Shortcuts to a functional adipose tissue: The role of small non-coding RNAs

Detalhes bibliográficos
Autor(a) principal: Brandao, Bruna B. [UNIFESP]
Data de Publicação: 2017
Outros Autores: Guerra, Beatriz A.[UNIFESP], Mori, Marcelo A. [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1016/j.redox.2017.01.020
https://repositorio.unifesp.br/handle/11600/53429
Resumo: Metabolic diseases such as type 2 diabetes are a major public health issue worldwide. These diseases are often linked to a dysfunctional adipose tissue. Fat is a large, heterogenic, pleiotropic and rather complex tissue. It is found in virtually all cavities of the human body, shows unique plasticity among tissues, and harbors many cell types in addition to its main functional unit - the adipocyte. Adipose tissue function varies depending on the localization of the fat depot, the cell composition of the tissue and the energy status of the organism. While the white adipose tissue (WAT) serves as the main site for triglyceride storage and acts as an important endocrine organ, the brown adipose tissue (BAT) is responsible for thermogenesis. Beige adipocytes can also appear in WAT depots to sustain heat production upon certain conditions, and it is becoming clear that adipose tissue depots can switch phenotypes depending on cell autonomous and non-autonomous stimuli. To maintain such degree of plasticity and respond adequately to changes in the energy balance, three basic processes need to be properly functioning in the adipose tissue: i) adipogenesis and adipocyte turnover, ii) metabolism, and iii) signaling. Here we review the fundamental role of small non-coding RNAs (sncRNAs) in these processes, with focus on microRNAs, and demonstrate their importance in adipose tissue function and whole body metabolic control in mammals.
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spelling Shortcuts to a functional adipose tissue: The role of small non-coding RNAsAdipose tissueMicroRNAsSmall non-coding RNAsObesityDiabetesMetabolic diseases such as type 2 diabetes are a major public health issue worldwide. These diseases are often linked to a dysfunctional adipose tissue. Fat is a large, heterogenic, pleiotropic and rather complex tissue. It is found in virtually all cavities of the human body, shows unique plasticity among tissues, and harbors many cell types in addition to its main functional unit - the adipocyte. Adipose tissue function varies depending on the localization of the fat depot, the cell composition of the tissue and the energy status of the organism. While the white adipose tissue (WAT) serves as the main site for triglyceride storage and acts as an important endocrine organ, the brown adipose tissue (BAT) is responsible for thermogenesis. Beige adipocytes can also appear in WAT depots to sustain heat production upon certain conditions, and it is becoming clear that adipose tissue depots can switch phenotypes depending on cell autonomous and non-autonomous stimuli. To maintain such degree of plasticity and respond adequately to changes in the energy balance, three basic processes need to be properly functioning in the adipose tissue: i) adipogenesis and adipocyte turnover, ii) metabolism, and iii) signaling. Here we review the fundamental role of small non-coding RNAs (sncRNAs) in these processes, with focus on microRNAs, and demonstrate their importance in adipose tissue function and whole body metabolic control in mammals.Univ Fed Sao Paulo, Program Mol Biol, Sao Paulo, BrazilUniv Estadual Campinas, Dept Biochem & Tissue Biol, Campinas, SP, BrazilUniv Estadual Campinas, Program Genet & Mol Biol, Campinas, BrazilUniv Fed Sao Paulo, Program Mol Biol, Sao Paulo, BrazilWeb of ScienceFundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)Fundo de Apoio ao Ensino, a Pesquisa e Extensao (FAEPEX/UNICAMP)FAPESP: 2015/01316-7FAPESP: 2015/03292-8CNPq: 444424/2014-8FAEPEX/UNICAMP: 2408/16Elsevier Science Bv2020-06-26T16:30:13Z2020-06-26T16:30:13Z2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion82-102application/pdfhttp://dx.doi.org/10.1016/j.redox.2017.01.020Redox Biology. Amsterdam, v. 12, p. 82-102, 2017.10.1016/j.redox.2017.01.020WOS000403328700008.pdf2213-2317https://repositorio.unifesp.br/handle/11600/53429WOS:000403328700008engRedox BiologyAmsterdaminfo:eu-repo/semantics/openAccessBrandao, Bruna B. [UNIFESP]Guerra, Beatriz A.[UNIFESP]Mori, Marcelo A. [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-03T03:16:40Zoai:repositorio.unifesp.br/:11600/53429Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-03T03:16:40Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Shortcuts to a functional adipose tissue: The role of small non-coding RNAs
title Shortcuts to a functional adipose tissue: The role of small non-coding RNAs
spellingShingle Shortcuts to a functional adipose tissue: The role of small non-coding RNAs
Brandao, Bruna B. [UNIFESP]
Adipose tissue
MicroRNAs
Small non-coding RNAs
Obesity
Diabetes
title_short Shortcuts to a functional adipose tissue: The role of small non-coding RNAs
title_full Shortcuts to a functional adipose tissue: The role of small non-coding RNAs
title_fullStr Shortcuts to a functional adipose tissue: The role of small non-coding RNAs
title_full_unstemmed Shortcuts to a functional adipose tissue: The role of small non-coding RNAs
title_sort Shortcuts to a functional adipose tissue: The role of small non-coding RNAs
author Brandao, Bruna B. [UNIFESP]
author_facet Brandao, Bruna B. [UNIFESP]
Guerra, Beatriz A.[UNIFESP]
Mori, Marcelo A. [UNIFESP]
author_role author
author2 Guerra, Beatriz A.[UNIFESP]
Mori, Marcelo A. [UNIFESP]
author2_role author
author
dc.contributor.author.fl_str_mv Brandao, Bruna B. [UNIFESP]
Guerra, Beatriz A.[UNIFESP]
Mori, Marcelo A. [UNIFESP]
dc.subject.por.fl_str_mv Adipose tissue
MicroRNAs
Small non-coding RNAs
Obesity
Diabetes
topic Adipose tissue
MicroRNAs
Small non-coding RNAs
Obesity
Diabetes
description Metabolic diseases such as type 2 diabetes are a major public health issue worldwide. These diseases are often linked to a dysfunctional adipose tissue. Fat is a large, heterogenic, pleiotropic and rather complex tissue. It is found in virtually all cavities of the human body, shows unique plasticity among tissues, and harbors many cell types in addition to its main functional unit - the adipocyte. Adipose tissue function varies depending on the localization of the fat depot, the cell composition of the tissue and the energy status of the organism. While the white adipose tissue (WAT) serves as the main site for triglyceride storage and acts as an important endocrine organ, the brown adipose tissue (BAT) is responsible for thermogenesis. Beige adipocytes can also appear in WAT depots to sustain heat production upon certain conditions, and it is becoming clear that adipose tissue depots can switch phenotypes depending on cell autonomous and non-autonomous stimuli. To maintain such degree of plasticity and respond adequately to changes in the energy balance, three basic processes need to be properly functioning in the adipose tissue: i) adipogenesis and adipocyte turnover, ii) metabolism, and iii) signaling. Here we review the fundamental role of small non-coding RNAs (sncRNAs) in these processes, with focus on microRNAs, and demonstrate their importance in adipose tissue function and whole body metabolic control in mammals.
publishDate 2017
dc.date.none.fl_str_mv 2017
2020-06-26T16:30:13Z
2020-06-26T16:30:13Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.redox.2017.01.020
Redox Biology. Amsterdam, v. 12, p. 82-102, 2017.
10.1016/j.redox.2017.01.020
WOS000403328700008.pdf
2213-2317
https://repositorio.unifesp.br/handle/11600/53429
WOS:000403328700008
url http://dx.doi.org/10.1016/j.redox.2017.01.020
https://repositorio.unifesp.br/handle/11600/53429
identifier_str_mv Redox Biology. Amsterdam, v. 12, p. 82-102, 2017.
10.1016/j.redox.2017.01.020
WOS000403328700008.pdf
2213-2317
WOS:000403328700008
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Redox Biology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 82-102
application/pdf
dc.coverage.none.fl_str_mv Amsterdam
dc.publisher.none.fl_str_mv Elsevier Science Bv
publisher.none.fl_str_mv Elsevier Science Bv
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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