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Helminth infection modulates number and function of adipose tissue Tregs in high fat diet-induced obesity

BACKGROUND: Epidemiological and experimental studies have shown a protective effect of helminth infections in weight gain and against the development of metabolic dysfunctions in the host. However, the mechanisms Treg cells exert in the helminth-obesity interface has been poorly investigated. The pr...

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Autores principales: Queiroz-Glauss, Camila P., Vieira, Mariana S., Gonçalves-Pereira, Marcela Helena, Almeida, Stephanie S., Freire, Rachel H., Gomes, Maria A., Alvarez-Leite, Jacqueline I., Santiago, Helton C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098094/
https://www.ncbi.nlm.nih.gov/pubmed/35499991
http://dx.doi.org/10.1371/journal.pntd.0010105
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author Queiroz-Glauss, Camila P.
Vieira, Mariana S.
Gonçalves-Pereira, Marcela Helena
Almeida, Stephanie S.
Freire, Rachel H.
Gomes, Maria A.
Alvarez-Leite, Jacqueline I.
Santiago, Helton C.
author_facet Queiroz-Glauss, Camila P.
Vieira, Mariana S.
Gonçalves-Pereira, Marcela Helena
Almeida, Stephanie S.
Freire, Rachel H.
Gomes, Maria A.
Alvarez-Leite, Jacqueline I.
Santiago, Helton C.
author_sort Queiroz-Glauss, Camila P.
collection PubMed
description BACKGROUND: Epidemiological and experimental studies have shown a protective effect of helminth infections in weight gain and against the development of metabolic dysfunctions in the host. However, the mechanisms Treg cells exert in the helminth-obesity interface has been poorly investigated. The present study aimed to verify the influence of Heligmosomoides polygyrus infection in early stages of high fat diet-induced obesity. PRINCIPAL FINDINGS: The presence of infection was able to prevent exacerbated weight gain in mice fed with high fat diet when compared to non-infected controls. In addition, infected animals displayed improved insulin sensitivity and decreased fat accumulation in the liver. Obesity-associated inflammation was reduced in the presence of infection, demonstrated by lower levels of leptin and resistin, lower infiltration of Th1 and Th17 cells in adipose tissue, higher expression of IL10 and adiponectin, increased infiltration of Th2 and eosinophils in adipose tissue of infected animals. Of note, the parasite infection was associated with increased Treg frequency in adipose tissue which showed higher expression of cell surface markers of function and activation, like LAP and CD134. The infection could also increase adipose Treg suppressor function in animals on high fat diet. CONCLUSION: These data suggest that H. polygyrus modulates adipose tissue Treg cells with implication for weight gain and metabolic syndrome.
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spelling pubmed-90980942022-05-13 Helminth infection modulates number and function of adipose tissue Tregs in high fat diet-induced obesity Queiroz-Glauss, Camila P. Vieira, Mariana S. Gonçalves-Pereira, Marcela Helena Almeida, Stephanie S. Freire, Rachel H. Gomes, Maria A. Alvarez-Leite, Jacqueline I. Santiago, Helton C. PLoS Negl Trop Dis Research Article BACKGROUND: Epidemiological and experimental studies have shown a protective effect of helminth infections in weight gain and against the development of metabolic dysfunctions in the host. However, the mechanisms Treg cells exert in the helminth-obesity interface has been poorly investigated. The present study aimed to verify the influence of Heligmosomoides polygyrus infection in early stages of high fat diet-induced obesity. PRINCIPAL FINDINGS: The presence of infection was able to prevent exacerbated weight gain in mice fed with high fat diet when compared to non-infected controls. In addition, infected animals displayed improved insulin sensitivity and decreased fat accumulation in the liver. Obesity-associated inflammation was reduced in the presence of infection, demonstrated by lower levels of leptin and resistin, lower infiltration of Th1 and Th17 cells in adipose tissue, higher expression of IL10 and adiponectin, increased infiltration of Th2 and eosinophils in adipose tissue of infected animals. Of note, the parasite infection was associated with increased Treg frequency in adipose tissue which showed higher expression of cell surface markers of function and activation, like LAP and CD134. The infection could also increase adipose Treg suppressor function in animals on high fat diet. CONCLUSION: These data suggest that H. polygyrus modulates adipose tissue Treg cells with implication for weight gain and metabolic syndrome. Public Library of Science 2022-05-02 /pmc/articles/PMC9098094/ /pubmed/35499991 http://dx.doi.org/10.1371/journal.pntd.0010105 Text en © 2022 Queiroz-Glauss et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Queiroz-Glauss, Camila P.
Vieira, Mariana S.
Gonçalves-Pereira, Marcela Helena
Almeida, Stephanie S.
Freire, Rachel H.
Gomes, Maria A.
Alvarez-Leite, Jacqueline I.
Santiago, Helton C.
Helminth infection modulates number and function of adipose tissue Tregs in high fat diet-induced obesity
title Helminth infection modulates number and function of adipose tissue Tregs in high fat diet-induced obesity
title_full Helminth infection modulates number and function of adipose tissue Tregs in high fat diet-induced obesity
title_fullStr Helminth infection modulates number and function of adipose tissue Tregs in high fat diet-induced obesity
title_full_unstemmed Helminth infection modulates number and function of adipose tissue Tregs in high fat diet-induced obesity
title_short Helminth infection modulates number and function of adipose tissue Tregs in high fat diet-induced obesity
title_sort helminth infection modulates number and function of adipose tissue tregs in high fat diet-induced obesity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098094/
https://www.ncbi.nlm.nih.gov/pubmed/35499991
http://dx.doi.org/10.1371/journal.pntd.0010105
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