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Stromal β-catenin overexpression contributes to the pathogenesis of renal dysplasia
Felix J Boivin1, Sanjay Sarin1, Pari Dabas1
1Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Canada.
Insights
Overexpression of beta-catenin (β-catenin) in kidney stromal cells causes renal dysplasia, a leading cause of kidney failure in children. This study reveals disrupted stromal cell differentiation and vascular development contribute to this condition.
Area of Science:
- Developmental Biology
- Pathology
- Genetics
Background:
- Renal dysplasia is the primary cause of kidney failure in pediatric patients.
- Its pathogenesis involves disrupted collecting duct branching and stromal expansion, but the stroma's role is unclear.
- Beta-catenin (β-catenin), a crucial transcriptional co-activator in renal development, is upregulated in human dysplastic kidney stroma.
Purpose of the Study:
- To investigate the role of beta-catenin (β-catenin) in the renal stroma during kidney development.
- To determine if stromal beta-catenin (β-catenin) overexpression can induce renal dysplasia.
- To elucidate the specific cellular and molecular mechanisms underlying beta-catenin (β-catenin)-induced renal dysplasia.
Main Methods:
- Generated a mouse model overexpressing beta-catenin (β-catenin) specifically in renal stromal progenitors (β-cat(GOF-S)).
- Performed histopathological analysis of kidneys from β-cat(GOF-S) mice and human dysplastic tissue.
- Characterized renal stroma, gene expression (Wnt4, Bmp4), and renal vasculature in the mouse model.
Main Results:
- β-cat(GOF-S) mice exhibited expanded fibroblast-like cells and altered stromal differentiation, mimicking human renal dysplasia.
- These stromal cells overexpressed ectopic Wnt4 and Bmp4, crucial for blood vessel formation.
- Disrupted endothelial cell migration, organization, and vascular morphogenesis were observed in β-cat(GOF-S) mice, mirroring human dysplastic kidneys.
Conclusions:
- Stromal beta-catenin (β-catenin) overexpression is sufficient to cause renal dysplasia.
- Disrupted stromal differentiation and aberrant vascular morphogenesis are key pathogenic mechanisms in renal dysplasia.
- This study establishes a direct link between stromal beta-catenin (β-catenin) and the development of renal dysplasia.
Abstract:
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.
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