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尿路上皮在正常和异常泌尿道发育中的作用。

Roles for urothelium in normal and aberrant urinary tract development.

机构信息

Nephrology and Urology Research Affinity Group, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.

Center for Clinical and Translational Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.

出版信息

Nat Rev Urol. 2020 Aug;17(8):459-468. doi: 10.1038/s41585-020-0348-2. Epub 2020 Jul 9.

DOI:10.1038/s41585-020-0348-2
PMID:32647226
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8966489/
Abstract

Congenital anomalies of the kidney and urinary tract (CAKUTs) represent the leading cause of chronic kidney disease and end-stage kidney disease in children. Increasing evidence points to critical roles for the urothelium in the developing urinary tract and in the genesis of CAKUTs. The involvement of the urothelium in patterning the urinary tract is supported by evidence that CAKUTs can arise as a result of abnormal urothelial development. Emerging evidence indicates that congenital urinary tract obstruction triggers urothelial remodelling that stabilizes the obstructed kidney and limits renal injury. Finally, the diagnostic potential of radiological findings and urinary biomarkers derived from the urothelium of patients with CAKUTs might aid their contribution to clinical care.

摘要

先天性肾和尿路畸形(CAKUT)是儿童慢性肾脏病和终末期肾病的主要原因。越来越多的证据表明尿路上皮在发育中的尿路和 CAKUT 的发生中起着关键作用。CAKUT 可因尿路上皮发育异常而发生,这一证据支持了尿路上皮在尿路形成中的作用。新出现的证据表明,先天性尿路梗阻引发尿路上皮重塑,从而稳定梗阻肾脏并限制肾损伤。最后,CAKUT 患者的影像学表现和源自尿路上皮的尿生物标志物的诊断潜力可能有助于它们为临床护理做出贡献。

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本文引用的文献

1
A Primer on Congenital Anomalies of the Kidneys and Urinary Tracts (CAKUT).肾脏和泌尿道先天异常(CAKUT)概论。
Clin J Am Soc Nephrol. 2020 May 7;15(5):723-731. doi: 10.2215/CJN.12581019. Epub 2020 Mar 18.
2
Krt5 urothelial cells are developmental and tissue repair progenitors in the kidney.Krt5 尿路上皮细胞是肾脏中的发育和组织修复祖细胞。
Am J Physiol Renal Physiol. 2019 Sep 1;317(3):F757-F766. doi: 10.1152/ajprenal.00171.2019. Epub 2019 Jul 19.
3
Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction.BNC2 中的罕见变异与常染色体显性遗传先天性下尿路梗阻有关。
Am J Hum Genet. 2019 May 2;104(5):994-1006. doi: 10.1016/j.ajhg.2019.03.023.
4
TBX2 and TBX3 act downstream of canonical WNT signaling in patterning and differentiation of the mouse ureteric mesenchyme.TBX2 和 TBX3 在经典 WNT 信号通路下游调控小鼠输尿管间质的模式形成和分化。
Development. 2018 Nov 26;145(23):dev171827. doi: 10.1242/dev.171827.
5
Uroplakins play conserved roles in egg fertilization and acquired additional urothelial functions during mammalian divergence.尿路上皮素在卵子受精中发挥保守作用,并在哺乳动物进化过程中获得了额外的尿路上皮功能。
Mol Biol Cell. 2018 Dec 15;29(26):3128-3143. doi: 10.1091/mbc.E18-08-0496. Epub 2018 Oct 10.
6
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.全外显子组测序鉴定出具有肾和泌尿道先天异常家族的致病突变。
J Am Soc Nephrol. 2018 Sep;29(9):2348-2361. doi: 10.1681/ASN.2017121265. Epub 2018 Aug 24.
7
The uroplakin plaque promotes renal structural integrity during congenital and acquired urinary tract obstruction.尿路上皮板层在先天性和获得性尿路梗阻中促进肾脏结构完整性。
Am J Physiol Renal Physiol. 2018 Oct 1;315(4):F1019-F1031. doi: 10.1152/ajprenal.00173.2018. Epub 2018 Jun 13.
8
Urinary antimicrobial peptides: Potential novel biomarkers of obstructive uropathy.尿抗菌肽:梗阻性尿路病的潜在新型生物标志物。
J Pediatr Urol. 2018 Jun;14(3):238.e1-238.e6. doi: 10.1016/j.jpurol.2018.03.006. Epub 2018 Mar 29.
9
IL-33/ST2 axis mediates hyperplasia of intrarenal urothelium in obstructive renal injury.IL-33/ST2 轴介导梗阻性肾损伤中肾内尿路上皮的增生。
Exp Mol Med. 2018 Apr 20;50(4):1-11. doi: 10.1038/s12276-018-0047-8.
10
Protein Kinase 2 Is Expressed in Neural Crest-Derived Urinary Pacemaker Cells and Required for Pyeloureteric Contraction.蛋白激酶 2 在神经嵴衍生的尿起搏细胞中表达,并对肾盂输尿管收缩起作用。
J Am Soc Nephrol. 2018 Apr;29(4):1198-1209. doi: 10.1681/ASN.2017090951. Epub 2018 Feb 7.