National Clinical Research Center of Kidney Disease, Nanfang Hospital, Southern Medical University, Guangzhou, People's Republic of China.
University of California Davis, Sacramento, CA, United States.
Prog Mol Biol Transl Sci. 2018 Jan;153:181-207. doi: 10.1016/bs.pmbts.2017.11.019. Epub 2017 Dec 30.
Wnt signal cascade is an evolutionarily conserved, developmental pathway that regulates embryogenesis, injury repair, and pathogenesis of human diseases. It is well established that Wnt ligands transmit their signal via canonical, β-catenin-dependent and noncanonical, β-catenin-independent mechanisms. Mounting evidence has revealed that Wnt signaling plays a key role in controlling early nephrogenesis and is implicated in the development of various kidney disorders. Dysregulations of Wnt expression cause a variety of developmental abnormalities and human diseases, such as congenital anomalies of the kidney and urinary tract, cystic kidney, and renal carcinoma. Multiple Wnt ligands, their receptors, and transcriptional targets are upregulated during nephron formation, which is crucial for mediating the reciprocal interaction between primordial tissues of ureteric bud and metanephric mesenchyme. Renal cysts are also associated with disrupted Wnt signaling. In addition, Wnt components are important players in renal tumorigenesis. Activation of Wnt/β-catenin is instrumental for tubular repair and regeneration after acute kidney injury. However, sustained activation of this signal cascade is linked to chronic kidney diseases and renal fibrosis in patients and experimental animal models. Mechanistically, Wnt signaling controls a diverse array of biologic processes, such as cell cycle progression, cell polarity and migration, cilia biology, and activation of renin-angiotensin system. In this chapter, we have reviewed recent findings that implicate Wnt signaling in kidney development and diseases. Targeting this signaling may hold promise for future treatment of kidney disorders in patients.
Wnt 信号级联是一种进化上保守的发育途径,调节胚胎发生、损伤修复和人类疾病的发病机制。现已明确,Wnt 配体通过经典的β-连环蛋白依赖性和非经典的β-连环蛋白非依赖性机制传递其信号。越来越多的证据表明,Wnt 信号在控制早期肾发生中起关键作用,并与各种肾脏疾病的发展有关。Wnt 表达的失调导致多种发育异常和人类疾病,如肾和尿路先天性异常、囊性肾病和肾细胞癌。多种 Wnt 配体、其受体和转录靶标在肾单位形成过程中上调,这对于介导输尿管芽和后肾间充质原始组织之间的相互作用至关重要。肾囊肿也与 Wnt 信号的破坏有关。此外,Wnt 成分是肾肿瘤发生的重要参与者。Wnt/β-连环蛋白的激活对于急性肾损伤后的肾小管修复和再生至关重要。然而,该信号级联的持续激活与患者和实验动物模型中的慢性肾脏病和肾纤维化有关。从机制上讲,Wnt 信号控制着多种生物学过程,如细胞周期进程、细胞极性和迁移、纤毛生物学以及肾素-血管紧张素系统的激活。在本章中,我们回顾了最近的发现,即 Wnt 信号参与肾脏发育和疾病。针对该信号可能为未来治疗患者的肾脏疾病提供希望。