首页> 外文期刊>Cell discovery. >LncRNA lncLy6C induced by microbiota metabolite butyrate promotes differentiation of Ly6C high to Ly6C int/neg macrophages through lncLy6C /C/EBPβ/Nr4A1 axis
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LncRNA lncLy6C induced by microbiota metabolite butyrate promotes differentiation of Ly6C high to Ly6C int/neg macrophages through lncLy6C /C/EBPβ/Nr4A1 axis

机译:Microbiota代谢物诱导的LNCRNA LNCLY6C通过LNCLY6C / C /EBPβ/ NR4A1轴促进Ly6C高至Ly6C Int / Neg巨噬细胞的分化

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Macrophages are mainly divided into two populations, which play a different role in physiological and pathological conditions. The differentiation of these cells may be regulated by transcription factors. However, it is unclear how to modulate these transcription factors to affect differentiation of these cells. Here, we found that lncLy6C, a novel ultraconserved lncRNA, promotes differentiation of Ly6Chigh inflammatory monocytes into Ly6Clow/neg resident macrophages. We demonstrate that gut microbiota metabolites butyrate upregulates the expression of lncLy6C. LncLy6C deficient mice had markedly increased Ly6Chigh pro-inflammatory monocytes and reduced Ly6Cneg resident macrophages. LncLy6C not only bound with transcription factor C/EBPβ but also bound with multiple lysine methyltransferases of H3K4me3 to specifically promote the enrichment of C/EBPβ and H3K4me3 marks on the promoter region of Nr4A1, which can promote Ly6Chigh into Ly6Cneg macrophages. As a result, lncLy6C causes the upregulation of Nr4A1 to promote Ly6Chigh inflammatory monocytes to differentiate into Ly6Cint/neg resident macrophages.
机译:巨噬细胞主要分为两种群体,在生理和病理条件下发挥着不同的作用。可以通过转录因子调节这些细胞的分化。然而,目前尚不清楚如何调节这些转录因子以影响这些细胞的分化。在这里,我们发现LNCLY6C,一种新型超级超法的LNCRNA,促进Ly6chigh炎性单核细胞的分化为Ly6clow / Neg常规巨噬细胞。我们证明肠道微生物酵母代谢物丁酸盐上调LNCLY6C的表达。 LNCLY6C缺陷小鼠显着增加了Ly6chigh促炎单核细胞和减少的Ly6cneg常规巨噬细胞。 LNCLY6C不仅与转录因子C /EBPβ结合,还与H3K4ME3的多个赖氨酸甲基转移酶结合,以特异性地促进C /EBPβ和H3K4ME3的富集在NR4A1的启动子区上,其可以促进Ly6Chigh进入Ly6cneg巨噬细胞。结果,LNCLY6C导致NR4A1的上调促进Ly6chhigh炎性单核细胞以区分Ly6cint / Neg常规巨噬细胞。

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