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雌激素受体激活有助于帕金森病模型中RNF146的表达和神经保护作用。

Estrogen receptor activation contributes to RNF146 expression and neuroprotection in Parkinson's disease models.

作者信息

Kim Hyojung, Ham Sangwoo, Lee Joon Yeop, Jo Areum, Lee Gum Hwa, Lee Yun-Song, Cho MyoungLae, Shin Heung-Mook, Kim Donghoon, Pletnikova Olga, Troncoso Juan C, Shin Joo-Ho, Lee Yun-Il, Lee Yunjong

机构信息

Division of Pharmacology, Department of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Samsung Biomedical Research Institute, Suwon 440-746, Republic of Korea.

National Development Institute of Korean Medicine, Gyeongsan 38540, Republic of Korea.

出版信息

Oncotarget. 2017 Oct 11;8(63):106721-106739. doi: 10.18632/oncotarget.21828. eCollection 2017 Dec 5.

Abstract

RNF146 is an E3 ubiquitin ligase that specifically recognizes and polyubiquitinates poly (ADP-ribose) (PAR)-conjugated substrates for proteasomal degradation. RNF146 has been shown to be neuroprotective against PAR polymerase-1 (PARP1)-induced cell death during stroke. Here we report that RNF146 expression and RNF146 inducers can prevent cell death elicited by Parkinson's disease (PD)-associated and PARP1-activating stimuli. In SH-SY5Y cells, RNF146 expression conferred resistance to toxic stimuli that lead to PARP1 activation. High-throughput screen using a luciferase construct harboring the RNF146 promoter identified liquiritigenin as an RNF146 inducer. We found that RNF146 expression by liquiritigenin was mediated by estrogen receptor activation and contributed to cytoprotective effect of liquiritigenin. Finally, RNF146 expression by liquiritigenin in mouse brains provided dopaminergic neuroprotection in a 6-hydroxydopamine PD mouse model. Given the presence of PARP1 activity and RNF146 deficits in PD, it could be a potential therapeutic strategy to restore RNF146 expression by natural compounds or estrogen receptor activation.

摘要

RNF146是一种E3泛素连接酶,它能特异性识别并将多聚(ADP-核糖)(PAR)共轭底物多聚泛素化,以便蛋白酶体进行降解。RNF146已被证明在中风期间对PAR聚合酶-1(PARP1)诱导的细胞死亡具有神经保护作用。在此,我们报告RNF146的表达及其诱导剂可预防帕金森病(PD)相关及PARP1激活刺激所引发的细胞死亡。在SH-SY5Y细胞中,RNF146的表达赋予了对导致PARP1激活的毒性刺激的抗性。使用含有RNF146启动子的荧光素酶构建体进行的高通量筛选确定了甘草素为RNF146诱导剂。我们发现甘草素诱导的RNF146表达是由雌激素受体激活介导的,并促成了甘草素的细胞保护作用。最后,甘草素在小鼠脑中诱导的RNF146表达在6-羟基多巴胺PD小鼠模型中提供了多巴胺能神经保护作用。鉴于PD中存在PARP1活性和RNF146缺陷,通过天然化合物或雌激素受体激活来恢复RNF146表达可能是一种潜在的治疗策略。

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