粪便中的 hsa-miR-7704 通过抑制 ProB 来抑制长双歧杆菌的生长和粘附,并加重肝性脑病。

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY npj Biofilms and Microbiomes Pub Date : 2024-02-24 DOI:10.1038/s41522-024-00487-8
Yuchong Wang, Yuyu Li, Longxian Lv, Liying Zhu, Liang Hong, Xueyao Wang, Yu Zhang, Xin Wang, Hongyan Diao
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引用次数: 0

摘要

肠道微生物组和微RNA(miRNA)在肝性脑病(HE)的发病过程中都起着一定的作用。然而,人们对粪便中微生物组和宿主衍生的 miRNA 之间的功能联系仍知之甚少。在本研究中,与慢性乙型肝炎患者相比,肝性脑病患者的肠道微生物组和粪便中的 miRNA 发生了改变。将肝性脑病患者的粪便和粪便中的 miRNA 转移给受体小鼠会加重硫代乙酰胺诱导的肝性脑病。口服 hsa-miR-7704(一种在 HE 患者粪便中高度富集的宿主来源 miRNA)会以微生物依赖的方式加重小鼠的 HE。从机制上讲,hsa-miR-7704 通过抑制 proB 来抑制长双歧杆菌的生长和粘附。长双歧杆菌及其代谢产物乙酸盐通过抑制微神经胶质细胞的活化和氨的产生来缓解 HE。我们的研究结果揭示了 miRNA-微生物组轴在 HE 中的作用,并表明粪便中的 hsa-miR-7704 是 HE 进展的潜在调节因子。
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Faecal hsa-miR-7704 inhibits the growth and adhesion of Bifidobacterium longum by suppressing ProB and aggravates hepatic encephalopathy.

Both gut microbiome and microRNAs (miRNAs) play a role in the development of hepatic encephalopathy (HE). However, the functional link between the microbiome and host-derived miRNAs in faeces remains poorly understood. In the present study, patients with HE had an altered gut microbiome and faecal miRNAs compared with patients with chronic hepatitis B. Transferring faeces and faecal miRNAs from patients with HE to the recipient mice aggravated thioacetamide-induced HE. Oral gavage of hsa-miR-7704, a host-derived miRNA highly enriched in faeces from patients with HE, aggravated HE in mice in a microbiome-dependent manner. Mechanistically, hsa-miR-7704 inhibited the growth and adhesion of Bifidobacterium longum by suppressing proB. B. longum and its metabolite acetate alleviated HE by inhibiting microglial activation and ammonia production. Our findings reveal the role of miRNA-microbiome axis in HE and suggest that faecal hsa-miR-7704 are potential regulators of HE progression.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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