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Pyruvate Dehydrogenase Kinase 1 inhibition mediated oxidative phosphorylation enhancement in cartilage promotes osteoarthritis progression

Xian‐Wen Yang, Qingsong Jiang, Tiankuo Luan, Yu Chao, Zhibo Liu, Ting Wang, Jingyuan Wan, Jiayu Huang, Ke Li

2023BMC Musculoskeletal Disorders14 citationsDOIOpen Access PDF

Abstract

Osteoarthritis (OA) is a common disease characterized by cartilage degradation. Growing evidence showed that glucose metabolism impacts joint homeostasis and an imbalance between glycolysis and oxidative phosphorylation (OXPHOS) may exacerbate OA progression, however, a definitive link is yet to be established. Here, we report that pyruvate metabolism and oxidative phosphorylation pathway is enriched in OA cartilage through gene set enrichment analysis (GSEA) and expression of Pyruvate Dehydrogenase Kinase 1 (PDK1), an enzyme that can phosphorylate Pyruvate Dehydrogenase (PDH), and inhibit pyruvate fluxes into the tricarboxylic acid (TCA) cycle and to OXPHOS, in articular cartilage is notably reduced through destabilization of medial meniscus (DMM). Moreover, by inhibiting PDK1, cartilage loss is markedly accelerated in DMM-induced OA through extracellular matrix (ECM) degradation and apoptosis of chondrocytes. These results indicate that PDK1 is involved in the progression of OA through accelerating cartilage matrix degradation and synovium inflammation to ameliorate cartilage degeneration.

Topics & Concepts

Pyruvate dehydrogenase complexPyruvate dehydrogenase kinasePKM2Pyruvate decarboxylationGlycolysisCitric acid cycleCartilageOxidative phosphorylationOsteoarthritisCell biologyBiochemistryMedicineEndocrinologyPyruvate kinaseInternal medicineChemistryBiologyMetabolismPathologyEnzymeAnatomyAlternative medicineOsteoarthritis Treatment and MechanismsPeroxisome Proliferator-Activated ReceptorsChemokine receptors and signaling
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