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Mitochondrial-epigenetic crosstalk as an integrative standpoint into gut microbiome dysbiosis and related diseases

dc.contributor.authorSimão, Vinícius Augusto [UNESP]
dc.contributor.authorChuffa, Luiz Gustavo De Almeida [UNESP]
dc.contributor.authorFerder, León
dc.contributor.authorInserra, Felipe
dc.contributor.authorManucha, Walter
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionCiudad Autónoma de Buenos Aires
dc.contributor.institutionUniversidad Nacional de Cuyo
dc.contributor.institutionConsejo Nacional de Investigaciones Científicas y Tecnológicas (CONICET)
dc.date.accessioned2025-04-29T18:05:11Z
dc.date.issued2024-01-01
dc.description.abstractThe interplay between mitochondria, epigenetics, and the microbiota is intricately linked to both health and disease. Within our cells, a complex molecular dance occurs, where these components intertwine in a mesmerizing ballet that plays a decisive role in our health. Mitochondria, beyond being energy powerhouses, modulate nuclear gene expression through messengers like reactive oxidative stress (ROS) and calcium. Epigenetics, acting as the molecular conductor, regulates the expression of both nuclear and mitochondrial genes through modifications like DNA methylation. The intestinal microbiota itself produces short-chain fatty acids (SCFAs) that influence mitochondrial activity. SCFA-induced epigenetic modifications, like histone acetylation, impact mitochondrial function which may lead to disease. Mitochondrial dysfunction generates retrograde signals that alter nuclear gene expression, as evidenced by increased histone H3 lysine 27 acetylation (H3K27ac) in genes essential for neuronal differentiation and mitochondrial reprogramming. Alterations in the mitochondrial-nuclear-microbiota axis are associated with diseases including diabetes, neurodegeneration, and cancer. Modulating the intestinal microbiota with probiotics or prebiotics can restore balance while intervening in mitochondrial pathways, which can be a therapeutic strategy. Additionally, using epigenetic agents like histone deacetylase (HDAC) inhibitors can reprogram gene expression and improve mitochondrial function. Finally, the present review aims to explore the central interplay between mitochondria, epigenetics modifications, and microbiota in a complex and dynamic molecular context that plays a fundamental role in human health. Specifically, it will examine the impact of microbiome components and metabolites generated from normobiosis and dysbiosis on mitochondria and epigenetic modifications across different diseases and metabolic conditions. This integrated understanding of the molecular players and their interactions provides a deeper perspective on how to promote health and potentially combat disease.en
dc.description.affiliationDepartment of Structural and Functional Biology UNESP São Paulo State University Institute of Biosciences, Botucatu
dc.description.affiliationDepartamento de Tecnología Médica Universidad Maimónides Ciudad Autónoma de Buenos Aires, Buenos
dc.description.affiliationÁrea de Farmacología Departamento de Patología Facultad de Ciencias Médicas Universidad Nacional de Cuyo
dc.description.affiliationInstituto de Medicina y Biología Experimental de Cuyo (IMBECU Consejo Nacional de Investigaciones Científicas y Tecnológicas (CONICET)
dc.description.affiliationUnespDepartment of Structural and Functional Biology UNESP São Paulo State University Institute of Biosciences, Botucatu
dc.format.extent1429-1442
dc.identifierhttp://dx.doi.org/10.32604/biocell.2024.053478
dc.identifier.citationBiocell, v. 48, n. 10, p. 1429-1442, 2024.
dc.identifier.doi10.32604/biocell.2024.053478
dc.identifier.issn1667-5746
dc.identifier.issn0327-9545
dc.identifier.scopus2-s2.0-85205904231
dc.identifier.urihttps://hdl.handle.net/11449/296971
dc.language.isoeng
dc.relation.ispartofBiocell
dc.sourceScopus
dc.subjectDysbiosis
dc.subjectEpigenetic regulation
dc.subjectGut microbiota
dc.subjectMetabolic disorders
dc.subjectMitochondria
dc.subjectNeurological diseases
dc.titleMitochondrial-epigenetic crosstalk as an integrative standpoint into gut microbiome dysbiosis and related diseasesen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationab63624f-c491-4ac7-bd2c-767f17ac838d
relation.isOrgUnitOfPublication.latestForDiscoveryab63624f-c491-4ac7-bd2c-767f17ac838d
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt

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