【摘 要】
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Objective: To investigate the potential role of p62, a characterized adaptor protein for selective autophagy, in RANKLinduced osteoclastogenesis.Methods: Real-time quantitative PCR and western blot an
【机 构】
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School & Hospital of Stomatology,Wuhan University 237# Luoyu Road,Hongshan District,Wuhan,China
【出 处】
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11th Asian Congress on Oeal and Maxillofacial Surgery(第十一届亚洲
论文部分内容阅读
Objective: To investigate the potential role of p62, a characterized adaptor protein for selective autophagy, in RANKLinduced osteoclastogenesis.Methods: Real-time quantitative PCR and western blot analyses were used to evaluate the expression levels of autophagy-related markers during RANKL-induced osteoclastogenesis in mouse macrophage-like RAW264.7 cells.Meanwhile, the potential relationship between p62/LC3 localization and F-actin ring formation was tested using double-labeling immunofluorescence.Then, the expression of p62 in RAW264.7 cells was knocked down using smallinterfering RNA (siRNA), followed by detecting its influence on RANKL-induced autophagy activation, osteoclast differentiation, and F-actin ring formation.
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