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The ADF/Cofilin-Pathway and Actin Dynamics in Podocyte Injury

机译:足细胞损伤中的ADF / Cofilin途径和肌动蛋白动力学

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ADF/cofilins are the major regulators of actin dynamics in mammalian cells. The activation of ADF/cofilins is controlled by a variety of regulatory mechanisms. Dysregulation of ADF/cofilin may result in loss of a precisely organized actin cytoskeletal architecture and can reduce podocyte migration and motility. Recent studies suggest that cofilin-1 can be regulated through several extracellular signals and slit diaphragm proteins. Cofilin knockdown and knockout animal models show dysfunction of glomerular barrier and filtration with foot process effacement and loss of secondary foot processes. This indicates that cofilin-1 is necessary for modulating actin dynamics in podocytes. Podocyte alterations in actin architecture may initiate or aid the progression of a large variety of glomerular diseases, and cofilin activity is required for reorganization of an intact filtration barrier. Since almost all proteinuric diseases result from a similar phenotype with effacement of the foot processes, we propose that cofilin-1 is at the centre stage of the development of proteinuria and thus may be an attractive drug target for antiproteinuric treatment strategies.
机译:ADF / cofilins是哺乳动物细胞中肌动蛋白动力学的主要调节剂。 ADF / cofilins的激活受多种调控机制控制。 ADF / cofilin的失调可能导致精确组织的肌动蛋白细胞骨架结构的丧失,并可能减少足细胞的迁移和运动。最近的研究表明,cofilin-1可以通过几种细胞外信号和裂膜蛋白来调节。 Cofilin基因敲除和基因敲除动物模型显示肾小球屏障功能障碍和滤过功能,伴有足突消失和继发性足突丧失。这表明cofilin-1是调节足细胞中肌动蛋白动力学所必需的。肌动蛋白结构中的足细胞改变可能引发或帮助多种肾小球疾病的进展,重组完整的滤过屏障需要cofilin活性。由于几乎所有蛋白尿疾病均来自相似的表型并伴有脚突,因此我们建议cofilin-1处于蛋白尿发展的中心阶段,因此可能是抗蛋白尿治疗策略的诱人药物靶标。

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