Hypoxic culture conditions as a solution for mesenchymal stem cell based regenerative therapy

Cell-based regenerative therapies, based on in vitro propagation of stem cells, offer tremendous hope to many individuals suffering from degenerative diseases that were previously deemed untreatable. Due to the self-renewal capacity, multilineage potential, and immunosuppressive property, mesenchyma...

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Main Authors: Haque, Nazmul, Rahman, Mohammad Tariqur, Abu Kasim, Noor Hayaty, Alabsi, Aied Mohammed
Format: Article
Language:English
Published: Hindawi Publishing Corporation 2013
Subjects:
Online Access:http://irep.iium.edu.my/35324/
http://irep.iium.edu.my/35324/
http://irep.iium.edu.my/35324/
http://irep.iium.edu.my/35324/1/632972.pdf
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spelling iium-353242014-02-05T03:00:35Z http://irep.iium.edu.my/35324/ Hypoxic culture conditions as a solution for mesenchymal stem cell based regenerative therapy Haque, Nazmul Rahman, Mohammad Tariqur Abu Kasim, Noor Hayaty Alabsi, Aied Mohammed RM270 Serum therapy. Immunotherapy Cell-based regenerative therapies, based on in vitro propagation of stem cells, offer tremendous hope to many individuals suffering from degenerative diseases that were previously deemed untreatable. Due to the self-renewal capacity, multilineage potential, and immunosuppressive property, mesenchymal stem cells (MSCs) are considered as an attractive source of stem cells for regenerative therapies. However, poor growth kinetics, early senescence, and genetic instability during in vitro expansion and poor engraftment after transplantation are considered to be among the major disadvantages of MSC-based regenerative therapies. A number of complex inter- and intracellular interactive signaling systems control growth, multiplication, and differentiation of MSCs in their niche. Common laboratory conditions for stem cell culture involve ambient O2 concentration (20%) in contrast to their niche where they usually reside in 2–9% O2. Notably, O2 plays an important role in maintaining stem cell fate in terms of proliferation and differentiation, by regulating hypoxia-inducible factor-1 (HIF-1) mediated expression of different genes. This paper aims to describe and compare the role of normoxia (20% O2) and hypoxia (2–9% O2) on the biology of MSCs. Finally it is concluded that a hypoxic environment can greatly improve growth kinetics, genetic stability, and expression of chemokine receptors during in vitro expansion and eventually can increase efficiency of MSC-based regenerative therapies. ,1,2 ,3 ,1,2 and Hindawi Publishing Corporation 2013-07 Article PeerReviewed application/pdf en http://irep.iium.edu.my/35324/1/632972.pdf Haque, Nazmul and Rahman, Mohammad Tariqur and Abu Kasim, Noor Hayaty and Alabsi, Aied Mohammed (2013) Hypoxic culture conditions as a solution for mesenchymal stem cell based regenerative therapy. The Scientific World Journal , 2013 (632972). pp. 1-12. ISSN 1537-744X http://www.hindawi.com/journals/tswj/2013/632972/ http://dx.doi.org/10.1155/2013/632972
repository_type Digital Repository
institution_category Local University
institution International Islamic University Malaysia
building IIUM Repository
collection Online Access
language English
topic RM270 Serum therapy. Immunotherapy
spellingShingle RM270 Serum therapy. Immunotherapy
Haque, Nazmul
Rahman, Mohammad Tariqur
Abu Kasim, Noor Hayaty
Alabsi, Aied Mohammed
Hypoxic culture conditions as a solution for mesenchymal stem cell based regenerative therapy
description Cell-based regenerative therapies, based on in vitro propagation of stem cells, offer tremendous hope to many individuals suffering from degenerative diseases that were previously deemed untreatable. Due to the self-renewal capacity, multilineage potential, and immunosuppressive property, mesenchymal stem cells (MSCs) are considered as an attractive source of stem cells for regenerative therapies. However, poor growth kinetics, early senescence, and genetic instability during in vitro expansion and poor engraftment after transplantation are considered to be among the major disadvantages of MSC-based regenerative therapies. A number of complex inter- and intracellular interactive signaling systems control growth, multiplication, and differentiation of MSCs in their niche. Common laboratory conditions for stem cell culture involve ambient O2 concentration (20%) in contrast to their niche where they usually reside in 2–9% O2. Notably, O2 plays an important role in maintaining stem cell fate in terms of proliferation and differentiation, by regulating hypoxia-inducible factor-1 (HIF-1) mediated expression of different genes. This paper aims to describe and compare the role of normoxia (20% O2) and hypoxia (2–9% O2) on the biology of MSCs. Finally it is concluded that a hypoxic environment can greatly improve growth kinetics, genetic stability, and expression of chemokine receptors during in vitro expansion and eventually can increase efficiency of MSC-based regenerative therapies. ,1,2 ,3 ,1,2 and
format Article
author Haque, Nazmul
Rahman, Mohammad Tariqur
Abu Kasim, Noor Hayaty
Alabsi, Aied Mohammed
author_facet Haque, Nazmul
Rahman, Mohammad Tariqur
Abu Kasim, Noor Hayaty
Alabsi, Aied Mohammed
author_sort Haque, Nazmul
title Hypoxic culture conditions as a solution for mesenchymal stem cell based regenerative therapy
title_short Hypoxic culture conditions as a solution for mesenchymal stem cell based regenerative therapy
title_full Hypoxic culture conditions as a solution for mesenchymal stem cell based regenerative therapy
title_fullStr Hypoxic culture conditions as a solution for mesenchymal stem cell based regenerative therapy
title_full_unstemmed Hypoxic culture conditions as a solution for mesenchymal stem cell based regenerative therapy
title_sort hypoxic culture conditions as a solution for mesenchymal stem cell based regenerative therapy
publisher Hindawi Publishing Corporation
publishDate 2013
url http://irep.iium.edu.my/35324/
http://irep.iium.edu.my/35324/
http://irep.iium.edu.my/35324/
http://irep.iium.edu.my/35324/1/632972.pdf
first_indexed 2023-09-18T20:50:39Z
last_indexed 2023-09-18T20:50:39Z
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