Introduction

Biomedical Reports

2049-9434 2049-9442

D.A. Spandidos

10.3892/br.2019.1247

BR-0-0-1247

Articles

Transcriptional factor Nrf2 is essential for aggresome formation during proteasome inhibition

Qin

Siyue

1 2 3 Jiang

Changan

2 3 Gao

2 3 4

1Department of Neurobiology, Shandong Provincial Key Laboratory of Mental Disorders, School of Medicine, Shandong University, Jinan, Shandong 250012, P.R. China 2Key Laboratory of Obstetrics, Gynecologic and Pediatric Diseases and Birth Defects, Ministry of Education, Sichuan University, Chengdu, Sichuan 610065, P.R. China 3Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610065, P.R. China 4The United Innovation of Mengchao Hepatobiliary Technology Key Laboratory of Fujian Province, Mengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou, Fujian 350002, P.R. China

Correspondence to: Dr Ju Gao or Professor Changan Jiang, Department of Pediatrics, West China Second University Hospital, Sichuan University, 24 South Section, 1 Yihuan Road, Chengdu, Sichuan 610065, P.R. China jugao204@gmail.com ca.jiang@siat.ac.cn

12 2019

21 10 2019

11 6 241 252 11 02 2019 18 09 2019

2019

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

Aggrephagy, the aggresome-related protein degradation system, represents a protective cellular response to shuttle misfolded proteins into the microtubule-organizing center for degradation through the autophagic pathway during stress conditions, including heat shock, oxidative stress and proteasome inhibition. In response to proteasome failure, many genes are transcriptionally activated to facilitate ubiquitinated proteins to be cleared via the aggrephagy pathway. Although many regulators involved in aggresome formation have been identified, the mechanism how transcriptional activation promotes aggresome formation remains unknown. Here, we have demonstrated that nuclear factor erythroid 2-related factor 2 (Nrf2) accumulated in the nucleus and activated the transcription of sequestosome-1 (p62) during proteasome inhibition in 293 cells. Loss of Nrf2 resulted in failure of aggresome formation and cell death; whereas overexpression of p62 alleviated Nrf2 knockdown-induced aggresome formation defects and promoted cell survival. Notably, blocking Nrf2 activation using a p38/MAPK inhibitor prevented proteasome inhibitor-induced aggresome formation. These findings suggested that Nrf2 may be a critical regulator of aggresome formation, which protects cells from proteasome dysfunction-induced stress.

nuclear factor erythroid 2-related factor 2 transcription p62 aggresome p38/MAPK

Introduction

The term aggresome refers to a stress sensitive subcellular structure, containing misfolded proteins, heat-shock proteins (HSPs) and proteasomal components, and it is formed when the protein-degradation system is overwhelmed (1). Aggresome formation requires an intact microtubule system and the distinct presence of γ-tubulin (2-4), which ultimately terminates in lysosomal degradation (5,6). Therefore, the aggresome pathway likely provides a backup system for delivery of aggregated proteins from the cytoplasm to lysosomes for degradation (4). Various stress conditions, including oxidative stress (7), proteasome inhibition (3) and heat shock (8), induce aggresome formation through different molecular mechanisms. In response to failure of ubiquitin proteasome system (UPS), p62 assembles the polyubiquitinated proteins into microaggregates through binding to their ubiquitin chains with its C-terminal ubiquitin binding domain and oligomerizing at its N-terminal PB1 domain (9). These microaggregates are then recognized by histone deacetylase 6 (HDAC6) and retrogradely transported via the microtubule network to the microtubule-organizing center for aggresome formation (3,10). Hence, proteasome inhibition-induced aggresome formation represents a highly organized biological process to switch polyubiquitinated proteins from the UPS to the autophagy pathway.

The aggrephagy pathway alleviates proteasome proteolysis failure-induced cell death under various stress conditions (5). Loss of aggresome formation regulators, such as p62, HDAC6 or PTEN-induced kinase 1 (PINK1), causes apoptosis in various cell types during proteasome inhibition (3,11,12). Consistently, toxicity of aggregated proteins is strongly enhanced by inhibition of the microtubule-dependent transport machineries, which are required for microaggregate transportation (4). More importantly, Parkinson's disease associated proteins, such as α-synuclein, leucine rich repeat kinase 2 and mutant DJ1, have been reported to be degraded via aggrephagy, suggesting that abnormalities in this backup protein degradation system may cause neurodegeneration (13-15). However, the mechanism underlying the activation of this compensatory pathway and the cellular factors that regulate aggresome formation remain unknown.

Transcriptional control of stress-responsive genes is a crucial part of the cell response to a wide variety of stresses (16). In response to oxidative stress, nuclear factor erythroid 2-related factor 2 (Nrf2), encoded by the NFE2L2 gene, binds to the antioxidant response elements (ARE) sequence within the promoter of detoxifying and antioxidant enzymes and activates their transcription (17). Interestingly, the induction of p62 by oxidative stress is mediated by Nrf2 and, at the same time, p62 competitively binds to Kelch-like ECH-associated protein 1 (Keap1) to activate Nrf2 (18-20). Although Nrf2 and p62 are essential for the oxidative stress response, the function of Nrf2 in aggresome formation during proteasome inhibition has not been determined.

Here, we showed that the loss of Nrf2 impaired aggresome formation and caused a hypersensitivity to proteasome inhibition in stressed cells, which was restored by the overexpression of p62. This study established Nrf2 as a major transcriptional mediator for proteasome stress-induced activation of the aggresome-autophagy pathway.

Materials and methods <sec> <title>Plasmid construction

The human Nrf2 and p62 full-length cDNA was obtained from Addgene, Inc. Nrf2 cDNA was amplified by Phusion high-fidelity DNA polymerase (Thermo Fischer Scientific, Inc.). A total of 30 cycles of PCR amplification were performed (98˚C for 5 sec, 55˚C for 5 sec and 72˚C for 90 sec). PCR products were digested by BamHI and XbaI. The digested fragment was cloned into pTango-CFlag vector (BioAtom Technology) linearized with BamHI/XbaI. The resulting construct is further referred to as Flag-Nrf2. p62 was amplified by PCR as described above (30 cycles of 98˚C for 5 sec, 55˚C for 5 sec and 72˚C for 80 sec) and cloned into pTango-NFlag (BioAtom Technology) after digestion with EcoRI and XbaI. The resulting construct is further referred to as Flag-p62. The human p62 promoter (-1781/+46) was obtained from genomic DNA purified from 293 cells based using publicly available sequence data (https://www.ncbi.nlm.nih.gov/gene/8878). Two fragments, namely the p62/SQSTM promoter (PCR, 30 cycles of 98˚C for 5 sec, 55˚C for 5 sec and 72˚C for 40 sec) digested by BamHI/EcoRI and the enhanced (E) GFP (PCR, 30 cycles of 98˚C for 5 sec, 55˚C for 5 sec and 72˚C for 30 sec) digested by EcoRI/XbaI, were cloned into an BamHI/XbaI-digested pBluescript II vector (Addgene, Inc.). The resulting construct was a fused EGFP sequence downstream of the p62 promoter region. All constructs were confirmed by sequencing. Detailed information for the primers is presented in Table SI.

Cell lines and reagents

MG132, anisomycin (ANI), actinomycin D (ActD), TAK715 and N-acetyl-cysteine were obtained from Tocris Bioscience. 293 cells were obtained from the American Type Culture Collection and were cultured in DMEM (Gibco; Thermo Fischer Scientific, Inc.) with 10% heat-inactivated fetal bovine serum (FBS; Gibco; Thermo Fischer Scientific, Inc.) and 1% penicillin/streptomycin (Gibco; Thermo Fischer Scientific, Inc.) at 37˚C with 5% CO₂.

For the chemical treatment, 50,000 cells were cultured for 24 h before treatment in 24-well plates at 80% confluence. Change the medium containing MG132 (2 µM), ANI (5 µg/ml), ActD (2 µg/ml), MG132 (2 µM) + ANI (5 µg/ml), MG132 (2 µM) + ActD (2 µg/ml), MG132 (2 µM) + TAK715 (10 µM) or MG132 (2 µM) + N-acetyl-cysteine (1 mM) and treat for 12 h. In time-dependent experiments, 293 cells were cultured in MG132 (2 µM)-containing medium for 12 h and ANI (5 µg/ml) was added at 0, 2, 4 or 6 h. To evaluate dose dependent effects of MG132 on Nrf2 accumulation, 293 cells were treated with 0.1, 0.5, 1, 2 and 10 µM MG132 for 12 h.

Transient transfection of 293 cells was performed using Mega-tran 1.0 (OriGene Technologies, Inc.) according to the manufacturer's instructions. Briefly, 50,000 cells were plated in 24-well plates 24 h prior to transfection (80% confluence). Medium was replaced with 0.5 ml of complete medium containing FBS and antibiotics 1 h before transfection. DNA (0.5 µg) was diluted in 50 µl of serum-free DMEM, mixed and 1.5 µl of MegaTran 1.0 was added and gently mixed. The resulting solution was incubated for 15 min at room temperature and added to the cells. Medium was replaced 5 h after adding the transfection solution. Transfection efficiency was checked 24 h post transfection by western blot.

Generation of Nrf2 knockout (nrf2-/-) cells

Nrf2 knockout cells were generated from 293 cells with a CRISPR/Cas9 system designed in our lab. pSpCas9(BB)-2A-Puro (PX459) V2.0 was a gift (cat. no. 62988; Addgene, Inc.) (21). All single guide (sg) RNA targeting sequences were predicted as first hits using the CRISPR guide design website (https://benchling.com). The 293 cells were first transfected with two PX459 vectors, which targeted 5'-CTTTTTTTGTCTTAAACAT-3' and 5'-GAAAGTTATGGCAGGTTTA-3', to delete the first exons of the NFE2L2 gene. After 24 h, cells were diluted and seeded in 96-well plates at 1 cell/well to isolate monoclonal cells without Nrf2 expression, as determined by quantitative (q) PCR and western blot analysis. Genomic DNA was extracted from cells by using PureLink Genomic DNA kit (Invitrogen; Thermo Fischer Scientific, Inc.). Further PCR analysis (as above; 30 cycles of 98˚C for 5 sec, 55˚C for 5 sec and 72˚C for 30 sec) was performed to validate the deletion of exon2 of the NFE2L2 gene in the monoclonal cells; primer sequences are presented in Table SI.

Generation of stable expression cells

The coding sequences Flag-p62 and Flag-Nrf2 were cloned into the plenti6-LVP lentiviral vectors (Thermo Fischer Scientific, Inc.). Viruses were generated and used to transduce nrf2^-/- cells as described previously (12). Briefly, plenti6-Flag-p62 and plenti6-Flag-Nrf2 plasmids were co-transfected with lentiviral packaging mix into 293 cells using Mega-tran 1.0. Supernatant containing lentivirus was harvested and cellular debris was removed by centrifugation (500 x g, 10 min, room temperature). A total of 10,000 nrf2^-/- cells was added to 24-well plates and transduced at an MOI of 5. Three days after transduction, puromycin (2 µg/ml) was added to the culture medium to generate stable nrf2^-/-[Flag-Nrf2] and nrf2^-/-[Flag-p62] cell lines. After puromycin selection, single cell clones were verified by qPCR analysis to validate the expression of exogenous Nrf2 and p62. Transfection controls were prepared with empty vector (plenti6-LVP). To evaluate the aggresome formation efficiency, nrf2^+/+, nrf2^-/-[Vector], [nrf2^-/-[Flag-Nrf2] and nrf2^-/-[Flag-p62] cells were treated with MG132 (2 µM) for 14 h.

Cell death assay

Cell death-inducing effects of proteasomal inhibition were measured with CF488A-Annexin V (ANXA5) and propidium iodide (PI) Apoptosis kits (cat. no. 30061; Biotium, Inc.) as described previously (12). A total of 100,000 cells/cm² were grown in 10 cm dishes. After 24 h, they were treated with DMSO (0.1%) or 2 µM MG132 (in DMSO) for 20 h. Cells were then harvested by digestion with 0.05% trypsin-EDTA, washed twice with ANXA5-Binding buffer and resuspended in 100 µl of this buffer. To each sample, 15 µl CF488A-ANXA5 and 5 µl PI were added and incubated in the dark for 30 min at room temperature. Unbound dyes were washed off with binding buffer, cells were mounted onto slides. All and images were captured using a fluorescence microscope (magnification, x40).

RNA extraction and reverse transcription-quantitative (RT-q) PCR

Total RNA was extracted from cells using the Qiagen All-Prep DNA/RNA/miRNA Universal kit (Qiagen, Inc.) according to manufacturer's protocols. RNA samples were subjected to DNase digestion using the Turbo DNA-free™ kit (Ambion; Thermo Fischer Scientific, Inc.). cDNA was synthesized by using ReverTra Ace^® qPCR RT kit (Toyobo Life Science) with a random primer (30˚C for 10 min, 42˚C for 20 min and 99˚C for 5 min). qPCR was performed using SYBR Premix Ex Taq (Takara Bio, Inc.) in a CFX96 real-time PCR system (Bio-Rad Laboratories, Inc.) following the manufacturer's protocol; thermocycling conditions were as follows: 95˚C for 30 sec, followed by 40 cycles of 95˚C for 5 sec and 60˚C for 30 sec. Levels of Nrf2 and p62 were normalized to GAPDH using the 2^-ΔΔCq method (22). The primers used for RT-qPCR were shown in Table SI.

Immunoblotting and immunocytochemistry analyses

Proteins were extracted from cells by 1% NP-40 in Tris buffer (50 mM Tris, 150 mM NaCl, pH 8.0, with protease and phosphatase inhibitors; Thermo Fischer Scientific, Inc.). The protein concentration was determined by BCA. Proteins (20 µg) were separated on 10% SDS-PAGE gels and transferred to PVDF membranes. Membranes were blocked with 5% non-fat milk in PBST (PBS pH 7.4 with 0.2% Tween-20) for h at room temperature, followed by incubation at 4˚C overnight with primary antibodies and washes with PBST (3x10 min at room temperature). Membranes were then incubated with 0.1 µg/ml Dylight 800 anti-rabbit (cat. no. 5230-0412; KPL, Inc.) or Dylight 680 anti-mouse (cat. no. 5230-0406; KPL, Inc.) secondary antibodies in the dark for 2 h at room temperature. After washing with PBST (3x10 min), images were acquired using a Li-Cor Odyssey Clx Infrared Imaging System (LI-COR Biosciences).

The following primary antibodies were used: Anti-Nrf2 (cat. no. ab137550; 1:2,000; Abcam), anti-p62 (cat.no. 18420-1-AP; 1:3,000; ProteinTech Group, Inc.), anti-FlagTag (cat. no. ANT-146; 1:5,000; Prospec-Tany TechnoGene, Ltd.), anti-phospho-p38 MAPK (Thr180/Tyr182; cat. no. 9211; 1:1,000; Cell Signaling Technology, Inc.), anti-p38 MAPK (D13E1) XP (cat. no. 8690; 1:1,000; Cell Signaling Technology, Inc.), anti-β-actin (cat. no. 60008-1-Ig; 1:5,000; ProteinTech Group, Inc.) and anti-GAPDH (cat. no. 10494-1-AP; 1:5,000; ProteinTech Group, Inc.).

For the immunocytochemistry, sterilized coverslips were placed in 24-well plates. Cells (30,000) were seeded and cultured for 24 h before treatment. After treatment, cover slips were washed with PBS (3x10 min at room temperature) and fixed with 4% paraformaldehyde for 15 min at room temperature. Cells were then permeabilized with 0.2% Triton X-100 for 15 min and blocked with 5% goat serum (Thermo Fischer Scientific, Inc.) for 1 h at room temperature. Samples were incubated with primary anti-ubiquitin Lys 48 (cat. no. 05-1307; 1:100; EMD Millipore) and anti-FlagTag antibodies (cat. no. ANT-146; 1:500; Prospec-Tany TechnoGene, Ltd.) at 4˚C overnight. After washing with PBS (3x10 min at room temperature), cells were incubated with goat anti-mouse Alexa Flour 488- (cat. no. A32723; 1:300) or goat anti-rabbit Alexa Fluor 568-conjugated secondary antibodies (cat. no. A-11011; 1:300; Thermo Fischer Scientific, Inc.) for 2 h at room temperature, stained with DAPI (1 µg/ml) for 5 min at room temperature and mounted for fluorescence microscopy examination. Fluorescent microscopy was performed with a confocal microscope (magnification, x63), with ≥20 observations per experiment.

Statistical analysis

Data are presented as the mean ± SEM. All the experiments were repeated ≥3 times. Statistical analysis was performed using one-way ANOVA followed by Tukey's multiple comparison test using GraphPad Prism 8 (GraphPad Software, Inc.). Detailed information about statistical analysis for each experiment are presented in the figure legends. P<0.05 was considered to indicate a statistically significant difference.

Results <sec> <title>Inhibition of protein synthesis blocks MG132-induced aggresome formation and Nrf2 accumulation

Previous studies have demonstrated that UbK48-linked polyubiquitin conjugates are proximal substrates of proteasomal proteolysis (23). During proteasomal stress, UbK48-linked polyubiquitinated proteins accumulate and package to form aggresome, which are recognized by antibodies. UbK48-positive structures are co-localized with other aggresome markers, such as p62, HDAC6 and PINK1S (13,24,25). To examine the role of just synthesized proteins in aggresome formation, we studied aggresome formation efficiency in MG132-treated cells after blocking transcription by ActD or translation by ANI. Immunostaining showed that 58.4% of cells formed UbK48-positive aggresomes in MG132-treated 293 cells and 4.4% of positive staining was observed in MG132+ANI-treated cells. ActD+MG132 treatment did not completely inhibit aggresome formation; however, there was a significant decrease in the number of aggresome containing cells after treatment with MG132+ActD compared with the MG132-treated cells (Fig. 1A). ActD treatment resulted in an accumulation of poly-ubiquitinated proteins in the nucleus, which may be caused by recruitment of ubiquitin E3 ligase into nuclear, such as murine double minute protein (26). We further examined aggresome formation efficiency by treating cells with MG132 and adding ANI at different incubation times (Fig. 1B). Inhibition of protein translation by ANI added after 2 h of MG132 pretreatment blocked aggresome formation in 293 cells. Aggresome formation efficiency increased to 37.9% when translation was blocked after 4 h of MG132 pretreatment and after 6 h of MG132 pretreatment, ANI had no effect on aggresome formation efficiency compared with the MG132-terated cells (Fig. 1B). These data indicated that protein translation in the first hours during proteasomal stress was critical for aggresome formation.

Immunoblotting analysis revealed that of protein translation induced by ANI prevented Nrf2 accumulation at early stages of stress, compared with the MG132-treated cells (Fig. 1C), and Nrf2 was localized in the nucleus after MG132 treatment (Fig. 1D). Furthermore, 0.1 to 10 µM MG132 treatment showed that Nrf2 accumulated in a dose-dependent manner (Fig. S1). Levels of p62, critical for poly-ubiquitinated proteins to form microaggresomes during proteasome inhibition, were higher in MG132-treated cells compared with ANI+MG132-treated groups (Fig. 1C). These results suggested that stress-induced protein synthesis, including the synthesis of Nrf2 and p62, may be essential for aggresome formation.

Loss of Nrf2 results in failure of aggresome formation

If Nrf2 was required for MG132-induced aggresome formation, we hypothesized that knockout of Nrf2 may interfere with aggresome formation and cell survival after MG132 treatment. To test this, we generated Nrf2 knockout cell lines using CRISPR/Cas9 (Fig. S2A) (21). Nrf2 is rapidly processed by UPS (27,28), but protein levels were detected by western blot in 293 cells following MG132 treatment to induce rapid accumulation of Nrf2 (Fig. S2B). As expected, deleting the first exon of NEL2L resulted in loss of Nrf2 protein expression in nrf2^-/- cells (Fig. S2B). Further PCR analysis of the monoclonal cell lines without Nrf2 expression showed that the first exon of NEL2L was successfully deleted (Fig. S2C and D). To determine aggresome formation efficiency in nrf2^+/+ and nrf2^-/- cells, MG132 was used to induce the aggresome formation. A 14 h treatment with 2 µM MG132 induced aggresome formation in 68% of nrf2^+/+ and 12.5% of nrf2^-/- cells (Fig. 2A). It has been reported that loss of Nrf2 induces increased reactive oxygen species (ROS) production in cultured cells and mouse brains (28,29), we wanted to evaluate whether aggresome formation defects were caused by increased intracellular ROS in nrf2^-/- cells. To reduce intracellular ROS level, we treated nrf2^+/+ and nrf2^-/- cells with N-acetyl-cysteine (NAC), an aminothiol and synthetic precursor of intracellular cysteine and GSH (30). NAC treatment had no significant effect on the aggresome formation in nrf2^+/+ and nrf2^-/- cells, suggesting that ROS levels may not influence aggresome formation during proteasome inhibition (Fig. S2E and F).

To explore the time-dependent manner of MG132 induced cell death, we treated 293 cells with 2 µM MG132 and analyzed cytotoxicity with FITC-Annexin V and PI assays. After 20 h treatment with MG132, changes in viability were significant in 293 cells (Fig. S3). We further treated nrf2^+/+ and nrf2^-/- cells with 2 µM MG132 for 20 h to induce apoptosis and necrosis. The cell viability assay demonstrated that the loss of Nrf2 significantly increased the cells susceptibility towards proteasomal inhibition-triggered cell death following MG132 treatment (Fig. 2B). MG132 treatment induced apoptosis in 8.7% and necrosis in 5.8% of nrf2^+/+ cells, and in nrf2^-/- cells, apoptosis and necrosis rates increased to 17.7 and 12.7%, respectively.

Transcriptional upregulation of p62 during proteasome inhibition is dependent on Nrf2

The presence of the ARE in the p62 gene suggests that p62 may be transcriptionally activated by Nrf2 during proteasome inhibition (17). To test this hypothesis, we examined mRNA and protein levels of p62 in nrf2^+/+ and nrf2^-/- cells. mRNA and protein levels of p62 were significantly increased in nrf2^+/+ cells when treated with MG132 and this response was inhibited by Nrf2 knockout (Fig. 3A and B). Similar to p62, heme oxygenase-1, a gene regulated by Nrf2 during proteasome inhibition (31), expression decreased in nrf2^-/- cells compared with nrf2^+/+ cells following MG132 treatment (Fig. S4A and B). This further indicated that Nrf2 may be essential for the transcriptional activation of stress-response genes. To exclude the possibility that Nrf2 may affect the activity of other transcriptional factors, we evaluate protein levels of HSP70, samples in which the transcriptional activation was driven by HSF1 during MG132 treatment (32). Loss of Nrf2 had no effect on HSP70 expression compared with nrf2^+/+ cells (Fig. S4C and D).

To further examine the transcriptional regulation of p62 by Nrf2, we cloned ~1.8 kb of the human p62 promoter region upstream of EGFP (33). The reporter gene was expressed in nrf2^+/+ and nrf2^-/- cells, and MG132 treatment significantly increased EGFP expression in nrf2^+/+ but not nrf2^-/- cells (Fig. 3C). The loss of Nrf2 inhibited aggresome formation and p62 transcriptional activation during proteasome inhibition.

Expression of p62 rescues proteasomal stress response defects in Nrf2 knockout cells

Proteasome inhibition stimulates p62 ubiquitin binding activity by phosphorylation and assembles ubiquitinated cargos into microaggregates through self-oligomerization (13,34,35). Loss of p62 suppresses the formation of aggresomes and clearance of poly-ubiquitinated proteins during MG132 treatment in 293 cells (12). If the Nrf2 knockout induced proteasome formation, defects may be dependent on the loss of p62 in 293 cells, overexpression of p62 in nrf2^-/- cells may rescue these defects. To this end, we generated nrf2^-/-[Flag-Nrf2] and nrf2^-/-[Flag-p62] stable cell lines by lentivirus-transduction (Fig. S5).

A 14 h treatment with 2 µM MG132 induced aggresome formation in 68.8% of nrf2^+/+ cells, but aggresome-containing cells in the nrf2^-/-[Vector] cell line was decreased to 17.1% (Fig. 4A). In nrf2^-/- cells, overexpression of Flag-Nrf2 rescued aggresome formation in 72.5% of cells and overexpression of Flag-p62 rescued aggresome formation efficiency to 51%, suggesting that p62 protein levels may be critical for aggresome formation. The aggresome formation efficiency in nrf2^-/-[Flag-p62] cells lower than that of the nrf2^-/- [Flag-Nrf2] cells, indicating that other targets regulated by Nrf2 are involved in aggresome formation. A 20 h treatment with 2 µM MG132 induced apoptosis in 19.5% and necrosis in 11.2% of the nrf2^-/-[Vector] cells, and in nrf2^-/-[Flag-Nrf2] cells, apoptosis and necrosis rates were reduced to 13.2 and 9.7%, respectively (Fig. 4B). Overexpression of Flag-p62 in nrf2^-/- cells decreased apoptosis and necrosis rates to 8.1 and 5.1%, respectively, suggesting that Nrf2-mediated transcriptional activation of p62 was required to minimize proteasomal stress-induced necrosis and apoptosis. Immunoblotting analysis showed that overexpression of Flag-Nrf2 rescued MG132-induced transcriptional activation of p62 deficits in nrf2^-/-[Vector] cells (Fig. 4C). Exogenous expressed Flag-Nrf2 in nrf2^-/- cells significantly increased after MG132 treatment compared with the unstressed condition, further supporting that Nrf2 was sensitive to proteasome inhibition (Fig. 4C). Together, these results confirmed that Nrf2-mediated transcriptional activation of p62 was essential for aggresome formation during proteasome dysfunction.

Nrf2 mediated aggresome formation depends on p38/MAPK kinase activity

It has been reported that Nrf2 activation is p38/MAPK-dependent, which compromises the cytotoxic effects through activating transcription of downstream targeting genes during proteasome inhibition (36). We blocked p38/MAPK activity using the specific inhibitor TAK715 to examine, if Nrf2-mediated aggresome formation in MG132-treated cells was dependent on the p38/MAPK pathway. Consistent with the previous study, p38 inhibitor TAK715 partially inhibited activation of p38-induced by proteasomal inhibition; the efficiency of aggresome formation in MG132+TAK715-treated cells decreased by 50% compared with the MG132-treated cells (Fig. 5A). Western blot analysis confirmed that protein levels of Nrf2 and p62 significantly decreased in MG132+TAK715-treated cells compared with the MG132-treated cells (Fig. 5B). Taken together, blocking Nrf2 activation through suppression of the p38/MAPK signaling pathway may decrease the efficiency of aggresome formation.

Discussion

The aggresome has emerged as a key stress-response subcellular structure in the clearance of misfolded protein aggregates during many stress conditions, which are often linked with cell death in neurodegenerative diseases (37). Despite the potential importance of the aggresome in managing the stress response and its association with disease, few proteins critical for aggresome formation have been identified (38-40). In this study, we reported that Nrf2 was crucial for aggresome formation and cell survival in response to proteasome inhibition-induced stress. Based on our results, we proposed a model, which described that Nrf2-mediated mRNA transcription may be induced through cellular stress and mediated by proteasome dysfunction (Fig. 6).

During mRNA translation, the synthesized polypeptide chain is elongated by the ribosome with the linear chain folding into its three dimensional structure and then being targeted to a precise intracellular location. If misfolded, the polypeptides are rapidly degraded by UPS (41,42). However, when UPS is impaired or overwhelmed, misfolded polypeptides are sequestered into microaggregates and then retrogradely transported to the microtubule-organizing center to form aggresomes (43,44). How does the UPS dysfunction activate downstream signals to form the aggresome? As shown in previous studies, during proteasome inhibition, newly synthesized proteins play a special regulatory role in the initiation of aggresome formation (40,45). Therefore, we hypothesized that inhibitors of transcription and translation may suppress aggresome formation. Inhibition of protein translation by ANI completely inhibited aggresome formation, whereas transcriptional inhibitor ActD, which prevents mRNA synthesis, only partially reduced the efficiency of aggresome formation. These data supported the notion that translational regulation provided immediate and effective changes in protein levels involved in aggresome formation. However, transcriptional regulation is essential in mediating the strength of stress response (46).

Cells activate mechanisms to regulate gene expression after exposure to environmental stress, largely at the transcriptional level. These stress responses enable cells to cope with and adapt to stressful situations, such as starvation, oxidative and DNA damage (47). A central mechanism for the regulation of stress-induced transcription is mediated by activation of the specific transcriptional factors (48). Transcriptional factor Nrf2 is the major regulator of cytoprotective responses to oxidative and electrophilic stress (49). Nrf2 is rapidly turned over by UPS, with a short half-life under physiological conditions (7-15 min) that is increased to 30-100 min in the presence of a stress inducer (50,51). Proteasome inhibitors, such as clasto-lactacystin, β-lactone, MG132 and MG115, lead to the rapid accumulation of Nrf2 in the nuclei (52,53). Here, we showed that MG132, at low concentration, such as 0.5 µM and 1 µM, induced Nrf2 accumulation, indicating that Nrf2 was extremely sensitive to proteasome inhibition making it a potential candidate to serve as an upstream modulator in the proteasomal stress response. Nrf2 knockout cells displayed reduced efficiency in aggresome formation, as well as increased cell death. This phenotype was suppressed by the overexpression of Nrf2 and p62, suggesting that the reduced aggresome formation efficiency in nrf2^-/- cells may be due to their lack of p62. These results supported claims of a major role of Nrf2 in the transduction of proteasome impairment signaling to the downstream aggresome-autophagy machinery.

Loss the Nrf2 expression caused decreases in aggresome formation efficiency (68.7 and 17.1% for nrf2^+/+ and nrf2^-/-, respectively), while transcriptional inhibitor ActD only reduced the efficiency to 37.9%. The data suggested that Nrf2 regulated aggresome formation not only through transcriptional upregulation of targeting mRNA, such as p62, but also through an unknown pathway. Loss of Nrf2 leads to mitochondrial depolarization, decreased ATP levels and impaired respiration (54). Microaggregate transport, through the microtubule mediated by HDAC6, is an energy-consuming process (3), and decreased ATP levels may contribute to aggresome formation defects in nrf2^-/- cells, a process which is independent of Nrf2-regulated transcriptional reprogramming. Although overexpression of p62 restored aggresome formation efficiency to 51%, levels were still different compared with nrf2^-/-[Flag-Nrf2] cells (72.5%), indicating that Nrf2 influenced aggresome formation through multiple pathways. Genetic activation of Nrf2 by deletion of Keap1 increases the mitochondrial membrane potential and ATP levels, the rate of respiration and the efficiency of oxidative phosphorylation (54). This may explain the small increase of aggresome formation efficiency in Nrf2 overexpressing in nrf2^-/- cells compared with the nrf2^+/+[Vector] cells. Further studies are needed to evaluate the association between Nrf2-mediated mitochondrial function and aggresome formation.

Proteasome inhibitors have been shown to induce aggresome formation in many cell types, including 293, MEF, as well as neuronal-like cells PC12 and N2A, in a time- and dose-dependent manner (26,55-57). However, some misfolded proteins form dispersed aggregates rather than aggresomes during proteasome inhibition, such as HeLa, Huh7 and Cos7 (55,58). In contrast to aggresomes formed around MTOC, dispersed aggregates are distributed in the cells and do not result in cytoskeleton rearrangements, suggesting that dispersed aggregates may represent intermediate particles during aggresome assembly (24,58). The defects of aggresome formation in these cells may be caused by the lack of critical regulators of aggresome assembly, such as the subtype of p38 kinase (24). Due to their biochemical and morphological similarities to the protein inclusion bodies in neurodegenerative diseases, aggresomes have received much attention in the past twenty years (41,59). Aggresomes have been thought to play a critical role in protein surveillance and the pathogenesis of neurodegenerative diseases (60). Induction of aggresome formation can increase cell survival when overexpressing a mutant huntingtin fragment in primary cultured neuronal cells (61). Reducing the load of aggresomes by genetically inhibiting ubiquitination enhances polyQ-mediated neuronal death in a mouse model (62). An Nrf2-mediated aggresome formation mechanism may not only explain the activation of autophagy by proteasome dysfunction, but also implicate the inefficient switch between different protein degradation pathways, as one pathological mechanism of neurodegenerative diseases.

In summary, our study revealed transcriptional events associated with Nrf2 as critical signaling modules for the perinuclear aggresome formation during proteasomal stress (Fig. 6). These findings supported claims that the stress-induced aggresome-autophagy pathway may be critical for cell survival during proteasomal failure. Given that protein aggregation and accumulation is related to many diseases (63), our findings suggested the p38/Nrf2/p62 pathway as an important therapeutic target.

Supplementary Material

Low levels of MG132 induce Nrf2 accumulation. (A) Representative immunoblots and (B) quantification of Nrf2 in cells treated with varying amounts of MG132. Data are presented as the mean ± SEM representative of three independent experiments and were assessed using one-way ANOVA followed by Tukey's test. **P<0.01 and ***P<0.001. Nrf2, nuclear factor erythroid 2-related factor 2.

Generation of Nrf2 knockout cells. (A) Schematic diagram of CRISPR/Cas9 genome editing of <italic>NEF2L2</italic>. (B) Representative immunoblots of Nrf2 in <italic>nrf2</italic>+/+ and <italic>nrf2</italic>-/- cells treated with MG132 (2 μM) for 12 h. (C) Representative images of <italic>NEF2L2</italic> gene fragments in <italic>nrf2</italic>+/+ and <italic>nrf2</italic>-/- cells; amplified genomic DNA covered the sgRNA-targeting sequence. (D) DNA sequences of PCR fragments in created by PCR. (E) Representative images and (F) quantification of aggresomes in MG132 or MG132+NAC (1 mM) treated cells; anti-ubiquitin Lys 48 visualizes aggresomes; scale bar, 20 μm. Data are presented as the mean± SEM representative of three independent experiments and were assessed using one-way ANOVA followed by Tukey's test. ***P<0.001. Nrf2, nuclear factor erythroid 2-related factor 2; NS, not significant; sgRNA, single guide RNA; <italic>nrf2</italic>-/-, Nrf2 knockout 293 cells; NAC, N-acetyl-cysteine.

MG132 induces cell death in 293 cells. Representative quantification of viable 293 cells stained with Annexin V and PI at different time points after MG132 (2 μM) treatment; live cells, Annexin V-PI-. Data are presented as the mean ± SEM representative of three independent experiments and were assessed using one-way ANOVA followed by Tukey's test. *P<0.05, ***P<0.001 and ****P<0.0001. Nrf2, nuclear factor erythroid 2-related factor 2; PI, propidium iodide.

Loss of Nrf2 reduces HO1 expression without affecting other stress-induced genes during proteasomal inhibition. (A) Representative immunoblots and (B) quantification of HO1 in cells treated with DMSO or MG132 (2 μM) for 12 h. (C) Representative immunoblots and (D) quantification of HSP70 in cells treated with DMSO or MG132 (2 μM) for 12 h. Data are presented as the mean ± SEM representative of three independent experiments and were assessed using one-way ANOVA followed by Tukey's test. **P<0.01. Nrf2, nuclear factor erythroid 2-related factor 2; <italic>nrf2</italic>-/-, Nrf2 knockout 293 cells; HO1, heme oxygenase-1; HSP70, 70-kDa heat shock protein.

Generation of <italic>nrf2</italic>-/-[Flag-p62] and <italic>nrf2</italic>-/-[Flag-Nrf2] cells. (A) Nrf2 mRNA levels in <italic>nrf2</italic>+/+, <italic>nrf2</italic>-/-, <italic>nrf2</italic>-/-[Flag-Nrf2], <italic>nrf2</italic>+/+[Vector] and <italic>nrf2</italic>-/-[Vector] cells. (B) p62 mRNA levels in <italic>nrf2</italic>+/+, <italic>nrf2</italic>-/-, <italic>nrf2</italic>-/-[Flag-p62], <italic>nrf2</italic>+/+[Vector] and <italic>nrf2</italic>-/-[Vector] cells. Data are presented as the mean ± SEM representative of three independent experiments and were assessed using one-way ANOVA followed by Tukey's test. ***P<0.001, ****P<0.0001. Nrf2, nuclear factor erythroid 2-related factor 2; <italic>nrf2</italic>-/-, Nrf2 knockout 293 cells; [], transfection construct.

Primers used in this study.

Acknowledgements

Not applicable.

Funding

This work was supported by the National Natural Science Foundation of China (grant nos. 30871032 and 31600616), the Natural Science Foundation of Fujian Province (grant no. 2017J05142), the Scientific Foundation of Fuzhou Health Department (grant no. 2016-S-124-10) and the Scientific Foundation of Fujian Provincial Health Commission (grant no. 2016-1-87).

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors' contributions

CJ and JG conceived and designed the experiments. SQ and JG performed experiments and analyzed the data. JG wrote the paper. All authors read and approved the final manuscript.

Ethics approval and consent to participate

Not applicable.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

References 1

Corboy

Thomas

Wigley

Aggresome formation

Methods Mol Biol3013053272005

15917642

10.1385/1-59259-895-1:305

Johnston

Ward

Kopito

Aggresomes: A cellular response to misfolded proteins

J Cell Biol143188318981998

9864362

10.1083/jcb.143.7.1883

Kawaguchi

Kovacs

McLaurin

Vance

Ito

Yao

The deacetylase HDAC6 regulates aggresome formation and cell viability in response to misfolded protein stress

Cell1157277382003

14675537

10.1016/s0092-8674(03)00939-5

Webb

Ravikumar

Rubinsztein

Microtubule disruption inhibits autophagosome-lysosome fusion: Implications for studying the roles of aggresomes in polyglutamine diseases

Int J Biochem Cell Biol36254125502004

15325591

10.1016/j.biocel.2004.02.003

Tanaka

Kim

Lee

Junn

Iwatsubo

Mouradian

Aggresomes formed by alpha-synuclein and synphilin-1 are cytoprotective

J Biol Chem279462546312004

14627698

10.1074/jbc.M310994200

Rubinsztein

Ravikumar

Acevedo-Arozena

Imarisio

O'Kane

Brown

Dyneins, autophagy, aggregation and neurodegeneration

Autophagy11771782005

16874055

10.4161/auto.1.3.2050

Marambio

Toro

Sanhueza

Troncoso

Parra

Verdejo

García

Quiroga

Munafo

Díaz-Elizondo

Glucose deprivation causes oxidative stress and stimulates aggresome formation and autophagy in cultured cardiac myocytes

Biochim Biophys Acta18025095182010

20176105

10.1016/j.bbadis.2010.02.002

Kovacs

Lentini

Ingano

Kovacs

Presenilin 1 forms aggresomal deposits in response to heat shock. Journal of molecular neuroscience

J Mol Neurosci299192006

16757805

10.1385/JMN:29:1:29

Ang

Pavlos

Rea

Chai

Walsh

Ratajczak

Zheng

Proteasome inhibitors impair RANKL-induced NF-kappaB activity in osteoclast-like cells via disruption of p62, TRAF6, CYLD, and IkappaBalpha signaling cascades

J Cell Physiol2204504592009

19365810

10.1002/jcp.21787

Kirkin

McEwan

Novak

Dikic

A role for ubiquitin in selective autophagy

Mol Cell342592692009

19450525

10.1016/j.molcel.2009.04.026

Pankiv

Clausen

Lamark

Brech

Bruun

Outzen

Øvervatn

Bjørkøy

Johansen

p62/SQSTM1 binds directly to Atg8/LC3 to facilitate degradation of ubiquitinated protein aggregates by autophagy

J Biol Chem28224131241452007

17580304

10.1074/jbc.M702824200

Gao

Qin

Zhang

Jiang

Deng

Zhang

You

Cytosolic PINK1 promotes the targeting of ubiquitinated proteins to the aggresome-autophagy pathway during proteasomal stress

Autophagy126326472016

27050454

10.1080/15548627.2016.1147667

Olzmann

Chudaev

Chen

Perez

Palmiter

Chin

Parkin-mediated K63-linked polyubiquitination targets misfolded DJ-1 to aggresomes via binding to HDAC6

J Cell Biol178102510382007

17846173

10.1083/jcb.200611128

Waxman

Covy

Bukh

Dawson

Giasson

Leucine-rich repeat kinase 2 expression leads to aggresome formation that is not associated with alpha-synuclein inclusions

J Neuropathol Exp Neurol687857962009

19535993

10.1097/NEN.0b013e3181aaf4fd

McLean

Ribich

Hyman

Subcellular localization of alpha-synuclein in primary neuronal cultures: Effect of missense mutations

J Neural Transm Suppl5853632000

11128613

10.1007/978-3-7091-6284-2_5

Harding

Novoa

Zhang

Zeng

Wek

Schapira

Ron

Regulated translation initiation controls stress-induced gene expression in mammalian cells

Mol Cell6109911082000

11106749

10.1016/s1097-2765(00)00108-8

Jain

Lamark

Sjøttem

Larsen

Awuh

Øvervatn

McMahon

Hayes

Johansen

p62/SQSTM1 is a target gene for transcription factor NRF2 and creates a positive feedback loop by inducing antioxidant response element-driven gene transcription

J Biol Chem28522576225912010

20452972

10.1074/jbc.M110.118976

Lau

Zheng

Tao

Wang

Whitman

White

Zhang

Arsenic inhibits autophagic flux, activating the Nrf2-Keap1 pathway in a p62-dependent manner

Mol Cell Biol33243624462013

23589329

10.1128/MCB.01748-12

Ichimura

Waguri

Sou

Kageyama

Hasegawa

Ishimura

Saito

Yang

Kouno

Fukutomi

Phosphorylation of p62 activates the Keap1-Nrf2 pathway during selective autophagy

Mol Cell516186312013

24011591

10.1016/j.molcel.2013.08.003

Komatsu

Kurokawa

Waguri

Taguchi

Kobayashi

Ichimura

Sou

Ueno

Sakamoto

Tong

The selective autophagy substrate p62 activates the stress responsive transcription factor Nrf2 through inactivation of Keap1

Nat Cell Biol122132232010

20173742

10.1038/ncb2021

Ran

Hsu

Wright

Agarwala

Scott

Zhang

Genome engineering using the CRISPR-Cas9 system

Nat Protoc8228123082013

24157548

10.1038/nprot.2013.143

Livak

Schmittgen

Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method

Methods254024082001

11846609

10.1006/meth.2001.1262

Pickart

Fushman

Polyubiquitin chains: Polymeric protein signals

Curr Opin Chem Biol86106162004

15556404

10.1016/j.cbpa.2004.09.009

Zhang

Gao

Deng

Jiang

p38δ MAPK regulates aggresome biogenesis by phosphorylating SQSTM1 in response to proteasomal stress

J Cell Sci1311312018

29930081

10.1242/jcs.216671

Hao

Nanduri

Rao

Panichelli

Ito

Yoshida

Yao

Proteasomes activate aggresome disassembly and clearance by producing unanchored ubiquitin chains

Mol Cell518198282013

24035499

10.1016/j.molcel.2013.08.016

Mekhail

Khacho

Carrigan

Hache

Gunaratnam

Lee

Regulation of ubiquitin ligase dynamics by the nucleolus

J Cell Biol1707337442005

16129783

10.1083/jcb.200506030

Cui

Lai

Janicki

Wang

Nuclear factor erythroid-2 related factor 2 (Nrf2)-mediated protein quality control in cardiomyocytes

Front Biosci211922022016

26709769

Hochmuth

Biteau

Bohmann

Jasper

Redox regulation by Keap1 and Nrf2 controls intestinal stem cell proliferation in Drosophila

Cell Stem Cell81881992011

21295275

10.1016/j.stem.2010.12.006

Kovac

Angelova

Holmström

Zhang

Dinkova-Kostova

Abramov

Nrf2 regulates ROS production by mitochondria and NADPH oxidase

Biochim Biophys Acta18507948012015

25484314

10.1016/j.bbagen.2014.11.021

Arakawa

Ito

N-acetylcysteine and neurodegenerative diseases: Basic and clinical pharmacology

Cerebellum63083142007

17853088

10.1080/14734220601142878

Sheng

Chien

Kang

Liou

Lee

Antagonism of proteasome inhibitor-induced heme oxygenase-1 expression by PINK1 mutation

PLoS One12e01830762017

28806787

10.1371/journal.pone.0183076

Kim

Proteasome inhibitors MG132 and lactacystin hyperphosphorylate HSF1 and induce hsp70 and hsp27 expression

Biochem Biophys Res Commun2542642681999

9920768

10.1006/bbrc.1998.9840

Vadlamudi

Shin

Genomic structure and promoter analysis of the p62 gene encoding a non-proteasomal multiubiquitin chain binding protein

FEBS Lett4351381421998

9762895

10.1016/s0014-5793(98)01021-7

Lim

Lachenmayer

Liu

Kundu

Wang

Komatsu

Zhao

Yue

Proteotoxic stress induces phosphorylation of p62/SQSTM1 by ULK1 to regulate selective autophagic clearance of protein aggregates

PLoS Genet11e10049872015

25723488

10.1371/journal.pgen.1004987

Matsumoto

Wada

Okuno

Kurosawa

Nukina

Serine 403 phosphorylation of p62/SQSTM1 regulates selective autophagic clearance of ubiquitinated proteins

Mol Cell442792892011

22017874

10.1016/j.molcel.2011.07.039

Yan

Zhang

Liu

Gao

Niu

Meng

Wang

Proteasome inhibition induces a p38 MAPK pathway-dependent antiapoptotic program via Nrf2 in thyroid cancer cells

J Clin Endocrinol Metab96E763E7712011

21346076

10.1210/jc.2010-2642

Kopito

Aggresomes, inclusion bodies and protein aggregation

Trends Cell Biol105245302000

11121744

10.1016/s0962-8924(00)01852-3

Szebenyi

Wigley

Hall

Didier

Thomas

Krämer

Hook2 contributes to aggresome formation

BMC Cell Biol8192007

17540036

10.1186/1471-2121-8-19

Bolhuis

Richter-Landsberg

Effect of proteasome inhibition by MG-132 on HSP27 oligomerization, phosphorylation, and aggresome formation in the OLN-93 oligodendroglia cell line

J Neurochem1149609712010

20089131

10.1111/j.1471-4159.2010.06600.x

Meriin

Zaarur

Sherman

Association of translation factor eEF1A with defective ribosomal products generates a signal for aggresome formation

J Cell Sci125266526742012

22357952

10.1242/jcs.098954

Hyttinen

Amadio

Viiri

Pascale

Salminen

Kaarniranta

Clearance of misfolded and aggregated proteins by aggrephagy and implications for aggregation diseases

Ageing Res Rev1816282014

25062811

10.1016/j.arr.2014.07.002

Lamark

Johansen

Aggrephagy: Selective disposal of protein aggregates by macroautophagy

Int J Cell Biol20127369052012

22518139

10.1155/2012/736905

Takalo

Salminen

Soininen

Hiltunen

Haapasalo

Protein aggregation and degradation mechanisms in neurodegenerative diseases

Am J Neurodegener Dis21142013

23516262

Brüning

Jückstock

Misfolded proteins: From little villains to little helpers in the fight against cancer

Front Oncol5472015

25759792

10.3389/fonc.2015.00047

Park

Ryu

Choi

Lee

Kim

Choe

Lee

Misfolded polypeptides are selectively recognized and transported toward aggresomes by a CED complex

Nat Commun8157302017

28589942

10.1038/ncomms15730

Liu

Qian

Translational reprogramming in cellular stress response

Wiley Interdiscip Rev RNA53013152014

24375939

10.1002/wrna.1212

Sonenberg

Hinnebusch

Regulation of translation initiation in eukaryotes: Mechanisms and biological targets

Cell1367317452009

19239892

10.1016/j.cell.2009.01.042

Espinosa-Diez

Miguel

Mennerich

Kietzmann

Sánchez-Pérez

Cadenas

Lamas

Antioxidant responses and cellular adjustments to oxidative stress

Redox Biol61831972015

26233704

10.1016/j.redox.2015.07.008

Baird

Dinkova-Kostova

The cytoprotective role of the Keap1-Nrf2 pathway

Arch Toxicol852412722011

21365312

10.1007/s00204-011-0674-5

McMahon

Thomas

Itoh

Yamamoto

Hayes

Redox-regulated turnover of Nrf2 is determined by at least two separate protein domains, the redox-sensitive Neh2 degron and the redox-insensitive Neh6 degron

J Biol Chem27931556315672004

15143058

10.1074/jbc.M403061200

Nguyen

Sherratt

Huang

Yang

Pickett

Increased protein stability as a mechanism that enhances Nrf2-mediated transcriptional activation of the antioxidant response element. Degradation of Nrf2 by the 26 S proteasome

J Biol Chem278453645412003

12446695

10.1074/jbc.M207293200

Itoh

Wakabayashi

Katoh

Ishii

O'Connor

Yamamoto

Keap1 regulates both cytoplasmic-nuclear shuttling and degradation of Nrf2 in response to electrophiles

Genes Cells83793912003

12653965

10.1046/j.1365-2443.2003.00640.x

Furukawa

Xiong

BTB protein Keap1 targets antioxidant transcription factor Nrf2 for ubiquitination by the Cullin 3-Roc1 ligase

Mol Cell Biol251621712005

15601839

10.1128/MCB.25.1.162-171.2005

Holmström

Baird

Zhang

Hargreaves

Chalasani

Land

Stanyer

Yamamoto

Dinkova-Kostova

Abramov

Nrf2 impacts cellular bioenergetics by controlling substrate availability for mitochondrial respiration

Biol Open27617702013

23951401

10.1242/bio.20134853

Pilecka

Sadowski

Kalaidzidis

Miaczynska

Recruitment of APPL1 to ubiquitin-rich aggresomes in response to proteasomal impairment

Exp Cell Res317109311072011

21320486

10.1016/j.yexcr.2011.02.002

Salemi

Almawi

Lefebvre

Schild-Poulter

Aggresome formation is regulated by RanBPM through an interaction with HDAC6

Biol Open34184302014

24795145

10.1242/bio.20147021

Dron

Dandoy-Dron

Farooq

Salamat MK

Laude

Proteasome inhibitors promote the sequestration of PrPSc into aggresomes within the cytosol of prion-infected CAD neuronal cells

J Gen Virol90205020602009

19339478

10.1099/vir.0.010082-0

Beaudoin

Goggin

Bissonnette

Grenier

Roucou

Aggresomes do not represent a general cellular response to protein misfolding in mammalian cells

BMC Cell Biol9592008

18937858

10.1186/1471-2121-9-59

Dantuma

Bott

The ubiquitin-proteasome system in neurodegenerative diseases: Precipitating factor, yet part of the solution

Front Mol Neurosci7702014

25132814

10.3389/fnmol.2014.00070

Cummings

Mancini

Antalffy

DeFranco

Orr

Zoghbi

Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1

Nat Genet191481541998

9620770

10.1038/502

Arrasate

Mitra

Schweitzer

Segal

Finkbeiner

Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death

Nature4318058102004

15483602

10.1038/nature02998

Cummings

Reinstein

Sun

Antalffy

Jiang

Ciechanover

Orr

Beaudet

Zoghbi

Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 mice

Neuron248798921999

10624951

10.1016/s0896-6273(00)81035-1

Gandhi

Antonelli

Afridi

Vatsia

Joshi

Romanov

Murray

Khan

Protein misfolding and aggregation in neurodegenerative diseases: A review of pathogeneses, novel detection strategies, and potential therapeutics

Rev Neurosci303393582019

30742586

10.1515/revneuro-2016-0035

Figure 1.

Inhibition of protein synthesis blocks proteasome inhibitor-induced aggresome formation. (A) Representative images and quantification of aggresomes in DMSO, MG132, MG132+ANI and MG132+ActD treated cells. 293 cells were treated with ANI (5 µg/ml), ActD (2 µg/ml) and/or MG132 (2 µM) for 12 h and stained with anti-UbK48 to visualize aggresomes (arrowheads); scale bar, 20 µm. (B) Representative images and quantification of aggresomes in cells treated with MG132 (2 µM) and/or ANI (5 µg/ml) for the indicated periods and aggresomes were stained with anti-UbK48 (arrowheads); scale bar, 20 µm. (C) Representative immunoblots and quantification of Nrf2 and p62 in cells treated by MG132 (2 µM) and/or ANI (5 µg/ml). (D) Representative images and quantification of Nrf2 in DMSO and MG132 treated cells. The 293 cells were treated with MG132 (2 µM) for 12 h and stained with anti-Nrf2 antibody to visualize the localization of endogenous Nrf2; DAPI was used to detect nuclei; scale bar, 20 µm. Data are presented as the mean ± SEM and were assessed using one-way ANOVA followed by Tukey's test. ^***P<0.001. Nrf2, nuclear factor erythroid 2-related factor 2; UbK48, ubiquitin Lys 48; ANI, anisomycin; ActD, actinomycin D.

Figure 2.

Loss of Nrf2 results in failure of proteasome inhibition-induced aggresome formation. (A) Representative images and quantification of aggresomes in nrf2^+/+ and nrf2^-/- cells after 14 h treatment with MG132 (2 µM). Anti-UbK48 was used to visualize aggresomes (arrowheads) and DAPI staining was used to detect nuclei; scale bar, 20 µm. (B) Representative images and quantification of nrf2^+/+ and nrf2^-/- cells stained with Annexin V (green) and PI (red) after 20 h treatment with DMSO or MG132 (2 µM). Live cells, Annexin V^-PI^-; early apoptotic cells, Annexin V⁺PI^-; necrotic cells, Annexin V^-PI⁺; late apoptotic cells, Annexin V⁺PI⁺; scale bar, 100 µm. Data are presented as the mean ± SEM representative of three independent experiments and were assessed using one-way ANOVA followed by Tukey's test. ^*P<0.05 and ^**P<0.01. Nrf2, nuclear factor erythroid 2-related factor 2; PI, propidium iodide; nrf2^-/-, Nrf2 knockout 293 cells; UbK48, ubiquitin Lys 48.

Figure 3.

Transcriptional upregulation of p62 during proteasome inhibition is dependent on Nrf2. (A) Representative images and quantification of p62 mRNA in nrf2^+/+ and nrf2^-/- cells treated with DMSO or MG132 for 12 h. (B) Representative immunoblots and quantification of p62 levels in nrf2^+/+ and nrf2^-/- cells treated with DMSO or MG132 (12 h). (C) Representative images and quantification of EGFP expression driven by the p62 promoter in nrf2^+/+ and nrf2^-/- cells treated with DMSO or MG132 (12 h). Data are presented as the mean ± SEM representative of three independent experiments and were assessed using one-way ANOVA followed by Tukey's test. ^*P<0.05 and ^***P<0.001. Nrf2, nuclear factor erythroid 2-related factor 2; nrf2^-/-, Nrf2 knockout 293 cells; EGFP, enhanced GFP.

Figure 4.

Expression of p62 rescues the defects of proteasomal stress response in Nrf2 knockout cells. (A) Representative images and quantification of aggresomes in nrf2^+/+, nrf2^-/-[Vector], nrf2^-/-[Flag-Nrf2] and nrf2^-/-[Flag-p62] cells after 14 h treatment with MG132 (2 µM). Anti-UbK48 was used to visualize ubiquitin-containing aggresomes (arrowheads), anti-Flag was used to visualize exogenous Nrf2 and p62, and DAPI was used to detect nuclei; scale bar, 20 µm. (B) Representative images and quantification of nrf2^+/+, nrf2^-/-[Vector], nrf2^-/-[Flag-Nrf2] and nrf2^-/-[Flag-p62] cells stained with Annexin V (green) and PI (red) after 20 h treatment with DMSO or MG132. Live cells, Annexin V^-PI^-; early apoptotic cells, Annexin V⁺PI^-; necrotic cells, Annexin V^-PI⁺; late apoptotic cells, Annexin V⁺PI⁺; scale bar, 100 µm. (C) Representative immunoblots and quantification of p62 and Nrf2 levels in nrf2^+/+, nrf2^-/-[Vector], nrf2^-/-[Flag-Nrf2] and nrf2^-/-[Flag-p62]. Data are presented as the mean ± SEM representative of three independent experiments and were assessed using one-way ANOVA followed by Tukey's test. ^*P<0.05, ^**P<0.01 and ^***P<0.001. Nrf2, nuclear factor erythroid 2-related factor 2; PI, propidium iodide; nrf2^-/-, Nrf2 knockout 293 cells; UbK48, ubiquitin Lys 48; [], transfection construct.

Figure 5.

MAPK/p38 inhibitor attenuates aggresome formation through Nrf2-mediated transcriptional activation. (A) Representative images and quantification of aggresomes in DMSO, MG132 or MG132+TAK715 treated cells (12 h). Anti-UbK48 was used to visualize aggresomes (arrowheads) and DAPI was used to detect nuclei; scale bar, 20 µm. (B) Representative immunoblots and quantification of Nrf2 and p62 in treated cells. Data are presented as the mean ± SEM representative of three independent experiments and were assessed using one-way ANOVA followed by Tukey's test. ^*P<0.05 and ^***P<0.001. Nrf2, nuclear factor erythroid 2-related factor 2; UbK48, ubiquitin Lys 48; p-, phosphorylated.

Figure 6.

Schematic model for the induction of aggresome formation by NRF2 during proteasome inhibition. Under physiological conditions, Nrf2 is degraded by the Ub proteasome system. In cells with reduced proteasome activity, Nrf2 is stabilized and accumulates in the nuclei. Through transcriptional activation of p62, Nrf2 promotes aggresomes formation. Through functioning as a sensor of cytosolic proteasome activity and an activator of aggresome formation, Nrf2 alleviates cell damages caused by proteasomal stress. Nrf2, nuclear factor erythroid 2-related factor 2; ARE, antioxidant response elements; Ub, ubiquitin.