Hypoxia enhances self-renewal properties and markers of mesenchymal stem cells

Background Mesenchymal stem cells (MSCs) are multipotent stromal cells that express CD73, CD90, and CD105 surface markers, but not CD14, CD45, CD34, CD11b, and HLA-DR. MSCs under hypoxic conditions have the essential role of maintaining the stemness capacity by releasing several growth factors into...

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Main Authors: Vivi Yustianingsih, Titiek Sumarawati, Agung Putra
Format: Article
Language:English
Published: Faculty of Medicine Trisakti University 2019-10-01
Series:Universa Medicina
Subjects:
MSC
Online Access:https://univmed.org/ejurnal/index.php/medicina/article/view/715
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spelling doaj-dab2b949ed1e4be8afa2fec95863676b2021-08-15T06:22:13ZengFaculty of Medicine Trisakti UniversityUniversa Medicina1907-30622407-22302019-10-0138310.18051/UnivMed.2019.v38.164-171386Hypoxia enhances self-renewal properties and markers of mesenchymal stem cellsVivi Yustianingsih0Titiek Sumarawati1Agung Putra2Postgraduate Biomedical Science Program, Medical Faculty, Sultan Agung Islamic University, SemarangDepartment of Postgraduate Biomedical Science, Medical Faculty, Sultan Agung Islamic University, SemarangDepartment of Pathological Anatomy of Medical Faculty of Sultan Agung Islamic University, Semarang Stem Cell and Cancer Research Laboratory of Medical Faculty of Sultan Agung Islamic UniversityBackground Mesenchymal stem cells (MSCs) are multipotent stromal cells that express CD73, CD90, and CD105 surface markers, but not CD14, CD45, CD34, CD11b, and HLA-DR. MSCs under hypoxic conditions have the essential role of maintaining the stemness capacity by releasing several growth factors into their medium, known as hypoxia conditioned medium (HCM). This study was performed to compare the effect of percentage of HCM to normoxic medium (NM) in increasing MSC proliferation marked by proliferation rate and surface marker expression. Methods This study was of post-test only control group design using human umbilical cord-MSCs (hUC-MSCs) as subjects. The HCM treatment group was obtained by culturing MSCs under 5% O2, whereas the NM control group was grown under 20% O2. The hUC-MSCs were divided into 4 groups with different dose ratios of HCM to NM (25%:75%; 50%:50%; 75%:25% for P1, P2 and P3, respectively and 100% of NM for the controls). All of these groups were maintained at 37oC and the data was collected after 72 hours incubation. MSC marker expression of CD73, CD90 and CD105 was analyzed using flow cytometry and MSC proliferation by trypan blue assay. Result There were significant differences in MSC marker expression of CD73, CD90 and CD105 and proliferation at all dose ratios of HCM to NM (p<0.05). Conclusion Low oxygen concentration promotes MSC proliferation and stemness thus it might be beneficial for maintaining the MSC physiologic niche in-vitro.https://univmed.org/ejurnal/index.php/medicina/article/view/715MSCMSC-HCMproliferationstemness
collection DOAJ
language English
format Article
sources DOAJ
author Vivi Yustianingsih
Titiek Sumarawati
Agung Putra
spellingShingle Vivi Yustianingsih
Titiek Sumarawati
Agung Putra
Hypoxia enhances self-renewal properties and markers of mesenchymal stem cells
Universa Medicina
MSC
MSC-HCM
proliferation
stemness
author_facet Vivi Yustianingsih
Titiek Sumarawati
Agung Putra
author_sort Vivi Yustianingsih
title Hypoxia enhances self-renewal properties and markers of mesenchymal stem cells
title_short Hypoxia enhances self-renewal properties and markers of mesenchymal stem cells
title_full Hypoxia enhances self-renewal properties and markers of mesenchymal stem cells
title_fullStr Hypoxia enhances self-renewal properties and markers of mesenchymal stem cells
title_full_unstemmed Hypoxia enhances self-renewal properties and markers of mesenchymal stem cells
title_sort hypoxia enhances self-renewal properties and markers of mesenchymal stem cells
publisher Faculty of Medicine Trisakti University
series Universa Medicina
issn 1907-3062
2407-2230
publishDate 2019-10-01
description Background Mesenchymal stem cells (MSCs) are multipotent stromal cells that express CD73, CD90, and CD105 surface markers, but not CD14, CD45, CD34, CD11b, and HLA-DR. MSCs under hypoxic conditions have the essential role of maintaining the stemness capacity by releasing several growth factors into their medium, known as hypoxia conditioned medium (HCM). This study was performed to compare the effect of percentage of HCM to normoxic medium (NM) in increasing MSC proliferation marked by proliferation rate and surface marker expression. Methods This study was of post-test only control group design using human umbilical cord-MSCs (hUC-MSCs) as subjects. The HCM treatment group was obtained by culturing MSCs under 5% O2, whereas the NM control group was grown under 20% O2. The hUC-MSCs were divided into 4 groups with different dose ratios of HCM to NM (25%:75%; 50%:50%; 75%:25% for P1, P2 and P3, respectively and 100% of NM for the controls). All of these groups were maintained at 37oC and the data was collected after 72 hours incubation. MSC marker expression of CD73, CD90 and CD105 was analyzed using flow cytometry and MSC proliferation by trypan blue assay. Result There were significant differences in MSC marker expression of CD73, CD90 and CD105 and proliferation at all dose ratios of HCM to NM (p<0.05). Conclusion Low oxygen concentration promotes MSC proliferation and stemness thus it might be beneficial for maintaining the MSC physiologic niche in-vitro.
topic MSC
MSC-HCM
proliferation
stemness
url https://univmed.org/ejurnal/index.php/medicina/article/view/715
work_keys_str_mv AT viviyustianingsih hypoxiaenhancesselfrenewalpropertiesandmarkersofmesenchymalstemcells
AT titieksumarawati hypoxiaenhancesselfrenewalpropertiesandmarkersofmesenchymalstemcells
AT agungputra hypoxiaenhancesselfrenewalpropertiesandmarkersofmesenchymalstemcells
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