| Literature DB >> 32464093 |
Gotaro Toda1, Kotaro Soeda1, Yukiko Okazaki1, Naoki Kobayashi2, Yukari Masuda3, Naoko Arakawa1, Hirotsugu Suwanai3, Yosuke Masamoto4, Yoshihiko Izumida3, Nozomu Kamei3, Takayoshi Sasako3, Ryo Suzuki3, Tetsuya Kubota3, Naoto Kubota3, Mineo Kurokawa4, Kazuyuki Tobe5, Tetsuo Noda6, Kenya Honda7, Domenico Accili8, Toshimasa Yamauchi3, Takashi Kadowaki9, Kohjiro Ueki10.
Abstract
The physiological role of immune cells in the regulation of postprandial glucose metabolism has not been fully elucidated. We have found that adipose tissue macrophages produce interleukin-10 (IL-10) upon feeding, which suppresses hepatic glucose production in cooperation with insulin. Both elevated insulin and gut-microbiome-derived lipopolysaccharide in response to feeding are required for IL-10 production via the Akt/mammalian target of rapamycin (mTOR) pathway. Indeed, myeloid-specific knockout of the insulin receptor or bone marrow transplantation of mutant TLR4 marrow cells results in increased expression of gluconeogenic genes and impaired glucose tolerance. Furthermore, myeloid-specific Akt1 and Akt2 knockout results in similar phenotypes that are rescued by additional knockout of TSC2, an inhibitor of mTOR. In obesity, IL-10 production is impaired due to insulin resistance in macrophages, whereas adenovirus-mediated expression of IL-10 ameliorates postprandial hyperglycemia. Thus, the orchestrated response of the endogenous hormone and gut environment to feeding is a key regulator of postprandial glycemia.Entities:
Keywords: Akt; gut microbiome; insulin; interleukin-10; lipopolysaccharide; macrophages; mammalian target of rapamycin; postprandial gluconeogenesis
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Year: 2020 PMID: 32464093 DOI: 10.1016/j.molcel.2020.04.033
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 19.328