The Role of Autophagy in White Adipose Tissue Function: Implications for Metabolic Health
White adipose tissue (WAT) is a highly adaptive endocrine organ that continuously remodels in response to nutritional cues. WAT expands to store excess energy by increasing adipocyte number and/or size. Failure in WAT expansion has serious consequences on metabolic health resulting in altered lipid,...
| Autores: | , , , , |
|---|---|
| Formato: | artículo |
| Fecha de publicación: | 2020 |
| País: | España |
| Recursos: | Instituto de Salud Carlos III (ISCIII) |
| Repositorio: | Repisalud |
| Idioma: | inglés |
| OAI Identifier: | oai:repisalud.isciii.es:20.500.12105/18038 |
| Acesso em linha: | http://hdl.handle.net/20.500.12105/18038 |
| Access Level: | acceso abierto |
| Palavra-chave: | Adipose tissue Adipocyte Autophagy Obesity Diabetes Metabolism Tejido adiposo Adipocitos Autofagia Obesidad Diabetes Mellitus Metabolismo Adipose Tissue Adipocytes Adipogenesis Humans Homeostasis Fibrosis Inflammation Lipids Glucose |
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The Role of Autophagy in White Adipose Tissue Function: Implications for Metabolic HealthClemente-Postigo, MercedesTinahones, AlbertoEl Bekay, RajaaMalagón, María M.Tinahones, Francisco J.Adipose tissueAdipocyteAutophagyObesityDiabetesMetabolismTejido adiposoAdipocitosAutofagiaObesidadDiabetes MellitusMetabolismoAdipose TissueAdipocytesAutophagyObesityDiabetes MellitusMetabolismAdipogenesisHumansHomeostasisFibrosisInflammationLipidsGlucoseWhite adipose tissue (WAT) is a highly adaptive endocrine organ that continuously remodels in response to nutritional cues. WAT expands to store excess energy by increasing adipocyte number and/or size. Failure in WAT expansion has serious consequences on metabolic health resulting in altered lipid, glucose, and inflammatory profiles. Besides an impaired adipogenesis, fibrosis and low-grade inflammation also characterize dysfunctional WAT. Nevertheless, the precise mechanisms leading to impaired WAT expansibility are yet unresolved. Autophagy is a conserved and essential process for cellular homeostasis, which constitutively allows the recycling of damaged or long-lived proteins and organelles, but is also highly induced under stress conditions to provide nutrients and remove pathogens. By modulating protein and organelle content, autophagy is also essential for cell remodeling, maintenance, and survival. In this line, autophagy has been involved in many processes affected during WAT maladaptation, including adipogenesis, adipocyte, and macrophage function, inflammatory response, and fibrosis. WAT autophagy dysregulation is related to obesity and diabetes. However, it remains unclear whether WAT autophagy alteration in obese and diabetic patients are the cause or the consequence of WAT malfunction. In this review, current data regarding these issues are discussed, focusing on evidence from human studies.Multidisciplinary Digital Publishing Institute (MDPI)[Clemente-Postigo,M; Malagón,MM] Department of Cell Biology, Physiology and Immunology, Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC)-Reina Sofia University Hospital, University of Cordoba, Edificio IMIBIC, Córdoba, Spain. [Tinahones,A; Tinahones,FJ] Unidad de Gestión Clínica de Endocrinología y Nutrición (Hospital Universitario Virgen de la Victoria), Instituto de Investigación Biomédica de Málaga (IBIMA), Universidad de Málaga, Málaga, Spain. [El Bekay,R] Unidad de Gestión Clínica de Endocrinología y Nutrición (Hospital Universitario Regional de Málaga), Instituto de Investigación Biomédica de Málaga (IBIMA), Universidad de Málaga, Málaga, Spain. [El Bekay,R; Malagón,MM; Tinahones,FJ] Centro de Investigación Biomédica en Red (CIBER) Fisiopatología de la Obesidad y Nutrición (CIBEROBN), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.20242024-02-1220202020-04-3020202020-04-30review articlehttp://purl.org/coar/resource_type/c_dcae04bcVoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articlehttp://hdl.handle.net/20.500.12105/18038reponame:Repisaludinstname:Instituto de Salud Carlos III (ISCIII)Inglésengopen accesshttp://purl.org/coar/access_right/c_abf2Attribution 4.0 Internationalhttp://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessoai:repisalud.isciii.es:20.500.12105/180382026-06-12T12:43:37Z |
| dc.title.none.fl_str_mv |
The Role of Autophagy in White Adipose Tissue Function: Implications for Metabolic Health |
| title |
The Role of Autophagy in White Adipose Tissue Function: Implications for Metabolic Health |
| spellingShingle |
The Role of Autophagy in White Adipose Tissue Function: Implications for Metabolic Health Clemente-Postigo, Mercedes Adipose tissue Adipocyte Autophagy Obesity Diabetes Metabolism Tejido adiposo Adipocitos Autofagia Obesidad Diabetes Mellitus Metabolismo Adipose Tissue Adipocytes Autophagy Obesity Diabetes Mellitus Metabolism Adipogenesis Humans Homeostasis Fibrosis Inflammation Lipids Glucose |
| title_short |
The Role of Autophagy in White Adipose Tissue Function: Implications for Metabolic Health |
| title_full |
The Role of Autophagy in White Adipose Tissue Function: Implications for Metabolic Health |
| title_fullStr |
The Role of Autophagy in White Adipose Tissue Function: Implications for Metabolic Health |
| title_full_unstemmed |
The Role of Autophagy in White Adipose Tissue Function: Implications for Metabolic Health |
| title_sort |
The Role of Autophagy in White Adipose Tissue Function: Implications for Metabolic Health |
| dc.creator.none.fl_str_mv |
Clemente-Postigo, Mercedes Tinahones, Alberto El Bekay, Rajaa Malagón, María M. Tinahones, Francisco J. |
| author |
Clemente-Postigo, Mercedes |
| author_facet |
Clemente-Postigo, Mercedes Tinahones, Alberto El Bekay, Rajaa Malagón, María M. Tinahones, Francisco J. |
| author_role |
author |
| author2 |
Tinahones, Alberto El Bekay, Rajaa Malagón, María M. Tinahones, Francisco J. |
| author2_role |
author author author author |
| dc.contributor.none.fl_str_mv |
[Clemente-Postigo,M; Malagón,MM] Department of Cell Biology, Physiology and Immunology, Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC)-Reina Sofia University Hospital, University of Cordoba, Edificio IMIBIC, Córdoba, Spain. [Tinahones,A; Tinahones,FJ] Unidad de Gestión Clínica de Endocrinología y Nutrición (Hospital Universitario Virgen de la Victoria), Instituto de Investigación Biomédica de Málaga (IBIMA), Universidad de Málaga, Málaga, Spain. [El Bekay,R] Unidad de Gestión Clínica de Endocrinología y Nutrición (Hospital Universitario Regional de Málaga), Instituto de Investigación Biomédica de Málaga (IBIMA), Universidad de Málaga, Málaga, Spain. [El Bekay,R; Malagón,MM; Tinahones,FJ] Centro de Investigación Biomédica en Red (CIBER) Fisiopatología de la Obesidad y Nutrición (CIBEROBN), Instituto de Salud Carlos III (ISCIII), Madrid, Spain. |
| dc.subject.none.fl_str_mv |
Adipose tissue Adipocyte Autophagy Obesity Diabetes Metabolism Tejido adiposo Adipocitos Autofagia Obesidad Diabetes Mellitus Metabolismo Adipose Tissue Adipocytes Autophagy Obesity Diabetes Mellitus Metabolism Adipogenesis Humans Homeostasis Fibrosis Inflammation Lipids Glucose |
| topic |
Adipose tissue Adipocyte Autophagy Obesity Diabetes Metabolism Tejido adiposo Adipocitos Autofagia Obesidad Diabetes Mellitus Metabolismo Adipose Tissue Adipocytes Autophagy Obesity Diabetes Mellitus Metabolism Adipogenesis Humans Homeostasis Fibrosis Inflammation Lipids Glucose |
| description |
White adipose tissue (WAT) is a highly adaptive endocrine organ that continuously remodels in response to nutritional cues. WAT expands to store excess energy by increasing adipocyte number and/or size. Failure in WAT expansion has serious consequences on metabolic health resulting in altered lipid, glucose, and inflammatory profiles. Besides an impaired adipogenesis, fibrosis and low-grade inflammation also characterize dysfunctional WAT. Nevertheless, the precise mechanisms leading to impaired WAT expansibility are yet unresolved. Autophagy is a conserved and essential process for cellular homeostasis, which constitutively allows the recycling of damaged or long-lived proteins and organelles, but is also highly induced under stress conditions to provide nutrients and remove pathogens. By modulating protein and organelle content, autophagy is also essential for cell remodeling, maintenance, and survival. In this line, autophagy has been involved in many processes affected during WAT maladaptation, including adipogenesis, adipocyte, and macrophage function, inflammatory response, and fibrosis. WAT autophagy dysregulation is related to obesity and diabetes. However, it remains unclear whether WAT autophagy alteration in obese and diabetic patients are the cause or the consequence of WAT malfunction. In this review, current data regarding these issues are discussed, focusing on evidence from human studies. |
| publishDate |
2020 |
| dc.date.none.fl_str_mv |
2020 2020-04-30 2020 2020-04-30 2024 2024-02-12 |
| dc.type.none.fl_str_mv |
review article http://purl.org/coar/resource_type/c_dcae04bc VoR http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| dc.type.openaire.fl_str_mv |
info:eu-repo/semantics/article |
| format |
article |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/20.500.12105/18038 |
| url |
http://hdl.handle.net/20.500.12105/18038 |
| dc.language.none.fl_str_mv |
Inglés eng |
| language_invalid_str_mv |
Inglés |
| language |
eng |
| dc.rights.none.fl_str_mv |
open access http://purl.org/coar/access_right/c_abf2 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ |
| dc.rights.openaire.fl_str_mv |
info:eu-repo/semantics/openAccess |
| rights_invalid_str_mv |
open access http://purl.org/coar/access_right/c_abf2 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ |
| eu_rights_str_mv |
openAccess |
| dc.publisher.none.fl_str_mv |
Multidisciplinary Digital Publishing Institute (MDPI) |
| publisher.none.fl_str_mv |
Multidisciplinary Digital Publishing Institute (MDPI) |
| dc.source.none.fl_str_mv |
reponame:Repisalud instname:Instituto de Salud Carlos III (ISCIII) |
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Instituto de Salud Carlos III (ISCIII) |
| reponame_str |
Repisalud |
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Repisalud |
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1869403763624640512 |
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15.811543 |