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Jiangtao Hu,Qianhong Gao,Lu Xu,Minglei Wang,Maojiang Zhang,Kuo Zhang,Xiaojing Guo,Weihua Liu,Guozhong Wu 한국섬유공학회 2018 Fibers and polymers Vol.19 No.7
Herein we report a simple and reproducible method for fabricating highly durable and robust superhydrophobic and superoleophilic cotton fabrics via simultaneous radiation-induced graft polymerization of glycidyl methacrylate and subsequent chemical modifications with aminopropyltriethoxysilane and hexamethyldisilazane. The chemical structure and the surface topography of the pristine and the modified cotton fabrics were investigated in detail by ATR-FTIR, XPS, and 29Si NMR, and a grafting layer was successfully immobilized onto the surface of the cotton fabric by forming covalent bonds. Multi-dimensional surface roughness was created by combining micro-sized fibers of the cotton fabric, nanoscaled protuberances of the grafting chain, and molecular level spherical projection points of silicon methyl. The superhydrophobic cotton fabric exhibited long-term stability, ultra-high durability and robustness, and maintained its properties even after 25 wash cycles. The fabric also showed excellent water repellency with a water contact angle of 153 o and a high efficiency of oil/water separation (98 %). The superhydrophobic/superoleophilic cotton fabric developed in the present work exhibits important potential applications in superhydrophobic textiles and oil/water separation.
BK Channel Deficiency in Osteoblasts Reduces Bone Formation via the Wnt/β-Catenin Pathway
Jiang, Lan,Yang, Qianhong,Gao, Jianjun,Yang, Jiahong,He, Jiaqi,Xin, Hong,Zhang, Xuemei Korean Society for Molecular and Cellular Biology 2021 Molecules and cells Vol.44 No.8
Global knockout of the BK channel has been proven to affect bone formation; however, whether it directly affects osteoblast differentiation and the mechanism are elusive. In the current study, we further investigated the role of BK channels in bone development and explored whether BK channels impacted the differentiation and proliferation of osteoblasts via the canonical Wnt signaling pathway. Our findings demonstrated that knockout of Kcnma1 disrupted the osteogenesis of osteoblasts and inhibited the stabilization of β-catenin. Western blot analysis showed that the protein levels of Axin1 and USP7 increased when Kcnma1 was deficient. Together, this study confirmed that BK ablation decreased bone mass via the Wnt/β-catenin signaling pathway. Our findings also showed that USP7 might have the ability to stabilize the activity of Axin1, which would increase the degradation of β-catenin in osteoblasts.