BMP-2 and BMP-9 promotes chondrogenic differentiation of human multipotential mesenchymal cells and overcomes the inhibitory effect of IL-1
Bone morphogenetic proteins play important roles in connective tissue morphogenesis. In this study, we used human multipotential mesenchymal cells as a target to analyze the effect of bone morphogenetic proteins on chondrogenesis. We also analyzed the effect of proinflammatory cytokine interleukin‐1...
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Published in | Journal of cellular physiology Vol. 189; no. 3; pp. 275 - 284 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
New York
John Wiley & Sons, Inc
01.12.2001
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Abstract | Bone morphogenetic proteins play important roles in connective tissue morphogenesis. In this study, we used human multipotential mesenchymal cells as a target to analyze the effect of bone morphogenetic proteins on chondrogenesis. We also analyzed the effect of proinflammatory cytokine interleukin‐1 on chondrogenic‐differentiated cells and the interaction of IL‐1β with bone morphogenetic proteins. Cells placed in a 3‐dimensional matrix of alginate beads and cultured in a serum‐free media with bone morphogenetic protein‐2 and ‐9 induced expression of type II collagen (Col2A1) mRNA and increased expression of aggrecan and cartilage oligomeric matrix protein suggesting chondrogenic differentiation of the cells. The transcription factor Sox‐9 that regulates both Col2A1 and aggrecan gene expression showed increased expression with BMP treatment. Chondrogenic differentiated cells treated with interleukin‐1 decreased Sox‐9, Col2A1 and aggrecan gene expression. Removal of interleukin‐1 and further addition of bone morphogenetic proteins resulted in returned expression of chondrogenic markers. Chondrogenic differentiated cells cultured in the presence of different concentrations of bone morphogenetic proteins and interleukin‐1 showed that bone morphogenetic proteins were able to partially block the suppressive effect of interleukin‐1. This study shows that bone morphogenetic proteins play an important role in chondrogenesis and may prove to be potential therapeutics in cartilage repair. © 2001 Wiley‐Liss, Inc. |
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AbstractList | Bone morphogenetic proteins play important roles in connective tissue morphogenesis. In this study, we used human multipotential mesenchymal cells as a target to analyze the effect of bone morphogenetic proteins on chondrogenesis. We also analyzed the effect of proinflammatory cytokine interleukin-1 on chondrogenic-differentiated cells and the interaction of IL-1beta with bone morphogenetic proteins. Cells placed in a 3-dimensional matrix of alginate beads and cultured in a serum-free media with bone morphogenetic protein-2 and -9 induced expression of type II collagen (Col2A1) mRNA and increased expression of aggrecan and cartilage oligomeric matrix protein suggesting chondrogenic differentiation of the cells. The transcription factor Sox-9 that regulates both Col2A1 and aggrecan gene expression showed increased expression with BMP treatment. Chondrogenic differentiated cells treated with interleukin-1 decreased Sox-9, Col2A1 and aggrecan gene expression. Removal of interleukin-1 and further addition of bone morphogenetic proteins resulted in returned expression of chondrogenic markers. Chondrogenic differentiated cells cultured in the presence of different concentrations of bone morphogenetic proteins and interleukin-1 showed that bone morphogenetic proteins were able to partially block the suppressive effect of interleukin-1. This study shows that bone morphogenetic proteins play an important role in chondrogenesis and may prove to be potential therapeutics in cartilage repair. Abstract Bone morphogenetic proteins play important roles in connective tissue morphogenesis. In this study, we used human multipotential mesenchymal cells as a target to analyze the effect of bone morphogenetic proteins on chondrogenesis. We also analyzed the effect of proinflammatory cytokine interleukin‐1 on chondrogenic‐differentiated cells and the interaction of IL‐1β with bone morphogenetic proteins. Cells placed in a 3‐dimensional matrix of alginate beads and cultured in a serum‐free media with bone morphogenetic protein‐2 and ‐9 induced expression of type II collagen ( Col2A1 ) mRNA and increased expression of aggrecan and cartilage oligomeric matrix protein suggesting chondrogenic differentiation of the cells. The transcription factor Sox‐9 that regulates both Col2A1 and aggrecan gene expression showed increased expression with BMP treatment. Chondrogenic differentiated cells treated with interleukin‐1 decreased Sox‐9, Col2A1 and aggrecan gene expression. Removal of interleukin‐1 and further addition of bone morphogenetic proteins resulted in returned expression of chondrogenic markers. Chondrogenic differentiated cells cultured in the presence of different concentrations of bone morphogenetic proteins and interleukin‐1 showed that bone morphogenetic proteins were able to partially block the suppressive effect of interleukin‐1. This study shows that bone morphogenetic proteins play an important role in chondrogenesis and may prove to be potential therapeutics in cartilage repair. © 2001 Wiley‐Liss, Inc. Bone morphogenetic proteins play important roles in connective tissue morphogenesis. In this study, we used human multipotential mesenchymal cells as a target to analyze the effect of bone morphogenetic proteins on chondrogenesis. We also analyzed the effect of proinflammatory cytokine interleukin‐1 on chondrogenic‐differentiated cells and the interaction of IL‐1β with bone morphogenetic proteins. Cells placed in a 3‐dimensional matrix of alginate beads and cultured in a serum‐free media with bone morphogenetic protein‐2 and ‐9 induced expression of type II collagen (Col2A1) mRNA and increased expression of aggrecan and cartilage oligomeric matrix protein suggesting chondrogenic differentiation of the cells. The transcription factor Sox‐9 that regulates both Col2A1 and aggrecan gene expression showed increased expression with BMP treatment. Chondrogenic differentiated cells treated with interleukin‐1 decreased Sox‐9, Col2A1 and aggrecan gene expression. Removal of interleukin‐1 and further addition of bone morphogenetic proteins resulted in returned expression of chondrogenic markers. Chondrogenic differentiated cells cultured in the presence of different concentrations of bone morphogenetic proteins and interleukin‐1 showed that bone morphogenetic proteins were able to partially block the suppressive effect of interleukin‐1. This study shows that bone morphogenetic proteins play an important role in chondrogenesis and may prove to be potential therapeutics in cartilage repair. © 2001 Wiley‐Liss, Inc. |
Author | Wang, Eunice Morris, Elisabeth Ann Majumdar, Manas Kumar |
Author_xml | – sequence: 1 givenname: Manas Kumar surname: Majumdar fullname: Majumdar, Manas Kumar email: mmajumdar@genetics.com organization: Genetics Institute, Inc., Cambridge, Massachusetts – sequence: 2 givenname: Eunice surname: Wang fullname: Wang, Eunice organization: Genetics Institute, Inc., Cambridge, Massachusetts – sequence: 3 givenname: Elisabeth Ann surname: Morris fullname: Morris, Elisabeth Ann organization: Genetics Institute, Inc., Cambridge, Massachusetts |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/11748585$$D View this record in MEDLINE/PubMed |
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Snippet | Bone morphogenetic proteins play important roles in connective tissue morphogenesis. In this study, we used human multipotential mesenchymal cells as a target... Abstract Bone morphogenetic proteins play important roles in connective tissue morphogenesis. In this study, we used human multipotential mesenchymal cells as... |
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StartPage | 275 |
SubjectTerms | Aggrecans Biomarkers - analysis Bone Morphogenetic Protein 2 Bone Morphogenetic Proteins - pharmacology Cell Differentiation Cells, Cultured Chondrocytes - physiology Chondrogenesis Collagen Type II - biosynthesis Collagen Type II - genetics Drug Antagonism Extracellular Matrix Proteins Growth Differentiation Factor 2 Growth Differentiation Factors High Mobility Group Proteins - biosynthesis High Mobility Group Proteins - genetics Humans Interleukin-1 - pharmacology Kinetics Lectins, C-Type Mesoderm - physiology Proteoglycans - biosynthesis Proteoglycans - genetics RNA, Messenger - biosynthesis SOX9 Transcription Factor Stem Cells - drug effects Stem Cells - physiology Transcription Factors - biosynthesis Transcription Factors - genetics Transforming Growth Factor beta |
Title | BMP-2 and BMP-9 promotes chondrogenic differentiation of human multipotential mesenchymal cells and overcomes the inhibitory effect of IL-1 |
URI | https://api.istex.fr/ark:/67375/WNG-C0T9P6Q0-H/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjcp.10025 https://www.ncbi.nlm.nih.gov/pubmed/11748585 |
Volume | 189 |
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