| Literature DB >> 33820962 |
Hyo Shin Yoon1, Chung Hwan Cho1, Myeong Sik Yun1, Sung Jae Jang1, Hyun Ju You1,2,3,4, Jun-Hyeong Kim5, Dohyun Han6, Kwang Hyun Cha7, Sung Hyun Moon1,5, Kiuk Lee5, Yeon-Ji Kim8, Sung-Joon Lee8, Tae-Wook Nam5, GwangPyo Ko9,10,11,12.
Abstract
The gut microbiota, which includes Akkermansia muciniphila, is known to modulate energy metabolism, glucose tolerance, immune system maturation and function in humans1-4. Although A. muciniphila is correlated with metabolic diseases and its beneficial causal effects were reported on host metabolism5-8, the molecular mechanisms involved have not been identified. Here, we report that A. muciniphila increases thermogenesis and glucagon-like peptide-1 (GLP-1) secretion in high-fat-diet (HFD)-induced C57BL/6J mice by induction of uncoupling protein 1 in brown adipose tissue and systemic GLP-1 secretion. We apply fast protein liquid chromatography and liquid chromatography coupled to mass spectrophotometry analysis to identify an 84 kDa protein, named P9, that is secreted by A. muciniphila. Using L cells and mice fed on an HFD, we show that purified P9 alone is sufficient to induce GLP-1 secretion and brown adipose tissue thermogenesis. Using ligand-receptor capture analysis, we find that P9 interacts with intercellular adhesion molecule 2 (ICAM-2). Interleukin-6 deficiency abrogates the effects of P9 in glucose homeostasis and downregulates ICAM-2 expression. Our results show that the interactions between P9 and ICAM-2 could be targeted by therapeutics for metabolic diseases.Entities:
Mesh:
Substances:
Year: 2021 PMID: 33820962 DOI: 10.1038/s41564-021-00880-5
Source DB: PubMed Journal: Nat Microbiol ISSN: 2058-5276 Impact factor: 17.745