Suppr超能文献

6-羟多巴胺通过自噬相关非经典分泌途径诱导 PARK7/DJ-1 的分泌。

6-Hydroxydopamine induces secretion of PARK7/DJ-1 via autophagy-based unconventional secretory pathway.

机构信息

a Department of Medical Life Systems, Faculty of Life and Medical Sciences , Doshisha University , Kyoto , Japan.

出版信息

Autophagy. 2018;14(11):1943-1958. doi: 10.1080/15548627.2018.1493043. Epub 2018 Aug 16.

Abstract

UNLABELLED

PARK7/DJ-1 is a Parkinson disease- and cancer-associated protein that functions as a multifunctional protein involved in gene transcription regulation and anti-oxidative defense. Although PARK7 lacks the secretory signal sequence, it is secreted and plays important physiological and pathophysiological roles. Whereas secretory proteins that lack the endoplasmic reticulum-targeting signal sequence are secreted from cells by way of what is called the unconventional secretion mechanism, the specific processes responsible for causing PARK7 to be secreted across the plasma membrane have remained unclear. In the present study, we found that PARK7 secretion was increased by treatment with 6-OHDA via the unconventional secretory pathway in human neuroblastoma SH-SY5Y cells and MEF cells. We also found that 6-OHDA-induced PARK7 secretion was suppressed in Atg5-, Atg9-, or Atg16l1-deficient MEF cells or ATG16L1 knockdown SH-SY5Y cells, indicating that the autophagy-based unconventional secretory pathway is involved in PARK7 secretion. We moreover observed that 6-OHDA-derived electrophilic quinone induced oxidative stress as indicated by a decrease in glutathione levels, and that this was suppressed by pretreatment with antioxidant NAC. We further found that NAC treatment suppressed autophagy and PARK7 secretion. We also observed that 6-OHDA-induced autophagy was associated with activation of AMPK and ULK1 via a pathway which was independent of MTOR. Collectively these results suggest that electrophilic 6-OHDA quinone enhances oxidative stress, and that this is followed by AMPK-ULK1 pathway activation and induction of secretory autophagy to produce unconventional secretion of PARK7.

ABBREVIATIONS

6-OHDA: 6-hydroxydopamine; AMPK: AMP-activated protein kinase; ATG: autophagy related; CAV1: caveolin 1; ER: endoplasmic reticulum; FN1: fibronectin 1; GSH: glutathione; IDE: insulin degrading enzyme; IL: interleukin; LDH: lactate dehydrogenase; MAP1LC3B/LC3B: microtubule associated protein 1 light chain 3 beta; MEF: mouse embryonic fibroblast; MTOR: mechanistic target of rapamycin kinase; NAC: N-acetyl-L-cysteine; PARK7/DJ-1: Parkinsonism associated deglycase; PD: Parkinson disease; RPS6KB1/p70S6K: ribosomal protein S6 kinase B1; RPN1: ribophorin I; ROS: reactive oxygen species; ULK1: unc-51 like autophagy activating kinase 1; WT: wild-type.

摘要

未标记

PARK7/DJ-1 是一种帕金森病和癌症相关蛋白,作为一种多功能蛋白,参与基因转录调控和抗氧化防御。尽管 PARK7 缺乏分泌信号序列,但它被分泌并发挥着重要的生理和病理生理作用。缺乏内质网靶向信号序列的分泌蛋白通过所谓的非经典分泌机制从细胞中分泌出来,但是导致 PARK7 穿过质膜分泌的具体过程仍不清楚。在本研究中,我们发现 6-OHDA 通过非经典分泌途径在人神经母细胞瘤 SH-SY5Y 细胞和 MEF 细胞中增加 PARK7 的分泌。我们还发现,在 Atg5-、Atg9- 或 Atg16l1 缺陷型 MEF 细胞或 ATG16L1 敲低 SH-SY5Y 细胞中,6-OHDA 诱导的 PARK7 分泌受到抑制,表明自噬为基础的非经典分泌途径参与 PARK7 分泌。此外,我们观察到 6-OHDA 衍生的亲电醌诱导氧化应激,表现为谷胱甘肽水平降低,而抗氧化剂 NAC 的预处理可抑制该作用。我们进一步发现,NAC 处理抑制自噬和 PARK7 的分泌。我们还观察到 6-OHDA 诱导的自噬与 AMPK 和 ULK1 的激活有关,该途径独立于 MTOR。总的来说,这些结果表明亲电 6-OHDA 醌增强氧化应激,随后 AMPK-ULK1 途径的激活和分泌自噬的诱导导致 PARK7 的非经典分泌。

缩写

6-OHDA:6-羟多巴胺;AMPK:AMP 激活的蛋白激酶;ATG:自噬相关;CAV1:窖蛋白 1;ER:内质网;FN1:纤连蛋白 1;GSH:谷胱甘肽;IDE:胰岛素降解酶;IL:白细胞介素;LDH:乳酸脱氢酶;MAP1LC3B/LC3B:微管相关蛋白 1 轻链 3β;MEF:小鼠胚胎成纤维细胞;MTOR:雷帕霉素靶蛋白激酶;NAC:N-乙酰-L-半胱氨酸;PARK7/DJ-1:帕金森病相关去糖基化酶;PD:帕金森病;RPS6KB1/p70S6K:核糖体蛋白 S6 激酶 B1;RPN1:核糖体蛋白 I;ROS:活性氧;ULK1:UNC-51 样自噬激活激酶 1;WT:野生型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cead/6152502/8a1714ae5045/kaup-14-11-1493043-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验