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High-Resolution Respirometry in Assessment of Mitochondrial Function in Neuroblastoma SH-SY5Y Intact Cells.高分辨率呼吸测定法在神经母细胞瘤 SH-SY5Y 完整细胞中线粒体功能评估中的应用。
J Membr Biol. 2020 Apr;253(2):129-136. doi: 10.1007/s00232-020-00107-4. Epub 2020 Jan 22.
2
The Impairments of α-Synuclein and Mechanistic Target of Rapamycin in Rotenone-Induced SH-SY5Y Cells and Mice Model of Parkinson's Disease.α-突触核蛋白和雷帕霉素作用机制靶点在鱼藤酮诱导的帕金森病SH-SY5Y细胞及小鼠模型中的损伤
Front Neurosci. 2019 Sep 24;13:1028. doi: 10.3389/fnins.2019.01028. eCollection 2019.
3
Presence of insoluble Tau following rotenone exposure ameliorates basic pathways associated with neurodegeneration.鱼藤酮暴露后不溶性 Tau 的存在改善了与神经退行性变相关的基本通路。
IBRO Rep. 2016 Sep 26;1:32-45. doi: 10.1016/j.ibror.2016.09.001. eCollection 2016 Dec.
4
The Close Encounter Between Alpha-Synuclein and Mitochondria.α-突触核蛋白与线粒体的亲密接触
Front Neurosci. 2018 Jun 7;12:388. doi: 10.3389/fnins.2018.00388. eCollection 2018.
5
SIRT3 Protects Rotenone-induced Injury in SH-SY5Y Cells by Promoting Autophagy through the LKB1-AMPK-mTOR Pathway.SIRT3通过LKB1-AMPK-mTOR途径促进自噬,保护鱼藤酮诱导的SH-SY5Y细胞损伤。
Aging Dis. 2018 Apr 1;9(2):273-286. doi: 10.14336/AD.2017.0517. eCollection 2018 Apr.
6
Is Parkinson's disease a lysosomal disorder?帕金森病是否是溶酶体疾病?
Brain. 2018 Aug 1;141(8):2255-2262. doi: 10.1093/brain/awy147.
7
Mitochondrial Dysfunction in Parkinson's Disease: New Mechanistic Insights and Therapeutic Perspectives.帕金森病中的线粒体功能障碍:新的发病机制及治疗展望。
Curr Neurol Neurosci Rep. 2018 Apr 3;18(5):21. doi: 10.1007/s11910-018-0829-3.
8
ER-mitochondria signaling in Parkinson's disease.帕金森病中的内质网-线粒体信号转导。
Cell Death Dis. 2018 Mar 1;9(3):337. doi: 10.1038/s41419-017-0079-3.
9
The respiratory chain inhibitor rotenone affects peroxisomal dynamics via its microtubule-destabilising activity.呼吸链抑制剂鱼藤酮通过其破坏微管的活性影响过氧化物酶体动力学。
Histochem Cell Biol. 2017 Sep;148(3):331-341. doi: 10.1007/s00418-017-1577-1. Epub 2017 May 18.
10
Englerin A induces an acute inflammatory response and reveals lipid metabolism and ER stress as targetable vulnerabilities in renal cell carcinoma.恩格勒因A诱导急性炎症反应,并揭示脂质代谢和内质网应激是肾细胞癌中可靶向的脆弱点。
PLoS One. 2017 Mar 15;12(3):e0172632. doi: 10.1371/journal.pone.0172632. eCollection 2017.

鱼藤酮诱导的 SH-SY5Y 细胞发病机制对亚细胞结构的易感性。

Vulnerability of subcellular structures to pathogenesis induced by rotenone in SH-SY5Y cells.

机构信息

Biomedical Center Martin, Martin, Slovak Republic.

出版信息

Physiol Res. 2021 Mar 17;70(1):89-99. doi: 10.33549/physiolres.934477. Epub 2021 Jan 14.

DOI:10.33549/physiolres.934477
PMID:33453717
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8820512/
Abstract

Numerous pathological changes of subcellular structures are characteristic hallmarks of neurodegeneration. The main research has focused to mitochondria, endoplasmic reticulum, Golgi apparatus, lysosomal networks as well as microtubular system of the cell. The sequence of specific organelle damage during pathogenesis has not been answered yet. Exposition to rotenone is used for simulation of neurodegenerative changes in SH-SY5Y cells, which are widely used for in vitro modelling of Parkinson´s disease pathogenesis. Intracellular effects were investigated in time points from 0 to 24 h by confocal microscopy and biochemical analyses. Analysis of fluorescent images identified the sensitivity of organelles towards rotenone in this order: microtubular cytoskeleton, mitochondrial network, endoplasmic reticulum, Golgi apparatus and lysosomal network. All observed morphological changes of intracellular compartments were identified before alphaS protein accumulation. Therefore, their potential as an early diagnostic marker is of interest. Understanding of subcellular sensitivity in initial stages of neurodegeneration is crucial for designing new approaches and a management of neurodegenerative disorders.

摘要

细胞亚结构的大量病变是神经退行性变的特征性标志。主要的研究集中在细胞的线粒体、内质网、高尔基体、溶酶体网络以及微管系统。然而,在发病机制中特定细胞器损伤的顺序尚未得到解答。鱼藤酮的暴露被用于模拟 SH-SY5Y 细胞的神经退行性变化,这些细胞被广泛用于帕金森病发病机制的体外建模。通过共聚焦显微镜和生化分析,在 0 到 24 小时的时间点研究了细胞内的效应。荧光图像分析确定了细胞器对鱼藤酮的敏感性顺序为:微管细胞骨架、线粒体网络、内质网、高尔基体和溶酶体网络。在αS 蛋白积累之前,所有观察到的细胞内隔室的形态变化都被识别出来。因此,它们作为早期诊断标志物的潜力引起了人们的兴趣。了解神经退行性变初始阶段的细胞亚结构敏感性对于设计新方法和管理神经退行性疾病至关重要。