The anterior disc displacement (ADD) leads to temporomandibular joint osteoarthritis (TMJOA) and mandibular growth retardation in adolescents. To investigate the potential functional role of fibrocartilage stem cells (FCSCs) during the process, a surgical ADD-TMJOA mouse model was established. From 1 week after model generation, ADD mice exhibited aggravated mandibular growth retardation with osteoarthritis (OA)-like joint cartilage degeneration, manifesting with impaired chondrogenic differentiation and loss of subchondral bone homeostasis. Lineage tracing using Gli1-CreER+; Tmfl/-mice and Sox9-CreER+;Tmfl/-mice showed that ADD interfered with the chondrogenic capacity of Gli1+ FCSCs as well as osteogenic differentiation of Sox9+ lineage, mainly in the middle zone of TMJ cartilage. Then, a surgically induced disc reposition (DR) mouse model was generated. The inhibited FCSCs capacity was significantly alleviated by DR treatment in ADD mice. And both the ADD mice and adolescent ADD patients had significantly relieved OA phenotype and improved condylar growth after DR treatment. In conclusion, ADD-TMJOA leads to impaired chondrogenic progenitor capacity and osteogenesis differentiation of FCSCs lineage, resulting in cartilage degeneration and loss of subchondral bone homeostasis, finally causing TMJ growth retardation. DR at an early stage could significantly alleviate cartilage degeneration and restore TMJ cartilage growth potential.
Discrimination of the catalytic ability of heterogeneous biochar components is often challenging. Herein, a sewage sludge-derived biochar (SDBC) was prepared to activate peroxydisulfate (PDS) for tetracycline (TC) degradation. To verify the contribution of different carbon components, SDBC was bleached with NaClO2 and CH3COOH to remove noncondensed aromatic carbon (NAC) contained in biochar, which was confirmed by 13C Nuclear Magnetic Resonance. The batch degradation experiment revealed that NAC removal decreased TC degradation by SDBC from 84.1% to 33.2% within 2 h, indicating its significant role in PDS activation. The quenching and electron paramagnetic resonance experiments suggested a very minor contribution of radical pathway in TC degradation. Instead, the electron transfer pathway predominated TC degradation mechanism as inferred by electrochemical tests. This is likely ascribed to formation of a biochar-PDS metastable complex, facilitating electron transfer from tetracycline-like compounds. An X-ray photoelectron spectroscopy confirmed that the percent of graphitic N in SDBC decreased after the degradation reaction, which suggested graphitic N is an important active site in biochar. Besides, acid-washed SDBC did not change TC degradation behavior excluding significant contribution of minerals in SDBC to PDS activation. Thus, the roles of biochar components in catalyzing PDS were quantified for the first time, proving insight for selection and manipulation of biochar in catalyzing PDS in environmental application.
Abstract The anterior disc displacement (ADD) leads to temporomandibular joint osteoarthritis (TMJOA) and mandibular growth retardation in adolescent. To investigate the potential functional role of fibrocartilage stem cells (FCSCs) during the process, a surgical ADD-TMJOA mouse model was established. From 1 week after model generation, ADD mice exhibited aggravated mandibular growth retardation with osteoarthritis (OA)-like joint cartilage degeneration, manifesting with impaired chondrogenic differentiation and loss of subchondral bone homeostasis. Lineage tracing using Gli1-CreER + ; Tm fl/− mice and Sox9-CreER + ; Tm fl/− mice showed that ADD interfered the chondrogenic capacity of Gli1 + FCSCs as well as osteogenic differentiation of Sox9 + lineage, mainly in the middle zone of TMJ cartilage. Then, a surgically induced disc reposition (DR) mouse model was generated. The inhibited FCSCs capacity were significantly alleviated by DR treatment in ADD mice. And both the ADD mice and adolescent ADD patients had significantly relieved OA phenotype and improved condylar growth after DR treatment. In conclusion, ADD-TMJOA leads to impaired chondrogenic progenitor capacity and osteogenesis differentiation of FCSCs lineage, results in cartilage degeneration and loss of subchondral bone homeostasis, finally causes TMJ growth retardation. DR at an early stage could significantly alleviate cartilage degeneration and restore TMJ cartilage growth potential.
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