Shortcuts to a functional adipose tissue: The role of small non-coding RNAs
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , |
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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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 |
_version_ |
1814268461562462208 |