Fan Lian, Chen Hui-Hua, Liu Hua-Jun, Chen Hui-Juan, Zhu Ling-Ling, Zhang Ting
The Teaching and Research Office for Fundamentals of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, 1200 Cailun Road, Shanghai 201203, China.
Evid Based Complement Alternat Med. 2022 Jul 31;2022:6761453. doi: 10.1155/2022/6761453. eCollection 2022.
Renal fibrosis could lead to chronic kidney disease (CKD) developing into the end-stage with its pathological manifestation is the deposition of extracellular matrix (ECM). Danggui Shaoyao San (DSS) is one of the widely used herbal formulas in ancient China, which has been proven to have efficacy in the treatment of CKD. The experiment employed TGF-1 to stimulate the NRK-52E cells to establish a renal fibrosis model. With rapamycin (RAPA) used as the positive control, we detected the expression of fibronectin (FN), caspase-3, and autophagy-related proteins in the NRK-52E cells treated with DSS by Western blot and immunofluorescence assay. In order to further verify autophagy-promoting effects of DSS, we adopted 3-MA to inhibit autophagy. The experiment has found that DSS can lower the protein levels of FN and caspase-3 in the NRK-52E cells induced by TGF-1. After TGF-1 stimulation, the expression of LC3 II/I and Beclin 1 has decreased, and the protein levels of mTOR and p62 have increased. Consistent with rapamycin, DSS has significantly reduced these effects of TGF-1. It has also been found that DSS can increase the expression of LC3 II/I and Beclin 1 proteins and can reduce the level of mTOR in cells treated with 3-MA, suggesting that DSS can promote autophagy. In conclusion, DSS has been proved to reduce the apoptosis and fibrosis of NRK-52E cells induced by TGF-1, which may be achieved by promoting autophagy.
肾纤维化可导致慢性肾脏病(CKD)发展至终末期,其病理表现为细胞外基质(ECM)沉积。当归芍药散(DSS)是中国古代广泛应用的中药方剂之一,已被证明对CKD有治疗作用。本实验采用转化生长因子-β1(TGF-β1)刺激NRK-52E细胞建立肾纤维化模型。以雷帕霉素(RAPA)作为阳性对照,通过蛋白质免疫印迹法和免疫荧光法检测DSS处理的NRK-52E细胞中纤连蛋白(FN)、半胱天冬酶-3(caspase-3)及自噬相关蛋白的表达。为进一步验证DSS的促自噬作用,采用3-甲基腺嘌呤(3-MA)抑制自噬。实验发现,DSS可降低TGF-β1诱导的NRK-52E细胞中FN和caspase-3的蛋白水平。TGF-β1刺激后,微管相关蛋白1轻链3Ⅱ/Ⅰ(LC3Ⅱ/Ⅰ)和Beclin 1的表达降低,雷帕霉素靶蛋白(mTOR)和p62的蛋白水平升高。与雷帕霉素一致,DSS显著减轻了TGF-β1的这些作用。还发现DSS可增加3-MA处理细胞中LC3Ⅱ/Ⅰ和Beclin 1蛋白的表达,并降低mTOR水平,表示DSS可促进自噬。综上所述,已证明DSS可减少TGF-β1诱导的NRK-52E细胞凋亡和纤维化,这可能是通过促进自噬实现的。