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Air Pollution–Mediated Susceptibility to Inflammation and Insulin Resistance: Influence of CCR2 Pathways in Mice

Background: Epidemiologic and experimental studies support an association between PM(2.5) exposure and insulin resistance (IR). Innate immune cell activation has been suggested to play a role in the pathogenesis of these effects. Objectives: We sought to evaluate the role of CC-chemokine receptor 2...

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Autores principales: Liu, Cuiqing, Xu, Xiaohua, Bai, Yuntao, Wang, Tse-Yao, Rao, Xiaoquan, Wang, Aixia, Sun, Lixian, Ying, Zhekang, Gushchina, Liubov, Maiseyeu, Andrei, Morishita, Masako, Sun, Qinghua, Harkema, Jack R., Rajagopalan, Sanjay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Institute of Environmental Health Sciences 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888572/
https://www.ncbi.nlm.nih.gov/pubmed/24149114
http://dx.doi.org/10.1289/ehp.1306841
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author Liu, Cuiqing
Xu, Xiaohua
Bai, Yuntao
Wang, Tse-Yao
Rao, Xiaoquan
Wang, Aixia
Sun, Lixian
Ying, Zhekang
Gushchina, Liubov
Maiseyeu, Andrei
Morishita, Masako
Sun, Qinghua
Harkema, Jack R.
Rajagopalan, Sanjay
author_facet Liu, Cuiqing
Xu, Xiaohua
Bai, Yuntao
Wang, Tse-Yao
Rao, Xiaoquan
Wang, Aixia
Sun, Lixian
Ying, Zhekang
Gushchina, Liubov
Maiseyeu, Andrei
Morishita, Masako
Sun, Qinghua
Harkema, Jack R.
Rajagopalan, Sanjay
author_sort Liu, Cuiqing
collection PubMed
description Background: Epidemiologic and experimental studies support an association between PM(2.5) exposure and insulin resistance (IR). Innate immune cell activation has been suggested to play a role in the pathogenesis of these effects. Objectives: We sought to evaluate the role of CC-chemokine receptor 2 (CCR2) in PM(2.5)-mediated inflammation and IR. Methods: Wild-type C57BL/6 and CCR2(–/–) male mice were fed a high-fat diet and exposed to either concentrated ambient PM(2.5) or filtered air for 17 weeks via a whole-body exposure system. We evaluated glucose tolerance and insulin sensitivity. At euthanasia, blood, spleen, and visceral adipose tissue (VAT) were collected, and inflammatory cells were measured using flow cytometry. We used standard immunoblots, immunohistochemical methods, and quantitative PCR (polymerase chain reaction) to assess pathways of interest involving insulin signaling, inflammation, and lipid and glucose metabolism in various organs. Vascular function was assessed using myography. Results: PM(2.5) exposure resulted in whole-body IR and increased hepatic lipid accumulation in the liver, which was attenuated in CCR2(–/–) mice by inhibiting SREBP1c-mediated transcriptional programming, decreasing fatty acid uptake, and suppressing p38 MAPK activity. Abnormal phosphorylation levels of AKT, AMPK in VAT, and adipose tissue macrophage content in wild-type mice were not present in CCR2(–/–) mice. However, the impaired whole-body glucose tolerance and reduced GLUT-4 in skeletal muscle in response to PM(2.5) was not corrected by CCR2 deficiency. Conclusions: PM(2.5) mediates IR by regulating VAT inflammation, hepatic lipid metabolism, and glucose utilization in skeletal muscle via both CCR2-dependent and -independent pathways. These findings provide new mechanistic links between air pollution and metabolic abnormalities underlying IR. Citation: Liu C, Xu X, Bai Y, Wang TY, Rao X, Wang A, Sun L, Ying Z, Gushchina L, Maiseyeu A, Morishita M, Sun Q, Harkema JR, Rajagopalan S. 2014. Air pollution–mediated susceptibility to inflammation and insulin resistance: influence of CCR2 pathways in mice. Environ Health Perspect 122:17–26; http://dx.doi.org/10.1289/ehp.1306841
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spelling pubmed-38885722014-01-21 Air Pollution–Mediated Susceptibility to Inflammation and Insulin Resistance: Influence of CCR2 Pathways in Mice Liu, Cuiqing Xu, Xiaohua Bai, Yuntao Wang, Tse-Yao Rao, Xiaoquan Wang, Aixia Sun, Lixian Ying, Zhekang Gushchina, Liubov Maiseyeu, Andrei Morishita, Masako Sun, Qinghua Harkema, Jack R. Rajagopalan, Sanjay Environ Health Perspect Research Background: Epidemiologic and experimental studies support an association between PM(2.5) exposure and insulin resistance (IR). Innate immune cell activation has been suggested to play a role in the pathogenesis of these effects. Objectives: We sought to evaluate the role of CC-chemokine receptor 2 (CCR2) in PM(2.5)-mediated inflammation and IR. Methods: Wild-type C57BL/6 and CCR2(–/–) male mice were fed a high-fat diet and exposed to either concentrated ambient PM(2.5) or filtered air for 17 weeks via a whole-body exposure system. We evaluated glucose tolerance and insulin sensitivity. At euthanasia, blood, spleen, and visceral adipose tissue (VAT) were collected, and inflammatory cells were measured using flow cytometry. We used standard immunoblots, immunohistochemical methods, and quantitative PCR (polymerase chain reaction) to assess pathways of interest involving insulin signaling, inflammation, and lipid and glucose metabolism in various organs. Vascular function was assessed using myography. Results: PM(2.5) exposure resulted in whole-body IR and increased hepatic lipid accumulation in the liver, which was attenuated in CCR2(–/–) mice by inhibiting SREBP1c-mediated transcriptional programming, decreasing fatty acid uptake, and suppressing p38 MAPK activity. Abnormal phosphorylation levels of AKT, AMPK in VAT, and adipose tissue macrophage content in wild-type mice were not present in CCR2(–/–) mice. However, the impaired whole-body glucose tolerance and reduced GLUT-4 in skeletal muscle in response to PM(2.5) was not corrected by CCR2 deficiency. Conclusions: PM(2.5) mediates IR by regulating VAT inflammation, hepatic lipid metabolism, and glucose utilization in skeletal muscle via both CCR2-dependent and -independent pathways. These findings provide new mechanistic links between air pollution and metabolic abnormalities underlying IR. Citation: Liu C, Xu X, Bai Y, Wang TY, Rao X, Wang A, Sun L, Ying Z, Gushchina L, Maiseyeu A, Morishita M, Sun Q, Harkema JR, Rajagopalan S. 2014. Air pollution–mediated susceptibility to inflammation and insulin resistance: influence of CCR2 pathways in mice. Environ Health Perspect 122:17–26; http://dx.doi.org/10.1289/ehp.1306841 National Institute of Environmental Health Sciences 2013-10-22 2014-01-01 /pmc/articles/PMC3888572/ /pubmed/24149114 http://dx.doi.org/10.1289/ehp.1306841 Text en http://creativecommons.org/publicdomain/mark/1.0/ Publication of EHP lies in the public domain and is therefore without copyright. All text from EHP may be reprinted freely. Use of materials published in EHP should be acknowledged (for example, “Reproduced with permission from Environmental Health Perspectives”); pertinent reference information should be provided for the article from which the material was reproduced. Articles from EHP, especially the News section, may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright.
spellingShingle Research
Liu, Cuiqing
Xu, Xiaohua
Bai, Yuntao
Wang, Tse-Yao
Rao, Xiaoquan
Wang, Aixia
Sun, Lixian
Ying, Zhekang
Gushchina, Liubov
Maiseyeu, Andrei
Morishita, Masako
Sun, Qinghua
Harkema, Jack R.
Rajagopalan, Sanjay
Air Pollution–Mediated Susceptibility to Inflammation and Insulin Resistance: Influence of CCR2 Pathways in Mice
title Air Pollution–Mediated Susceptibility to Inflammation and Insulin Resistance: Influence of CCR2 Pathways in Mice
title_full Air Pollution–Mediated Susceptibility to Inflammation and Insulin Resistance: Influence of CCR2 Pathways in Mice
title_fullStr Air Pollution–Mediated Susceptibility to Inflammation and Insulin Resistance: Influence of CCR2 Pathways in Mice
title_full_unstemmed Air Pollution–Mediated Susceptibility to Inflammation and Insulin Resistance: Influence of CCR2 Pathways in Mice
title_short Air Pollution–Mediated Susceptibility to Inflammation and Insulin Resistance: Influence of CCR2 Pathways in Mice
title_sort air pollution–mediated susceptibility to inflammation and insulin resistance: influence of ccr2 pathways in mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888572/
https://www.ncbi.nlm.nih.gov/pubmed/24149114
http://dx.doi.org/10.1289/ehp.1306841
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