宿主通过粪miRNA对肠道菌群进行塑形

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研究亮点

Ø  miRNA是鼠类以及人类粪便中的正常组份;
Ø  宿主肠上皮细胞以及Hopx+细胞是粪miRNA的主要来源;
Ø  miRNA进入细菌内并调节细菌基因表达及生长;
Ø  粪miRNA是维持正常肠道菌群所必需的。
 
宿主如何对肠道菌群进行塑形尚不清楚。本研究发现粪miRNA来源于肠上皮细胞以及Hopx+细胞。这类miRNA可以调节细菌基因表达及生长,粪miRNA丢失可导致肠道菌群失调以及结肠炎加重。

宿主的肠道菌群随着物种以及个体的变化而变化,但在某一特定个体内却保持相对稳定。然而,宿主如何对肠道菌群进行选择性塑形基本尚未阐明。在此,发现粪miRNA介导的物种间基因调控有利于宿主对肠道菌群的控制。miRNA在鼠类以及人类有着大量表达并以胞外小泡出现。细胞特异性miRNA加工酶(Dicer)敲除鉴定出肠上皮细胞(IEC)以及Hopx+细胞是粪miRNA的主要来源。这类miRNA可进入细菌,如F. nucleatumE. coli,特异性调节细菌基因转录本,并影响到细菌的生长。IEC-miRNA表达缺陷(Dicer1IEC)小鼠出现肠道菌群生长失控以及结肠炎加重,移植入野生型小鼠miRNA可以重塑肠道菌群并减轻结肠炎症程度。此发现揭示了粪miRNA对肠道菌群进行塑形这一生理学功能并揭示了操控微生物组的可能策略。
 
摘自:
Cell Host & Microbe 2016; 19: 32–43

Highlights

  • miRNAs are normal constituents of murine and human feces
  • Host gut epithelial cells and Hopx+ cells are the main sources of fecal miRNA
  • miRNAs enter bacteria and regulate bacterial gene expression and growth
  • Fecal miRNAs are essential for the maintenance of normal gut microbiota

Summary

The host gut microbiota varies across species and individuals but is relatively stable over time within an individual. How the host selectively shapes the microbiota is largely unclear. Here, we show that fecal microRNA (miRNA)-mediated inter-species gene regulation facilitates host control of the gut microbiota. miRNAs are abundant in mouse and human fecal samples and present within extracellular vesicles. Cell-specific loss of the miRNA-processing enzyme, Dicer, identified intestinal epithelial cells (IEC) and Hopx-positive cells as predominant fecal miRNA sources. These miRNAs can enter bacteria, such as F. nucleatum and E. coli, specifically regulate bacterial gene transcripts, and affect bacterial growth. IEC-miRNA-deficient (Dicer1ΔIEC) mice exhibit uncontrolled gut microbiota and exacerbated colitis, and WT fecal miRNA transplantation restores fecal microbes and ameliorates colitis. These findings identify both a physiologic role by which fecal miRNA shapes the gut microbiota and a potential strategy for manipulating the microbiome.


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