Monosodium urate (MSU) crystals activate inflammatory pathways that overlap with interleukin-1β (IL-1β) signaling. However, the post-translational mechanisms involved and the role of signaling proteins in this activation are unknown. In the present study, we investigated the intracellular signaling mechanisms involved in MSU-induced activation of THP-1 macrophages and human nondiseased synovial fibroblasts (NLSFs) and the in vivo efficacy of an inhibitor of tumor growth factor-β (TGF-β)-activated kinase 1 (TAK1), 5Z-7-oxozeaenol, in MSU-induced paw inflammation in C57BL/6 mice. THP-1 macrophage activation with MSU crystals (25–200 µg/ml) resulted in the rapid and sustained phosphorylation of interleukin-1 receptor-activated kinase 1 (IRAK1 Thr209) and TAK1 (Thr184/187) and their association with the E3 ubiquitin ligase TRAF6. At the cellular level, MSU inhibited the deubiquitinases A20 and UCHL2 and increased 20s proteasomal activity, leading to a global decrease in K63-linked ubiquitination and increase in K48-linked ubiquitination in THP-1 macrophages. While MSU did not stimulate cytokine production in NLSFs, it significantly amplified IL-1β-induced IL-6, IL-8, and ENA-78/CXCL5 production. Docking studies and MD simulations followed by TAK1 in vitro kinase assays revealed that uric acid molecules are capable of arresting TAK1 in an active-state conformation, resulting in sustained TAK1 kinase activation. Importantly, MSU-induced proinflammatory cytokine production was completely inhibited by 5Z-7-oxozeaenol but not IRAK1/4 or TRAF6 inhibitors. Administration of 5Z-7-oxozeaenol (5 or 15 mg/kg; orally) significantly inhibited MSU-induced paw inflammation in C57BL/6 mice. Our study identifies a novel post-translational mechanism of TAK1 activation by MSU and suggests the therapeutic potential of TAK1 in regulating MSU-induced inflammation.
Gout is characterized by painful and progressive attacks of acute inflammation due to the deposition of monosodium urate (MSU) crystals in joints and periarticular tissues. Current therapies for the management of gout include uric acid-lowering therapies (ULTs), such as allopurinol or febuxostat, and colchicine, which inhibits inflammation.1 Although the prevalence of gout is increasing, the management strategies for gout remain suboptimal.2 This discrepancy is partly attributed to a limited understanding of the underlying mechanisms exploited by MSU crystals to induce gouty inflammation and tissue destruction. Studies suggest that MSU utilizes the Toll-like/interleukin-1β (IL-1β) receptor (TIR) signaling system, in which adaptor proteins such as Myd88 and IL-1R1 are essential to trigger an acute inflammatory response to IL-1β.3,4 Studies also suggest that MSU crystals activate the NALP3 inflammasome to expedite IL-1β processing.5
The centrality of IL-1β in mediating MSU-induced acute inflammation has triggered interest in the clinical testing of IL-1β inhibitors.6,7 While the short-term use of these IL-1 inhibitors seems promising, problems such as efficacy limited to a subset of the patient population, increased risk of infection with long-term use, and socioeconomic challenges associated with delivery not observed with conventional medications emphasize the need for novel therapeutic approaches.2 Moreover, the underlying mechanism through which MSU crystals activate resident cells in the joints such as synovial fibroblasts remains unclear.
Post-translational modifications (PTMs) play an essential role in relaying cellular signals initiated by TLRs, cytokines, or growth factors.8 One such PTM, ubiquitination, plays an important role in the TLR, IL-1β, and tumor necrosis factor-α (TNF-α) signaling pathways by either stabilizing signaling proteins via K63-linked ubiquitin chains or initiating proteasomal degradation by tagging proteins with K48-linked ubiquitin chains.9 The ubiquitination process is mediated by E3 ubiquitin ligases such as TNF receptor-associated factor (TRAF2 or TRAF6) that receive signals from adaptor proteins proximal to IL-1 or TNF receptors to activate the downstream nuclear factor-κB (NF-κB) and mitogen-activated protein kinase (MAPK) pathways.8,9 The central position of TGF-β-activated kinase 1 (TAK1) in the cytokine and TLR signaling pathways makes it an attractive therapeutic target.10,11,12 Whether MSU crystals, which are known to bind IL-1R1 and Myd88, utilize PTMs to activate IL-1β inflammatory signaling is not known.
Materials and methods
Antibodies and reagents
Please see detailed information in the Supplementary Materials and methods section.
Cell culture and stimulation
Human monocytic leukemia (THP-1) cells were maintained in RPMI-1640 culture medium with 10% fetal bovine serum and antibiotics. For the experiments, THP-1 cells were differentiated into macrophages with phorbol 12-myristate 13-acetate (250 ng/ml) for 3 h by a method described previously,13,14 followed by medium replacement with fresh Opti-MEM overnight. The next day, differentiated THP-1 cells (2 × 106) were stimulated with different concentrations (25–200 μg/ml) of endotoxin-free MSU crystals (Cat#: Tlrl-25; Invivogen) for different time periods. THP-1 macrophages (1 × 104 per well) were seeded in 96-well plates and stimulated with MSU (25–200 μg/ml) for 24 h to evaluate the effect of MSU on cell viability by a previously described method.15
For inhibitor experiments, THP-1 macrophages were pretreated with interleukin-1 receptor-activated kinase 1 (IRAK1) inhibitors [N-(2-morpholinylethyl)-2-(3-nitrobenzoylamido)-benzimidazole; 0.5–10 µM], TAK1 [5Z-7-oxozeaenol; 0.05–5 µM], TRAF6 inhibitor peptide [10–20 µM], or control peptide [10–20 µM] for 2 h in fresh Opti-MEM, followed by MSU (100 μg/ml) stimulation for either 30 min for Western blotting or 24 h to measure released cytokines.
Primary human synovial fibroblasts from nondiseased (NLSFs) donors and donors with rheumatoid arthritis (RASFs) were obtained from synovial tissues under an Institutional Review Board-approved protocol and cultured using a previously described method.16 Confluent cells (2 × 106 in 35 mm dishes) were serum-starved overnight and stimulated with different concentrations (25–100 μg/ml) of endotoxin-free MSU for 30 min to study the signaling mechanisms or 24 h to determine the effect of MSU on protein release. MSU (25–100 μg/ml) was also added to the cells in the presence of a low concentration of IL-1β (1 ng/ml) for 24 h to determine their combined effect on cytokine production.
Individual cytokine levels in the conditioned media were measured using DuoSet ELISA (enzyme-linked immunosorbent assay) kits for human IL-1β, TNF-α, IL-8, and monocyte chemoattractant protein-1 (MCP-1) (R&D Systems, MN).
THP-1 cells (1 × 107) in 100 mm dishes were starved overnight with Opti-MEM, pretreated with 5Z-7-oxozeaenol for 2 h, and finally stimulated with MSU (100 µg/ml) for 30 min. Immunoprecipitation using mouse monoclonal antibodies against FK2, TRAF6, and TAK1 at the specified dilutions was performed as previously described.12
In vitro TAK1 kinase assay
An in vitro TAK1 kinase assay was performed using a TAK1/TAB1 fusion protein. Specific details of TAK1/TAB1 fusion protein expression, purification, and utilization in the kinase assay are provided in the Supplementary Materials and methods section.
Small interfering RNA (siRNA) method
Predesigned small interfering RNA (siRNA) sequences for IRAK1 (SASI_Hs01_00017884 and SASI_Hs02_00307425), TRAF6 (SASI_Hs01_00116399 and SASI_Hs01_00116390), IL-1β (SASI_Hs01_00028205 and SASI_Hs01_00028206), and TAK1 (SASI_Hs01_00166582, SASI_Hs02_00365229, and SASI_Hs02_00365227) were purchased from Sigma MISSION. THP-1 macrophages were transfected with 120 pmol of scrambled (SIC001) or targeted siRNAs with Lipofectamine 2000 for 48 h using a recently described method.18 After 48 h of transfection, cells were serum-starved overnight prior to MSU simulation for 24 h.
Molecular modeling studies and ligand preparation
All computational studies were performed using different modules of Schrodinger suite 15.3 as described previously.12,19 A detailed procedure is provided in the Supplementary Materials and methods section.
Human peripheral blood mononuclear cell-derived macrophage culture
Human peripheral blood mononuclear cells (PBMCs) obtained from a commercial source (Zen-Bio, Inc., Research Triangle, NC, USA) were differentiated into macrophages by a method described earlier.20 Experimental details are provided in the Supplementary Material and Methods section.
All animal experiments were approved by the Washington State University IACUC committee (protocol approval number: 04775). We chose C57BL/6 male mice since they are susceptible to the development of paw inflammation when injected with a suspension of MSU crystals (0.5 mg, Invivogen) in 20 µl of endotoxin-free phosphate-buffered saline using 27-gauge syringes (Cat#: 705SN, Hamilton, NY) as described recently.21 A detailed procedure is provided in the Supplementary Materials and Methods section. Paw circumference was calculated using a previously described method.17
Histological analysis of ankles
Fresh-frozen sections (6 μm) of joints from experimental mice were stained with hematoxylin & eosin (H&E) and processed as previously described.17 For an objective evaluation of synovitis and inflammation, slides were analyzed by a pathologist for the following parameters: polymorphonuclear inflammation, immune cell infiltration (lymphocytes, plasma cells, and macrophages), neovascularization, and fibrosis (Supplementary Table 1), as described in our recent study.22
The Student’s t test was performed to calculate the statistical significance of differences between the means of different protein variables obtained from in vivo findings. P values <0.05 (two-tailed) indicated significance.
MSU crystals induce the autophosphorylation of IL-1β signaling proteins
THP-1 macrophages treated with MSU (25–200 µg/ml) for 30 min showed a gradual increase in the autophosphorylation of IRAK1 (Thr387) that peaked with an MSU concentration of ~100 μg/ml (Fig. 1a). In contrast to canonical IL-1β or TLR signaling, in which IRAK1 degrades, MSU induced the activation of p-IRAK1 (Thr387). To our surprise, we observed the increased phosphorylation of TAK1 at the Thr184/187 position, which is essential for its kinase activation.23 Furthermore, MSU induced a time-dependent increase in the phosphorylation of IRAK1 at Thr209/387 and TAK1 at Thr184/187 in THP-1 macrophages that peaked at ~60 min without affecting their viability (Fig. 1b; densitometric analysis in Supplementary Fig. S1A–C and viability data in Fig. S2A). To verify that this early effect is not governed by released IL-1β, we carried out different experimental approaches. First, we activated undifferentiated THP-1 monocytes with MSU for 30 min and observed by Western blot analysis that MSU can effectively induce the phosphorylation of IRAK1 (Thr387) and TAK1 (Thr184/187) (Fig. S2B) in monocytic cells that do not produce IL-1β (data not shown). Second, we evaluated the temporal production of IL-β and TNF-α in differentiated THP-1 macrophages treated with MSU (100 μg/ml). Our results rule out the role of IL-1β in TAK1 or IRAK1 activation since MSU induced significant and detectable levels of IL-1β or TNF-α as early as 6 h (Fig. S2C).
To further rule out any canonical IL-1β signaling by MSU, we determined the expression levels the IL-1R1, Pellino, NEMO, and IL-1Ra (an IL-1R antagonist) proteins in THP-1 macrophages and compared them to their expression levels in NLSFs and RASFs. Western blot analysis showed that THP-1 macrophages express no or negligible levels of IL-1R1 compared to those in NLSFs and RASFs; however, THP-1 macrophages expressed the Pellino and NEMO proteins at levels comparable to those observed in NLSFs and RASFs (Fig. 1c). To exclude the possible role of IL-1β in the MSU-induced activation of signaling kinases, we treated THP-1 macrophages with IL-1β or negative control (NC) siRNA prior to MSU (100 μg/ml) stimulation for 24 h. Western blotting showed that IL-1β knockdown had no effect on the ability of MSU to induce TAK1 activation (Fig. S3A). In addition, evaluation of the conditioned media from the same treated samples showed that IL-1β siRNA significantly inhibited IL-1β production, but had no effect on MSU-induced TNF-α production (Fig. S3B, C). Furthermore, THP-1 macrophages pretreated with exogenous IL-1Ra (500 ng/ml) showed no marked inhibition of MSU-induced IL-1β, MCP-1, and IL-8 production, but a modestly reduction in TNF-α production (Fig. 1d), suggesting that MSU-induced signaling activation is independent of IL-1R or synthesized IL-1β.
MSU activates primary human macrophages and synovial fibroblasts and facilitates cytokine production
To extend our observations of IL-1β signaling activation in THP-1 macrophages to primary human cells, we stimulated human PBMC-derived macrophages with MSU (50–200 μg/ml) for 30 min. Western blot analysis of lysates showed that MSU activated the phosphorylation of IRAK1 (Thr387) and TAK1 (Thr184/187) in a dose-dependent manner (Fig. 2a). To understand the detrimental effects of MSU crystals on resident nonhematopoietic cells, we treated primary human NLSFs with MSU (25–100 µg/ml) for 30 min and evaluated signaling pathways (Fig. 2). MSU induced the phosphorylation of IRAK1 (Thr209 and Thr387), and phosphorylated IRAK1 levels were comparable to those following activation by IL-1β (Fig. 2b; Fig. S4A). However, the MSU-induced activation of TRAF6, TAK1 (Thr184/187), TAK1 (Ser439), and TAB2 (Ser372) was strikingly different from the canonical activation mechanism driven by IL-1β in human SFs.12 To gain further insight into this difference, we treated NLSFs with a low dose of IL-1β (1 ng/ml) and/or MSU (25–100 µg/ml) for 24 h (Fig. 2c–f). Evaluation of released inflammatory proteins in the conditioned media showed that MSU alone had no effect on their induction (Fig. 2c); however, MSU further significantly enhanced the IL-1β-induced production of IL-6, IL-8, and ENA-78/CXCL5 (Fig. 2c–f; p < 0.05, p < 0.01).
MSU exploits the protein ubiquitin system to relay IL-1β-like signaling
THP-1 macrophages treated with different concentrations of MSU for 4 h showed a concentration-dependent increase in K48-linked ubiquitination and concomitant decrease in K63-linked ubiquitination, even at the lowest MSU concentration of 25 µg/ml (Fig. 3a). We extended our studies to primary human macrophages and observed that treated with MSU (25–200 μg/ml) for 24 h reduced K63-linked ubiquitination in these cells as well (Fig. S4B). To confirm the generality of this effect of MSU, we treated human NLSFs with varying concentrations of MSU and observed that MSU is indeed able to activate K48-linked ubiquitination in human NLSFs, with a modest concentration-dependent decrease in K63-linked ubiquitination (Fig. 3b). We evaluated the impact of MSU (25–100 µg/ml) on deubiquitinases in THP-1 macrophages and found that MSU inhibited the expression of the deubiquitinases A20 and UCHL2, but increased 26s proteasomal subunit PSMD13 expression in a dose-dependent manner (Fig. 3c; p < 0.05, densitometric analysis). These findings suggest that MSU can accelerate proteasome activity in THP-1 macrophages to induce inflammatory mediators. To confirm this finding, the results of an in vitro kinase assay showed that MSU at a concentration as low as 25 µg/ml significantly increased proteasome activity by more than 25% and that this effect plateaued at up to 100 µg/ml MSU (Fig. 3d).
TAK1 inhibition suppresses MSU-induced cytokine production
To understand the importance of IRAK1/4, TRAF6, and TAK1 in MSU-induced inflammation, we pretreated THP-1 macrophages with chemical inhibitors of IRAK1/4 or TAK1 and a peptide inhibitor of TRAF6, followed by MSU (100 µg/ml) stimulation for 24 h (Fig. 4). Our ELISA results showed that the IRAK1/4 inhibitor had no significant inhibitory effect on MSU-induced TNF-α, IL-1β, and IL-8 production, whereas 5Z-7-oxozeaenol completely inhibited the ability of MSU to induce expression of these cytokines and chemokines, suggesting the critical role of TAK1 in MSU-induced inflammation (Fig. 4a–d). We further confirmed these findings using siRNA targeting IRAK1, TRAF6, and TAK1. Our ELISA results showed that IRAK1, TRAF6, and TAK1 siRNA successfully inhibited MSU-induced IL-1β and TNF-α production in THP-1 macrophages, but had no effect on MCP-1 and IL-8 production (Fig. S5A, B; p < 0.05). While these results partly confirmed those of inhibitor experiments, they also suggested that the use of siRNA to study the role of kinases does not provide conclusive results.
5Z-7-oxozeanol modulates MSU-induced IL-1β expression and ubiquitination
To understand the impact of the TAK1 inhibitor 5Z-7-oxozeanol on IL-1β production, we stimulated THP-1 macrophages with MSU for 30 min with or without 5Z-7-oxozeaenol pretreatment. Western blot analysis showed that MSU induced both the proform and mature form of IL-1β (Fig. 4e). Interestingly, pretreatment with 5Z-7-oxozeaenol inhibited both constitutive and MSU-induced IL-1β expression. 5Z-7-oxozeaenol pretreatment also downregulated IL-1β maturation, as confirmed by reduced expression of a cleaved IL-1β (Asp116) fragment (Fig. 4e), which was almost completely inhibited by 4 h of MSU stimulation (Fig. 4f). To determine whether this effect is due to proteasomal degradation, we treated THP-1 macrophages with 5Z-7-oxozeaenol in the presence of the proteasome inhibitor MG132 (10 μM). MG132 pretreatment rescued 5Z-7-oxozeaenol-induced pro-IL-1β protein degradation (Fig. 4g). Furthermore, our results in primary human macrophages showed that pretreatment with 5Z-7-oxozeaenol had no inhibitory effect on the phosphorylation of IRAK1 (Thr387), but markedly suppressed pro-IL-1β expression (Fig. 4h). This novel finding suggests that TAK1 plays an important role in the stability of IL-1β and that TAK1 inhibitors limit the role of mature or released IL-1β by reducing pro-IL-1β expression.
MSU crystals activate TAK1 kinase activity
MSU crystals in solution exist as tautomeric urate forms,24 and these forms are equally capable of inducing IL-1β production.25 To determine whether soluble uric acid molecules can bind with TAK1 and induce its kinase activity, we simulated the placement of six molecules of uric acid in and around the active site of TAK1 in a TAK1-TAB1 fusion protein using Glide and submitted the final docked complex for molecular dynamics (MD) simulation. Up to four molecules of uric acid were found to occupy the active site of the TAK1-TAB1 protein without causing any significant changes in the secondary structure of the TAK1 protein (Fig. 5a, b; Fig. S6A–D). Furthermore, the phosphorylation loop of TAK1, which is far from the binding pocket, is stabilized by the binding of a uric acid molecule in the active site, thereby stabilizing the active conformation of TAK1 or delaying its dephosphorylation. A closer look at the interaction demonstrates the stable binding of one uric acid molecule in the binding pocket through the formation of H-bonds with V42, R44, E105, and the side chain of D175 (Fig. 5b), which is stabilized by hydrophobic interactions with the side chains of V50, M104, and L163 This site is proximal to the C174 site, which is occupied by 5Z-7-oxozeaenol through covalent bonds, causing the irreversible inhibition of TAK1 kinase activity.23 The stability of uric acid binding to the TAK1-TAB1 complex is further enhanced through the formation of cooperative π–π interactions and the assistance of water molecules that form a bridge between uric acid and protein residues in the binding site (Fig. 5b). Confirming the MD simulation findings, our in vitro kinase assay showed that TAK1 kinase activity is induced by MSU (1, 5, 10, and 50 µg per reaction) in a dose-dependent manner, and TAK1 kinase activity was increased by almost 10-fold by 10 μg MSU when compared to the control values (Fig. 5c; p < 0.05).
Furthermore, all ubiquitinated proteins were immunoprecipitated with anti-FK2 antibody and probed for K63-linked ubiquitination. 5Z-7-oxozeaenol treatment, alone or in combination with MSU, restored global K63-linked ubiquitination (Fig. 5d). However, immunoprecipitation of TAK1 and subsequent Western blot analysis showed that 5Z-7-oxozeaenol effectively inhibited the constitutive and MSU-induced K63-linked ubiquitination of TAK1 in THP-1 macrophages (Fig. 5e).
IRAK1, TRAF6, and TAK1 form an activation complex essential for activating the downstream MAPK and NF-κB pathways.8,10,26 In our studies, MSU markedly enhanced the association of IRAK1/TRAF6/TAK1 as an activation complex (Fig. 5f). Interestingly, 5Z-7-oxozeaenol significantly inhibited the ability of TRAF6 to associate with IRAK1 (Fig. 5f, g; p < 0.05). These findings provide evidence that 5Z-7-oxozeaenol also reduces the ability of TRAF6 to associate with IRAK1 and disrupts the formation of an activation complex, which is essential for TAK1 activation.12,27 These effects result in the marked inhibition in MAPK activation and NF-κBp65 and p-c-Jun nuclear translocation (Fig. S7A, B).
5Z-7-oxozeaenol suppresses MSU-induced paw inflammation
We evaluated the therapeutic potential of targeting TAK1 in a mouse model of MSU-induced inflammation.21 The injection of MSU (0.5 mg/20 µl) near the metatarsal joint resulted in paw swelling within 24 h, which resolved after ~96 h (Fig. S8). Based on these findings, mice injected with MSU served as the experimental control and were compared to groups of mice administered 5Z-7-oxozeaenol (5 or 15 mg/kg, per os (p.o.)) 2 h prior to MSU injection (Fig. 6a). Interestingly, 5Z-7-oxozeaenol at 5 and 15 mg/kg markedly inhibited MSU-induced paw inflammation. Histological analysis showed that MSU injection induced the massive infiltration of inflammatory cells, as indicated by a significant increase in the inflammation score, which was inhibited upon 5Z-7-oxozeaenol or febuxostat treatment (Fig. 6b; p < 0.01). Histopathological evaluation of joints and periarticular connective tissue using H&E staining showed extensive acute and chronic inflammation of the joints and periarticular connective tissue, with associated severe synovitis, erosion of articular cartilage, loss of subchondral bone, pannus formation, and fibrous ankylosis. In contrast, treatment with 5Z-7-oxozeaenol or febuxostat significantly abrogated all the features of acute and chronic inflammation induced by MSU (Fig. 6c; Supplementary Table 1). Western blot analysis of joint homogenates showed that MSU crystals can induce the phosphorylation of TAK1 (Thr184/187) in vivo, which was significantly inhibited by 5Z-7-oxozeaenol treatment (Fig. 6d). Furthermore, MSU crystals markedly induced global K48-linked polyubiquitination in vivo, which was markedly reduced by 5Z-7-oxozeaenol (Fig. 6e).
This study sheds light on the previously undescribed role of TAK1 and PTMs in mediating MSU-induced inflammation. In particular, we identified that MSU facilitates IRAK1/TAK1/TRAF6 complex formation by activating the K63-polyubiquitination of TAK1 and occupying its binding pocket to induce TAK1 kinase activity. The inhibition of MSU-induced cytokine/chemokine production by 5Z-7-oxozeaenol suggests that TAK1 can serve as a therapeutic target to suppress MSU-induced inflammatory conditions, such as gout.
Studies so far have focused on the downstream events triggered by MSU crystals, with special attention to IL-1β production and its therapeutic regulation.2,28 While some studies have pointed at the role of MyD88 and TLR2 in MSU-activated inflammation, we provide evidence that MSU can exploit the ubiquitin proteasome system to relay IL-1β-like inflammatory signals and intensify inflammation. In particular, the temporal activation of IRAK1 by MSU allows the relay of constant cellular signals, thereby permitting association with the E3 ligase TRAF6 and the prolonged activation of downstream TAK1, which controls the MAPK and NF-κB pathways in macrophages and synovial fibroblasts. In addition, the finding that only 5Z-7-oxozeaenol among the signaling inhibitors tested can shut down MSU-induced IL-1β, TNF-α, IL-8, and MCP-1 production suggest TAK1 as a target for gout. While the observed differences in cytokine/chemokine inhibition by small-molecule inhibitors vs. siRNA are open to interpretation, this divergence may be attributed to protein–protein interactions.29 Proteins treated with a small-molecule inhibitor may still act as scaffolds for protein–protein interactions, whereas the treatment of siRNAs with a small-molecule inhibitor can disrupt their biological function and activity. Therefore, the ability of small molecules to target kinase activity without affecting stoichiometry make them a powerful tool for regulating the pathological role of kinases in inflammatory conditions. However, further rigorous experiments related to the dose efficacy and target specificity of TAK1 inhibitors are essential to validate the pharmacological effects identified in this study.
The ubiquitin protein system is responsible for a well-described PTM in cytokine and TLR signaling molecules; however, the means by which MSU crystals exploit this mechanism remain unknown. K48-linked proteins are primed for 26s proteasomal degradation, while K63-linked proteins are rescued from 26s proteasome degradation, facilitating stable signal transduction and cellular trafficking.9 Studies also suggest that some deubiquitination enzymes (DUBs) play an important role in removing K48-linked polyubiquitin chains from proteins “primed” for degradation, thereby reducing or retarding downstream signaling networks.30 Among these DUBs, A20 and CYLD are important in IL-1β and TNF-α signaling and inflammatory regulation,31,32,33,34,35 but the role of UCHL2 in cytokine signaling has not yet been studied. Our finding that MSU significantly inhibits A20 and UCHL2 expression in conjunction with increased K48-linked ubiquitination suggests that MSU directly upregulates the ubiquitin proteasome system to trigger multicytokine-driven signaling events and inflammasome activity in macrophages. Furthermore, this notion is supported by increased 20s proteasome activity and 26s proteasome subunit PSMD13 expression in MSU-stimulated samples. Importantly, the inhibition of TAK1, which is an important signaling mediator activated by MSU, resulted in the marked inhibition of the release of cytokines and chemokines essential for inflammation.
MSU crystal-induced pathological events have been primarily studied in human monocytes or THP-1-activated macrophages. While some studies have shown the role of MSU in inducing chemokine, nitric oxide and matrix metalloproteinase (MMP) production in synovial fibroblasts or chondrocytes,36,37,38 this is the first study that provides evidence of the role of TAK1 and exploitation of ubiquitination by MSU crystals to cause inflammation. Our findings also provide evidence that MSU can activate TAK1 in human synovial fibroblasts and coordinate with IL-1β at a low concentration to synergistically induce inflammation. Since synovial fibroblasts are a major source of chemokines and MMPs and our recent findings provide evidence of TAK1 as a critical kinase in the IL-1β signaling pathway,12 these findings suggest that the inhibition of TAK1 significantly impedes the overlapping MSU-IL-1β signaling networks to downregulate chronic inflammation and tissue destruction.
While several clinical trials have shown the therapeutic efficacy of IL-1 inhibitors such as anakinra and, more recently, rilonacept,39,40,41 others have acknowledged their limitations in the treatment of gout.2,7,41 These challenges provide an opportunity to design novel targeted therapeutic approaches to address these limitations and provide ease of delivery as well. While the findings of this study are open to interpretation, we believe that TAK1 inhibitors provide a platform for target validation and drug discovery for the treatment of gout. This belief is further supported by our MD simulation studies, which illustrated the direct interaction of uric acid molecules with the TAK1-TAB1 fusion protein and their ability to stabilize the phosphorylation state of TAK1. This interaction potentially results in sustained downstream signaling that may be the underlying cause of the increased frequency of gouty attacks and accelerated joint destruction.
TAK1 has mostly been ignored due to the fact that TAK1-null mice die at an early embryonic developmental stage.42 However, recent studies suggest TAK1 as a therapeutic target in autoimmune diseases governed by IL-1β, such as rheumatoid arthritis, type I diabetes, and multiple sclerosis.10,11,43,44 Interestingly, Brown et al.45 recently suggested that, unlike other serine threonine kinases, TAK1 possesses a glycine-rich loop positioned opposite the adenosine-binding region of the ATP-binding pocket that exhibits high stoichiometric flexibility (up to 9 Å or 6.6 Å).45 This spatial independence allows urate molecules to bind to the TAK1-TAB1 fusion protein and potentially activate TAK1 kinase for a prolonged period, as evidenced by the increased activity of TAK1 in our kinase assay. In addition, the marked inhibition of the MSU-induced synthesis of IL-1β precursor and its maturation by 5Z-7-oxozeaenol suggests that TAK1 inhibition also transcriptionally suppresses IL-1β synthesis, thereby limiting its role in inflammation.
Research on targeting IL-1 signaling proteins for therapeutic purposes in inflammatory diseases has gained significant attention, and the targeting of IRAKs has shown some promise.46 However, a recent study using IRAK1 knock-in mice showed no effect on the secretion of inflammatory mediators (IL-6, TNF-α, or IL-10), suggesting that IRAK1 catalytic activity is not a rate-limiting step.47 Furthermore, the observation that IRAK1-deficient human fibroblasts demonstrate efficient IL-1R-mediated responses48 suggests that IRAK1 is not a therapeutic target for crystallopathies. While IRAK1/4 are centrally involved in IL-1β signaling, other proinflammatory cytokines (TNF-α, RANKL) or TLRs may not rely on IRAKs for effective signal transduction. In contrast, TAK1 plays a crucial role in signaling induced by most of these proinflammatory factors.10 The results of these studies, taken together with our findings, suggest that TAK1 inhibition has a consistent regulatory impact on MSU-induced inflammation and potentially gout.
Overall, we provide novel insights into the pathogenic effects of MSU crystals on the ubiquitin proteasome system to generate inflammatory responses while highlighting the therapeutic potential of targeting TAK1 to suppress MSU-induced inflammatory events that cannot be regulated by IL-1 inhibitors alone.
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We thank the National Disease Research Interchange, Philadelphia, PA and the Cooperative Human Tissue Network (CHTN), Columbus, OH for providing synovial tissues. We would also like to thank Sadiq Umar and Bhanupriya Madarampalli for providing technical support in animal experiments. We also thank Ruby Siegel for critical reading of the manuscript. This study was supported by start-up funds from Washington State University.
The authors declare no competing interests.
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Singh, A.K., Haque, M., O’Sullivan, K. et al. Suppression of monosodium urate crystal-induced inflammation by inhibiting TGF-β-activated kinase 1-dependent signaling: role of the ubiquitin proteasome system. Cell Mol Immunol 18, 162–170 (2021). https://doi.org/10.1038/s41423-019-0284-3
- Monosodium urate crystals
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