亚油酸的宿主细胞特异性代谢控制着弓形虫在细胞培养中的生长。

IF 2.9 3区 医学 Q3 IMMUNOLOGY
Nicole D Hryckowian, Carlos J Ramírez-Flores, Caitlin Zinda, Sung Chul Park, Martin T Kelty, Laura J Knoll
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引用次数: 0

摘要

弓形虫(Toxoplasma gondii)是一种强制性细胞内寄生虫,可以感染并复制到迄今为止测试过的任何温血细胞中,但我们对弓形虫细胞生物学的了解大多来自一种宿主细胞类型:人类包皮成纤维细胞(HFFs)。为了扩大我们对宿主-寄生虫脂质相互作用的了解,我们研究了肠上皮细胞中的淋球菌,这是口腔感染后宿主-寄生虫接触的第一个部位,也是猫科动物宿主中寄生虫性发育的唯一部位。我们发现,即使使用高浓度的亚油酸(LA)(一种多不饱和脂肪酸(PUFA),它能杀死 HFFs 中的寄生虫)处理 Caco-2 细胞,高代谢性的 Caco-2 细胞也能允许淋球菌生长。Caco-2细胞似乎能将LA从寄生虫体内封存起来,防止膜破坏和脂毒性,而这正是LA诱导寄生虫在HFFs中死亡的特征。我们的工作是了解猫肠道上皮细胞中宿主与寄生虫相互作用的重要一步,猫肠道上皮细胞是淋球菌生命周期中未被充分研究但却很重要的细胞类型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Host cell-specific metabolism of linoleic acid controls Toxoplasma gondii growth in cell culture.

The obligate intracellular parasite Toxoplasma gondii can infect and replicate in any warm-blooded cell tested to date, but much of our knowledge about T. gondii cell biology comes from just one host cell type: human foreskin fibroblasts (HFFs). To expand our knowledge of host-parasite lipid interactions, we studied T. gondii in intestinal epithelial cells, the first site of host-parasite contact following oral infection and the exclusive site of parasite sexual development in feline hosts. We found that highly metabolic Caco-2 cells are permissive to T. gondii growth even when treated with high levels of linoleic acid (LA), a polyunsaturated fatty acid (PUFA) that kills parasites in HFFs. Caco-2 cells appear to sequester LA away from the parasite, preventing membrane disruptions and lipotoxicity that characterize LA-induced parasite death in HFFs. Our work is an important step toward understanding host-parasite interactions in feline intestinal epithelial cells, an understudied but important cell type in the T. gondii life cycle.

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来源期刊
Infection and Immunity
Infection and Immunity 医学-传染病学
CiteScore
6.00
自引率
6.50%
发文量
268
审稿时长
3 months
期刊介绍: Infection and Immunity (IAI) provides new insights into the interactions between bacterial, fungal and parasitic pathogens and their hosts. Specific areas of interest include mechanisms of molecular pathogenesis, virulence factors, cellular microbiology, experimental models of infection, host resistance or susceptibility, and the generation of innate and adaptive immune responses. IAI also welcomes studies of the microbiome relating to host-pathogen interactions.
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