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本文引用的文献

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Targeting Inflammation in So-Called Acute Kidney Injury.针对所谓急性肾损伤中的炎症反应
Semin Nephrol. 2016 Jan;36(1):17-30. doi: 10.1016/j.semnephrol.2016.01.006.
2
Partial podocyte replenishment in experimental FSGS derives from nonpodocyte sources.实验性局灶节段性肾小球硬化症中足细胞的部分补充来源于非足细胞来源。
Am J Physiol Renal Physiol. 2016 Jun 1;310(11):F1397-413. doi: 10.1152/ajprenal.00369.2015. Epub 2016 Apr 13.
3
The impact of hypoxia on nephrogenesis.缺氧对肾发生的影响。
Curr Opin Nephrol Hypertens. 2016 May;25(3):180-6. doi: 10.1097/MNH.0000000000000211.
4
Structure and Function of the Kidney in Septic Shock. A Prospective Controlled Experimental Study.脓毒性休克患者肾脏结构与功能的前瞻性对照实验研究
Am J Respir Crit Care Med. 2016 Sep 15;194(6):692-700. doi: 10.1164/rccm.201511-2285OC.
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Zinc Attenuates Tubulointerstitial Fibrosis in Diabetic Nephropathy Via Inhibition of HIF Through PI-3K Signaling.锌通过PI-3K信号通路抑制缺氧诱导因子,减轻糖尿病肾病中的肾小管间质纤维化。
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6
Necroptosis in acute kidney injury: a shedding light.急性肾损伤中的坏死性凋亡:新的见解
Cell Death Dis. 2016 Mar 3;7(3):e2125. doi: 10.1038/cddis.2016.37.
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Sox9-Positive Progenitor Cells Play a Key Role in Renal Tubule Epithelial Regeneration in Mice.Sox9阳性祖细胞在小鼠肾小管上皮再生中起关键作用。
Cell Rep. 2016 Feb 2;14(4):861-871. doi: 10.1016/j.celrep.2015.12.071. Epub 2016 Jan 14.
8
Vascular growth factors play critical roles in kidney glomeruli.血管生长因子在肾小球中发挥着关键作用。
Clin Sci (Lond). 2015 Dec;129(12):1225-36. doi: 10.1042/CS20150403.
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Icariin protects rats against 5/6 nephrectomy-induced chronic kidney failure by increasing the number of renal stem cells.淫羊藿苷通过增加肾干细胞数量保护大鼠免受5/6肾切除诱导的慢性肾衰竭。
BMC Complement Altern Med. 2015 Oct 21;15:378. doi: 10.1186/s12906-015-0909-8.
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Intrinsic Age-Dependent Changes and Cell-Cell Contacts Regulate Nephron Progenitor Lifespan.内在的年龄依赖性变化和细胞间接触调节肾单位祖细胞寿命。
Dev Cell. 2015 Oct 12;35(1):49-62. doi: 10.1016/j.devcel.2015.09.009.

肾脏修复会重现肾脏发育过程吗?

Does Renal Repair Recapitulate Kidney Development?

作者信息

Little Melissa Helen, Kairath Pamela

机构信息

Murdoch Children's Research Institute, Melbourne, Australia; and

Department of Pediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne, Australia.

出版信息

J Am Soc Nephrol. 2017 Jan;28(1):34-46. doi: 10.1681/ASN.2016070748. Epub 2016 Oct 26.

DOI:10.1681/ASN.2016070748
PMID:27798243
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5198297/
Abstract

Over a decade ago, it was proposed that the regulation of tubular repair in the kidney might involve the recapitulation of developmental pathways. Although the kidney cannot generate new nephrons after birth, suggesting a low level of regenerative competence, the tubular epithelial cells of the nephrons can proliferate to repair the damage after AKI. However, the debate continues over whether this repair involves a persistent progenitor population or any mature epithelial cell remaining after injury. Recent reports have highlighted the expression of Sox9, a transcription factor critical for normal kidney development, during postnatal epithelial repair in the kidney. Indeed, the proliferative response of the epithelium involves expression of several pathways previously described as being involved in kidney development. In some instances, these pathways are also apparently involved in the maladaptive responses observed after repeated injury. Whether development and repair in the kidney are the same processes or we are misinterpreting the similar expression of genes under different circumstances remains unknown. Here, we review the evidence for this link, concluding that such parallels in expression may more correctly represent the use of the same pathways in a distinct context, likely triggered by similar stressors.

摘要

十多年前,有人提出肾脏中肾小管修复的调控可能涉及发育途径的重演。尽管出生后肾脏无法生成新的肾单位,这表明其再生能力较低,但肾单位的肾小管上皮细胞可以增殖以修复急性肾损伤后的损伤。然而,关于这种修复是涉及持续存在的祖细胞群体还是损伤后残留的任何成熟上皮细胞,争论仍在继续。最近的报告强调了Sox9(一种对正常肾脏发育至关重要的转录因子)在出生后肾脏上皮修复过程中的表达。事实上,上皮细胞的增殖反应涉及先前描述的几种参与肾脏发育的途径的表达。在某些情况下,这些途径显然也参与了反复损伤后观察到的适应性不良反应。肾脏的发育和修复是相同的过程,还是我们在不同情况下对相似基因表达的解读有误,目前尚不清楚。在这里,我们回顾了这种联系的证据,得出结论认为,这种表达上的相似性可能更正确地代表了相同途径在不同背景下的使用,可能是由相似的应激源触发的。