首页> 外文期刊>International Journal of Experimental Diabetes Research: Experimental Diabesity Research >Involvement of F-Actin in Chaperonin-Containing t-Complex 1 Beta Regulating Mouse Mesangial Cell Functions in a Glucose-Induction Cell Model
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Involvement of F-Actin in Chaperonin-Containing t-Complex 1 Beta Regulating Mouse Mesangial Cell Functions in a Glucose-Induction Cell Model

机译:F-肌动蛋白参与伴侣蛋白的t复杂1 Beta调节葡萄糖诱导细胞模型中的小鼠系膜细胞功能。

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The aim of this study is to investigate the role of chaperonin-containing t-complex polypeptide 1 beta (CCT2) in the regulation of mouse mesangial cell (mMC) contraction, proliferation, and migration with filamentous/globular-(F/G-) actin ratio under high glucose induction. A low CCT2 mMC model induced by treatment of small interference RNA was established. Groups with and without low CCT2 induction examined in normal and high (H) glucose conditions revealed the following major results (1) low CCT2 or H glucose showed the ability to attenuate F/G-actin ratio; (2) groups with low F/G-actin ratio all showed less cell contraction; (3) suppression of CCT2 may reduce the proliferation and migration which were originally induced by H glucose. In conclusion, CCT2 can be used as a specific regulator for mMC contraction, proliferation, and migration affected by glucose, which mechanism may involve the alteration of F-actin, particularly for cell contraction.
机译:这项研究的目的是调查伴侣蛋白的t-复合多肽1β(CCT2)在调节小鼠系膜细胞(mMC)收缩,增殖和丝状/球状(F / G-)迁移中的作用高葡萄糖诱导下的肌动蛋白比。建立了通过处理小干扰RNA诱导的低CCT2 mMC模型。在正常和高(H)葡萄糖条件下检查有无CCT2诱导的组显示以下主要结果:(1)低CCT2或H葡萄糖具有减弱F / G-肌动蛋白比率的能力; (2)F / G-肌动蛋白比率低的组均显示较少的细胞收缩; (3)抑制CCT2可以减少最初由H葡萄糖诱导的增殖和迁移。总之,CCT2可以用作受葡萄糖影响的mMC收缩,增殖和迁移的特异性调节剂,该机制可能涉及F-肌动蛋白的改变,尤其是细胞收缩。

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