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足细胞细胞膜动力学的活体和肾切片成像

Intravital and Kidney Slice Imaging of Podocyte Membrane Dynamics.

作者信息

Brähler Sebastian, Yu Haiyang, Suleiman Hani, Krishnan Gokul M, Saunders Brian T, Kopp Jeffrey B, Miner Jeffrey H, Zinselmeyer Bernd H, Shaw Andrey S

机构信息

Department of Pathology and Immunology and.

Kidney Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland.

出版信息

J Am Soc Nephrol. 2016 Nov;27(11):3285-3290. doi: 10.1681/ASN.2015121303. Epub 2016 Apr 1.

Abstract

In glomerular disease, podocyte injury results in a dramatic change in cell morphology known as foot process effacement. Remodeling of the actin cytoskeleton through the activity of small GTPases was identified as a key mechanism in effacement, with increased membrane activity and motility in vitro However, whether podocytes are stationary or actively moving cells in vivo remains debated. Using intravital and kidney slice two-photon imaging of the three-dimensional structure of mouse podocytes, we found that uninjured podocytes remained nonmotile and maintained a canopy-shaped structure over time. On expression of constitutively active Rac1, however, podocytes changed shape by retracting processes and clearly exhibited domains of increased membrane activity. Constitutive activation of Rac1 also led to podocyte detachment from the glomerular basement membrane, and we detected detached podocytes crawling on the surface of the tubular epithelium and occasionally, in contact with peritubular capillaries. Podocyte membrane activity also increased in the inflammatory environment of immune complex-mediated GN. Our results provide evidence that podocytes transition from a static to a dynamic state in vivo, shedding new light on mechanisms in foot process effacement.

摘要

在肾小球疾病中,足细胞损伤会导致细胞形态发生显著变化,即足突消失。通过小GTP酶的活性对肌动蛋白细胞骨架进行重塑被确定为足突消失的关键机制,在体外会增加膜活性和运动性。然而,足细胞在体内是静止细胞还是活跃移动细胞仍存在争议。利用对小鼠足细胞三维结构的活体和肾切片双光子成像,我们发现未受损的足细胞保持不运动状态,并随着时间推移维持伞状结构。然而,在组成型活性Rac1表达时,足细胞通过缩回突起改变形状,并明显表现出膜活性增加的区域。Rac1的组成型激活还导致足细胞从肾小球基底膜脱离,并且我们检测到脱离的足细胞在肾小管上皮表面爬行,偶尔与肾小管周围毛细血管接触。在免疫复合物介导的肾小球肾炎的炎症环境中,足细胞膜活性也会增加。我们的结果提供了证据,表明足细胞在体内从静态转变为动态状态,为足突消失的机制提供了新的线索。

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