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Hypoxia Rapidly Induces the Expression of Cardiomyogenic Factors in Human Adipose-Derived Adherent Stromal Cells

Background: The efficacy of interstitial vascular fraction (SVF) transplantation in the treatment of heart disease has been proven in a variety of in vivo studies. In a previous study, we found that bone marrow-derived mesenchymal stem cells (BM-MSCs) altered their expression of several cardiomyogen...

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Autores principales: Choi, Jung-Won, Moon, Hanbyeol, Jung, Seung Eun, Lim, Soyeon, Lee, Seahyoung, Kim, Il-Kwon, Lee, Hoon-Bum, Lee, Jiyun, Song, Byeong-Wook, Kim, Sang Woo, Hwang, Ki-Chul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6723458/
https://www.ncbi.nlm.nih.gov/pubmed/31443313
http://dx.doi.org/10.3390/jcm8081231
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author Choi, Jung-Won
Moon, Hanbyeol
Jung, Seung Eun
Lim, Soyeon
Lee, Seahyoung
Kim, Il-Kwon
Lee, Hoon-Bum
Lee, Jiyun
Song, Byeong-Wook
Kim, Sang Woo
Hwang, Ki-Chul
author_facet Choi, Jung-Won
Moon, Hanbyeol
Jung, Seung Eun
Lim, Soyeon
Lee, Seahyoung
Kim, Il-Kwon
Lee, Hoon-Bum
Lee, Jiyun
Song, Byeong-Wook
Kim, Sang Woo
Hwang, Ki-Chul
author_sort Choi, Jung-Won
collection PubMed
description Background: The efficacy of interstitial vascular fraction (SVF) transplantation in the treatment of heart disease has been proven in a variety of in vivo studies. In a previous study, we found that bone marrow-derived mesenchymal stem cells (BM-MSCs) altered their expression of several cardiomyogenic factors under hypoxic conditions. Methods: We hypothesized that hypoxia may also induce obtained adipose-derived adherent stromal cells (ADASs) from SVFs and adipose-derived stem cells (ASCs) to differentiate into cardiomyocytes and/or cells with comparable phenotypes. We examined the differentiation markers of cell lineages in ADASs and ASCs according to time by hypoxic stress and found that only ADASs expressed cardiomyogenic markers within 24 h under hypoxic conditions in association with the expression of hypoxia-inducible factor 1-α (HIF-1α). Results: Differentially secreted proteins in a conditioned medium (CM) from ASCs and ADASs under normoxic or hypoxic conditions were detected using an antibody assay and may be associated with a dramatic increase in the expression of cardiomyogenic markers in only ADASs. Furthermore, the cardiomyogenic factors were expressed more rapidly in ADASs than in ASCs under hypoxic conditions in association with the expression of HIF-1α, and angiogenin, fibroblast growth factor-19 (FGF-19) and/or macrophage inhibitory factor (MIF) are related. Conclusions: These results provide new insights into the applicability of ADASs preconditioned by hypoxic stress in cardiac diseases.
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spelling pubmed-67234582019-09-10 Hypoxia Rapidly Induces the Expression of Cardiomyogenic Factors in Human Adipose-Derived Adherent Stromal Cells Choi, Jung-Won Moon, Hanbyeol Jung, Seung Eun Lim, Soyeon Lee, Seahyoung Kim, Il-Kwon Lee, Hoon-Bum Lee, Jiyun Song, Byeong-Wook Kim, Sang Woo Hwang, Ki-Chul J Clin Med Article Background: The efficacy of interstitial vascular fraction (SVF) transplantation in the treatment of heart disease has been proven in a variety of in vivo studies. In a previous study, we found that bone marrow-derived mesenchymal stem cells (BM-MSCs) altered their expression of several cardiomyogenic factors under hypoxic conditions. Methods: We hypothesized that hypoxia may also induce obtained adipose-derived adherent stromal cells (ADASs) from SVFs and adipose-derived stem cells (ASCs) to differentiate into cardiomyocytes and/or cells with comparable phenotypes. We examined the differentiation markers of cell lineages in ADASs and ASCs according to time by hypoxic stress and found that only ADASs expressed cardiomyogenic markers within 24 h under hypoxic conditions in association with the expression of hypoxia-inducible factor 1-α (HIF-1α). Results: Differentially secreted proteins in a conditioned medium (CM) from ASCs and ADASs under normoxic or hypoxic conditions were detected using an antibody assay and may be associated with a dramatic increase in the expression of cardiomyogenic markers in only ADASs. Furthermore, the cardiomyogenic factors were expressed more rapidly in ADASs than in ASCs under hypoxic conditions in association with the expression of HIF-1α, and angiogenin, fibroblast growth factor-19 (FGF-19) and/or macrophage inhibitory factor (MIF) are related. Conclusions: These results provide new insights into the applicability of ADASs preconditioned by hypoxic stress in cardiac diseases. MDPI 2019-08-15 /pmc/articles/PMC6723458/ /pubmed/31443313 http://dx.doi.org/10.3390/jcm8081231 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Choi, Jung-Won
Moon, Hanbyeol
Jung, Seung Eun
Lim, Soyeon
Lee, Seahyoung
Kim, Il-Kwon
Lee, Hoon-Bum
Lee, Jiyun
Song, Byeong-Wook
Kim, Sang Woo
Hwang, Ki-Chul
Hypoxia Rapidly Induces the Expression of Cardiomyogenic Factors in Human Adipose-Derived Adherent Stromal Cells
title Hypoxia Rapidly Induces the Expression of Cardiomyogenic Factors in Human Adipose-Derived Adherent Stromal Cells
title_full Hypoxia Rapidly Induces the Expression of Cardiomyogenic Factors in Human Adipose-Derived Adherent Stromal Cells
title_fullStr Hypoxia Rapidly Induces the Expression of Cardiomyogenic Factors in Human Adipose-Derived Adherent Stromal Cells
title_full_unstemmed Hypoxia Rapidly Induces the Expression of Cardiomyogenic Factors in Human Adipose-Derived Adherent Stromal Cells
title_short Hypoxia Rapidly Induces the Expression of Cardiomyogenic Factors in Human Adipose-Derived Adherent Stromal Cells
title_sort hypoxia rapidly induces the expression of cardiomyogenic factors in human adipose-derived adherent stromal cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6723458/
https://www.ncbi.nlm.nih.gov/pubmed/31443313
http://dx.doi.org/10.3390/jcm8081231
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