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Different responses to mechanical injury in neonatal and adult ovine articular cartilage
BACKGROUND: Articular cartilage injury remains a major challenge in orthopedic surgery. This study aimed to identify differences in gene expression and molecular responses between neonatal and adult articular cartilage during the healing of an injury. METHODS: An established in vitro model was used...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3691644/ https://www.ncbi.nlm.nih.gov/pubmed/23773399 http://dx.doi.org/10.1186/1475-925X-12-53 |
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author | Xue, Xuhong Zheng, Qixin Wu, Hongbin Zou, Lixue Li, Peng |
author_facet | Xue, Xuhong Zheng, Qixin Wu, Hongbin Zou, Lixue Li, Peng |
author_sort | Xue, Xuhong |
collection | PubMed |
description | BACKGROUND: Articular cartilage injury remains a major challenge in orthopedic surgery. This study aimed to identify differences in gene expression and molecular responses between neonatal and adult articular cartilage during the healing of an injury. METHODS: An established in vitro model was used to compare the transcriptional response to cartilage injury in neonatal and adult sheep by microarray analysis of gene expression. Total RNA was isolated from tissue samples, linearly amplified, and 15,208 ovine probes were applied to cDNA microarray. Validation for selected genes was obtained by real-time quantitative polymerase chain reaction (RT-qPCR). RESULTS: We found 1,075 (11.6%) differentially expressed probe sets in adult injured cartilage relative to normal cartilage. A total of 1,016 (11.0%) probe sets were differentially expressed in neonatal injured cartilage relative to normal cartilage. A total of 1,492 (16.1%) probe sets were differentially expressed in adult normal cartilage relative to neonatal normal cartilage. A total of 1,411 (15.3%) probe sets were differentially expressed in adult injured cartilage relative to neonatal injured cartilage. Significant functional clusters included genes associated with wound healing, articular protection, inflammation, and energy metabolism. Selected genes (PPARG, LDH, TOM, HIF1A, SMAD7, and NF-κB) were also found and validated by RT-qPCR. CONCLUSIONS: There are significant differences in gene expression between neonatal and adult ovine articular cartilage following acute injury. They are partly due to intrinsic differences in the process of development, and partly to different biological responses to mechanical trauma between neonatal and adult articular cartilage. |
format | Online Article Text |
id | pubmed-3691644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36916442013-06-26 Different responses to mechanical injury in neonatal and adult ovine articular cartilage Xue, Xuhong Zheng, Qixin Wu, Hongbin Zou, Lixue Li, Peng Biomed Eng Online Research BACKGROUND: Articular cartilage injury remains a major challenge in orthopedic surgery. This study aimed to identify differences in gene expression and molecular responses between neonatal and adult articular cartilage during the healing of an injury. METHODS: An established in vitro model was used to compare the transcriptional response to cartilage injury in neonatal and adult sheep by microarray analysis of gene expression. Total RNA was isolated from tissue samples, linearly amplified, and 15,208 ovine probes were applied to cDNA microarray. Validation for selected genes was obtained by real-time quantitative polymerase chain reaction (RT-qPCR). RESULTS: We found 1,075 (11.6%) differentially expressed probe sets in adult injured cartilage relative to normal cartilage. A total of 1,016 (11.0%) probe sets were differentially expressed in neonatal injured cartilage relative to normal cartilage. A total of 1,492 (16.1%) probe sets were differentially expressed in adult normal cartilage relative to neonatal normal cartilage. A total of 1,411 (15.3%) probe sets were differentially expressed in adult injured cartilage relative to neonatal injured cartilage. Significant functional clusters included genes associated with wound healing, articular protection, inflammation, and energy metabolism. Selected genes (PPARG, LDH, TOM, HIF1A, SMAD7, and NF-κB) were also found and validated by RT-qPCR. CONCLUSIONS: There are significant differences in gene expression between neonatal and adult ovine articular cartilage following acute injury. They are partly due to intrinsic differences in the process of development, and partly to different biological responses to mechanical trauma between neonatal and adult articular cartilage. BioMed Central 2013-06-17 /pmc/articles/PMC3691644/ /pubmed/23773399 http://dx.doi.org/10.1186/1475-925X-12-53 Text en Copyright © 2013 Xue et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Xue, Xuhong Zheng, Qixin Wu, Hongbin Zou, Lixue Li, Peng Different responses to mechanical injury in neonatal and adult ovine articular cartilage |
title | Different responses to mechanical injury in neonatal and adult ovine articular cartilage |
title_full | Different responses to mechanical injury in neonatal and adult ovine articular cartilage |
title_fullStr | Different responses to mechanical injury in neonatal and adult ovine articular cartilage |
title_full_unstemmed | Different responses to mechanical injury in neonatal and adult ovine articular cartilage |
title_short | Different responses to mechanical injury in neonatal and adult ovine articular cartilage |
title_sort | different responses to mechanical injury in neonatal and adult ovine articular cartilage |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3691644/ https://www.ncbi.nlm.nih.gov/pubmed/23773399 http://dx.doi.org/10.1186/1475-925X-12-53 |
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