Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Canada.
Center for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, Maine, USA.
J Pathol. 2016 Jun;239(2):174-85. doi: 10.1002/path.4713. Epub 2016 Apr 23.
Renal dysplasia, the leading cause of renal failure in children, is characterized by disrupted branching of the collecting ducts and primitive tubules, with an expansion of the stroma, yet a role for the renal stroma in the genesis of renal dysplasia is not known. Here, we demonstrate that expression of β-catenin, a key transcriptional co-activator in renal development, is markedly increased in the expanded stroma in human dysplastic tissue. To understand its contribution to the genesis of renal dysplasia, we generated a mouse model that overexpresses β-catenin specifically in stromal progenitors, termed β-cat(GOF-S) . Histopathological analysis of β-cat(GOF) (-S) mice revealed a marked expansion of fibroblast cells surrounding primitive ducts and tubules, similar to defects observed in human dysplastic kidneys. Characterization of the renal stroma in β-cat(GOF) (-S) mice revealed altered stromal cell differentiation in the expanded renal stroma demonstrating that this is not renal stroma but instead a population of stroma-like cells. These cells overexpress ectopic Wnt4 and Bmp4, factors necessary for endothelial cell migration and blood vessel formation. Characterization of the renal vasculature demonstrated disrupted endothelial cell migration, organization, and vascular morphogenesis in β-cat(GOF) (-S) mice. Analysis of human dysplastic tissue demonstrated a remarkably similar phenotype to that observed in our mouse model, including altered stromal cell differentiation, ectopic Wnt4 expression in the stroma-like cells, and disrupted endothelial cell migration and vessel formation. Our findings demonstrate that the overexpression of β-catenin in stromal cells is sufficient to cause renal dysplasia. Further, the pathogenesis of renal dysplasia is one of disrupted stromal differentiation and vascular morphogenesis. Taken together, this study demonstrates for the first time the contribution of stromal β-catenin overexpression to the genesis of renal dysplasia. Copyright © 2016 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
肾发育不良是儿童肾衰竭的主要原因,其特征是集合管和原始小管的分支中断,基质扩张,但肾基质在肾发育不良的发生中的作用尚不清楚。在这里,我们证明了β-连环蛋白(在肾脏发育中起关键转录共激活因子作用)的表达在人发育不良组织中扩张的基质中明显增加。为了了解其对肾发育不良发生的贡献,我们生成了一种在基质祖细胞中特异性过表达β-连环蛋白的小鼠模型,称为β-cat(GOF-S)。β-cat(GOF-S)小鼠的组织病理学分析显示,原始导管和小管周围的成纤维细胞明显扩张,类似于人发育不良肾脏中观察到的缺陷。β-cat(GOF-S)小鼠的肾基质特征表明,在扩张的肾基质中,基质细胞分化发生改变,这不是肾基质,而是一群类似于基质的细胞。这些细胞过度表达异位 Wnt4 和 Bmp4,这是内皮细胞迁移和血管形成所必需的。对肾脏血管系统的特征分析表明,β-cat(GOF-S)小鼠的内皮细胞迁移、组织和血管形态发生受损。对人发育不良组织的分析表明,与我们的小鼠模型观察到的表型非常相似,包括基质细胞分化改变、基质样细胞中异位 Wnt4 表达以及内皮细胞迁移和血管形成受损。我们的研究结果表明,β-连环蛋白在基质细胞中的过表达足以导致肾发育不良。此外,肾发育不良的发病机制之一是基质分化和血管形态发生的破坏。总之,这项研究首次证明了基质β-连环蛋白过表达对肾发育不良发生的贡献。版权所有©2016 英国和爱尔兰病理学学会。由约翰威立父子公司出版。