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http://purl.uniprot.org/citations/28612031http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/28612031http://www.w3.org/2000/01/rdf-schema#comment"

Objective

Decreased expression of collagen type II in favour of collagen type I or X is one hallmark of chondrocyte phenotype changes in osteoarthritic (OA) cartilage. MicroRNA-(miR-) 29b was previously shown to target collagens in several tissues. We studied whether it could contribute to collagen imbalance in chondrocytes with an impaired phenotype.

Methods

After preliminary microarrays screening, miR-29b levels were measured by RT-quantitative PCR in in vitro models of chondrocyte phenotype changes (IL-1β challenge or serial subculturing) and in chondrocytes from OA and non-OA patients. Potential miR-29b targets identified in silico in 3'-UTRs of collagens mRNAs were tested with luciferase reporter assays. The impact of premiR-29b overexpression in ATDC5 cells was studied on collagen mRNA levels and synthesis (Sirius red staining) during chondrogenesis.

Results

MiR-29b level increased significantly in IL-1β-stimulated and weakly in subcultured chondrocytes. A 5.8-fold increase was observed in chondrocytes from OA versus non-OA patients. Reporter assays showed that miR-29b targeted COL2A1 and COL1A2 3'-UTRs although with a variable recovery upon mutation. In ATDC5 cells overexpressing premiR-29b, collagen production was reduced while mRNA levels increased.

Conclusions

By acting probably as a posttranscriptional regulator with a different efficacy on COL2A1 and COL1A2 expression, miR-29b can contribute to the collagens imbalance associated with an abnormal chondrocyte phenotype."xsd:string
http://purl.uniprot.org/citations/28612031http://purl.org/dc/terms/identifier"doi:10.1155/2017/9792512"xsd:string
http://purl.uniprot.org/citations/28612031http://purl.uniprot.org/core/author"Branlant C."xsd:string
http://purl.uniprot.org/citations/28612031http://purl.uniprot.org/core/author"Charpentier B."xsd:string
http://purl.uniprot.org/citations/28612031http://purl.uniprot.org/core/author"Salone V."xsd:string
http://purl.uniprot.org/citations/28612031http://purl.uniprot.org/core/author"Behm-Ansmant I."xsd:string
http://purl.uniprot.org/citations/28612031http://purl.uniprot.org/core/author"Clement T."xsd:string
http://purl.uniprot.org/citations/28612031http://purl.uniprot.org/core/author"Moulin D."xsd:string
http://purl.uniprot.org/citations/28612031http://purl.uniprot.org/core/author"Jouzeau J.Y."xsd:string
http://purl.uniprot.org/citations/28612031http://purl.uniprot.org/core/author"Koufany M."xsd:string
http://purl.uniprot.org/citations/28612031http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/28612031http://purl.uniprot.org/core/name"Biomed Res Int"xsd:string
http://purl.uniprot.org/citations/28612031http://purl.uniprot.org/core/pages"9792512"xsd:string
http://purl.uniprot.org/citations/28612031http://purl.uniprot.org/core/title"MicroRNA-29b Contributes to Collagens Imbalance in Human Osteoarthritic and Dedifferentiated Articular Chondrocytes."xsd:string
http://purl.uniprot.org/citations/28612031http://purl.uniprot.org/core/volume"2017"xsd:string
http://purl.uniprot.org/citations/28612031http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/28612031
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