The influence of osteogenic differentiation on the stem-like properties of adipose derived stem cells – an RT-qPCR study

Author:

Bryl Rut1,Dompe Claudia2,Jankowski Maurycy1,Stefańska Katarzyna3,Narenji Afsaneh Golkar4,Kulus Jakub5,Kulus Magdalena6,Wieczorkiewicz Maria7,Wąsiatycz Grzegorz6,Jaśkowski Jędrzej M.5,Kaczmarek Mariusz8,Petitte James N.4,Mozdziak Paul49,Antosik Paweł6,Bukowska Dorota5

Affiliation:

1. Department of Anatomy, Poznań University of Medical Sciences , Poznań , Poland

2. School of Medicine, Medical Sciences and Nutrition, University of Aberdeen , Aberdeen , UK

3. Department of Histology and Embryology, Poznań University of Medical Sciences , Poznań , Poland

4. Prestage Department of Poultry Science, North Carolina State University , Raleigh, NC , USA

5. Department of Diagnostics and Clinical Sciences, Institute of Veterinary Medicine, Nicolaus Copernicus University in Toruń , Toru , Poland

6. Department of Veterinary Surgery, Institute of Veterinary Medicine, Nicolaus Copernicus University in Toruń , Toruń , Poland

7. Department of Basic and Preclinical Sciences, Institute of Veterinary Medicine, Faculty of Biological and Veterinary Sciences, Nicolaus Copernicus University in Toruń , Toruń , Poland

8. Department of Cancer Immunology, Poznan University of Medical Sciences , Poznań , Poland

9. Physiology Graduate Program, North Carolina State University , Raleigh, NC , USA

Abstract

Abstract ADSCs are readily accessible and widely available. Isolated through a minimally invasive procedure from adipose depots, they can be found at diverse body location, where they served various functions, including energy homeostasis. They can be obtained upon surgeries from otherwise waste tissues, like after excision of fat tissue or liposuction. In addition, due to the possibility to isolate many ADSCs, in vitro proliferation can be performed in a short time period, resulting in cells showing more predictable results[1]. For this study ADSCs were obtained from waste material following routing sterilization procedures of dogs. This study aimed to analyse the expression of MSC specific markers before and after in vitro differentiation of ASCs. Three positive and three negative markers were analysed, CD105, CD73, CD90, CD34, CD14 and CD45. There were significant differences detected in the expression of all of the genes, with most of them exhibiting notable downregulation. The only exception, CD14 showed major upregulation after the process of differentiation. These changes confirm the success of differentiation, as well as suggest that this process significantly lowers the stem-like ability of ASCs. This knowledge should serve as a reference for further molecular and clinical studies, possibly aiding the understanding of the internal mechanisms governing the differentiation and stemness of ASCs, to enable their widespread and safe application in regenerative medicine. Running title: Mesenchymal markers during ASC osteogenic differentiation

Publisher

Walter de Gruyter GmbH

Subject

Cell Biology,Molecular Biology

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