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Gender-dimorphic effects of adipose-derived stromal vascular fractions on HUVECs exposed to oxidative stress

Stromal vascular fractions (SVFs) are a heterogeneous collection of cells within adipose tissue that are being studied for various clinical indications. In this study, we aimed to determine whether SVF transplantation into impaired tissues has differential effects on inflammatory and angiogenetic pr...

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Autores principales: Lim, Soyeon, Kim, Il-Kwon, Choi, Jung-Won, Seo, Hyang-Hee, Lim, Kyu Hee, Lee, Seahyoung, Lee, Hoon-Bum, Kim, Sang Woo, Hwang, Ki-Chul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562200/
https://www.ncbi.nlm.nih.gov/pubmed/28824330
http://dx.doi.org/10.7150/ijms.19998
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author Lim, Soyeon
Kim, Il-Kwon
Choi, Jung-Won
Seo, Hyang-Hee
Lim, Kyu Hee
Lee, Seahyoung
Lee, Hoon-Bum
Kim, Sang Woo
Hwang, Ki-Chul
author_facet Lim, Soyeon
Kim, Il-Kwon
Choi, Jung-Won
Seo, Hyang-Hee
Lim, Kyu Hee
Lee, Seahyoung
Lee, Hoon-Bum
Kim, Sang Woo
Hwang, Ki-Chul
author_sort Lim, Soyeon
collection PubMed
description Stromal vascular fractions (SVFs) are a heterogeneous collection of cells within adipose tissue that are being studied for various clinical indications. In this study, we aimed to determine whether SVF transplantation into impaired tissues has differential effects on inflammatory and angiogenetic properties with regard to gender. As reactive oxygen species have been implicated in cardiovascular disease development, we investigated differences in gene and protein expression related to inflammation and angiogenesis in HUVECs co-cultured with adipose-derived SVFs from male (M group) and female (F group) individuals under oxidative stress conditions. The expression of several inflammatory (interleukin (IL)-33) and angiogenetic (platelet-derived growth factor (PDGF)) factors differed dramatically between male and female donors. Anti-inflammatory and pro-angiogenetic responses were observed in HUVECs co-cultured with SVFs under oxidative stress conditions, and these characteristics may exhibit partially differential effects according to gender. Using network analysis, we showed that co-culturing HUVECs with SVFs ameliorated pyroptosis/apoptosis via an increase in oxidative stress. Activation of caspase-1 and IL-1B was significantly altered in HUVECs co-cultured with SVFs from female donors. These findings regarding gender-dimorphic regulation of adipose-derived SVFs provide valuable information that can be used for evidence-based gender-specific clinical treatment of SVF transplantation for understanding of cardiovascular disease, allowing for the development of additional treatment.
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spelling pubmed-55622002017-08-18 Gender-dimorphic effects of adipose-derived stromal vascular fractions on HUVECs exposed to oxidative stress Lim, Soyeon Kim, Il-Kwon Choi, Jung-Won Seo, Hyang-Hee Lim, Kyu Hee Lee, Seahyoung Lee, Hoon-Bum Kim, Sang Woo Hwang, Ki-Chul Int J Med Sci Research Paper Stromal vascular fractions (SVFs) are a heterogeneous collection of cells within adipose tissue that are being studied for various clinical indications. In this study, we aimed to determine whether SVF transplantation into impaired tissues has differential effects on inflammatory and angiogenetic properties with regard to gender. As reactive oxygen species have been implicated in cardiovascular disease development, we investigated differences in gene and protein expression related to inflammation and angiogenesis in HUVECs co-cultured with adipose-derived SVFs from male (M group) and female (F group) individuals under oxidative stress conditions. The expression of several inflammatory (interleukin (IL)-33) and angiogenetic (platelet-derived growth factor (PDGF)) factors differed dramatically between male and female donors. Anti-inflammatory and pro-angiogenetic responses were observed in HUVECs co-cultured with SVFs under oxidative stress conditions, and these characteristics may exhibit partially differential effects according to gender. Using network analysis, we showed that co-culturing HUVECs with SVFs ameliorated pyroptosis/apoptosis via an increase in oxidative stress. Activation of caspase-1 and IL-1B was significantly altered in HUVECs co-cultured with SVFs from female donors. These findings regarding gender-dimorphic regulation of adipose-derived SVFs provide valuable information that can be used for evidence-based gender-specific clinical treatment of SVF transplantation for understanding of cardiovascular disease, allowing for the development of additional treatment. Ivyspring International Publisher 2017-07-20 /pmc/articles/PMC5562200/ /pubmed/28824330 http://dx.doi.org/10.7150/ijms.19998 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Lim, Soyeon
Kim, Il-Kwon
Choi, Jung-Won
Seo, Hyang-Hee
Lim, Kyu Hee
Lee, Seahyoung
Lee, Hoon-Bum
Kim, Sang Woo
Hwang, Ki-Chul
Gender-dimorphic effects of adipose-derived stromal vascular fractions on HUVECs exposed to oxidative stress
title Gender-dimorphic effects of adipose-derived stromal vascular fractions on HUVECs exposed to oxidative stress
title_full Gender-dimorphic effects of adipose-derived stromal vascular fractions on HUVECs exposed to oxidative stress
title_fullStr Gender-dimorphic effects of adipose-derived stromal vascular fractions on HUVECs exposed to oxidative stress
title_full_unstemmed Gender-dimorphic effects of adipose-derived stromal vascular fractions on HUVECs exposed to oxidative stress
title_short Gender-dimorphic effects of adipose-derived stromal vascular fractions on HUVECs exposed to oxidative stress
title_sort gender-dimorphic effects of adipose-derived stromal vascular fractions on huvecs exposed to oxidative stress
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562200/
https://www.ncbi.nlm.nih.gov/pubmed/28824330
http://dx.doi.org/10.7150/ijms.19998
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