Academy of Scientific and Innovative Research (AcSIR), CSIR-IITR campus, Lucknow, India.
Developmental Toxicology Laboratory, Systems Toxicology and Health Risk Assessment Group, CSIR-Indian Institute of Toxicology Research (CSIR-IITR), Vishvigyan Bhavan, 31, Mahatma GandhiMarg, Lucknow, Uttar Pradesh, 226001, India.
Mol Neurobiol. 2018 Mar;55(3):2125-2149. doi: 10.1007/s12035-017-0469-7. Epub 2017 Mar 10.
We previously demonstrated that arsenic, cadmium, and lead mixture at environmentally relevant doses induces astrocyte apoptosis in the developing brain. Here, we investigated the mechanism and contribution of each metal in inducing the apoptosis. We hypothesized participation of transcription factor, peroxisome proliferator-activated receptor gamma (PPARγ), reported to affect astrocyte survival. We treated cultured rat astrocytes with single metals and their combinations and performed apoptosis assay and measured PPARγ expression levels. We found that cadmium demonstrated maximum increase in PPARγ as well as apoptosis, followed by arsenic and then lead. Interestingly, we observed that the metals mimicked PPARγ agonist, troglitazone, and enhanced PPARγ-transcriptional activity. Co-treatment with PPARγ-siRNA or PPARγ-antagonist, GW9662, suppressed the astrocyte apoptosis, suggesting a prominent participation of PPARγ in metal(s)-induced astrocyte loss. We explored PPARγ-transcriptional activity and identify its target gene in apoptosis, performed in silico screening. We spotted PPARγ-response elements (PPREs) within poly(ADP-ribose) polymerase (PARP) gene, and through gel-shift assay verified metal(s)-mediated increased PPARγ binding to PARP-PPREs. Chromatin-immunoprecipitation and luciferase-reporter assays followed by real-time PCR and Western blotting proved PPRE-mediated PARP expression, where cadmium contributed most and lead least, and the effects of metal mixture were comparable with troglitazone. Eventually, dose-dependent increased cleaved-PARP/PARP ratio confirmed astrocyte apoptosis. Additionally, we found that PPARγ and PARP expressions were c-Jun N-terminal kinases and cyclin-dependent kinase5-dependent. In vivo treatment of developing rats with the metals corroborated enhanced PPARγ-dependent PARP and astrocyte apoptosis, where yet again cadmium contributed most. Overall, our study enlightens a novel PPARγ-dependent mechanism of As-, Cd-, and Pb-induced astrocyte apoptosis.
我们之前已经证明,环境相关剂量的砷、镉和铅混合物会诱导发育中的大脑中的星形胶质细胞凋亡。在这里,我们研究了每种金属诱导凋亡的机制和贡献。我们假设转录因子过氧化物酶体增殖物激活受体γ(PPARγ)的参与,据报道,PPARγ 会影响星形胶质细胞的存活。我们用单一金属及其组合处理培养的大鼠星形胶质细胞,进行凋亡检测,并测量 PPARγ 表达水平。我们发现,镉表现出最大的 PPARγ 增加以及凋亡,其次是砷,然后是铅。有趣的是,我们观察到这些金属模拟了 PPARγ 激动剂曲格列酮,并增强了 PPARγ 的转录活性。用 PPARγ-siRNA 或 PPARγ 拮抗剂 GW9662 共同处理抑制了星形胶质细胞凋亡,表明 PPARγ 参与了金属诱导的星形胶质细胞丢失。我们探索了 PPARγ 的转录活性,并在凋亡中识别其靶基因,进行了计算机筛选。我们在多聚(ADP-核糖)聚合酶(PARP)基因内发现了 PPARγ 反应元件(PPREs),并通过凝胶迁移实验验证了金属介导的 PPARγ 与 PARP-PPREs 的结合增加。染色质免疫沉淀和荧光素酶报告基因检测,以及实时 PCR 和 Western blot 证实了 PPRE 介导的 PARP 表达,其中镉的作用最大,铅的作用最小,金属混合物的作用与曲格列酮相当。最终,剂量依赖性增加的裂解 PARP/PARP 比值证实了星形胶质细胞凋亡。此外,我们发现 PPARγ 和 PARP 的表达依赖于 c-Jun N-末端激酶和细胞周期依赖性激酶 5。对发育中的大鼠进行金属体内处理证实了 PPARγ 依赖性 PARP 和星形胶质细胞凋亡的增强,其中镉的作用最大。总的来说,我们的研究揭示了一种新的 As、Cd 和 Pb 诱导星形胶质细胞凋亡的 PPARγ 依赖性机制。