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North American ginseng influences adipocyte–macrophage crosstalk regulation of inflammatory gene expression

BACKGROUND: Adipocyte–macrophage communication plays a critical role regulating white adipose tissue (WAT) inflammatory gene expression. Because WAT inflammation contributes to the development of metabolic diseases, there is significant interest in understanding how exogenous compounds regulate the...

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Autores principales: Garbett, Jaime, Wilson, Sarah A.F., Ralston, Jessica C., De Boer, Anna A., Lui, Ed M.K., Wright, David C., Mutch, David M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4845049/
https://www.ncbi.nlm.nih.gov/pubmed/27158235
http://dx.doi.org/10.1016/j.jgr.2015.07.001
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author Garbett, Jaime
Wilson, Sarah A.F.
Ralston, Jessica C.
De Boer, Anna A.
Lui, Ed M.K.
Wright, David C.
Mutch, David M.
author_facet Garbett, Jaime
Wilson, Sarah A.F.
Ralston, Jessica C.
De Boer, Anna A.
Lui, Ed M.K.
Wright, David C.
Mutch, David M.
author_sort Garbett, Jaime
collection PubMed
description BACKGROUND: Adipocyte–macrophage communication plays a critical role regulating white adipose tissue (WAT) inflammatory gene expression. Because WAT inflammation contributes to the development of metabolic diseases, there is significant interest in understanding how exogenous compounds regulate the adipocyte–macrophage crosstalk. An aqueous (AQ) extract of North American (NA) ginseng (Panax quinquefolius) was previously shown to have strong inflammo-regulatory properties in adipocytes. This study examined whether different ginseng extracts influence adipocyte–macrophage crosstalk, as well as WAT inflammatory gene expression. METHODS: The effects of AQ and ethanol (EtOH) ginseng extracts (5 μg/mL) on adipocyte and macrophage inflammatory gene expression were studied in 3T3-L1 and RAW264.7 cells, respectively, using real-time reverse transcription polymerase chain reaction. Adipose tissue organ culture was also used to examine the effects of ginseng extracts on epididymal WAT (EWAT) and inguinal subcutaneous WAT (SWAT) inflammatory gene expression. RESULTS: The AQ extract caused significant increases in the expression of common inflammatory genes (e.g., Mcp1, Ccl5, Tnf-α, Nos2) in both cell types. Culturing adipocytes in media from macrophages treated with the AQ extract, and vice versa, also induced inflammatory gene expression. Adipocyte Ppar-γ expression was reduced with the AQ extract. The AQ extract strongly induced inflammatory gene expression in EWAT, but not in SWAT. The EtOH extract had no effect on inflammatory gene expression in either both cell types or WAT. CONCLUSION: These findings provide important new insights into the inflammo-regulatory role of NA ginseng in WAT.
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spelling pubmed-48450492016-05-06 North American ginseng influences adipocyte–macrophage crosstalk regulation of inflammatory gene expression Garbett, Jaime Wilson, Sarah A.F. Ralston, Jessica C. De Boer, Anna A. Lui, Ed M.K. Wright, David C. Mutch, David M. J Ginseng Res Research Article BACKGROUND: Adipocyte–macrophage communication plays a critical role regulating white adipose tissue (WAT) inflammatory gene expression. Because WAT inflammation contributes to the development of metabolic diseases, there is significant interest in understanding how exogenous compounds regulate the adipocyte–macrophage crosstalk. An aqueous (AQ) extract of North American (NA) ginseng (Panax quinquefolius) was previously shown to have strong inflammo-regulatory properties in adipocytes. This study examined whether different ginseng extracts influence adipocyte–macrophage crosstalk, as well as WAT inflammatory gene expression. METHODS: The effects of AQ and ethanol (EtOH) ginseng extracts (5 μg/mL) on adipocyte and macrophage inflammatory gene expression were studied in 3T3-L1 and RAW264.7 cells, respectively, using real-time reverse transcription polymerase chain reaction. Adipose tissue organ culture was also used to examine the effects of ginseng extracts on epididymal WAT (EWAT) and inguinal subcutaneous WAT (SWAT) inflammatory gene expression. RESULTS: The AQ extract caused significant increases in the expression of common inflammatory genes (e.g., Mcp1, Ccl5, Tnf-α, Nos2) in both cell types. Culturing adipocytes in media from macrophages treated with the AQ extract, and vice versa, also induced inflammatory gene expression. Adipocyte Ppar-γ expression was reduced with the AQ extract. The AQ extract strongly induced inflammatory gene expression in EWAT, but not in SWAT. The EtOH extract had no effect on inflammatory gene expression in either both cell types or WAT. CONCLUSION: These findings provide important new insights into the inflammo-regulatory role of NA ginseng in WAT. Elsevier 2016-04 2015-07-18 /pmc/articles/PMC4845049/ /pubmed/27158235 http://dx.doi.org/10.1016/j.jgr.2015.07.001 Text en Copyright 2015, The Korean Society of Ginseng, Published by Elsevier. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Garbett, Jaime
Wilson, Sarah A.F.
Ralston, Jessica C.
De Boer, Anna A.
Lui, Ed M.K.
Wright, David C.
Mutch, David M.
North American ginseng influences adipocyte–macrophage crosstalk regulation of inflammatory gene expression
title North American ginseng influences adipocyte–macrophage crosstalk regulation of inflammatory gene expression
title_full North American ginseng influences adipocyte–macrophage crosstalk regulation of inflammatory gene expression
title_fullStr North American ginseng influences adipocyte–macrophage crosstalk regulation of inflammatory gene expression
title_full_unstemmed North American ginseng influences adipocyte–macrophage crosstalk regulation of inflammatory gene expression
title_short North American ginseng influences adipocyte–macrophage crosstalk regulation of inflammatory gene expression
title_sort north american ginseng influences adipocyte–macrophage crosstalk regulation of inflammatory gene expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4845049/
https://www.ncbi.nlm.nih.gov/pubmed/27158235
http://dx.doi.org/10.1016/j.jgr.2015.07.001
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