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1
Toward the development of podocyte-specific drugs.致力于开发足细胞特异性药物。
Kidney Int. 2010 Apr;77(8):662-8. doi: 10.1038/ki.2009.559. Epub 2010 Feb 3.
2
Targeting podocyte-associated diseases.靶向足细胞相关疾病。
Adv Drug Deliv Rev. 2010 Nov 30;62(14):1325-36. doi: 10.1016/j.addr.2010.08.012. Epub 2010 Sep 7.
3
New insights into the role of podocytes in proteinuria.足细胞在蛋白尿中作用的新见解。
Nat Rev Nephrol. 2009 Aug;5(8):463-8. doi: 10.1038/nrneph.2009.108. Epub 2009 Jul 7.
4
Urine podocyte mRNAs mark progression of renal disease.尿足细胞信使核糖核酸标志着肾脏疾病的进展。
J Am Soc Nephrol. 2009 May;20(5):1041-52. doi: 10.1681/ASN.2007121328. Epub 2009 Apr 23.
5
Role of the podocyte in proteinuria.足细胞在蛋白尿中的作用。
Pediatr Nephrol. 2011 Oct;26(10):1775-80. doi: 10.1007/s00467-010-1725-5. Epub 2010 Dec 24.
6
A preclinical overview of emerging therapeutic targets for glomerular diseases.肾小球疾病新兴治疗靶点的临床前概述。
Expert Opin Ther Targets. 2019 Jul;23(7):593-606. doi: 10.1080/14728222.2019.1626827. Epub 2019 Jun 12.
7
Targeting the podocyte cytoskeleton: from pathogenesis to therapy in proteinuric kidney disease.靶向足细胞细胞骨架:从蛋白尿性肾病的发病机制到治疗
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Podocytes: recent biomolecular developments.足细胞:近期生物分子研究进展
Biomol Concepts. 2014 Aug;5(4):319-30. doi: 10.1515/bmc-2014-0020.
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Vitamin D down-regulates TRPC6 expression in podocyte injury and proteinuric glomerular disease.维生素 D 下调足细胞损伤和蛋白尿性肾小球疾病中 TRPC6 的表达。
Am J Pathol. 2013 Apr;182(4):1196-204. doi: 10.1016/j.ajpath.2012.12.011. Epub 2013 Feb 4.
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Update on the podocyte.足细胞的最新进展。
Curr Opin Nephrol Hypertens. 2009 May;18(3):206-11. doi: 10.1097/mnh.0b013e328326f3ca.

引用本文的文献

1
Still finding ways to augment the existing management of acute and chronic kidney diseases with targeted gene and cell therapies: Opportunities and hurdles.仍在寻找通过靶向基因和细胞疗法增强急性和慢性肾脏病现有管理的方法:机遇与障碍。
Front Med (Lausanne). 2023 Mar 7;10:1143028. doi: 10.3389/fmed.2023.1143028. eCollection 2023.
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KIBRA upregulation increases susceptibility to podocyte injury and glomerular disease progression.KIBRA 上调增加了足细胞损伤和肾小球疾病进展的易感性。
JCI Insight. 2023 Apr 10;8(7):e165002. doi: 10.1172/jci.insight.165002.
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Silver nanoparticle modified surfaces induce differentiation of mouse kidney-derived stem cells.银纳米颗粒修饰的表面诱导小鼠肾源性干细胞分化。
RSC Adv. 2018 Jun 4;8(36):20334-20340. doi: 10.1039/c8ra02145g. eCollection 2018 May 30.
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Renal cell markers: lighthouses for managing renal diseases.肾细胞标志物:管理肾脏疾病的灯塔。
Am J Physiol Renal Physiol. 2021 Dec 1;321(6):F715-F739. doi: 10.1152/ajprenal.00182.2021. Epub 2021 Oct 11.
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Tangeretin Ameliorates Glucose-Induced Podocyte Injury through Blocking Epithelial to Mesenchymal Transition Caused by Oxidative Stress and Hypoxia.橘红素通过阻断氧化应激和低氧引起的足细胞上皮间质转化改善葡萄糖诱导的足细胞损伤。
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Establishment and functional characterization of the reversibly immortalized mouse glomerular podocytes (imPODs).可逆性永生化小鼠肾小球足细胞(imPODs)的建立及功能特性研究
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High-content screening assay-based discovery of paullones as novel podocyte-protective agents.基于高通量筛选的新型足细胞保护剂保罗内酯的发现。
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The Hippo pathway regulator KIBRA promotes podocyte injury by inhibiting YAP signaling and disrupting actin cytoskeletal dynamics.Hippo 通路调节剂 KIBRA 通过抑制 YAP 信号通路和破坏肌动蛋白细胞骨架动力学促进足细胞损伤。
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Podocyturia: Potential applications and current limitations.足细胞尿:潜在应用及当前局限性
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A High-Content Screening Technology for Quantitatively Studying Podocyte Dynamics.一种用于定量研究足细胞动力学的高内涵筛选技术。
Adv Chronic Kidney Dis. 2017 May;24(3):183-188. doi: 10.1053/j.ackd.2017.04.001.

本文引用的文献

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M-type phospholipase A2 receptor as target antigen in idiopathic membranous nephropathy.M型磷脂酶A2受体作为特发性膜性肾病的靶抗原
N Engl J Med. 2009 Jul 2;361(1):11-21. doi: 10.1056/NEJMoa0810457.
2
The promise of well-being: stay in shape with N(i)ck.健康的承诺:与尼克一起保持身材。
J Am Soc Nephrol. 2009 Jul;20(7):1425-7. doi: 10.1681/ASN.2009040453. Epub 2009 Jun 4.
3
Introduction: cell-based assays for high-throughput screening.引言:用于高通量筛选的基于细胞的检测方法。
Methods Mol Biol. 2009;486:1-12. doi: 10.1007/978-1-60327-545-3_1.
4
The insect nephrocyte is a podocyte-like cell with a filtration slit diaphragm.昆虫肾细胞是一种具有滤过裂隙隔膜的足细胞样细胞。
Nature. 2009 Jan 15;457(7227):322-6. doi: 10.1038/nature07526. Epub 2008 Oct 29.
5
Tetracycline-inducible gene expression in conditionally immortalized mouse podocytes.四环素诱导的条件性永生化小鼠足细胞中的基因表达
Am J Nephrol. 2009;29(3):153-63. doi: 10.1159/000151770. Epub 2008 Aug 28.
6
The actin cytoskeleton of kidney podocytes is a direct target of the antiproteinuric effect of cyclosporine A.肾足细胞的肌动蛋白细胞骨架是环孢素A抗蛋白尿作用的直接靶点。
Nat Med. 2008 Sep;14(9):931-8. doi: 10.1038/nm.1857.
7
Cell-penetrating peptides: from molecular mechanisms to therapeutics.细胞穿透肽:从分子机制到治疗应用
Biol Cell. 2008 Apr;100(4):201-17. doi: 10.1042/BC20070116.
8
VEGF inhibition and renal thrombotic microangiopathy.血管内皮生长因子抑制与肾血栓性微血管病
N Engl J Med. 2008 Mar 13;358(11):1129-36. doi: 10.1056/NEJMoa0707330.
9
The Notch pathway in podocytes plays a role in the development of glomerular disease.足细胞中的Notch信号通路在肾小球疾病的发展中起作用。
Nat Med. 2008 Mar;14(3):290-8. doi: 10.1038/nm1731. Epub 2008 Mar 2.
10
Decreased tyrosine phosphorylation of nephrin in rat and human nephrosis.大鼠和人类肾病中nephrin的酪氨酸磷酸化降低。
Kidney Int. 2008 Apr;73(8):926-32. doi: 10.1038/ki.2008.19. Epub 2008 Feb 6.

致力于开发足细胞特异性药物。

Toward the development of podocyte-specific drugs.

机构信息

Division of Nephrology and Hypertension, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.

出版信息

Kidney Int. 2010 Apr;77(8):662-8. doi: 10.1038/ki.2009.559. Epub 2010 Feb 3.

DOI:10.1038/ki.2009.559
PMID:20130528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4089392/
Abstract

Most kidney diseases that ultimately lead to end-stage renal failure originate within the glomerulus and are associated with proteinuria. Treatment options are unspecific and offer partial cures at best because available therapies do not primarily treat glomerular cells but rather act systemically and thus cause many side effects. Most glomerulopathies directly stem from injury to podocytes, cells that have a key role in the maintenance of the glomerular filter. Thus, these cells constitute an obvious and promising target for the development of novel kidney-protective drugs. During the last decade, enormous advances have been made in the understanding of podocyte structure and function. A number of pathways that are altered during glomerular diseases may be targeted by novel small- and large-molecule drugs as well as biologicals that have been identified in nephrology and other areas of drug development. Cultured podocytes provide a valuable model for high-throughput drug screening assays. Furthermore, podocytes have been shown to possess many features that make them particularly good target cells for renal protection. This mini-review discusses some of the most recent promising data related to potential drug therapy for proteinuria and kidney disease through direct podocyte targeting.

摘要

大多数最终导致终末期肾衰竭的肾脏疾病起源于肾小球,并与蛋白尿有关。治疗选择是非特异性的,最多只能提供部分治愈,因为可用的疗法主要不是针对肾小球细胞,而是全身性作用,因此会引起许多副作用。大多数肾小球疾病直接源于足细胞的损伤,足细胞在维持肾小球滤过中起着关键作用。因此,这些细胞构成了开发新型肾脏保护药物的一个明显而有前途的靶点。在过去的十年中,人们对足细胞的结构和功能有了深入的了解。在肾小球疾病中发生改变的许多途径可以通过新型小分子和大分子药物以及在肾脏病学和药物开发的其他领域中发现的生物制剂来靶向。培养的足细胞为高通量药物筛选试验提供了有价值的模型。此外,已经表明足细胞具有许多使其成为肾脏保护特别理想的靶细胞的特征。这篇迷你综述讨论了一些与通过直接靶向足细胞治疗蛋白尿和肾脏疾病的潜在药物治疗相关的最新有希望的数据。