Effects of BIO on proliferation and chondrogenic differentiation of mouse marrow derived mesenchymal stem cells

In vitroexpansion of mesenchymal stem cell (MSCs) into large number is necessary fortheir application in cell-based treatment of articular cartilage defects. On the other hand,some studies have indicated that BIO (6-Bromoindirubin-3-Oxime) possesses mitogeniceffects on cell culture. The objective of...

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Main Authors: Nasrin Fallah, Mohamadreza Baghaban Eslami nejad
Format: Article
Language:English
Published: Urmia University 2013-06-01
Series:Veterinary Research Forum
Subjects:
BIO
Online Access:http://www.urmia.ac.ir/vrf/Shared%20Documents/pdf/vol-4%20no-2/69-76-0363.pdf
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spelling doaj-3ac7f7e3ad804ec48508155b143fd1cb2020-11-25T00:04:09ZengUrmia UniversityVeterinary Research Forum2008-81402013-06-01426976Effects of BIO on proliferation and chondrogenic differentiation of mouse marrow derived mesenchymal stem cellsNasrin FallahMohamadreza Baghaban Eslami nejadIn vitroexpansion of mesenchymal stem cell (MSCs) into large number is necessary fortheir application in cell-based treatment of articular cartilage defects. On the other hand,some studies have indicated that BIO (6-Bromoindirubin-3-Oxime) possesses mitogeniceffects on cell culture. The objective of the present study was to examine the effect of BIO onin vitro expansion and chondrogenic differentiation of mouse marrow-derived MSCs. Theculture was established using bone marrow tissue obtained from 10 NMRI mice. MSC natureof the isolated cells was verified according to the minimal criteria proposed for MSC.Passaged-3 cells were seeded in 24-well culture plates and treated by 0.05, 0.01, 0.1, 1.0 and1.5 μM BIO forsevendays. The culture without BIO was taken as the control. At the end ofcultivation period, the cultures were examinedfor viable cell number which was then used tocalculate population doubling time (PDT). The BIO with higher proliferation-promoting effectwas investigated for its chondrogenic effect on MSC culture. There was significantly moreviable cells at the cultures treated by 0.1 μM BIO. At this culture the cells tended to doubletheir population in rapid rate (each 43.07 hr) than the cells treated with the other BIOconcentrations (p< 0.05). Interestingly treatment of MSC chondrogenic culture with 0.1 μMBIO ledto the up-regulation of cartilage specific genes including aggrecan, collagen II andSox9. In conclusion BIO at 0.1 μM could enhance mouse MSC in vitro proliferation as well astheir chondrogenic differentiation. These findings would be of great importance for the fieldof regenerative medicine. http://www.urmia.ac.ir/vrf/Shared%20Documents/pdf/vol-4%20no-2/69-76-0363.pdfBIOCartilage differentiationMesenchymal stem cellsMouseProliferation
collection DOAJ
language English
format Article
sources DOAJ
author Nasrin Fallah
Mohamadreza Baghaban Eslami nejad
spellingShingle Nasrin Fallah
Mohamadreza Baghaban Eslami nejad
Effects of BIO on proliferation and chondrogenic differentiation of mouse marrow derived mesenchymal stem cells
Veterinary Research Forum
BIO
Cartilage differentiation
Mesenchymal stem cells
Mouse
Proliferation
author_facet Nasrin Fallah
Mohamadreza Baghaban Eslami nejad
author_sort Nasrin Fallah
title Effects of BIO on proliferation and chondrogenic differentiation of mouse marrow derived mesenchymal stem cells
title_short Effects of BIO on proliferation and chondrogenic differentiation of mouse marrow derived mesenchymal stem cells
title_full Effects of BIO on proliferation and chondrogenic differentiation of mouse marrow derived mesenchymal stem cells
title_fullStr Effects of BIO on proliferation and chondrogenic differentiation of mouse marrow derived mesenchymal stem cells
title_full_unstemmed Effects of BIO on proliferation and chondrogenic differentiation of mouse marrow derived mesenchymal stem cells
title_sort effects of bio on proliferation and chondrogenic differentiation of mouse marrow derived mesenchymal stem cells
publisher Urmia University
series Veterinary Research Forum
issn 2008-8140
publishDate 2013-06-01
description In vitroexpansion of mesenchymal stem cell (MSCs) into large number is necessary fortheir application in cell-based treatment of articular cartilage defects. On the other hand,some studies have indicated that BIO (6-Bromoindirubin-3-Oxime) possesses mitogeniceffects on cell culture. The objective of the present study was to examine the effect of BIO onin vitro expansion and chondrogenic differentiation of mouse marrow-derived MSCs. Theculture was established using bone marrow tissue obtained from 10 NMRI mice. MSC natureof the isolated cells was verified according to the minimal criteria proposed for MSC.Passaged-3 cells were seeded in 24-well culture plates and treated by 0.05, 0.01, 0.1, 1.0 and1.5 μM BIO forsevendays. The culture without BIO was taken as the control. At the end ofcultivation period, the cultures were examinedfor viable cell number which was then used tocalculate population doubling time (PDT). The BIO with higher proliferation-promoting effectwas investigated for its chondrogenic effect on MSC culture. There was significantly moreviable cells at the cultures treated by 0.1 μM BIO. At this culture the cells tended to doubletheir population in rapid rate (each 43.07 hr) than the cells treated with the other BIOconcentrations (p< 0.05). Interestingly treatment of MSC chondrogenic culture with 0.1 μMBIO ledto the up-regulation of cartilage specific genes including aggrecan, collagen II andSox9. In conclusion BIO at 0.1 μM could enhance mouse MSC in vitro proliferation as well astheir chondrogenic differentiation. These findings would be of great importance for the fieldof regenerative medicine.
topic BIO
Cartilage differentiation
Mesenchymal stem cells
Mouse
Proliferation
url http://www.urmia.ac.ir/vrf/Shared%20Documents/pdf/vol-4%20no-2/69-76-0363.pdf
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