The gut microbiota reprograms intestinal lipid metabolism through long noncoding RNA Snhg9 .
Yuhao WangMeng WangJiaxin ChenYun LiZheng KuangChaitanya DendePrithvi RajGabriella QuinnZehan HuTarun SrinivasanBrian HassellKelly A RuhnCassie L BehrendtJianpeng ShengXiaobing DouZhangfa SongLora V HooperPublished in: Science (New York, N.Y.) (2023)
The intestinal microbiota regulates mammalian lipid absorption, metabolism, and storage. We report that the microbiota reprograms intestinal lipid metabolism in mice by repressing the expression of long noncoding RNA (lncRNA) Snhg9 (small nucleolar RNA host gene 9) in small intestinal epithelial cells. Snhg9 suppressed the activity of peroxisome proliferator-activated receptor γ (PPARγ)-a central regulator of lipid metabolism-by dissociating the PPARγ inhibitor sirtuin 1 from cell cycle and apoptosis protein 2 (CCAR2). Forced expression of Snhg9 in the intestinal epithelium of conventional mice impaired lipid absorption, reduced body fat, and protected against diet-induced obesity. The microbiota repressed Snhg9 expression through an immune relay encompassing myeloid cells and group 3 innate lymphoid cells. Our findings thus identify an unanticipated role for a lncRNA in microbial control of host metabolism.
Keyphrases
- poor prognosis
- long noncoding rna
- long non coding rna
- cell cycle arrest
- cell cycle
- fatty acid
- induced apoptosis
- high fat diet induced
- insulin resistance
- endoplasmic reticulum stress
- type diabetes
- cell proliferation
- binding protein
- pi k akt
- dendritic cells
- microbial community
- bone marrow
- body mass index
- skeletal muscle
- weight gain
- amino acid
- genome wide identification