Differentiation of Bone Marrow Mesenchymal Stem Cells into Chondrocytes after Short Term Culture in Alkaline Medium

Background: Bone marrow mesenchymal stem cells (MSCs) are one of the undifferentiated multipotential cell sources of human body. Methods: MSCs have the capacity to form a variety of cell types, especially chondrocytes and osteocytes. Learning about responses of MSCs to external milieu and chemical f...

Full description

Bibliographic Details
Main Authors: Farshad Homayouni Moghadam, Tahereh Tayebi, Maryam Dehghan, Gilda Eslami, Hamid Nadri, Alireza Moradi, Hassanali Vahedian-Ardakani, Kazem Barzegar
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2014-12-01
Series:International Journal of Hematology-Oncology and Stem Cell Research
Subjects:
Online Access:https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/408
_version_ 1827845753755664384
author Farshad Homayouni Moghadam
Tahereh Tayebi
Maryam Dehghan
Gilda Eslami
Hamid Nadri
Alireza Moradi
Hassanali Vahedian-Ardakani
Kazem Barzegar
author_facet Farshad Homayouni Moghadam
Tahereh Tayebi
Maryam Dehghan
Gilda Eslami
Hamid Nadri
Alireza Moradi
Hassanali Vahedian-Ardakani
Kazem Barzegar
author_sort Farshad Homayouni Moghadam
collection DOAJ
description Background: Bone marrow mesenchymal stem cells (MSCs) are one of the undifferentiated multipotential cell sources of human body. Methods: MSCs have the capacity to form a variety of cell types, especially chondrocytes and osteocytes. Learning about responses of MSCs to external milieu and chemical factors such as pH could recommend new approaches for preparation of suitable scaffolds for bone and cartilage tissue engineering. In present study, the effect of alkaline medium on chondrogenic and osteogenic differentiation of rat MSCs was evaluated.MSCs were harvested from bone marrow of animals and then the response of passage1 and 2 of MSCs (P1 MSCs & P2 MSCs) to the culture in alkaline medium (pH: 8) was evaluated. Cytochemical and immunocytochemical staining were performed to distinguish chondrocytes and osteocytes. Real-time PCR was performed to evaluate the type II collagen and osteopontin mRNA levels. Results: Staining for type II collagen, a chondrocytic specific marker, revealed that after one-week culture in alkaline medium, a considerable amount of P1 MSCs had shown chondrocytic morphology. By prolonging the culture period up to 4 weeks, osteogenic cells with expanded matrix and mineralized areas around them were appeared. Results of real-time PCR showed that P1 MSCs after one week culture in alkaline medium expressed highest rate of type II collagen and osteopontin mRNA among all groups. Conclusion: This study demonstrated that alkaline medium is a potent chondrogenic differentiation inducer for MSCs in their first passage.
first_indexed 2024-03-12T09:02:51Z
format Article
id doaj.art-9bee0ddd977046459dd1903d85a080c5
institution Directory Open Access Journal
issn 2008-2207
language English
last_indexed 2024-03-12T09:02:51Z
publishDate 2014-12-01
publisher Tehran University of Medical Sciences
record_format Article
series International Journal of Hematology-Oncology and Stem Cell Research
spelling doaj.art-9bee0ddd977046459dd1903d85a080c52023-09-02T15:34:00ZengTehran University of Medical SciencesInternational Journal of Hematology-Oncology and Stem Cell Research2008-22072014-12-0184394Differentiation of Bone Marrow Mesenchymal Stem Cells into Chondrocytes after Short Term Culture in Alkaline MediumFarshad Homayouni Moghadam0Tahereh Tayebi1Maryam Dehghan2Gilda Eslami3Hamid Nadri4Alireza Moradi5Hassanali Vahedian-Ardakani6Kazem Barzegar7Department of Physiology, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. AND Neurobiomedical Research Center, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.Department of Physiology, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.Neurobiomedical Research Center, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.Department of Medical Parasitology and Mycology, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.Department of Medicinal Chemistry, School of Pharmacy, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.Department of Medicinal Chemistry, School of Pharmacy, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.Department of Internal Medicine, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.English Language Department, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.Background: Bone marrow mesenchymal stem cells (MSCs) are one of the undifferentiated multipotential cell sources of human body. Methods: MSCs have the capacity to form a variety of cell types, especially chondrocytes and osteocytes. Learning about responses of MSCs to external milieu and chemical factors such as pH could recommend new approaches for preparation of suitable scaffolds for bone and cartilage tissue engineering. In present study, the effect of alkaline medium on chondrogenic and osteogenic differentiation of rat MSCs was evaluated.MSCs were harvested from bone marrow of animals and then the response of passage1 and 2 of MSCs (P1 MSCs & P2 MSCs) to the culture in alkaline medium (pH: 8) was evaluated. Cytochemical and immunocytochemical staining were performed to distinguish chondrocytes and osteocytes. Real-time PCR was performed to evaluate the type II collagen and osteopontin mRNA levels. Results: Staining for type II collagen, a chondrocytic specific marker, revealed that after one-week culture in alkaline medium, a considerable amount of P1 MSCs had shown chondrocytic morphology. By prolonging the culture period up to 4 weeks, osteogenic cells with expanded matrix and mineralized areas around them were appeared. Results of real-time PCR showed that P1 MSCs after one week culture in alkaline medium expressed highest rate of type II collagen and osteopontin mRNA among all groups. Conclusion: This study demonstrated that alkaline medium is a potent chondrogenic differentiation inducer for MSCs in their first passage.https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/408Alkaline mediumChondrocyteMesenchymal stem cellOsteoblast
spellingShingle Farshad Homayouni Moghadam
Tahereh Tayebi
Maryam Dehghan
Gilda Eslami
Hamid Nadri
Alireza Moradi
Hassanali Vahedian-Ardakani
Kazem Barzegar
Differentiation of Bone Marrow Mesenchymal Stem Cells into Chondrocytes after Short Term Culture in Alkaline Medium
International Journal of Hematology-Oncology and Stem Cell Research
Alkaline medium
Chondrocyte
Mesenchymal stem cell
Osteoblast
title Differentiation of Bone Marrow Mesenchymal Stem Cells into Chondrocytes after Short Term Culture in Alkaline Medium
title_full Differentiation of Bone Marrow Mesenchymal Stem Cells into Chondrocytes after Short Term Culture in Alkaline Medium
title_fullStr Differentiation of Bone Marrow Mesenchymal Stem Cells into Chondrocytes after Short Term Culture in Alkaline Medium
title_full_unstemmed Differentiation of Bone Marrow Mesenchymal Stem Cells into Chondrocytes after Short Term Culture in Alkaline Medium
title_short Differentiation of Bone Marrow Mesenchymal Stem Cells into Chondrocytes after Short Term Culture in Alkaline Medium
title_sort differentiation of bone marrow mesenchymal stem cells into chondrocytes after short term culture in alkaline medium
topic Alkaline medium
Chondrocyte
Mesenchymal stem cell
Osteoblast
url https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/408
work_keys_str_mv AT farshadhomayounimoghadam differentiationofbonemarrowmesenchymalstemcellsintochondrocytesaftershorttermcultureinalkalinemedium
AT taherehtayebi differentiationofbonemarrowmesenchymalstemcellsintochondrocytesaftershorttermcultureinalkalinemedium
AT maryamdehghan differentiationofbonemarrowmesenchymalstemcellsintochondrocytesaftershorttermcultureinalkalinemedium
AT gildaeslami differentiationofbonemarrowmesenchymalstemcellsintochondrocytesaftershorttermcultureinalkalinemedium
AT hamidnadri differentiationofbonemarrowmesenchymalstemcellsintochondrocytesaftershorttermcultureinalkalinemedium
AT alirezamoradi differentiationofbonemarrowmesenchymalstemcellsintochondrocytesaftershorttermcultureinalkalinemedium
AT hassanalivahedianardakani differentiationofbonemarrowmesenchymalstemcellsintochondrocytesaftershorttermcultureinalkalinemedium
AT kazembarzegar differentiationofbonemarrowmesenchymalstemcellsintochondrocytesaftershorttermcultureinalkalinemedium