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• W2074325918 abstract "Histone deacetylase 4 (HDAC4) is a critical negative regulator for chondrocyte hypertrophy by binding to and inhibiting Runx2, a critical transcription factor for chondrocyte hypertrophy. It is unclear how HDAC4 expression and stability are regulated during growth plate development. We report here that inhibition of mitogen-activated protein kinase (MAPK) p38 by dominant negative p38 or p38 inhibitor prevents HDAC4 degradation. Mutation of a potential caspase-2 and 3 cleavage site Asp289 stabilizes HDAC4 in chondrocytes. In contrast, constitutively active MAPK kinase 6 (constitutive activator of p38) transgenic mice exhibit decreased HDAC4 content in vivo. We also observed that p38 stimulates caspase-3 activity in chondrocytes. Inhibition of p38 or caspases reduced HDAC4 degradation. HDAC4 inhibited Runx2 promoter activity in a dose-dependent manner and caspase inhibitors further enhanced this inhibition by preventing HDAC4 degradation. Overall, these results demonstrate that p38 promotes HDAC4 degradation by increasing caspase-mediated cleavage, which releases Runx2 from a repressive influence of HDAC4 and promotes the chondrocyte hypertrophy and bone formation." @default.
• W2074325918 created "2016-06-24" @default.
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• W2074325918 date "2015-02-01" @default.
• W2074325918 modified "2023-10-15" @default.
• W2074325918 title "Mitogen-activated protein kinase p38 induces HDAC4 degradation in hypertrophic chondrocytes" @default.
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• W2074325918 doi "https://doi.org/10.1016/j.bbamcr.2014.11.003" @default.
• W2074325918 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4289442" @default.
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