Suppr超能文献

萌芽与否:CAKUT中RET的视角

To bud or not to bud: the RET perspective in CAKUT.

作者信息

Davis T Keefe, Hoshi Masato, Jain Sanjay

出版信息

Pediatr Nephrol. 2014 Apr;29(4):597-608. doi: 10.1007/s00467-013-2606-5.

Abstract

Congenital anomalies of the kidneys or lower urinary tract (CAKUT) encompass a spectrum of anomalies that result from aberrations in spatio-temporal regulation of genetic, epigenetic, environmental, and molecular signals at key stages of urinary tract development. The Rearranged in Transfection (RET) tyrosine kinase signaling system is a major pathway required for normal development of the kidneys, ureters, peripheral and enteric nervous systems. In the kidneys, RET is activated by interaction with the ligand glial cell line-derived neurotrophic factor (GDNF) and coreceptor GFRα1. This activated complex regulates a number of downstream signaling cascades (PLCγ, MAPK, and PI3K) that control proliferation, migration, renewal, and apoptosis. Disruption of these events is thought to underlie diseases arising from aberrant RET signaling. RET mutations are found in 5-30 % of CAKUT patients and a number of Ret mouse mutants show a spectrum of kidney and lower urinary tract defects reminiscent of CAKUT in humans. The remarkable similarities between mouse and human kidney development and in defects due to RET mutations has led to using RET signaling as a paradigm for determining the fundamental principles in patterning of the upper and lower urinary tract and for understanding CAKUT pathogenesis. In this review, we provide an overview of studies in vivo that delineate expression and the functional importance of RET signaling complex during different stages of development of the upper and lower urinary tracts. We discuss how RET signaling balances activating and inhibitory signals emanating from its docking tyrosines and its interaction with upstream and downstream regulators to precisely modulate different aspects of Wolffian duct patterning and branching morphogenesis. We outline the diversity of cellular mechanisms regulated by RET, disruption of which causes malformations ranging from renal agenesis to multicystic dysplastic kidneys in the upper tract and vesicoureteral reflux or ureteropelvic junction obstruction in the lower tract.

摘要

肾脏或下尿路先天性异常(CAKUT)包括一系列异常情况,这些异常是由于尿路发育关键阶段的遗传、表观遗传、环境和分子信号的时空调节异常所致。转染重排(RET)酪氨酸激酶信号系统是肾脏、输尿管、外周和肠神经系统正常发育所需的主要途径。在肾脏中,RET通过与配体胶质细胞系源性神经营养因子(GDNF)和共受体GFRα1相互作用而被激活。这种激活的复合物调节许多下游信号级联反应(PLCγ、MAPK和PI3K),这些级联反应控制细胞增殖、迁移、更新和凋亡。这些事件的破坏被认为是RET信号异常引发疾病的基础。在5%-30%的CAKUT患者中发现了RET突变,许多Ret小鼠突变体表现出一系列肾脏和下尿路缺陷,类似于人类的CAKUT。小鼠和人类肾脏发育以及RET突变导致的缺陷之间的显著相似性,使得RET信号被用作确定上、下尿路模式形成的基本原理以及理解CAKUT发病机制的范例。在本综述中,我们概述了体内研究,这些研究描绘了RET信号复合物在上下尿路不同发育阶段的表达及其功能重要性。我们讨论了RET信号如何平衡来自其对接酪氨酸的激活和抑制信号,以及它与上游和下游调节因子的相互作用,以精确调节沃尔夫管模式形成和分支形态发生的不同方面。我们概述了由RET调节的细胞机制的多样性,其破坏会导致上尿路从肾缺如到多囊性发育不良肾等畸形,以及下尿路的膀胱输尿管反流或输尿管肾盂连接部梗阻。

相似文献

1
To bud or not to bud: the RET perspective in CAKUT.萌芽与否:CAKUT中RET的视角
Pediatr Nephrol. 2014 Apr;29(4):597-608. doi: 10.1007/s00467-013-2606-5.
9
The many faces of RET dysfunction in kidney.肾脏中 RET 功能障碍的多种表现形式。
Organogenesis. 2009 Oct;5(4):177-90. doi: 10.4161/org.5.4.10048.
10

引用本文的文献

1
Ureter development and associated congenital anomalies.输尿管发育及相关先天性异常。
Nat Rev Nephrol. 2025 Jun;21(6):366-382. doi: 10.1038/s41581-025-00951-4. Epub 2025 Mar 31.
2
Genomic testing for RET in the clinic: UK and global perspective.临床中RET基因检测:英国及全球视角
Endocr Relat Cancer. 2025 Apr 15;32(5). doi: 10.1530/ERC-24-0230. Print 2025 May 1.
6
The genetic etiologies of bilateral renal agenesis.双侧肾发育不全的遗传病因。
Prenat Diagn. 2024 Feb;44(2):205-221. doi: 10.1002/pd.6516. Epub 2024 Jan 5.

本文引用的文献

2
Structure and physiology of the RET receptor tyrosine kinase.REV 受体酪氨酸激酶的结构和生理学。
Cold Spring Harb Perspect Biol. 2013 Feb 1;5(2):a009134. doi: 10.1101/cshperspect.a009134.
3
Cell biology of ureter development.输尿管发育的细胞生物学。
J Am Soc Nephrol. 2013 Jan;24(1):19-25. doi: 10.1681/ASN.2012020127. Epub 2012 Nov 2.
6
KIF5B-RET fusions in lung adenocarcinoma.肺腺癌中的 KIF5B-RET 融合。
Nat Med. 2012 Feb 12;18(3):375-7. doi: 10.1038/nm.2644.
9
Receptor tyrosine kinases in kidney development.肾脏发育中的受体酪氨酸激酶
J Signal Transduct. 2011;2011:869281. doi: 10.1155/2011/869281. Epub 2011 Mar 3.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验