Regulation of intracellular proliferation of Salmonella typhimurium by CD63.

IF 1.7 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Genes & genomics Pub Date : 2025-09-01 Epub Date: 2025-08-12 DOI:10.1007/s13258-025-01659-2
Kwan Sik Park, In Sook Jeon, Jin Tae Hong, Bumhee Yang, Joong-Kook Choi
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引用次数: 0

Abstract

Background: Autophagy is an intracellular degradation process involving the lysosomal breakdown of unnecessary or abnormal cellular components. Targets of autophagy include pathogens, altered organelles, and protein aggregates, which are sequestered within double-membrane-limited vesicles known as autophagosomes. A variety of lysosomal membrane proteins play essential roles in numerous cellular processes, including lysosomal acidification, metabolite transport, and interaction with other membrane systems. Cluster of differentiation 63 (CD63), a member of the transmembrane 4 superfamily, is present on the cell surface and in intracellular membrane compartments, such as endosomal and lysosomal membranes. This protein is also associated with several diseases, including Hermansky-Pudlak syndrome and immunoglobulin E-mediated allergies. However, its role in the autophagy pathway and intracellular bacterial proliferation remains poorly understood.

Objective: This study aimed to investigate changes in CD63 expression in response to Salmonella infection and to analyze the effects of these changes on Salmonella proliferation.

Methods: Changes in CD63 expression were examined following Salmonella infection using cellular models. Expression regulation was assessed for dependence on nuclear factor kappa B signaling. Colocalization of CD63 was evaluated with green fluorescent protein-tagged Salmonella and the lysosomal marker LysoTracker. Intracellular Salmonella titers were measured and correlated with CD63 expression levels to determine impacts on bacterial survival.

Results: CD63 expression increased in response to Salmonella infection in a nuclear factor kappa B-dependent manner. CD63 colocalized with green fluorescent protein-tagged Salmonella and the lysosomal marker LysoTracker. The titer of intracellular Salmonella was inversely correlated with CD63 expression, suggesting that higher CD63 levels reduce bacterial survival.

Conclusion: CD63 contributes to the regulation of intracellular Salmonella survival through the autophagy pathway, specifically xenophagy (autophagy targeting pathogens). This is the first report documenting the inhibition of Salmonella proliferation via induction of CD63 expression and Xenophagy.

CD63对鼠伤寒沙门菌细胞内增殖的调控作用。
背景:自噬是一种细胞内降解过程,涉及溶酶体分解不必要的或异常的细胞成分。自噬的目标包括病原体、改变的细胞器和蛋白质聚集体,这些聚集体被隔离在称为自噬体的双膜限制囊泡中。多种溶酶体膜蛋白在许多细胞过程中发挥重要作用,包括溶酶体酸化、代谢物运输以及与其他膜系统的相互作用。CD63 (Cluster of differentiation 63, CD63)是跨膜4超家族的一员,存在于细胞表面和细胞膜间室,如内体和溶酶体膜。这种蛋白还与几种疾病有关,包括Hermansky-Pudlak综合征和免疫球蛋白e介导的过敏。然而,其在自噬途径和细胞内细菌增殖中的作用仍然知之甚少。目的:研究CD63在沙门氏菌感染后的表达变化,并分析其对沙门氏菌增殖的影响。方法:采用细胞模型检测沙门氏菌感染后CD63表达的变化。评估表达调控是否依赖核因子κ B信号传导。用绿色荧光蛋白标记的沙门氏菌和溶酶体标记物LysoTracker评估CD63的共定位。测量细胞内沙门氏菌滴度并与CD63表达水平相关,以确定对细菌存活的影响。结果:CD63在沙门氏菌感染后以核因子κ b依赖的方式表达增加。CD63与绿色荧光蛋白标记的沙门氏菌和溶酶体标记LysoTracker共定位。细胞内沙门氏菌滴度与CD63表达呈负相关,表明CD63水平升高会降低细菌存活率。结论:CD63通过自噬途径,特别是异噬(针对病原体的自噬)参与调节胞内沙门氏菌的存活。这是第一篇通过诱导CD63表达和异种噬体抑制沙门氏菌增殖的报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Genes & genomics
Genes & genomics 生物-生化与分子生物学
CiteScore
3.70
自引率
4.80%
发文量
131
审稿时长
6-12 weeks
期刊介绍: Genes & Genomics is an official journal of the Korean Genetics Society (http://kgenetics.or.kr/). Although it is an official publication of the Genetics Society of Korea, membership of the Society is not required for contributors. It is a peer-reviewed international journal publishing print (ISSN 1976-9571) and online version (E-ISSN 2092-9293). It covers all disciplines of genetics and genomics from prokaryotes to eukaryotes from fundamental heredity to molecular aspects. The articles can be reviews, research articles, and short communications.
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