肺部炎症与脂质沉积有关。

Daria M Potashnikova, Anna V Tvorogova, Alexey A Komissarov, Aleena A Saidova, Tatiana N Sotnikova, Valeria O Makarova, Eugene A Arifulin, Tatiana V Lipina, Olesya M Shirokova, Eugene S Melnikov, Tatiana A Rodina, Anna A Valyaeva, Anastasia A Zharikova, George O Zayratyants, Oleg V Zayratyants, Eugene V Sheval, Leonid B Margolis, Elena J Vasilieva
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引用次数: 0

摘要

肺部炎症,即肺炎,是最近在COVID-19大流行期间备受关注的各种病因的急性呼吸道疾病,因为肺部是SARS-CoV-2的主要目标之一。多种其他病原与肺炎有关。在这里,我们描述了一种新认识的病理,即死于COVID-19和非COVID-19肺炎的患者肺部的异常脂质沉积。我们对半薄和苏丹iii染色肺标本的分析显示,无论肺炎病因如何,细胞外和细胞内都有脂质沉积。最值得注意的是,脂质沉积位于炎症区域附近的血管内,在那里它们明显干扰了血液流动。从结构上看,炎症肺组织中的脂滴是均匀的,缺乏外膜。脂滴沉积区形态计量学分析使我们能够将非肺炎对照肺标本与肺炎肺的宏观完整区和肺炎肺的炎症区区分开来。我们的测量显示,脂质沉积的梯度向炎症区域。脂质分布模式证明了所有肺炎的普遍性。最后,通过脂肪酸分析和参与脂质转换的基因表达来评估肺组织中的脂质代谢。质谱分析显示,与来自同一个体的对照非炎症肺组织相比,炎症部位的不饱和脂肪酸含量升高。qPCR和RNA-seq分析显示,参与脂质代谢的基因表达在肺炎中发生改变。因此,各种病因的肺炎与特定的脂质异常有关;因此,脂质代谢可以被认为是新的治疗策略的目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lung lipid deposition in pneumonias of different etiologies.

Pneumonia is an acute respiratory disease of varying etiology that has drawn much attention during the COVID-19 pandemic. Among the many thoroughly studied aspects of pneumonia, lipid metabolism has not been sufficiently addressed. Here, we investigated lipid deposition in the post mortem lung specimens of patients who died from COVID-19 and non-COVID-19 pneumonias. We used semi-thin sections and cryosections stained with Sudan III to visualize lipid droplet deposition within cells and in the extracellular space, most notably in small lung vessels. Electron microscopy analysis of the ultrathin sections was used to confirm the homogeneous structure of the droplets. Morphometric analysis revealed that the area of lipid deposition was increased in pneumonia compared to control lung tissue. Likewise, it was increased in the macroscopically inflamed vs. the macroscopically intact area of the same pneumonia lung. The lipid profiling by chromato-mass spectrometry revealed that lipid droplet accumulation in pneumonia was associated with a specific fatty acid content of the inflamed lung tissue. The gene expression analysis pointed to changes of lipid metabolism in the inflamed lung tissue compared to control lungs. Taken together, our data indicate a number of morphologic and metabolic changes associated with inflammation and common for pneumonias of different etiologies that likely contribute to pneumonia pathogenesis. Therefore, targeting lipid metabolism can be considered a new therapeutic strategy.

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