Implications of zonal architecture on differential gene expression profiling and altered pathway expressions in mandibular condylar cartilage
Abstract Mandibular condylar cartilage (MCC) is a multi-zonal heterogeneous fibrocartilage containing different types of cells, but the factors/mechanisms governing the phenotypic transition across the zones have not been fully understood. The reliability of molecular studies heavily rely on the pro...
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doaj-37cdb1648bde4b6f8189d1c7daa5309a2021-08-22T11:25:02ZengNature Publishing GroupScientific Reports2045-23222021-08-0111111510.1038/s41598-021-96071-7Implications of zonal architecture on differential gene expression profiling and altered pathway expressions in mandibular condylar cartilageAisha M. Basudan0Mohammad Azhar Aziz1Yanqi Yang2Division of Orthodontics, Dental Services Department, KAMC/KAIMRC/King Saud bin Abdulaziz University for Health Sciences (KSAU-HS), Ministry of National Guard-Health Affairs (MNGHA)King Abdullah International Medical Research Center (KAIMRC)/King Saud bin Abdulaziz University for Health Sciences (KSAU-HS), Colorectal Cancer Research Program, MNGHADivision of Paediatric Dentistry and Orthodontics, Faculty of Dentistry, The University of Hong KongAbstract Mandibular condylar cartilage (MCC) is a multi-zonal heterogeneous fibrocartilage containing different types of cells, but the factors/mechanisms governing the phenotypic transition across the zones have not been fully understood. The reliability of molecular studies heavily rely on the procurement of pure cell populations from the heterogeneous tissue. We used a combined laser-capture microdissection and microarray analysis approach which allowed identification of differential zone-specific gene expression profiling and altered pathways in the MCC of 5-week-old rats. The bioinformatics analysis demonstrated that the MCC cells clearly exhibited distinguishable phenotypes from the articular chondrocytes. Additionally, a set of genes has been determined as potential markers to identify each MCC zone individually; Crab1 gene showed the highest enrichment while Clec3a was the most downregulated gene at the superficial layer, which consists of fibrous (FZ) and proliferative zones (PZ). Ingenuity Pathway Analysis revealed numerous altered signaling pathways; Leukocyte extravasation signaling pathway was predicted to be activated at all MCC zones, in particular mature and hypertrophic chondrocytes zones (MZ&HZ), when compared with femoral condylar cartilage (FCC). Whereas Superpathway of Cholesterol Biosynthesis showed predicted activation in both FZ and PZ as compared with deep MCC zones and FCC. Determining novel zone-specific differences of large group of potential genes, upstream regulators and pathways in healthy MCC would improve our understanding of molecular mechanisms on regional (zonal) basis, and provide new insights for future therapeutic strategies.https://doi.org/10.1038/s41598-021-96071-7 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Aisha M. Basudan Mohammad Azhar Aziz Yanqi Yang |
spellingShingle |
Aisha M. Basudan Mohammad Azhar Aziz Yanqi Yang Implications of zonal architecture on differential gene expression profiling and altered pathway expressions in mandibular condylar cartilage Scientific Reports |
author_facet |
Aisha M. Basudan Mohammad Azhar Aziz Yanqi Yang |
author_sort |
Aisha M. Basudan |
title |
Implications of zonal architecture on differential gene expression profiling and altered pathway expressions in mandibular condylar cartilage |
title_short |
Implications of zonal architecture on differential gene expression profiling and altered pathway expressions in mandibular condylar cartilage |
title_full |
Implications of zonal architecture on differential gene expression profiling and altered pathway expressions in mandibular condylar cartilage |
title_fullStr |
Implications of zonal architecture on differential gene expression profiling and altered pathway expressions in mandibular condylar cartilage |
title_full_unstemmed |
Implications of zonal architecture on differential gene expression profiling and altered pathway expressions in mandibular condylar cartilage |
title_sort |
implications of zonal architecture on differential gene expression profiling and altered pathway expressions in mandibular condylar cartilage |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-08-01 |
description |
Abstract Mandibular condylar cartilage (MCC) is a multi-zonal heterogeneous fibrocartilage containing different types of cells, but the factors/mechanisms governing the phenotypic transition across the zones have not been fully understood. The reliability of molecular studies heavily rely on the procurement of pure cell populations from the heterogeneous tissue. We used a combined laser-capture microdissection and microarray analysis approach which allowed identification of differential zone-specific gene expression profiling and altered pathways in the MCC of 5-week-old rats. The bioinformatics analysis demonstrated that the MCC cells clearly exhibited distinguishable phenotypes from the articular chondrocytes. Additionally, a set of genes has been determined as potential markers to identify each MCC zone individually; Crab1 gene showed the highest enrichment while Clec3a was the most downregulated gene at the superficial layer, which consists of fibrous (FZ) and proliferative zones (PZ). Ingenuity Pathway Analysis revealed numerous altered signaling pathways; Leukocyte extravasation signaling pathway was predicted to be activated at all MCC zones, in particular mature and hypertrophic chondrocytes zones (MZ&HZ), when compared with femoral condylar cartilage (FCC). Whereas Superpathway of Cholesterol Biosynthesis showed predicted activation in both FZ and PZ as compared with deep MCC zones and FCC. Determining novel zone-specific differences of large group of potential genes, upstream regulators and pathways in healthy MCC would improve our understanding of molecular mechanisms on regional (zonal) basis, and provide new insights for future therapeutic strategies. |
url |
https://doi.org/10.1038/s41598-021-96071-7 |
work_keys_str_mv |
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