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RASSF6 Expression in Adipocytes Is Down-Regulated by Interaction with Macrophages

Macrophage infiltration into adipose tissue is associated with obesity and the crosstalk between adipocytes and infiltrated macrophages has been investigated as an important pathological phenomenon during adipose tissue inflammation. Here, we sought to identify adipocyte mRNAs that are regulated by...

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Autores principales: Sanada, Yohei, Kumoto, Takahiro, Suehiro, Haruna, Nishimura, Fusanori, Kato, Norihisa, Hata, Yutaka, Sorisky, Alexander, Yanaka, Noriyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3633988/
https://www.ncbi.nlm.nih.gov/pubmed/23626755
http://dx.doi.org/10.1371/journal.pone.0061931
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author Sanada, Yohei
Kumoto, Takahiro
Suehiro, Haruna
Nishimura, Fusanori
Kato, Norihisa
Hata, Yutaka
Sorisky, Alexander
Yanaka, Noriyuki
author_facet Sanada, Yohei
Kumoto, Takahiro
Suehiro, Haruna
Nishimura, Fusanori
Kato, Norihisa
Hata, Yutaka
Sorisky, Alexander
Yanaka, Noriyuki
author_sort Sanada, Yohei
collection PubMed
description Macrophage infiltration into adipose tissue is associated with obesity and the crosstalk between adipocytes and infiltrated macrophages has been investigated as an important pathological phenomenon during adipose tissue inflammation. Here, we sought to identify adipocyte mRNAs that are regulated by interaction with infiltrated macrophages in vivo. An anti-inflammatory vitamin, vitamin B6, suppressed macrophage infiltration into white adipose tissue and altered mRNA expression. We identified >3500 genes whose expression is significantly altered during the development of obesity in db/db mice, and compared them to the adipose tissue mRNA expression profile of mice supplemented with vitamin B6. We identified PTX3 and MMP3 as candidate genes regulated by macrophage infiltration. PTX3 and MMP3 mRNA expression in 3T3-L1 adipocytes was up-regulated by activated RAW264.7 cells and these mRNA levels were positively correlated with macrophage number in adipose tissue in vivo. Next, we screened adipose genes down-regulated by the interaction with macrophages, and isolated RASSF6 (Ras association domain family 6). RASSF6 mRNA in adipocytes was decreased by culture medium conditioned by activated RAW264.7 cells, and RASSF6 mRNA level was negatively correlated with macrophage number in adipose tissue, suggesting that adipocyte RASSF6 mRNA expression is down-regulated by infiltrated macrophages in vivo. Finally, this study also showed that decreased RASSF6 expression up-regulates mRNA expression of several genes, such as CD44 and high mobility group protein HMGA2. These data provide novel insights into the biological significance of interactions between adipocytes and macrophages in adipose tissue during the development of obesity.
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spelling pubmed-36339882013-04-26 RASSF6 Expression in Adipocytes Is Down-Regulated by Interaction with Macrophages Sanada, Yohei Kumoto, Takahiro Suehiro, Haruna Nishimura, Fusanori Kato, Norihisa Hata, Yutaka Sorisky, Alexander Yanaka, Noriyuki PLoS One Research Article Macrophage infiltration into adipose tissue is associated with obesity and the crosstalk between adipocytes and infiltrated macrophages has been investigated as an important pathological phenomenon during adipose tissue inflammation. Here, we sought to identify adipocyte mRNAs that are regulated by interaction with infiltrated macrophages in vivo. An anti-inflammatory vitamin, vitamin B6, suppressed macrophage infiltration into white adipose tissue and altered mRNA expression. We identified >3500 genes whose expression is significantly altered during the development of obesity in db/db mice, and compared them to the adipose tissue mRNA expression profile of mice supplemented with vitamin B6. We identified PTX3 and MMP3 as candidate genes regulated by macrophage infiltration. PTX3 and MMP3 mRNA expression in 3T3-L1 adipocytes was up-regulated by activated RAW264.7 cells and these mRNA levels were positively correlated with macrophage number in adipose tissue in vivo. Next, we screened adipose genes down-regulated by the interaction with macrophages, and isolated RASSF6 (Ras association domain family 6). RASSF6 mRNA in adipocytes was decreased by culture medium conditioned by activated RAW264.7 cells, and RASSF6 mRNA level was negatively correlated with macrophage number in adipose tissue, suggesting that adipocyte RASSF6 mRNA expression is down-regulated by infiltrated macrophages in vivo. Finally, this study also showed that decreased RASSF6 expression up-regulates mRNA expression of several genes, such as CD44 and high mobility group protein HMGA2. These data provide novel insights into the biological significance of interactions between adipocytes and macrophages in adipose tissue during the development of obesity. Public Library of Science 2013-04-23 /pmc/articles/PMC3633988/ /pubmed/23626755 http://dx.doi.org/10.1371/journal.pone.0061931 Text en © 2013 Sanada et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Sanada, Yohei
Kumoto, Takahiro
Suehiro, Haruna
Nishimura, Fusanori
Kato, Norihisa
Hata, Yutaka
Sorisky, Alexander
Yanaka, Noriyuki
RASSF6 Expression in Adipocytes Is Down-Regulated by Interaction with Macrophages
title RASSF6 Expression in Adipocytes Is Down-Regulated by Interaction with Macrophages
title_full RASSF6 Expression in Adipocytes Is Down-Regulated by Interaction with Macrophages
title_fullStr RASSF6 Expression in Adipocytes Is Down-Regulated by Interaction with Macrophages
title_full_unstemmed RASSF6 Expression in Adipocytes Is Down-Regulated by Interaction with Macrophages
title_short RASSF6 Expression in Adipocytes Is Down-Regulated by Interaction with Macrophages
title_sort rassf6 expression in adipocytes is down-regulated by interaction with macrophages
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3633988/
https://www.ncbi.nlm.nih.gov/pubmed/23626755
http://dx.doi.org/10.1371/journal.pone.0061931
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