Cargando…

Effects of PCB126 on Adipose-to-Muscle Communication in an in Vitro Model

BACKGROUND: Exposure to coplanar polychlorinated biphenyls (PCBs) is linked to the development of insulin resistance. Previous studies suggested PCB126 alters muscle mitochondrial function through an indirect mechanism. Given that PCBs are stored in fat, we hypothesized that PCB126 alters adipokine...

Descripción completa

Detalles Bibliográficos
Autores principales: Caron, Audrey, Ahmed, Fozia, Peshdary, Vian, Garneau, Léa, Atlas, Ella, Aguer, Céline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Environmental Health Perspectives 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539676/
https://www.ncbi.nlm.nih.gov/pubmed/33026256
http://dx.doi.org/10.1289/EHP7058
_version_ 1783591093138358272
author Caron, Audrey
Ahmed, Fozia
Peshdary, Vian
Garneau, Léa
Atlas, Ella
Aguer, Céline
author_facet Caron, Audrey
Ahmed, Fozia
Peshdary, Vian
Garneau, Léa
Atlas, Ella
Aguer, Céline
author_sort Caron, Audrey
collection PubMed
description BACKGROUND: Exposure to coplanar polychlorinated biphenyls (PCBs) is linked to the development of insulin resistance. Previous studies suggested PCB126 alters muscle mitochondrial function through an indirect mechanism. Given that PCBs are stored in fat, we hypothesized that PCB126 alters adipokine secretion, which in turn affects muscle metabolism. OBJECTIVES: We determined a) the impacts of PCB126 exposure on adipocyte cytokine/adipokine secretion in vitro; b) whether adipocyte-derived factors alter glucose metabolism and mitochondrial function in myotubes when exposed to PCB126; and c) whether preestablished insulin resistance alters the metabolic responses of adipocytes exposed to PCB126 and the communication between adipocytes and myotubes. METHODS: 3T3-L1 adipocytes were exposed to PCB126 ([Formula: see text]) in two insulin sensitivity conditions [insulin sensitive (IS) and insulin resistant (IR) adipocytes], followed by the measurement of secreted adipokines, mitochondrial function, and insulin-stimulated glucose uptake. Communication between adipocytes and myotubes was reproduced by exposing C2C12 myotubes or mouse primary myotubes to conditioned medium (CM) derived from IS or IR 3T3-L1 adipocytes exposed to PCB126. Mitochondrial function and insulin-stimulated glucose uptake were then determined in myotubes. RESULTS: IR 3T3-L1 adipocytes treated with PCB126 had significantly higher adipokine (adiponectin, IL-6, MCP-1, [Formula: see text]) secretion and lower mitochondrial function, glucose uptake, and glycolysis. However, PCB126 did not significantly alter these parameters in IS adipocytes. Altered energy metabolism in IR 3T3-L1 adipocytes was linked to lower phosphorylation of AMP-activated protein kinase (p-AMPK) and higher superoxide dismutase 2 levels, an enzyme involved in reactive oxygen species detoxification. Myotubes exposed to the CM from PCB126-treated IR adipocytes had lower glucose uptake, with no alteration in glycolysis or mitochondrial function. Interestingly, p-AMPK levels were higher in myotubes exposed to the CM of PCB126-treated IR adipocytes. DISCUSSION: Taken together, these data suggest that increased adipokine secretion from IR adipocytes exposed to PCB126 might explain impaired glucose uptake in myotubes. https://doi.org/10.1289/EHP7058
format Online
Article
Text
id pubmed-7539676
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Environmental Health Perspectives
record_format MEDLINE/PubMed
spelling pubmed-75396762020-10-09 Effects of PCB126 on Adipose-to-Muscle Communication in an in Vitro Model Caron, Audrey Ahmed, Fozia Peshdary, Vian Garneau, Léa Atlas, Ella Aguer, Céline Environ Health Perspect Research BACKGROUND: Exposure to coplanar polychlorinated biphenyls (PCBs) is linked to the development of insulin resistance. Previous studies suggested PCB126 alters muscle mitochondrial function through an indirect mechanism. Given that PCBs are stored in fat, we hypothesized that PCB126 alters adipokine secretion, which in turn affects muscle metabolism. OBJECTIVES: We determined a) the impacts of PCB126 exposure on adipocyte cytokine/adipokine secretion in vitro; b) whether adipocyte-derived factors alter glucose metabolism and mitochondrial function in myotubes when exposed to PCB126; and c) whether preestablished insulin resistance alters the metabolic responses of adipocytes exposed to PCB126 and the communication between adipocytes and myotubes. METHODS: 3T3-L1 adipocytes were exposed to PCB126 ([Formula: see text]) in two insulin sensitivity conditions [insulin sensitive (IS) and insulin resistant (IR) adipocytes], followed by the measurement of secreted adipokines, mitochondrial function, and insulin-stimulated glucose uptake. Communication between adipocytes and myotubes was reproduced by exposing C2C12 myotubes or mouse primary myotubes to conditioned medium (CM) derived from IS or IR 3T3-L1 adipocytes exposed to PCB126. Mitochondrial function and insulin-stimulated glucose uptake were then determined in myotubes. RESULTS: IR 3T3-L1 adipocytes treated with PCB126 had significantly higher adipokine (adiponectin, IL-6, MCP-1, [Formula: see text]) secretion and lower mitochondrial function, glucose uptake, and glycolysis. However, PCB126 did not significantly alter these parameters in IS adipocytes. Altered energy metabolism in IR 3T3-L1 adipocytes was linked to lower phosphorylation of AMP-activated protein kinase (p-AMPK) and higher superoxide dismutase 2 levels, an enzyme involved in reactive oxygen species detoxification. Myotubes exposed to the CM from PCB126-treated IR adipocytes had lower glucose uptake, with no alteration in glycolysis or mitochondrial function. Interestingly, p-AMPK levels were higher in myotubes exposed to the CM of PCB126-treated IR adipocytes. DISCUSSION: Taken together, these data suggest that increased adipokine secretion from IR adipocytes exposed to PCB126 might explain impaired glucose uptake in myotubes. https://doi.org/10.1289/EHP7058 Environmental Health Perspectives 2020-10-07 /pmc/articles/PMC7539676/ /pubmed/33026256 http://dx.doi.org/10.1289/EHP7058 Text en https://ehp.niehs.nih.gov/about-ehp/license EHP is an open-access journal published with support from the National Institute of Environmental Health Sciences, National Institutes of Health. All content is public domain unless otherwise noted.
spellingShingle Research
Caron, Audrey
Ahmed, Fozia
Peshdary, Vian
Garneau, Léa
Atlas, Ella
Aguer, Céline
Effects of PCB126 on Adipose-to-Muscle Communication in an in Vitro Model
title Effects of PCB126 on Adipose-to-Muscle Communication in an in Vitro Model
title_full Effects of PCB126 on Adipose-to-Muscle Communication in an in Vitro Model
title_fullStr Effects of PCB126 on Adipose-to-Muscle Communication in an in Vitro Model
title_full_unstemmed Effects of PCB126 on Adipose-to-Muscle Communication in an in Vitro Model
title_short Effects of PCB126 on Adipose-to-Muscle Communication in an in Vitro Model
title_sort effects of pcb126 on adipose-to-muscle communication in an in vitro model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539676/
https://www.ncbi.nlm.nih.gov/pubmed/33026256
http://dx.doi.org/10.1289/EHP7058
work_keys_str_mv AT caronaudrey effectsofpcb126onadiposetomusclecommunicationinaninvitromodel
AT ahmedfozia effectsofpcb126onadiposetomusclecommunicationinaninvitromodel
AT peshdaryvian effectsofpcb126onadiposetomusclecommunicationinaninvitromodel
AT garneaulea effectsofpcb126onadiposetomusclecommunicationinaninvitromodel
AT atlasella effectsofpcb126onadiposetomusclecommunicationinaninvitromodel
AT aguerceline effectsofpcb126onadiposetomusclecommunicationinaninvitromodel