Key result
Tongxinluo ameliorated renal structure and function by regulating miR-21-induced epithelial-to-mesenchymal transition in diabetic nephropathy.
Why the study?
Does tongxinluo ameliorate renal structure and function by regulating miR-21-induced epithelial-to-mesenchymal transition in diabetic nephropathy?
Does tongxinluo ameliorate renal structure and function by regulating miR-21-induced epithelial-to-mesenchymal transition in diabetic nephropathy?
Tongxinluo ameliorates renal structure and function in diabetic nephropathy models by regulating miR-21-induced epithelial-to-mesenchymal transition.
Hypothesis-generating in diabetic nephropathy models; leaves open translation of tongxinluo effects to human renal outcomes.
Diabetic nephropathy (DN) is one of the most important diabetic microangiopathies. The epithelial-to-mesenchymal transition (EMT) plays an important role in DN. The physiological role of microRNA-21 (miR-21) was closely linked to EMT. However, it remained elusive whether tongxinluo (TXL) ameliorated renal structure and function by regulating miR-21-induced EMT in DN. This study aimed to determine the effect of TXL on miR-21-induced renal tubular EMT and to explore the relationship between miR-21 and TGF-β1/smads signals. Real-time RT-PCR, cell transfection, in situ hybridization (ISH), and laser confocal microscopy were used, respectively. Here, we revealed that TXL dose dependently lowered miR-21 expression in tissue, serum, and cells. Overexpression of miR-21 can enhance α-smooth muscle actin (SMA) expression and decrease E-cadherin expression by upregulating smad3/p-smad3 expression and downregulating smad7 expression. Interestingly, TXL also increased E-cadherin expression and decreased α-SMA expression by regulating miR-21 expression. More importantly, TXL decreased collagen IV, fibronectin, glomerular basement membrane, glomerular area, and the albumin/creatinine ratio, whereas it increased the creatinine clearance ratio. The results demonstrated that TXL ameliorated renal structure and function by regulating miR-21-induced EMT, which was one of the mechanisms to protect against DN, and that miR-21 may be one of the therapeutic targets for TXL in DN.
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Wang et al. (2013) studied Diabetic nephropathy. Tongxinluo (TXL) was evaluated on Renal structure and function, miR-21 expression, and EMT markers. Tongxinluo ameliorated renal structure and function by regulating miR-21-induced epithelial-to-mesenchymal transition in diabetic nephropathy.
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