Li Fengrui, Tian Xiaofei, Zhan Xiaoni, Wang Baojie, Ding Mei, Pang Hao
School of Forensic Medicine, China Medical University, No. 77 Puhe Road, Shenyang North New Area, Shenyang, 110122, People's Republic of China.
Department of Forensic Medicine, Baotou Medical University, Baotou, People's Republic of China.
Neurotox Res. 2017 Aug;32(2):204-217. doi: 10.1007/s12640-017-9722-0. Epub 2017 Mar 16.
The herbicide paraquat (PQ) is an exogenous toxin that allows the selective activation of dopaminergic neurons in the mesencephalon to induce injury and also causes its apoptosis in vitro. However, uptake mechanisms between PQ and neurons remain elusive. To address this issue, we undertook a study of PQ endocytosis in a dopaminergic SH-SY5Y cell line as well as explored the subsequent subcellular location and potential functional analysis of PQ. The PQ was found to bind the SH-SY5Y cell membrane and then became internalized via a clathrin-dependent pathway. PQ was internalized by many subcellular organelles in a time- and dose-dependent manner. Interestingly, the taken up PQ and secretogranin III (SCG3), which became dysregulated with PQ treatment that induced SH-SY5Y apoptosis in our previous study, colocalized in cytoplasmic vesicles. Taken together, our findings indicate that PQ is endocytosed by SH-SY5Y cells and that its multiple, subcellular localizations indicate PQ may potentially be involved in subcellular-level functions. More importantly, PQ distributing preferentially into SCG3-positive vesicles demonstrates its selective targeting which may affect SCG3 and cargoes carried by SCG3-positive vesicles. Therefore, it is reasonable to infer that PQ toxic insults may potentially interfere with neurotransmitter storage and transport associated with secretory granules.
除草剂百草枯(PQ)是一种外源性毒素,它能选择性激活中脑多巴胺能神经元以诱导损伤,并且在体外也会导致其凋亡。然而,PQ与神经元之间的摄取机制仍不清楚。为了解决这个问题,我们对多巴胺能SH-SY5Y细胞系中的PQ内吞作用进行了研究,并探索了PQ随后的亚细胞定位和潜在功能分析。发现PQ与SH-SY5Y细胞膜结合,然后通过网格蛋白依赖途径内化。PQ以时间和剂量依赖的方式被许多亚细胞器内化。有趣的是,摄取的PQ与分泌粒蛋白III(SCG3)在细胞质囊泡中共定位,在我们之前的研究中,SCG3在PQ处理诱导SH-SY5Y细胞凋亡时失调。综上所述,我们的研究结果表明,PQ被SH-SY5Y细胞内吞,其多个亚细胞定位表明PQ可能潜在地参与亚细胞水平的功能。更重要的是,PQ优先分布到SCG3阳性囊泡中,表明其选择性靶向作用,这可能会影响SCG3以及SCG3阳性囊泡携带的货物。因此,合理推断PQ毒性损伤可能潜在地干扰与分泌颗粒相关的神经递质储存和运输。