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• W2017130282 abstract "Mutations in cartilage oligomeric matrix protein (COMP), a large extracellular glycoprotein expressed in musculoskeletal tissues, cause two skeletal dysplasias, pseudoachondroplasia and multiple epiphyseal dysplasia. These mutations lead to massive intracellular retention of COMP, chondrocyte death and loss of growth plate chondrocytes that are necessary for linear growth. In contrast, COMP null mice have only minor growth plate abnormalities, normal growth and longevity. This suggests that reducing mutant and wild-type COMP expression in chondrocytes may prevent the toxic cellular phenotype causing the skeletal dysplasias. We tested this hypothesis using RNA interference to reduce steady state levels of COMP mRNA. A panel of shRNAs directed against COMP was tested. One shRNA (3B) reduced endogenous and recombinant COMP mRNA dramatically, regardless of expression levels. The activity of the shRNA against COMP mRNA was maintained for up to 10 weeks. We also demonstrate that this treatment reduced ER stress. Moreover, we show that reducing steady state levels of COMP mRNA alleviates intracellular retention of other extracellular matrix proteins associated with the pseudoachondroplasia cellular pathology. These findings are a proof of principle and the foundation for the development of a therapeutic intervention based on reduction of COMP expression." @default.
• W2017130282 created "2016-06-24" @default.
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• W2017130282 date "2010-04-22" @default.
• W2017130282 modified "2023-09-25" @default.
• W2017130282 title "RNAi Reduces Expression and Intracellular Retention of Mutant Cartilage Oligomeric Matrix Protein" @default.
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• W2017130282 doi "https://doi.org/10.1371/journal.pone.0010302" @default.
• W2017130282 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2858657" @default.
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