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Ndfip1可预防鱼藤酮诱导的SH-SY5Y细胞神经毒性及α-突触核蛋白上调。

Ndfip1 Prevents Rotenone-Induced Neurotoxicity and Upregulation of α-Synuclein in SH-SY5Y Cells.

作者信息

Liu Xin, Qu Le, Zhang Na, Yu Xiaoqi, Xiao Zhixin, Song Limei, Xie Junxia, Xu Huamin

机构信息

Shandong Provincial Key Laboratory of Pathogenesis and Prevention of Neurological Disorders and State Key Disciplines: Physiology, Department of Physiology, Medical College of Qingdao University, Qingdao, China.

Institute of Brain Science and Disease, Qingdao University, Qingdao, China.

出版信息

Front Mol Neurosci. 2021 Jan 5;13:613404. doi: 10.3389/fnmol.2020.613404. eCollection 2020.

Abstract

Nedd4 family interacting protein 1 (Ndfip1) is an adaptor of Nedd4-family ubiquitin ligases. Experimental results showed that Ndfip1 had a potential neuroprotective effect in neurology diseases. However, the neuroprotective effect and the underlying mechanisms of Ndfip1 in Parkinson's disease (PD) have not yet been fully elucidated. Therefore, in this study, we explored the neuroprotective effect of Ndfip1 against mitochondrial complex I inhibitor rotenone in a human dopaminergic neuroblastoma SH-SY5Y cell line and further elucidated its possible underlying mechanisms. Our results showed that rotenone could induce the up-regulation of α-synuclein (α-syn) in both mRNA and protein levels. The expression of Ndfip1 decreased at 24 h after rotenone treatment. Further study showed that high expression of Ndfip1 could protect SH-SY5Y cells against rotenone-induced neurotoxicity and antagonize the rotenone-induced increase in α-syn protein levels. In addition, high expression of Ndfip1 inhibited rotenone-induced increase in the protein levels of caspase-3 and decrease in tyrosine hydroxylase (TH). Further study showed that Ndfip1 did not affect the protein expression of iron regulatory protein 1 (IRP1), transferrin receptor 1 (TfR1), while antagonized the increase in protein levels of P62 and ferritin L caused by rotenone. Our findings provide specific identification of Ndfip1 proteins to inhibit the increase of α-syn in rotenone-induced SH-SY5Y cells. Ndfip1 might be a new theoretical drug target for the prevention and treatment of PD.

摘要

Nedd4家族相互作用蛋白1(Ndfip1)是Nedd4家族泛素连接酶的衔接蛋白。实验结果表明,Ndfip1在神经疾病中具有潜在的神经保护作用。然而,Ndfip1在帕金森病(PD)中的神经保护作用及其潜在机制尚未完全阐明。因此,在本研究中,我们探讨了Ndfip1对人多巴胺能神经母细胞瘤SH-SY5Y细胞系中线粒体复合物I抑制剂鱼藤酮的神经保护作用,并进一步阐明其可能的潜在机制。我们的结果表明,鱼藤酮可在mRNA和蛋白质水平上诱导α-突触核蛋白(α-syn)上调。鱼藤酮处理24小时后Ndfip1的表达降低。进一步研究表明,Ndfip1的高表达可保护SH-SY5Y细胞免受鱼藤酮诱导的神经毒性,并拮抗鱼藤酮诱导的α-syn蛋白水平升高。此外,Ndfip1的高表达抑制了鱼藤酮诱导的caspase-3蛋白水平升高和酪氨酸羟化酶(TH)降低。进一步研究表明,Ndfip1不影响铁调节蛋白1(IRP1)、转铁蛋白受体1(TfR1)的蛋白表达,同时拮抗鱼藤酮引起的P62和铁蛋白L蛋白水平升高。我们的研究结果明确了Ndfip1蛋白可抑制鱼藤酮诱导的SH-SY5Y细胞中α-syn的增加。Ndfip1可能是预防和治疗PD的新的理论药物靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/225a/7813998/489033b0047d/fnmol-13-613404-g0001.jpg

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