布鲁氏菌分泌蛋白 VceA 促进 FOXO1 进入细胞核,使宿主细胞的新陈代谢转向糖酵解。

IF 3.3 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Acta biochimica et biophysica Sinica Pub Date : 2024-11-22 DOI:10.3724/abbs.2024203
Shuzhu Cao, Xinxin Han, Xingmei Deng, Jia Guo, Liangbo Liu, Yu Zhang, Maratbek Suleimenov, Tianyi Zhao, Wei Li, Jian Ding, Songsong Xie, Hui Zhang
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引用次数: 0

摘要

糖酵解代谢增加是布鲁氏菌繁殖和诱发布鲁氏菌病的关键步骤,然而,人们对这一过程在感染期间是如何调节的知之甚少。叉头盒蛋白 O1(FOXO1)是一种调节能量代谢的转录因子。在本研究中,我们利用酵母双杂交系统(Y2H)和免疫沉淀(Co-IP)首次反向筛选了FOXO1,并确定了FOXO1与布鲁氏菌分泌蛋白VceA之间的相互作用。我们的研究结果表明,布鲁氏菌分泌蛋白 VceA 与 FOXO1 共同定位在细胞质中。此外,我们还观察到,流产布鲁氏菌 2308(S2308)感染巨噬细胞会促进 FOXO1 进入细胞核,导致巨噬细胞中的糖酵解水平显著上调。相反,在 VceA 突变株(S2308-ΔVceA)中,我们注意到 FOXO1 进入细胞核的能力显著下降,同时糖酵解水平也下降了。此外,布鲁氏菌通过分泌蛋白 VceA 与 FOXO1 相互作用,促进 FOXO1 进入细胞核,从而改变宿主的代谢模式。这项研究揭示了布鲁氏菌入侵宿主巨噬细胞并诱导独特代谢变化的机制。这些见解可能为开发代谢治疗策略,治疗和预防相关疾病提供了新的理论依据。
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Brucella secretory protein VceA promotes FOXO1 entry into the nucleus to shift host cell metabolism toward glycolysis.

Increased glycolytic metabolism is a key step in the reproduction of Brucella and the induction of brucellosis, however, little is known about how this process is regulated during infection. Forkhead box protein O1 (FOXO1) is a transcription factor that regulates energy metabolism. In this study, we employ the yeast two-hybrid system (Y2H) and immunoprecipitation (Co-IP) to reverse screen for the FOXO1 for the first time and identify interactions between FOXO1 and the Brucella secretory protein VceA. Our findings reveal that the Brucella secretory protein VceA colocalizes with FOXO1 in the cytoplasm. Additionally, we observe that infection of macrophages with Brucella abortus 2308 ( S2308) promotes FOXO1 entry into the nucleus, leading to a significant upregulation of glycolysis level in macrophage. Conversely, in a VceA mutant strain (S2308-ΔVceA), we note a significant reduction in the ability of FOXO1 to enter the nucleus, accompanied by a decrease in glycolysis level. Furthermore, Brucella interacts with FOXO1 through the secreted protein VceA, promoting the entry of FOXO1 into the nucleus and thereby altering host metabolic patterns. This study provides insights into the mechanisms by which Brucella invades host macrophages and induces unique metabolic changes. These insights may offer a novel rationale for developing metabolic therapeutic strategies for the treatment and prevention of related diseases.

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来源期刊
Acta biochimica et biophysica Sinica
Acta biochimica et biophysica Sinica 生物-生化与分子生物学
CiteScore
5.00
自引率
5.40%
发文量
170
审稿时长
3 months
期刊介绍: Acta Biochimica et Biophysica Sinica (ABBS) is an internationally peer-reviewed journal sponsored by the Shanghai Institute of Biochemistry and Cell Biology (CAS). ABBS aims to publish original research articles and review articles in diverse fields of biochemical research including Protein Science, Nucleic Acids, Molecular Biology, Cell Biology, Biophysics, Immunology, and Signal Transduction, etc.
期刊最新文献
Retraction: miR-129-5p suppresses proliferation, migration, and induces apoptosis in pancreatic cancer cells by targeting PBX3. Brucella secretory protein VceA promotes FOXO1 entry into the nucleus to shift host cell metabolism toward glycolysis. Ivermectin inhibits the growth of ESCC by activating the ATF4-mediated endoplasmic reticulum stress-autophagy pathway. RNA modifications: emerging players in the regulation of reproduction and development. Functions and applications of RNA interference and small regulatory RNAs.
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