| First Author | Beaton H | Year | 2016 |
| Journal | Am J Physiol Renal Physiol | Volume | 311 |
| Issue | 1 | Pages | F35-45 |
| PubMed ID | 27122540 | Mgi Jnum | J:320192 |
| Mgi Id | MGI:6869393 | Doi | 10.1152/ajprenal.00136.2016 |
| Citation | Beaton H, et al. (2016) Wnt6 regulates epithelial cell differentiation and is dysregulated in renal fibrosis. Am J Physiol Renal Physiol 311(1):F35-45 |
| abstractText | Diabetic nephropathy is the most common microvascular complication of diabetes mellitus, manifesting as mesangial expansion, glomerular basement membrane thickening, glomerular sclerosis, and progressive tubulointerstitial fibrosis leading to end-stage renal disease. Here we describe the functional characterization of Wnt6, whose expression is progressively lost in diabetic nephropathy and animal models of acute tubular injury and renal fibrosis. We have shown prominent Wnt6 and frizzled 7 (FzD7) expression in the mesonephros of the developing mouse kidney, suggesting a role for Wnt6 in epithelialization. Importantly, TCF/Lef reporter activity is also prominent in the mesonephros. Analysis of Wnt family members in human renal biopsies identified differential expression of Wnt6, correlating with severity of the disease. In animal models of tubular injury and fibrosis, loss of Wnt6 was evident. Wnt6 signals through the canonical pathway in renal epithelial cells as evidenced by increased phosphorylation of GSK3beta (Ser9), nuclear accumulation of beta-catenin and increased TCF/Lef transcriptional activity. FzD7 was identified as a putative receptor of Wnt6. In vitro Wnt6 expression leads to de novo tubulogenesis in renal epithelial cells grown in three-dimensional culture. Importantly, Wnt6 rescued epithelial cell dedifferentiation in response to transforming growth factor-beta (TGF-beta); Wnt6 reversed TGF-beta-mediated increases in vimentin and loss of epithelial phenotype. Wnt6 inhibited TGF-beta-mediated p65-NF-kappaB nuclear translocation, highlighting cross talk between the two pathways. The critical role of NF-kappaB in the regulation of vimentin expression was confirmed in both p65(-/-) and IKKalpha/beta(-/-) embryonic fibroblasts. We propose that Wnt6 is involved in epithelialization and loss of Wnt6 expression contributes to the pathogenesis of renal fibrosis. |
