Notch1-ADAM8 positive feed-back loop regulates the degradation of chondrogenic extracellular matrix and osteoarthritis progression
Autor: | Yan Liu, Xin-Yu Yun, Biao Duan, Zhe-Hai Li, Fu-Guo Shi, Yong Wang, He Hu, Xi-Rui Han, Ming-Yu Yan, An-Fu Chen, Ya-Long Liu, Hao Xue |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
ADAM8 Notch signaling pathway lcsh:Medicine Biochemistry Cell Line Extracellular matrix Rats Sprague-Dawley 03 medical and health sciences 0302 clinical medicine Chondrocytes Osteoarthritis Animals lcsh:QH573-671 Receptor Notch1 Extracellular Signal-Regulated MAP Kinases Molecular Biology Aggrecan 030203 arthritis & rheumatology Regulation of gene expression Feedback Physiological Gene knockdown Notch1 ECM lcsh:Cytology Chemistry Research lcsh:R NF-kappa B Membrane Proteins Cell Biology Chondrogenesis Cell biology Extracellular Matrix Rats Up-Regulation ErbB Receptors ADAM Proteins 030104 developmental biology Phenotype Gene Knockdown Techniques Disease Progression Signal transduction MMP-9 Signal Transduction |
Zdroj: | Cell Communication and Signaling : CCS Cell Communication and Signaling, Vol 17, Iss 1, Pp 1-17 (2019) |
ISSN: | 1478-811X |
Popis: | Background Osteoarthritis (OA) is one of the most prevalent joint disease, and there are still no effective therapeutic agents or clinical methods for the cure of this disease to date. The degradation of cartilage extracellular matrix (ECM) is a major cause of OA. Method IL-1β was used to induce chondrogenic degradation. Q-PCR and Western blotting were used to detect mRNA and protein level, respectively. ELISA was used to detect the secreted TNF-α and IL-6 level. Immunofluorescence was used to detect the protein level of Aggrecan, Collagen II and ki67. TUNEL and flow cytometry were used to examine cell apoptosis of chondrocytes. ChIP and luciferase assay were used to study molecular gene regulation. Osteoarthritic animal model and Safranin-O staining were used to determine the in vivo OA phenotype. Results The expression of ADAM8 was up-regulated in osteoarthritic chondrocytes. Knockdown of ADAM8 suppressed the OA phenotype in the in vitro OA cell model. ADAM8 regulated OA progression through the activation of EGFR/ERK/NF-κB signaling pathway. Inhibition of Notch signaling suppressed OA phenotype in the in vitro OA cell model. Notch signaling regulated the gene expression of ADAM8 directly via Hes1. Notch1-ADAM8 positive feedback loop promoted the progression of OA in vivo. Conclusion Notch1-ADAM8 feed-back loop regulates the degradation of chondrogenic extracellular matrix and osteoarthritis progression. |
Databáze: | OpenAIRE |
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