Journal of Nutrition, Год журнала: 2017, Номер 147(5), С. 727 - 745
Опубликована: Март 29, 2017
Язык: Английский
Journal of Nutrition, Год журнала: 2017, Номер 147(5), С. 727 - 745
Опубликована: Март 29, 2017
Язык: Английский
Cell, Год журнала: 2016, Номер 167(6), С. 1469 - 1480.e12
Опубликована: Дек. 1, 2016
Язык: Английский
Процитировано
2936Cell Research, Год журнала: 2020, Номер 30(6), С. 492 - 506
Опубликована: Май 20, 2020
Abstract The interplay between the commensal microbiota and mammalian immune system development function includes multifold interactions in homeostasis disease. microbiome plays critical roles training of major components host’s innate adaptive system, while orchestrates maintenance key features host-microbe symbiosis. In a genetically susceptible host, imbalances microbiota-immunity under defined environmental contexts are believed to contribute pathogenesis multitude immune-mediated disorders. Here, we review microbiome-immunity crosstalk their health disease, providing examples molecular mechanisms orchestrating these intestine extra-intestinal organs. We highlight aspects current knowledge, challenges limitations achieving causal understanding host immune-microbiome interactions, as well impact on diseases, discuss how insights may translate towards future microbiome-targeted therapeutic interventions.
Язык: Английский
Процитировано
2755Frontiers in Endocrinology, Год журнала: 2020, Номер 11
Опубликована: Янв. 31, 2020
A substantial body of evidence supports that the gut microbiota plays a pivotal role in regulation metabolic, endocrine and immune functions. In recent years, there has been growing recognition involvement modulation multiple neurochemical pathways through highly interconnected gut-brain axis. Although amazing scientific breakthroughs over last few years have expanded our knowledge on communication between microbes their hosts, underpinnings microbiota-gut-brain crosstalk remain to be determined. Short-chain fatty acids (SCFAs), main metabolites produced colon by bacterial fermentation dietary fibers resistant starch, are speculated play key neuro-immunoendocrine regulation. However, underlying mechanisms which SCFAs might influence brain physiology behavior not fully elucidated. this review, we will outline current about interactions. We also highlight how development future treatments for central nervous system (CNS) disorders can take advantage intimate mutual interactions with exploring function.
Язык: Английский
Процитировано
1942Cellular and Molecular Gastroenterology and Hepatology, Год журнала: 2018, Номер 6(2), С. 133 - 148
Опубликована: Янв. 1, 2018
Язык: Английский
Процитировано
1030Nature Reviews Gastroenterology & Hepatology, Год журнала: 2019, Номер 16(11), С. 690 - 704
Опубликована: Сен. 25, 2019
Язык: Английский
Процитировано
978Cell Research, Год журнала: 2019, Номер 29(10), С. 787 - 803
Опубликована: Сен. 6, 2019
Recently, increasing evidence has suggested the association between gut dysbiosis and Alzheimer's disease (AD) progression, yet role of microbiota in AD pathogenesis remains obscure. Herein, we provide a potential mechanistic link neuroinflammation progression. Using mouse models, discovered that, during alteration composition leads to peripheral accumulation phenylalanine isoleucine, which stimulates differentiation proliferation pro-inflammatory T helper 1 (Th1) cells. The brain-infiltrated Th1 immune cells are associated with M1 microglia activation, contributing AD-associated neuroinflammation. Importantly, elevation isoleucine concentrations increase cell frequency blood were also observed two small independent cohorts patients mild cognitive impairment (MCI) due AD. Furthermore, GV-971, sodium oligomannate that demonstrated solid consistent cognition improvement phase 3 clinical trial China, suppresses phenylalanine/isoleucine accumulation, harnesses reverses impairment. Together, our findings highlight dysbiosis-promoted progression suggest novel strategy for therapy by remodelling microbiota.
Язык: Английский
Процитировано
916Science, Год журнала: 2017, Номер 356(6344)
Опубликована: Июнь 23, 2017
The human gut microbiota makes key contributions to the metabolism of ingested compounds (xenobiotics), transforming hundreds dietary components, industrial chemicals, and pharmaceuticals into metabolites with altered activities, toxicities, lifetimes within body. chemistry microbial xenobiotic is often distinct from that host enzymes. Despite their important consequences for biology, microbes, genes, enzymes involved in are poorly understood. Linking these transformations elucidating biological effects undoubtedly challenging. However, recent studies demonstrate integrating traditional emerging technologies can enable progress toward this goal. Ultimately, a molecular understanding will guide personalized medicine nutrition, inform toxicology risk assessment, improve drug discovery development.
Язык: Английский
Процитировано
855Journal of Alzheimer s Disease, Год журнала: 2017, Номер 58(1), С. 1 - 15
Опубликована: Март 31, 2017
The gut microbiota comprises a complex community of microorganism species that resides in our gastrointestinal ecosystem and whose alterations influence not only various disorders but also central nervous system such as Alzheimer's disease (AD). AD, the most common form dementia, i s neurodegenerative disorder associated with impaired cognition cerebral accumulation amyloid-β peptides (Aβ). Most notably, microbiota-gut-brain axis is bidirectional communication fully understood, includes neural, immune, endocrine, metabolic pathways. Studies germ-free animals exposed to pathogenic microbial infections, antibiotics, probiotics, or fecal transplantation suggest role for host AD-related pathogenesis. increased permeability blood-brain barrier induced by dysbiosis may mediate affect AD pathogenesis other disorders, especially those aging. In addition, bacteria populating can secrete large amounts amyloids lipopolysaccharides, which might contribute modulation signaling pathways production proinflammatory cytokines AD. Moreover, imbalances induce inflammation obesity, type 2 diabetes mellitus, purpose this review summarize discuss current findings elucidate development Understanding underlying mechanisms provide new insights into novel therapeutic strategies
Язык: Английский
Процитировано
754Current Neurology and Neuroscience Reports, Год журнала: 2017, Номер 17(12)
Опубликована: Окт. 17, 2017
Язык: Английский
Процитировано
694Cell, Год журнала: 2017, Номер 172(3), С. 500 - 516.e16
Опубликована: Дек. 21, 2017
Microglia are embryonically seeded macrophages that contribute to brain development, homeostasis, and pathologies. It is thus essential decipher how microglial properties temporally regulated by intrinsic extrinsic factors, such as sexual identity the microbiome. Here, we found microglia undergo differentiation phases, discernable transcriptomic signatures chromatin accessibility landscapes, which can diverge in adult males females. Remarkably, absence of microbiome germ-free mice had a time sexually dimorphic impact both prenatally postnatally: were more profoundly perturbed male embryos female adults. Antibiotic treatment triggered biased responses revealing acute long-term effects microbiota depletion. Finally, human fetal exhibited significant overlap with murine signature. Our study shows respond environmental challenges sex- time-dependent manner from prenatal stages, major implications for our understanding contributions health disease.
Язык: Английский
Процитировано
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