Rudgalvyte Martina, Peltonen Juhani, Lakso Merja, Nass Richard, Wong Garry
A. I. Virtanen Institute for Molecular Sciences, Department of Neurobiology, University of Eastern Finland, Kuopio 70211, Finland.
Department of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
J Biochem Mol Toxicol. 2016 Feb;30(2):97-105. doi: 10.1002/jbt.21768. Epub 2015 Sep 29.
Manganese (Mn) is an essential nutrient; nonetheless, excessive amounts can accumulate in brain tissues causing manganism, a severe neurological condition. Previous studies have suggested oxidative stress, mitochondria dysfunction, and impaired metabolism pathways as routes for Mn toxicity. Here, we used the nematode Caenorhabditis elegans to analyze gene expression changes after acute Mn exposure using RNA-Seq. L1 stage animals were exposed to 50 mM MnCl2 for 30 min and analyzed at L4. We identified 746 up- and 1828 downregulated genes (FDR corrected p < 0.05; two-fold change) that included endoplasmic reticulum related abu and fkb family genes, as well as six of seven lipocalin-related (lpr) family members. These were also verified by qRT-PCR. RNA interference of lpr-5 showed a dramatic increase in whole body vulnerability to Mn exposure. Our studies demonstrate that Mn exposure alters gene transcriptional levels in different cell stress pathways that may ultimately contribute to its toxic effects.
锰(Mn)是一种必需营养素;然而,过量的锰会在脑组织中积累,导致锰中毒,这是一种严重的神经疾病。先前的研究表明,氧化应激、线粒体功能障碍和代谢途径受损是锰毒性的途径。在这里,我们使用线虫秀丽隐杆线虫,通过RNA测序分析急性锰暴露后的基因表达变化。将L1期动物暴露于50 mM氯化锰中30分钟,并在L4期进行分析。我们鉴定出746个上调基因和1828个下调基因(FDR校正p<0.05;两倍变化),其中包括内质网相关的abu和fkb家族基因,以及七个脂质运载蛋白相关(lpr)家族成员中的六个。这些结果也通过qRT-PCR得到了验证。对lpr-5进行RNA干扰显示,全身对锰暴露的易感性显著增加。我们的研究表明,锰暴露会改变不同细胞应激途径中的基因转录水平,这可能最终导致其毒性作用。