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金属硫蛋白是线虫暴露于铅和汞引起的神经行为毒性的交叉适应反应形成所必需的。

Metallothioneins are required for formation of cross-adaptation response to neurobehavioral toxicity from lead and mercury exposure in nematodes.

机构信息

College of Life Science and Technology, China Pharmaceutical University, Nanjing, China.

出版信息

PLoS One. 2010 Nov 18;5(11):e14052. doi: 10.1371/journal.pone.0014052.

Abstract

Metallothioneins (MTs) are small, cysteine-rich polypeptides, but the role of MTs in inducing the formation of adaptive response is still largely unknown. We investigated the roles of metallothionein genes (mtl-1 and mtl-2) in the formation of cross-adaptation response to neurobehavioral toxicity from metal exposure in Caenorhabditis elegans. Pre-treatment with mild heat-shock at L2-larva stage effectively prevented the formation of the neurobehavioral defects and the activation of severe stress response in metal exposed nematodes at concentrations of 50 and 100 µM, but pre-treatment with mild heat-shock did not prevent the formation of neurobehavioral defects in 200 µM of metal exposed nematodes. During the formation of cross-adaptation response, the induction of mtl-1 and mtl-2 promoter activity and subsequent GFP gene expression were sharply increased in 50 µM or 100 µM of metal exposed Pmtl-1::GFP and Pmtl-2::GFP transgenic adult animals after mild heat-shock treatment compared with those treated with mild heat-shock or metal exposure alone. Moreover, after pre-treatment with mild heat-shock, no noticeable increase of locomotion behaviors could be observed in metal exposed mtl-1 or mtl-2 mutant nematodes compared to those without mild heat-shock pre-treatment. The defects of adaptive response to neurobehavioral toxicity induced by metal exposure formed in mtl-1 and mtl-2 mutants could be completely rescued by the expression of mtl-1 and mtl-2 with the aid of their native promoters. Furthermore, over-expression of MTL-1 and MTL-2 at the L2-larval stage significantly suppressed the toxicity on locomotion behaviors from metal exposure at all examined concentrations. Therefore, the normal formation of cross-adaptation response to neurobehavioral toxicity induced by metal exposure may need the enough accumulation of MTs protein in animal tissues.

摘要

金属硫蛋白(MTs)是一种富含半胱氨酸的小分子多肽,但 MTs 在诱导适应性反应形成中的作用在很大程度上仍是未知的。我们研究了金属硫蛋白基因(mtl-1 和 mtl-2)在秀丽隐杆线虫暴露于金属后神经行为毒性的交叉适应反应形成中的作用。在 L2 幼虫阶段进行轻度热休克预处理可有效防止在 50 和 100µM 金属暴露的线虫中形成神经行为缺陷和严重应激反应的激活,但在 200µM 金属暴露的线虫中,轻度热休克预处理不能防止神经行为缺陷的形成。在交叉适应反应形成过程中,与单独进行轻度热休克或金属暴露处理相比,在 50µM 或 100µM 金属暴露的 Pmtl-1::GFP 和 Pmtl-2::GFP 转基因成年动物中,轻度热休克处理后 mtl-1 和 mtl-2 启动子活性的诱导和随后 GFP 基因的表达明显增加。此外,与未进行轻度热休克预处理的线虫相比,在轻度热休克预处理后,金属暴露的 mtl-1 或 mtl-2 突变线虫的运动行为没有明显增加。金属暴露诱导的神经行为毒性适应性反应的缺陷可通过其天然启动子辅助 mtl-1 和 mtl-2 的表达而完全得到挽救。此外,在 L2 幼虫阶段过表达 MTL-1 和 MTL-2 可显著抑制所有检测浓度的金属暴露对运动行为的毒性。因此,金属暴露诱导的神经行为毒性的交叉适应反应的正常形成可能需要动物组织中 MTs 蛋白的足够积累。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6d7/2987793/c2a8fc6c418e/pone.0014052.g001.jpg

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