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Global transcriptome analysis identifies weight regain-induced activation of adaptive immune responses in white adipose tissue of mice

OBJECTIVE: Studies have indicated that weight regain following weight loss predisposes obese individuals to metabolic disorders; however, the molecular mechanism of this potential adverse effect of weight regain is not fully understood. Here we investigated global transcriptome changes and the immun...

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Autores principales: Kyung, D S, Sung, H R, Kim, Y J, Kim, K D, Cho, S Y, Choi, J H, Lee, Y-H, Kim, I Y, Seong, J K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984075/
https://www.ncbi.nlm.nih.gov/pubmed/29762555
http://dx.doi.org/10.1038/ijo.2017.297
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author Kyung, D S
Sung, H R
Kim, Y J
Kim, K D
Cho, S Y
Choi, J H
Lee, Y-H
Kim, I Y
Seong, J K
author_facet Kyung, D S
Sung, H R
Kim, Y J
Kim, K D
Cho, S Y
Choi, J H
Lee, Y-H
Kim, I Y
Seong, J K
author_sort Kyung, D S
collection PubMed
description OBJECTIVE: Studies have indicated that weight regain following weight loss predisposes obese individuals to metabolic disorders; however, the molecular mechanism of this potential adverse effect of weight regain is not fully understood. Here we investigated global transcriptome changes and the immune response in mouse white adipose tissue caused by weight regain. DESIGN: We established a diet switch protocol to compare the effects of weight regain with those of weight gain without precedent weight loss, weight loss maintenance and chow diet. We conducted a time course analysis of global transcriptome changes in gonadal white adipose tissue (gWAT) during the weight fluctuation. Co-expression network analysis was used to identify functional modules associated with the weigh regain phenotype. Immune cell populations in gWAT were characterized by flow-cytometric immunophenotyping. Metabolic phenotypes were monitored by histological analysis of adipose tissue and liver, and blood-chemistry and body weight/composition analyses. RESULTS: In total, 952 genes were differentially expressed in the gWAT in the weight regain vs the weight gain group. Upregulated genes were associated with immune response and leukocyte activation. Co-expression network analysis showed that genes involved in major histocompatibility complex I and II-mediated antigen presentation and T-cell activation function were upregulated. Consistent with the transcriptome analysis results, flow cytometry demonstrated significant increases in subsets of T cells and proinflammatory M1 macrophages in the gWAT in the weight regain as compared to the weight gain group. In addition, upregulation of adaptive immune responses was associated with high incidence of adipocyte death and upregulation of high mobility group box 1, a well-known component of damage-associated molecular patterns. CONCLUSIONS: Our global transcriptome analysis identified weight regain-induced activation of adaptive immune responses in mouse white adipose tissue. Results suggest that activation of adipocyte death-associated adaptive immunity in adipose tissue may contribute to unfavorable metabolic effects of weight regain following weight loss.
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spelling pubmed-59840752018-06-04 Global transcriptome analysis identifies weight regain-induced activation of adaptive immune responses in white adipose tissue of mice Kyung, D S Sung, H R Kim, Y J Kim, K D Cho, S Y Choi, J H Lee, Y-H Kim, I Y Seong, J K Int J Obes (Lond) Original Article OBJECTIVE: Studies have indicated that weight regain following weight loss predisposes obese individuals to metabolic disorders; however, the molecular mechanism of this potential adverse effect of weight regain is not fully understood. Here we investigated global transcriptome changes and the immune response in mouse white adipose tissue caused by weight regain. DESIGN: We established a diet switch protocol to compare the effects of weight regain with those of weight gain without precedent weight loss, weight loss maintenance and chow diet. We conducted a time course analysis of global transcriptome changes in gonadal white adipose tissue (gWAT) during the weight fluctuation. Co-expression network analysis was used to identify functional modules associated with the weigh regain phenotype. Immune cell populations in gWAT were characterized by flow-cytometric immunophenotyping. Metabolic phenotypes were monitored by histological analysis of adipose tissue and liver, and blood-chemistry and body weight/composition analyses. RESULTS: In total, 952 genes were differentially expressed in the gWAT in the weight regain vs the weight gain group. Upregulated genes were associated with immune response and leukocyte activation. Co-expression network analysis showed that genes involved in major histocompatibility complex I and II-mediated antigen presentation and T-cell activation function were upregulated. Consistent with the transcriptome analysis results, flow cytometry demonstrated significant increases in subsets of T cells and proinflammatory M1 macrophages in the gWAT in the weight regain as compared to the weight gain group. In addition, upregulation of adaptive immune responses was associated with high incidence of adipocyte death and upregulation of high mobility group box 1, a well-known component of damage-associated molecular patterns. CONCLUSIONS: Our global transcriptome analysis identified weight regain-induced activation of adaptive immune responses in mouse white adipose tissue. Results suggest that activation of adipocyte death-associated adaptive immunity in adipose tissue may contribute to unfavorable metabolic effects of weight regain following weight loss. Nature Publishing Group 2018-04 2018-05-15 /pmc/articles/PMC5984075/ /pubmed/29762555 http://dx.doi.org/10.1038/ijo.2017.297 Text en Copyright © 2018 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Original Article
Kyung, D S
Sung, H R
Kim, Y J
Kim, K D
Cho, S Y
Choi, J H
Lee, Y-H
Kim, I Y
Seong, J K
Global transcriptome analysis identifies weight regain-induced activation of adaptive immune responses in white adipose tissue of mice
title Global transcriptome analysis identifies weight regain-induced activation of adaptive immune responses in white adipose tissue of mice
title_full Global transcriptome analysis identifies weight regain-induced activation of adaptive immune responses in white adipose tissue of mice
title_fullStr Global transcriptome analysis identifies weight regain-induced activation of adaptive immune responses in white adipose tissue of mice
title_full_unstemmed Global transcriptome analysis identifies weight regain-induced activation of adaptive immune responses in white adipose tissue of mice
title_short Global transcriptome analysis identifies weight regain-induced activation of adaptive immune responses in white adipose tissue of mice
title_sort global transcriptome analysis identifies weight regain-induced activation of adaptive immune responses in white adipose tissue of mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984075/
https://www.ncbi.nlm.nih.gov/pubmed/29762555
http://dx.doi.org/10.1038/ijo.2017.297
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