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本文引用的文献

1
Intravital imaging of podocyte calcium in glomerular injury and disease.肾小球损伤和疾病中足细胞钙的活体成像。
J Clin Invest. 2014 May;124(5):2050-8. doi: 10.1172/JCI71702. Epub 2014 Apr 8.
2
Two-photon microscopy reveals stationary podocytes in living zebrafish larvae.双光子显微镜揭示活体斑马鱼幼鱼中静止的足细胞。
J Am Soc Nephrol. 2014 Apr;25(4):681-6. doi: 10.1681/ASN.2013020178. Epub 2013 Dec 5.
3
Tracking the fate of glomerular epithelial cells in vivo using serial multiphoton imaging in new mouse models with fluorescent lineage tags.利用带有荧光谱系标签的新型小鼠模型中的连续多光子成像技术在体内追踪肾小球上皮细胞的命运。
Nat Med. 2013 Dec;19(12):1661-6. doi: 10.1038/nm.3405. Epub 2013 Nov 24.
4
Rac1 activation in podocytes induces rapid foot process effacement and proteinuria.Rac1 在足细胞中的激活导致足突融合和蛋白尿的快速发生。
Mol Cell Biol. 2013 Dec;33(23):4755-64. doi: 10.1128/MCB.00730-13. Epub 2013 Sep 23.
5
Divergent functions of the Rho GTPases Rac1 and Cdc42 in podocyte injury.Rho GTPases Rac1 和 Cdc42 在足细胞损伤中的功能分化。
Kidney Int. 2013 Nov;84(5):920-30. doi: 10.1038/ki.2013.175. Epub 2013 May 15.
6
PD-1 promotes immune exhaustion by inducing antiviral T cell motility paralysis.PD-1 通过诱导抗病毒 T 细胞运动麻痹促进免疫衰竭。
J Exp Med. 2013 Apr 8;210(4):757-74. doi: 10.1084/jem.20121416. Epub 2013 Mar 25.
7
An intact kidney slice model to investigate vasa recta properties and function in situ.一种用于原位研究直小血管特性和功能的完整肾切片模型。
Nephron Physiol. 2012;120(3):p17-31. doi: 10.1159/000339110. Epub 2012 Jul 20.
8
Activation of RhoA in podocytes induces focal segmental glomerulosclerosis.足细胞中 RhoA 的激活可导致局灶节段性肾小球硬化。
J Am Soc Nephrol. 2011 Sep;22(9):1621-30. doi: 10.1681/ASN.2010111146. Epub 2011 Jul 29.
9
Intestinal crypt homeostasis results from neutral competition between symmetrically dividing Lgr5 stem cells.肠隐窝稳态源自对称分裂的 Lgr5 干细胞之间的中性竞争。
Cell. 2010 Oct 1;143(1):134-44. doi: 10.1016/j.cell.2010.09.016.
10
A high-powered view of the filtration barrier.高倍视野下的滤过屏障。
J Am Soc Nephrol. 2010 Nov;21(11):1835-41. doi: 10.1681/ASN.2010040378. Epub 2010 Jun 24.

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.

DOI:10.1681/ASN.2015121303
PMID:27036737
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5084896/
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。