Dysbiosis-Induced Secondary Bile Acid Deficiency Promotes Intestinal Inflammation DOI Creative Commons
Sidhartha R. Sinha, Yeneneh Haileselassie, Linh P. Nguyen

и другие.

Cell Host & Microbe, Год журнала: 2020, Номер 27(4), С. 659 - 670.e5

Опубликована: Фев. 25, 2020

Язык: Английский

Parabacteroides distasonis Alleviates Obesity and Metabolic Dysfunctions via Production of Succinate and Secondary Bile Acids DOI Creative Commons
Kai Wang,

Mingfang Liao,

Nan Zhou

и другие.

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

891

Inflammaging and ‘Garb-aging’ DOI
Claudio Franceschi, Paolo Garagnani, Giovanni Vitale

и другие.

Trends in Endocrinology and Metabolism, Год журнала: 2016, Номер 28(3), С. 199 - 212

Опубликована: Окт. 24, 2016

Язык: Английский

Процитировано

806

Microbiota metabolite short chain fatty acids, GPCR, and inflammatory bowel diseases DOI Open Access
Mingming Sun, Wei Wu, Zhanju Liu

и другие.

Journal of Gastroenterology, Год журнала: 2016, Номер 52(1), С. 1 - 8

Опубликована: Июль 23, 2016

Язык: Английский

Процитировано

805

The intestinal microbiota fuelling metabolic inflammation DOI
Herbert Tilg, Niv Zmora, Timon E. Adolph

и другие.

Nature reviews. Immunology, Год журнала: 2019, Номер 20(1), С. 40 - 54

Опубликована: Авг. 6, 2019

Язык: Английский

Процитировано

795

The Short Chain Fatty Acid Butyrate Imprints an Antimicrobial Program in Macrophages DOI Creative Commons

Julie Schulthess,

Sumeet Pandey,

Melania Capitani

и другие.

Immunity, Год журнала: 2019, Номер 50(2), С. 432 - 445.e7

Опубликована: Янв. 25, 2019

Язык: Английский

Процитировано

790

The gut microbiome: Relationships with disease and opportunities for therapy DOI Creative Commons
Juliana Durack, Susan V. Lynch

The 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

746

Microbes, metabolites, and the gut–lung axis DOI Creative Commons
Anh Thu Dang, Benjamin J. Marsland

Mucosal Immunology, Год журнала: 2019, Номер 12(4), С. 843 - 850

Опубликована: Апрель 11, 2019

Язык: Английский

Процитировано

743

Intestinal barrier and gut microbiota: Shaping our immune responses throughout life DOI Open Access
Tatiana Takiishi, Camila Morales, Niels Olsen Saraiva Câmara

и другие.

Tissue 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

730

Intestinal microbiota-derived short-chain fatty acids regulation of immune cell IL-22 production and gut immunity DOI Creative Commons
Wenjing Yang, Tianming Yu, Xiangsheng Huang

и другие.

Nature 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

720

Understanding the Holobiont: How Microbial Metabolites Affect Human Health and Shape the Immune System DOI Creative Commons
Thomas S. Postler, Sankar Ghosh

Cell Metabolism, Год журнала: 2017, Номер 26(1), С. 110 - 130

Опубликована: Июнь 15, 2017

Язык: Английский

Процитировано

716