seen in the microtubule patterns in all liver cells tested, which could be related, depending on cell type, either to a direct LPS action or to [Ca+2]i dishomeostasis as well as free radical and cytokine (IL-1beta and TNF-alpha) production. Due to their features, proliferating rat liver cell cultures are used as a sensitive cell model to understand the effect of LPS on cytoskeleton organisation.

摘要

革兰氏阴性菌产生的内毒素(脂多糖,LPS)被认为是引发内毒素休克的介质,会导致严重的细胞代谢失衡。细胞毒性损伤以及功能和代谢紊乱主要发生在肝脏,肝脏是目标器官之一且具有LPS清除功能。为了探究内毒素休克的分子基础并提出一个实验模型,我们将这项研究聚焦于不同剂量内毒素在不同肝脏靶细胞中诱导的细胞骨架(微管和微丝)改变。通过免疫荧光和不同的显微镜技术(光学荧光显微镜和共聚焦激光扫描显微镜)研究微丝和微管,以提高细胞骨架研究的分辨率。LPS作用严重破坏了实质细胞和窦状细胞的形态,这与细胞骨架组织紊乱有关,在特定的增殖大鼠肝细胞培养中更为明显。在所有测试的肝细胞中,微管模式出现了最相关的变化,根据细胞类型的不同,这可能与LPS的直接作用、[Ca+2]i失衡以及自由基和细胞因子(IL-1β和TNF-α)的产生有关。由于其特性,增殖大鼠肝细胞培养物被用作敏感的细胞模型来理解LPS对细胞骨架组织的影响。

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