Wen-pi-tang-Hab-Wu-ling-san, an oriental herbal prescription, attenuates epithelial-mesenchymal transdifferentiation stimulated by TGF-β1 in kidney cells

被引:14
作者
Lee, Sang Il
Kim, Hyo Jung
Baek, Moon-Chang
Park, Kwon Moo
Park, Yongki
Yoon, Cheol Ho
Boo, Yong Chool
机构
[1] Kyungpook Natl Univ, Sch Med, Dept Mol Med, Taegu 700422, South Korea
[2] Kyungpook Natl Univ, Sch Med, Dept Anat, Taegu 700422, South Korea
[3] Dongguk Univ, Orient Med Coll, Dept Oriental Herbol, Kyungju 780714, Kyungbuk, South Korea
[4] Dongguk Univ, Orient Med Coll, Dept Internal Med, Kyungju 780714, Kyungbuk, South Korea
关键词
kidney fibrosis; herbal prescription; epithelial-mesenchymal transdifferentiation; alpha-smooth muscle actin; transforming growth factor-beta;
D O I
10.1002/ptr.2106
中图分类号
R914 [药物化学];
学科分类号
100701 [药物化学];
摘要
Wen-pi-tang-Hab-Wu-ling-san (WHW), an oriental herbal prescription, is currently used in oriental clinics for the treatment of chronic renal failure (CRF). While its effectiveness has been supported by a series of modern studies, the underlying mechanism remains poorly understood. CRF progression involves tubulointerstitial fibrosis where transforming growth factor-beta 1 (TGF-P 1) plays a critical role by inducing epithelial-mesenchymal transdifferentiation (EMT). This study examined whether WHW extract attenuated the TGF-fil-induced EMT in Madin-Darby canine kidney cells. When the cells were stimulated by TGF-beta 1 (2.5 ng/mL), they exhibited an elongated, spindle-shaped appearance but this morphological change was significantly suppressed by WHW extract (I mg/mL). The WHW extract did not show notable cytotoxicity and even mitigated the cytotoxic effects of TGF-beta 1. It inhibited the expression of a-smooth muscle actin (alpha-SMA), a marker of EMT, but not the secretion of matrix metalloproteinases stimulated by TGF-fil. The WHW extract also inhibited the phosphorylation of Smad2 that mediates TGF-beta signaling leading to a-SMA expression. The present study suggests that WHW extract may provide renal protective effects through modulation of the TGF-beta 1/ Smad2/alpha-SMA pathway involved in fibrosis. Copyright (C) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:548 / 553
页数:6
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