The innate immune receptor RP105 promotes metabolic syndrome by altering gut microbiota composition and intestinal barrier function

被引:0
|
作者
Kani, Koudai [1 ]
Kasai, Kaichi [1 ]
Tada, Yuki [1 ]
Ishibashi, Riko [1 ]
Takano, Shun [1 ]
Igarashi, Naoya [1 ]
Ichimura-Shimizu, Mayuko [2 ]
Tsuneyama, Koichi [2 ]
Furusawa, Yukihiro [1 ]
Nagai, Yoshinori [1 ]
机构
[1] Toyama Prefectural Univ, Fac Engn, Dept Pharmaceut Engn, 5180 Kurokawa, Imizu, Toyama 9390398, Japan
[2] Tokushima Univ, Dept Pathol & Lab Med, Grad Sch Biomed Sci, 3-8-15 Kuramoto Cho, Tokushima 7708503, Japan
基金
日本学术振兴会;
关键词
RP105; Innate immunity; Metabolic syndrome; Gut microbiota; Intestinal barrier dysfunction; DIET-INDUCED OBESITY; COMPLEX; INFLAMMATION; ENDOTOXEMIA; MD-1; RESPONSIVENESS; PROLIFERATION; MACROPHAGES; MOLECULE; ANTIBODY;
D O I
10.1016/j.bbrc.2023.04.068
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Radioprotective 105 (RP105) plays a key role in the development of high-fat diet (HFD)-induced meta-bolic disorders; however, the underlying mechanisms remain to be understood. Here, we aimed to uncover whether RP105 affects metabolic syndrome through the modification of gut microbiota. We confirmed that body weight gain and fat accumulation by HFD feeding were suppressed in Rp105-/- mice. Fecal microbiome transplantation from HFD-fed donor Rp105-/- mice into HFD-fed recipient wild-type mice significantly improved various abnormalities associated with metabolic syndrome, including body weight gain, insulin resistance, hepatic steatosis, macrophage infiltration and inflammation in the adipose tissue. In addition, HFD-induced intestinal barrier dysfunction was attenuated by fecal micro-biome transplantation from HFD-fed donor Rp105-/- mice. A 16S rRNA sequence analysis indicated that RP105 modified gut microbiota composition and was involved in the maintenance of its diversity. Thus, RP105 promotes metabolic syndrome by altering gut microbiota composition and intestinal barrier function. (c) 2023 Elsevier Inc. All rights reserved.
引用
收藏
页码:77 / 85
页数:9
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