Effects of High-Mobility Group A Protein Application on Canine Adipose-Derived Mesenchymal Stem Cells In Vitro

Multipotency and self-renewal are considered as most important features of stem cells to persist throughout life in tissues. In this context, the role of HMGA proteins to influence proliferation of adipose-derived mesenchymal stem cell (ASCs) while maintaining their multipotent and self-renewal cap...

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Main Authors: A. A. Ismail, S. Wagner, H. Murua Escobar, S. Willenbrock, K. A. Sterenczak, M. T. Samy, A. M. Abd El-Aal, I. Nolte, P. Wefstaedt
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:Veterinary Medicine International
Online Access:http://dx.doi.org/10.1155/2012/752083
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author A. A. Ismail
S. Wagner
H. Murua Escobar
S. Willenbrock
K. A. Sterenczak
M. T. Samy
A. M. Abd El-Aal
I. Nolte
P. Wefstaedt
author_facet A. A. Ismail
S. Wagner
H. Murua Escobar
S. Willenbrock
K. A. Sterenczak
M. T. Samy
A. M. Abd El-Aal
I. Nolte
P. Wefstaedt
author_sort A. A. Ismail
collection DOAJ
description Multipotency and self-renewal are considered as most important features of stem cells to persist throughout life in tissues. In this context, the role of HMGA proteins to influence proliferation of adipose-derived mesenchymal stem cell (ASCs) while maintaining their multipotent and self-renewal capacities has not yet been investigated. Therefore, extracellular HMGA1 and HMGA2 application alone (10–200 ng/mL) and in combination with each other (100, 200 ng/mL each) was investigated with regard to proliferative effects on canine ASCs (cASCs) after 48 hours of cultivation. Furthermore, mRNA expression of multipotency marker genes in unstimulated and HMGA2-stimulated cASCs (50, 100 ng/mL) was analyzed by RT-qPCR. HMGA1 significantly reduced cASCs proliferation in concentrations of 10–200 ng/mL culture medium. A combination of HMGA1 and HMGA2 protein (100 and 200 ng/mL each) caused the same effects, whereas no significant effect on cASCs proliferation was shown after HMGA2 protein application alone. RT-qPCR results showed that expression levels of marker genes including KLF4, SOX2, OCT4, HMGA2, and cMYC mRNAs were on the same level in both HMGA2-protein-stimulated and -unstimulated cASCs. Extracellular HMGA protein application might be valuable to control proliferation of cASCs in context with their employment in regenerative approaches without affecting their self-renewal and multipotency abilities.
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spelling doaj-art-7f8176b210ef407796ffa5d1c06b9e302025-08-20T03:35:20ZengWileyVeterinary Medicine International2090-81132042-00482012-01-01201210.1155/2012/752083752083Effects of High-Mobility Group A Protein Application on Canine Adipose-Derived Mesenchymal Stem Cells In VitroA. A. Ismail0S. Wagner1H. Murua Escobar2S. Willenbrock3K. A. Sterenczak4M. T. Samy5A. M. Abd El-Aal6I. Nolte7P. Wefstaedt8Small Animal Hospital, University of Veterinary Medicine Foundation, 30559 Hannover, GermanySmall Animal Hospital, University of Veterinary Medicine Foundation, 30559 Hannover, GermanySmall Animal Hospital, University of Veterinary Medicine Foundation, 30559 Hannover, GermanySmall Animal Hospital, University of Veterinary Medicine Foundation, 30559 Hannover, GermanySmall Animal Hospital, University of Veterinary Medicine Foundation, 30559 Hannover, GermanyDepartment of Surgery, Anesthesiology and Radiology, Faculty of Veterinary Medicine, Zagazig University, El-Sharkia, EgyptDepartment of Surgery, Anesthesiology and Radiology, Faculty of Veterinary Medicine, Zagazig University, El-Sharkia, EgyptSmall Animal Hospital, University of Veterinary Medicine Foundation, 30559 Hannover, GermanySmall Animal Hospital, University of Veterinary Medicine Foundation, 30559 Hannover, GermanyMultipotency and self-renewal are considered as most important features of stem cells to persist throughout life in tissues. In this context, the role of HMGA proteins to influence proliferation of adipose-derived mesenchymal stem cell (ASCs) while maintaining their multipotent and self-renewal capacities has not yet been investigated. Therefore, extracellular HMGA1 and HMGA2 application alone (10–200 ng/mL) and in combination with each other (100, 200 ng/mL each) was investigated with regard to proliferative effects on canine ASCs (cASCs) after 48 hours of cultivation. Furthermore, mRNA expression of multipotency marker genes in unstimulated and HMGA2-stimulated cASCs (50, 100 ng/mL) was analyzed by RT-qPCR. HMGA1 significantly reduced cASCs proliferation in concentrations of 10–200 ng/mL culture medium. A combination of HMGA1 and HMGA2 protein (100 and 200 ng/mL each) caused the same effects, whereas no significant effect on cASCs proliferation was shown after HMGA2 protein application alone. RT-qPCR results showed that expression levels of marker genes including KLF4, SOX2, OCT4, HMGA2, and cMYC mRNAs were on the same level in both HMGA2-protein-stimulated and -unstimulated cASCs. Extracellular HMGA protein application might be valuable to control proliferation of cASCs in context with their employment in regenerative approaches without affecting their self-renewal and multipotency abilities.http://dx.doi.org/10.1155/2012/752083
spellingShingle A. A. Ismail
S. Wagner
H. Murua Escobar
S. Willenbrock
K. A. Sterenczak
M. T. Samy
A. M. Abd El-Aal
I. Nolte
P. Wefstaedt
Effects of High-Mobility Group A Protein Application on Canine Adipose-Derived Mesenchymal Stem Cells In Vitro
Veterinary Medicine International
title Effects of High-Mobility Group A Protein Application on Canine Adipose-Derived Mesenchymal Stem Cells In Vitro
title_full Effects of High-Mobility Group A Protein Application on Canine Adipose-Derived Mesenchymal Stem Cells In Vitro
title_fullStr Effects of High-Mobility Group A Protein Application on Canine Adipose-Derived Mesenchymal Stem Cells In Vitro
title_full_unstemmed Effects of High-Mobility Group A Protein Application on Canine Adipose-Derived Mesenchymal Stem Cells In Vitro
title_short Effects of High-Mobility Group A Protein Application on Canine Adipose-Derived Mesenchymal Stem Cells In Vitro
title_sort effects of high mobility group a protein application on canine adipose derived mesenchymal stem cells in vitro
url http://dx.doi.org/10.1155/2012/752083
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