Gong Xuezhong, Ivanov Vladimir N, Hei Tom K
Department of Nephrology, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, 274 Zhijiang Middle Road, Shanghai, 200071, China.
Center for Radiological Research, College of Physician and Surgeons, Columbia University, 630 West 168th Street, New York, NY, 10032, USA.
Arch Toxicol. 2016 Sep;90(9):2187-2200. doi: 10.1007/s00204-015-1600-z. Epub 2015 Sep 24.
Our recent study demonstrated that sodium arsenite at a clinically relevant dose induced nephrotoxicity in human renal proximal tubular epithelial cell line HK-2, which could be inhibited by natural product 2,3,5,6-tetramethylpyrazine (TMP) with antioxidant activity. The present study demonstrated that arsenic exposure resulted in protein and enzymatic induction of heme oxygenase-1 (HO-1) in dose- and time-dependent manners in HK-2 cells. Blocking HO-1 enzymatic activity by zinc protoporphyrin (ZnPP) augmented arsenic-induced apoptosis, ROS production and mitochondrial dysfunction, suggesting a critical role for HO-1 as a renal protectant in this procession. On the other hand, TMP, upstream of HO-1, inhibited arsenic-induced ROS production and ROS-dependent HO-1 expression. TMP also prevented mitochondria dysfunction and suppressed activation of the intrinsic apoptotic pathway in HK-2 cells. Our results revealed that the regulation of arsenic-induced HO-1 expression was performed through multiple ROS-dependent signal pathways and the corresponding transcription factors, including p38 MAPK and JNK (but not ERK), AP-1, Nrf2 and NF-κB. TMP inhibited arsenic-induced activations of JNK, p38 MAPK, ERK, AP-1 and Nrf2 and block HO-1 protein expression. The present study, furthermore, demonstrated arsenic-induced expression of arsenic response protein 2 (ARS2) that was regulated by p38 MAPK, ERK and NF-κB. To our knowledge, this is the first report showing that ARS2 involved in arsenic-induced nephrotoxicity, while TMP pretreatment prevented such an up-regulation of ARS2 in HK-2 cells. Given ARS2 and HO-1 sharing the similar regulation mechanism, we speculated that ARS2 might also mediate cell survival in this procession. In summary, our study highlighted a role of HO-1 in the protection against arsenic-induced cytotoxicity downstream from the primary targets of TMP and further indicated that TMP may be used as a potential therapeutic agent in the treatment of arsenic-induced nephrotoxicity.
我们最近的研究表明,临床相关剂量的亚砷酸钠可诱导人肾近端小管上皮细胞系HK-2发生肾毒性,而具有抗氧化活性的天然产物2,3,5,6-四甲基吡嗪(TMP)可抑制这种毒性。本研究表明,砷暴露在HK-2细胞中以剂量和时间依赖性方式导致血红素加氧酶-1(HO-1)的蛋白和酶诱导。用锌原卟啉(ZnPP)阻断HO-1酶活性会增强砷诱导的细胞凋亡、活性氧(ROS)产生和线粒体功能障碍,这表明HO-1在这一过程中作为肾脏保护剂起着关键作用。另一方面,HO-1上游的TMP可抑制砷诱导的ROS产生和ROS依赖性HO-1表达。TMP还可防止HK-2细胞中的线粒体功能障碍,并抑制内源性凋亡途径的激活。我们的结果表明,砷诱导的HO-1表达的调节是通过多个ROS依赖性信号通路以及相应的转录因子进行的,包括p38丝裂原活化蛋白激酶(MAPK)和应激活化蛋白激酶(JNK)(而非细胞外信号调节激酶(ERK))、活化蛋白-1(AP-1)、核因子E2相关因子2(Nrf2)和核因子κB(NF-κB)。TMP可抑制砷诱导的JNK、p38 MAPK、ERK、AP-1和Nrf2的激活,并阻断HO-1蛋白表达。此外,本研究还表明砷诱导的砷反应蛋白2(ARS2)的表达受p38 MAPK、ERK和NF-κB的调节。据我们所知,这是首次报道ARS2参与砷诱导的肾毒性,而TMP预处理可防止HK-2细胞中ARS2的这种上调。鉴于ARS2和HO-1具有相似的调节机制,我们推测ARS2在这一过程中可能也介导细胞存活。总之,我们的研究突出了HO-1在保护细胞免受TMP主要靶点下游砷诱导的细胞毒性中的作用,并进一步表明TMP可能用作治疗砷诱导的肾毒性的潜在治疗剂。