a Instituto de Investigaciones Biomédicas "Alberto Sols" UAM-CSIC, Instituto de Investigación Sanitaria La Paz (IdiPaz) and Department of Biochemistry, Faculty of Medicine , Autonomous University of Madrid , Madrid , Spain.
b Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), ISCIII , Madrid , Spain.
Autophagy. 2018;14(8):1310-1322. doi: 10.1080/15548627.2018.1474992. Epub 2018 Jul 26.
Chaperone-mediated autophagy (CMA) is a selective degradative process for cytosolic proteins that contributes to the maintenance of proteostasis. The signaling mechanisms that control CMA are not fully understood but might involve response to stress conditions including oxidative stress. Considering the role of CMA in redoxtasis and proteostasis, we sought to determine if the transcription factor NFE2L2/NRF2 (nuclear factor, erythroid derived 2, like 2) has an impact on CMA modulation. In this work, we identified and validated 2 NFE2L2 binding sequences in the LAMP2 gene and demonstrated in several human and mouse cell types that NFE2L2 deficiency and overexpression was linked to reduced and increased LAMP2A levels, respectively. Accordingly, lysosomal LAMP2A levels were drastically reduced in nfe2l2-knockout hepatocytes, which also displayed a marked decrease in CMA activity. Oxidant challenge with paraquat or hydrogen peroxide, or pharmacological activation of NFE2L2 with sulforaphane or dimethyl fumarate also increased LAMP2A levels and CMA activity. Overall, our study identifies for the first time basal and inducible regulation of LAMP2A, and consequently CMA activity, by NFE2L2.
ACTB: actin, beta, ARE: antioxidant response element; ATG5: autophagy related 5; BACH1: BTB domain and CNC homolog 1; ChIP: chromatin immunoprecipitation; CMA: chaperone-mediated autophagy; DHE: dihydroethidium; DMF: dimethyl fumarate; ENCODE: Encyclopedia of DNA elements at the University of California, Santa Cruz; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GBA: glucosylceramidase beta; GFP: green fluorescent protein; HMOX1: heme oxygenase 1; HO: hydrogen peroxide; HSPA8/HSC70: heat shock protein family A (Hsp70) member 8; KEAP1: kelch like ECH associated protein 1; LAMP2A: lysosomal associated membrane protein 2A; LAMP2B: lysosomal associated membrane protein 2B; LAMP2C: lysosomal associated membrane protein 2C; LAMP1: lysosomal associated membrane protein 1; MAFF: MAF bZIP transcription factor F; MAFK: MAF bZIP transcription factor K; NFE2L2/NRF2: nuclear factor, erythroid derived 2, like 2; NQO1: NAD(P)H quinone dehydrogenase 1; PQ: paraquat; PI: protease inhibitors; qRT-PCR: quantitative real-time polymerase chain reaction; RNASE: ribonuclease A family member; SFN: sulforaphane; SQSTM1/p62: sequestosome 1; TBP: TATA-box binding protein.
伴侣介导的自噬(CMA)是一种细胞溶质蛋白的选择性降解过程,有助于维持蛋白质平衡。控制 CMA 的信号机制尚未完全了解,但可能涉及对包括氧化应激在内的应激条件的反应。考虑到 CMA 在 redoxtasis 和蛋白质平衡中的作用,我们试图确定转录因子 NFE2L2/NRF2(核因子,红细胞衍生 2 样 2)是否对 CMA 调节有影响。在这项工作中,我们在 LAMP2 基因中鉴定并验证了 2 个 NFE2L2 结合序列,并在几种人和鼠细胞类型中证明,NFE2L2 缺乏和过表达分别与 LAMP2A 水平的降低和升高有关。相应地,nfe2l2 敲除肝细胞中的溶酶体 LAMP2A 水平明显降低,CMA 活性也明显降低。百草枯或过氧化氢的氧化应激挑战,或用萝卜硫素或二甲基富马酸对 NFE2L2 的药理学激活也增加了 LAMP2A 水平和 CMA 活性。总的来说,我们的研究首次确定了 NFE2L2 对 LAMP2A 基础和诱导调节,进而对 CMA 活性的调节。
ACTB:肌动蛋白,β;ARE:抗氧化反应元件;ATG5:自噬相关 5;BACH1:BTB 结构域和 CNC 同源物 1;ChIP:染色质免疫沉淀;CMA:伴侣介导的自噬;DHE:二氢乙啶;DMF:二甲基富马酸;ENCODE:加利福尼亚大学圣克鲁兹分校的 DNA 元件百科全书;GAPDH:甘油醛-3-磷酸脱氢酶;GBA:β-葡萄糖脑苷脂酶;GFP:绿色荧光蛋白;HMOX1:血红素加氧酶 1;HO:过氧化氢;HSPA8/HSC70:热休克蛋白家族 A(Hsp70)成员 8;KEAP1:kelch 样 ECH 相关蛋白 1;LAMP2A:溶酶体相关膜蛋白 2A;LAMP2B:溶酶体相关膜蛋白 2B;LAMP2C:溶酶体相关膜蛋白 2C;LAMP1:溶酶体相关膜蛋白 1;MAFF:MAF bZIP 转录因子 F;MAFK:MAF bZIP 转录因子 K;NFE2L2/NRF2:核因子,红细胞衍生 2 样 2;NQO1:NAD(P)H 醌脱氢酶 1;PQ:百草枯;PI:蛋白酶抑制剂;qRT-PCR:实时定量聚合酶链反应;RNASE:核糖核酸酶 A 家族成员;SFN:萝卜硫素;SQSTM1/p62:自噬体 1;TBP:TATA 结合蛋白。