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Anguo Ying,Zhifeng Li,Yuxiang Ni,Songlin Xu,Hailiang Hou,Huanan Hu 한국공업화학회 2015 Journal of Industrial and Engineering Chemistry Vol.24 No.-
Four novel multiple-acidic ionic liquids based on triethanolamine (TEA) were prepared and used as efficient catalysts to synthesize bis-indolylmethanes at room temperature without any organic solvent. [TEOA][HSO4] showed the best catalytic performance. The optimal amount of catalyst was 10 mol%. Various aldehydes/ketones reacted with indole/substituted indole smoothly and afforded to corresponding products in 70–99% yields within minutes. Additionally, the ionic liquid could be reused up to five times with only a slight decrease in catalytic activity. Finally, a possible reaction mechanism was given. Techniques of acidity test and NMR were introduced to verify the proposed mechanism.
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Xinjie Gao,Heng Yang,Weiping Xiao,Jiabin Su,Yuwen Zhang,He Wang,Wei Ni,Yuxiang Gu 한국생체재료학회 2022 생체재료학회지 Vol.26 No.4
Background: Despite limited efficiency, modulation of microglia/macrophages has shown to attenuate neuroinflammation after intracerebral hemorrhage (ICH). In this context, we evaluated the efficacy of modified exosomal signal regulatory protein α (SIRPα) variants (SIRPα-v Exos) in microglia/macrophages and neuroinflammation-associated white matter injury after ICH. Methods: SIRPα-v Exos were engineered to block CD47-SIRPα interactions. After obtaining SIRPα-v Exos from lentivirus-infected mesenchymal stem cells, C57BL/6 mice suffering from ICH underwent consecutive intravenous injections of SIRPα-v Exos (6 mg/kg) for 14 days. Afterwards, the volume of hematoma and neurological dysfunctions were assessed in mice continuously until 35 days after ICH. In addition, demyelination, electrophysiology and neuroinflammation were evaluated. Furthermore, the mechanisms of microglial regulation by SIRPα-v Exos were investigated in vitro under coculture conditions. Results: The results demonstrated that the clearance of hematoma in mice suffering from ICH was accelerated after SIRPα-v Exo treatment. SIRPα-v Exos improved long-term neurological dysfunction by ameliorating white matter injury. In addition, SIRPα-v Exos recruited regulatory T cells (Tregs) to promote M2 polarization of microglia/macrophages in the peri-hematoma tissue. In vitro experiments further showed that SIRPα-v Exos regulated primary microglia in a direct and indirect manner in synergy with Tregs. Conclusion: Our studies revealed that SIRPα-v Exos could accelerate the clearance of hematoma and ameliorate secondary white matter injury after ICH through regulation of microglia/macrophages. SIRPα-v Exos may become a promising treatment for ICH in clinical practice.
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