
Cell Host & Microbe, Год журнала: 2020, Номер 27(4), С. 659 - 670.e5
Опубликована: Фев. 25, 2020
Язык: Английский
Cell Host & Microbe, Год журнала: 2020, Номер 27(4), С. 659 - 670.e5
Опубликована: Фев. 25, 2020
Язык: Английский
Cell Reports, Год журнала: 2019, Номер 26(1), С. 222 - 235.e5
Опубликована: Янв. 1, 2019
Highlights•Parabacteroides distasonis alleviates obesity and obesity-related dysfunctions in mice.•P. generates succinate secondary bile acids the gut.•P. activates intestinal gluconeogenesis (IGN) FXR pathways gut.•Succinate is a ligand of fructose-1,6-bisphosphatase, rate-limiting enzyme IGN.SummaryWe demonstrated metabolic benefits Parabacteroides (PD) on decreasing weight gain, hyperglycemia, hepatic steatosis ob/ob high-fat diet (HFD)-fed mice. Treatment with live P. (LPD) dramatically altered acid profile elevated lithocholic (LCA) ursodeoxycholic (UDCA) increased level gut. In vitro cultivation PD its capacity to transform production succinate. Succinate supplementation decreased hyperglycemia mice via activation (IGN). Gavage mixture LCA UDCA reduced hyperlipidemia by activating pathway repairing gut barrier integrity. Co-treatment LCA/UDCA mirrored LPD. The binding target was identified as IGN. produced played key roles modulation host metabolism.Graphical abstract
Язык: Английский
Процитировано
891Trends in Endocrinology and Metabolism, Год журнала: 2016, Номер 28(3), С. 199 - 212
Опубликована: Окт. 24, 2016
Язык: Английский
Процитировано
806Journal of Gastroenterology, Год журнала: 2016, Номер 52(1), С. 1 - 8
Опубликована: Июль 23, 2016
Язык: Английский
Процитировано
805Nature reviews. Immunology, Год журнала: 2019, Номер 20(1), С. 40 - 54
Опубликована: Авг. 6, 2019
Язык: Английский
Процитировано
795Immunity, Год журнала: 2019, Номер 50(2), С. 432 - 445.e7
Опубликована: Янв. 25, 2019
Язык: Английский
Процитировано
790The Journal of Experimental Medicine, Год журнала: 2018, Номер 216(1), С. 20 - 40
Опубликована: Окт. 15, 2018
Over the past decade, our view of human-associated microbes has expanded beyond that a few species toward an appreciation diverse and niche-specialized microbial communities develop in human host with chronological age. The largest reservoir exists distal gastrointestinal tract, both lumen, where facilitate primary secondary metabolism, on mucosal surfaces, they interact immune cell populations. While local microbial-driven immunomodulation gut is well described, more recent studies have demonstrated role for microbiome influencing remote organs hematopoietic function. Unsurprisingly, therefore, perturbation to composition function microbiota been associated chronic diseases ranging from inflammatory metabolic conditions neurological, cardiovascular, respiratory illnesses. Considerable effort currently focused understanding natural history development humans context health outcomes, parallel improving knowledge microbiome-host molecular interactions. These efforts ultimately aim effective approaches rehabilitate perturbed ecosystems as means restore or prevent disease. This review details modulating focus discusses strategies manipulating management prevention conditions.
Язык: Английский
Процитировано
746Mucosal Immunology, Год журнала: 2019, Номер 12(4), С. 843 - 850
Опубликована: Апрель 11, 2019
Язык: Английский
Процитировано
743Tissue Barriers, Год журнала: 2017, Номер 5(4), С. e1373208 - e1373208
Опубликована: Сен. 6, 2017
The gastrointestinal (GI) tract is considered the largest immunological organ in body having a central role regulating immune homeostasis. Contrary to earlier belief, intestinal epithelial barrier not static physical but rather strongly interacts with gut microbiome and cells of system. This intense communication between cells, will shape specific responses antigens, balancing tolerance effector functions. Recent studies indicate that composition affects system development modulates mediators, which turn affect barrier. Moreover, dysbiosis may favor disruption could be related increased susceptibility certain diseases. review focused on its function host defense how throughout life can this role.
Язык: Английский
Процитировано
730Nature Communications, Год журнала: 2020, Номер 11(1)
Опубликована: Сен. 8, 2020
Innate lymphoid cells (ILCs) and CD4+ T produce IL-22, which is critical for intestinal immunity. The microbiota central to IL-22 production in the intestines; however, factors that regulate by ILCs are not clear. Here, we show microbiota-derived short-chain fatty acids (SCFAs) promote through G-protein receptor 41 (GPR41) inhibiting histone deacetylase (HDAC). SCFAs upregulate promoting aryl hydrocarbon (AhR) hypoxia-inducible factor 1α (HIF1α) expression, differentially regulated mTOR Stat3. HIF1α binds directly Il22 promoter, increase binding promoter modification. SCFA supplementation enhances production, protects intestines from inflammation. human cell production. These findings establish roles of inducing maintain homeostasis.
Язык: Английский
Процитировано
720Cell Metabolism, Год журнала: 2017, Номер 26(1), С. 110 - 130
Опубликована: Июнь 15, 2017
Язык: Английский
Процитировано
716