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  • Title: Overexpression of BMP‑7 reverses TGF‑β1‑induced epithelial‑mesenchymal transition by attenuating the Wnt3/β‑catenin and TGF-β1/Smad2/3 signaling pathways in HK‑2 cells.
    Author: Song Y, Lv S, Wang F, Liu X, Cheng J, Liu S, Wang X, Chen W, Guan G, Liu G, Peng C.
    Journal: Mol Med Rep; 2020 Feb; 21(2):833-841. PubMed ID: 31974602.
    Abstract:
    Tubular epithelial cells undergoing epithelial‑mesenchymal transition (EMT) is a crucial event in the progression of renal interstitial fibrosis (RIF). Bone morphogenetic protein‑7 (BMP‑7) has been reported to exhibit anti‑fibrotic functions in various renal diseases. However, the function of BMP‑7 in regulating EMT and the progression of RIF remains largely unknown. The aim of the present study was to examine the potential effect of BMP‑7 on transforming growth factor β1 (TGF‑β1)‑induced EMT and the underlying mechanisms by which BMP‑7 exerted its effects. Human renal proximal tubular epithelial cells (HK‑2) were treated with TGF‑β1 for various time periods and at various concentrations and lentiviral vectors were used to overexpress BMP‑7. Cell Counting Kit‑8 and Transwell assays were used to evaluate the viability and migration of HK‑2 cells in vitro. EMT was estimated by assessing the changes in cell morphology and the expression of EMT markers. In addition, the activation of the Wnt3/β‑catenin and TGF‑β1/Smad2/3 signaling pathways were analyzed using western blotting. TGF‑β1 induced EMT in a time‑ and dose‑dependent manner in HK‑2 cells. Treatment with TGF‑β1 induced morphological changes, decreased cell viability and the expression of E‑cadherin, increased cell migration and the expression of α‑smooth muscle actin, fibroblast‑specific protein 1, collagen I and vimentin, and activated the Wnt3/β‑catenin and TGF‑β1/Smad2/3 signaling pathways in HK‑2 cells. However, BMP‑7 overexpression notably reversed all these effects. These results suggest that BMP‑7 effectively suppresses TGF‑β1‑induced EMT through the inhibition of the Wnt3/β‑catenin and TGF‑β1/Smad2/3 signaling pathways, highlighting a potential novel anti‑RIF strategy.
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