Transcriptional factor Nrf2 is essential for aggresome formation during proteasome inhibition.

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. Copyright: © Qin et al.

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

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

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.

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.

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).

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.

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).

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.

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.

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.

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.

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.

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).

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.

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.