Reduction of Silent Information Regulator 1 Activates Interleukin-33/ST2 Signaling and Contributes to Neuropathic Pain Induced by Spared Nerve Injury in Rats
Yanyan Zeng1† 
Yu Shi1† 
Hongrui Zhan1,2 
Wei Liu1 
Guiyuan Cai1 Haili Zhong1 Yaping Wang1 Shangjie Chen3* Shimin Huang1 
Wen Wu1*- 1Department of Rehabilitation, Zhujiang Hospital, Southern Medical University, Guangzhou, China
- 2Department of Rehabilitation, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, China
- 3Department of Rehabilitation, Baoan Hospital, Southern Medical University, Shenzhen, China
Emerging studies have demonstrated that interleukin (IL)-33 and its receptor ST2 act as key factors in inflammatory diseases. Moreover, accumulating evidence has suggested that cytokines, including tumor necrosis factor (TNF)-α and IL-1β, trigger an inflammatory cascade. SIRT1 has been shown to suppress the expression of inflammatory cytokines. However, the effects of SIRT1 on IL-33/ST2 signaling and initiation of the inflammatory cascade via modulation of TNF-α and IL-1β by IL-33 remain unclear. In the present study, we found that the dorsal root ganglion (DRG) IL-33 and ST2 were upregulated in a rat model of spared nerve injury (SNI) and intrathecal injection of either IL-33 or ST2 antibodies alleviated mechanical allodynia and downregulated TNF-α and IL-1β induced by SNI. In addition, activation of SIRT1 decreased enhanced DRG IL-33/ST2 signaling in SNI rats. Artificial inactivation of SIRT1 via intrathecal injection of an SIRT1 antagonist could induce mechanical allodynia and upregulate IL-33 and ST2. These results demonstrated that reduction in SIRT1 could induce upregulation of DRG IL-33 and ST2 and contribute to mechanical allodynia induced by SNI in rats.
Introduction
Chronic pain, often characterized by allodynia, hyperalgesia, and spontaneous pain affects approximately one-third of the world’s population (Alford et al., 2008). In the United States, direct and indirect costs of chronic pain have been estimated to be approximately $100 billion annually, which is more than the combined costs of cancer, heart disease, and diabetes (Pizzo and Clark, 2012). It is well established that peripheral and central sensitizations are the basic mechanisms of chronic pain (Meacham et al., 2017). Inflammation has been extensively reported to be associated with peripheral and central sensitization (Ji et al., 2018). However, the type of inflammatory cytokine that triggers the inflammation cascade remains controversial.
Interleukin (IL)-33 belongs to a member of the IL-1 family and exerts its effects via binding to its receptor ST2 (Xu et al., 2019). It has been demonstrated that IL-33 plays a vital role in many inflammatory conditions, including septic shock (Ding et al., 2019), atherosclerosis (Buckley et al., 2019) and rheumatoid arthritis (Pinto et al., 2019). Furthermore, other studies have suggested that IL-33 modulates cutaneous hyper-nociception in inflammatory pain in mice (Verri et al., 2008) and has been implicated in activating astrocytes in the spinal cord in mouse models of bone pain (Zhao et al., 2013). However, the role of IL-33 in the dorsal root ganglion (DRG) in neuropathic pain remains unclear.
The silent information regulator 1 (SIRT1) is an NAD+-dependent deacetylase belonging to the SIRT family (Hattori and Ihara, 2016). Among SIRT family, SIRT1 has been validated to be most related in this family and function as deacetylating and regulating histones (Ling et al., 2018) as well as a wide range of non-histone substrates, such as NF-κB (Kauppinen et al., 2013), p53 (Nakamura et al., 2017), FOXO (Brunet et al., 2004), ERK (Han et al., 2017), peroxisome proliferator-activated receptor γ (PPARγ) and others (Kauppinen et al., 2013). With regulating this protein, SIRT1 plays a central role in regulating cellular processes, including apoptosis (Ling et al., 2017), cellular proliferation (Jablonska et al., 2016), and inflammation (Zhang et al., 2017). In the nervous system, SIRT1 suppress the neurodegenerative diseases such as Alzheimer’s disease and Parkinson’s disease via anti-apoptosis, anti-inflammation (Singh et al., 2017; Gomes et al., 2018). Recently, several studies have reported that the activation of SIRT1 in the spinal cord alleviates neuropathic pain induced by chronic constriction injury (CCI) surgery in rats and mice via inhibition of the inflammatory cascade (Shao et al., 2014; Lv et al., 2015). In addition, SIRT1 in the spinal cord epigenetically upregulates inflammasome NALP1 expression and contributes to the chronic pain induced by the chemotherapeutic drug bortezomib (Chen et al., 2018). However, whether SIRT1 modulates the inflammatory cytokine IL-33 remains unclear.
In the present study, we performed spared nerve injury (SNI) surgery in rats to establish a neuropathic pain model and hypothesized that downregulation of SIRT1 in the DRG induced by SNI enhances IL-33/ST2 signaling and triggers a downstream inflammatory cascade leading to mechanical allodynia.
Materials and Methods
Animals
Male Sprague-Dawley rats, weighing 200–250 g, were obtained from the Institute of Experimental Animals of Southern Medical University (Guangzhou, China; Approval number: SCXK 2016-0041). The animals were housed in standard cages in a temperature-controlled (24 ± 1°C) colony room under a 12 h light/dark cycle regimen, with ad libitum access to food and water. The experimental protocols were approved by the Southern Medical University Animal Care and Use Committee and were performed in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals.
Surgery and Drug Administration
SNI model rats were developed in accordance with previously described procedures (Decosterd and Woolf, 2000). Briefly, after making an incision on the skin at the lateral surface of the thigh, a section was made directly through the biceps femoris muscle to expose the sciatic nerve and its three terminal branches, the sural, common peroneal, and tibial nerves. The SNI procedure involves axotomy and ligation of the tibial and common peroneal nerves but leaves the sural nerve intact. The common peroneal and tibial nerves were tightly ligated using 5.0 silk and transected distal to the ligation, removing approximately 4 mm of the distal nerve stump. Care was taken to avoid any damage to the nearby sural nerve. After surgery, all wounds were irrigated with sterile saline and closed in layers. In the sham group, an identical procedure was performed to expose the sciatic nerve and its three terminal branches, but without any nerve injury. For intrathecal delivery of the SIRT1 agonist SRT1720, the animals were implanted with catheters during the same surgery, as previously reported (Hirai et al., 2014). Briefly, a sterile catheter filled with saline was inserted through the lumbar (L) 5/6 intervertebral space, and the tip of the tube was positioned at the lumbosacral spinal level. Animals that exhibited hind limb paralysis or paresis after surgery were excluded. For animals without movement disorders, lidocaine (2%) was administered through the catheter to verify the intraspinal location. An immediate bilateral hind limb paralysis (within 15 s) lasting 20–30 min confirmed the correct catheterization. Animals without the aforementioned features were not used in the experiments that followed. The SIRT1 agonist SRT1720 and antagonist EX-527 were dissolved in DMSO and intrathecal administration at concentration of 15 mg/kg and 10 mg/kg respectively. IL-33 (rIL-33; 3626-ML) and ST2- neutralizing antibody (AF1004) were purchased from R&D Systems (Minneapolis, MN, USA). The rIL-33 and ST2 antibodies were diluted in sterile phosphate buffer solution (PBS).
Behavioral Test
Mechanical sensitivity was assessed using von Frey hairs and the up-down method, as previously described (Chaplan et al., 1994). Briefly, after acclimatization to the testing environment for 2 h per day on three consecutive days, the rats were placed in separate transparent testing chambers positioned on a wire mesh floor. After a 10-min adaptation period, each stimulus consisted of a 2–3 s application of von Frey hairs to the middle of the plantar surface of the hind paws and the lateral surface of ipsilateral hind paws for SNI rats, with a 5-min interval between consecutive tests. Quick withdrawal or licking of the paw in response to the stimulus was considered a positive response. The operator performing the behavioral tests was blinded to the study design.
Immunohistochemistry
The animals were deeply anesthetized using 50 mg/kg sodium pentobarbital (intraperitoneal) and perfused through the ascending aorta with saline, followed by 4% paraformaldehyde in 0.1 M phosphate buffer (4°C, pH 7.4), as previously described. After perfusion, the L4, L5, and L6 DRGs were removed and post-fixed in the same fixative for 3 h, which was subsequently replaced with 30% sucrose (in 0.1 M PBS) overnight. Frozen tissues were sectioned in the longitudinal plane with a thickness of 16 mm using a microtome and processed for immunofluorescence staining. All sections were blocked with 3% donkey serum in 0.3% Triton X-100 for 1 h at room temperature and incubated over two nights at 4°C with primary antibodies. After incubation with primary antibodies, the tissue sections were washed three times in 0.01 M PBS and then incubated in Cy3-conjugated donkey anti-rabbit IgG (diluted 1:300; Jackson ImmunoResearch, West Grove, PA, USA) for 1 h at room temperature. For double immunofluorescence staining, tissue sections were incubated with a mixture of anti-SIRT1 [1:200, Cell Signaling Technologies (CST), Danvers, MA, USA] antibody with neurofilament-200 [NF-200 (a marker for myelinated A-fibers), 1:200; Chemicon/Thermo-Fisher Scientific, Waltham, MA, USA], IB4 [FITC-conjugated (a marker for nonpeptidergic C-type neurons), 20 mg/ml (Sigma)], anti-calcitonin gene-related peptide [CGRP (a marker of peptidergic C-type neurons), 1:500, Abcam, Cambridge, MA, USA], IL-33 (1:300, Abcam, Cambridge, MA, USA), ST2 (1:400, Abcam, Cambridge, MA, USA) over two nights at 4°C. Except for isolectin-B4 (IB4)-treated tissue sections, all of the aforementioned sections were treated with a mixture of FITC and Cy3-conjugated secondary antibodies for 1 h at room temperature. The sections were rinsed with 0.01 M PBS three times and mounted on gelatin-coated slides and air-dried. The stained sections were examined using a fluorescence microscope (Leica, Wetzlar, Germany) and images were captured using a charge-coupled device spot camera.
Western Blotting
Western blotting was performed according to the method described in a previous study (Hnasko and Hnasko, 2015). Briefly, L4–L6 DRG tissues of animals were removed and homogenized in 15 mmol/L Tris containing a cocktail of proteinase inhibitors after the animals were anesthetized with 50 mg/kg sodium pentobarbital (intraperitoneal). Next, the L4–L6 DRG lysates were prepared and separated using sodium dodecyl polyacrylamide gel electrophoresis and transferred to a polyvinylidene fluoride membrane. The membranes were then pre-incubated with blocking buffer for 1 h at room temperature. After incubating with diluted primary antibodies against SIRT1 (1:1,000, CST), IL-33 (1:1,000, Abcam), ST2 (1:1,000, Abcam), tumor necrosis factor (TNF)-α (1:1,000, Abcam), and/or β-actin (1:2,000, Abcam) overnight at 4°C, the membranes were incubated in horseradish peroxidase-conjugated secondary antibody for 1 h at room temperature. Finally, protein bands on the membranes were visualized using a commercially available enhanced chemiluminescence assay (Pierce, USA) according to the manufacturer’s instructions. The bands were subsequently quantified using a computer-assisted imaging analysis system.
Statistical Analysis
All data are expressed as mean ± standard error of the mean (SEM). Statistical analysis was performed using SPSS version 20.0 (IBM Corporation, Armonk, NY, USA). For the behavior test, one- or two-way analysis of variance (ANOVA) with repeated measures, followed by a Tukey post hoc test, was performed. Western blot was analyzed using one-way ANOVA followed by the Turkey post hoc test. Differences with p 0.05 were considered statistically significant.
Results
IL-33 and Its Receptor ST2 in DRG Were Induced and Upregulated by SNI in Rats
Consistent with the results of a previous study (Boccella et al., 2018), the mechanical withdrawal threshold was significantly reduced in SNI rats (Figure 1A). To further study the role of IL-33/ST2 signaling in neuropathic pain induced by SNI, western blot assay was performed to analyze protein expression of IL-33 and ST2. As shown in Figures 1B,C, IL-33, and ST2 in DRG (L4-L6) was markedly increased on day 1 following SNI surgery and lasted at least until day 14.
Figure 1. Spared nerve injury (SNI) induced mechanical allodynia and enhanced expression of interleukin (IL)-33 and ST2 in dorsal root ganglion (DRG) of rats. (A) SNI induced mechanical allodynia in the ipsilateral but not contralateral hind paw (n = 6), but the sham operation did not induce changes in bilateral hind paw(n = 6). (B,C) Compared with the sham rats, expression of IL-33 and its receptor ST2 increased in L4-L6 DRG since day 1 and persisted till day 14 after SNI (n = 4). *p < 0.05, ***p < 0.001 compared with the sham group.
Enhanced IL-33 and ST2 Expression Contributed to Mechanical Allodynia Induced by SNI
We determined whether the increased expression of IL-33 and ST2 was involved in the development of mechanical allodynia in SNI rats. We investigated the behavior response after intrathecally injecting IL-33 and ST2 neutralizing antibodies. The results revealed that both IL-33 and ST2 neutralizing antibodies alleviated mechanical allodynia induced by SNI surgery for seven consecutive days (Figures 2A,B). Studies have reported that TNF-α and IL-1β activate the inflammatory cascade (Cavaillon et al., 2003; Iwawaki, 2017) and that IL-33 may also play an important role in it. To determine the role of IL-33 in the inflammation, we used the western blot assay to quantify the expression of TNF-α and IL-1β after intrathecal administration of IL-33 antibodies. The results revealed that both TNF-α and IL-1β levels were significantly decreased in the DRG (Figure 2).
Figure 2. Intrathecal injection both IL-33 and its receptor ST2 neutralization antibody ameliorated mechanical allodynia and reversed the increased expression of tumor necrosis factor (TNF)-α and IL-1β. (A,B) Intrathecal application of IL-33 or ST2 neutralization antibody alleviated SNI-induced mechanical allodynia but IgG treatment did not show effects on mechanical allodynia induced by SNI. The dose of IL-33 or ST2 neutralization antibody was 100 ng for consecutive 10 days and 250 ng for consecutive 10 days, respectively. The time point for intrathecal injection was 15 min before SNI surgery, n = 6/group. (C,D) Upregulation of TNF-α and IL-1β was blocked after intrathecal injection of IL-33 neutralization antibody on day 7 (n = 4/group). ***p < 0.001 compared with sham group, #p < 0.05, ##p < 0.01, ###p < 0.001 compared with SNI+IgG group.
Reduction of SIRT1 Is Involved in the Mechanical Allodynia Induced by SNI
SIRT1 plays an important role in synaptic plasticity and chronic pain. The levels of SIRT1 protein in the DRG started to decrease on day 1 following SNI surgery, which lasted until at least day 14 (Figure 3B). Meanwhile, behavior testing demonstrated that intrathecal administration of the SIRT1 agonist SRT1720 remarkably decreased the paw withdraw thresholds induced by SNI in rats (Figure 3A).
Figure 3. SNI reduced expression of DRG SIRT1 and intrathecal administration of SIRT1 agonist alleviated SNI-induced mechanical allodynia. (A) Intrathecal injection of SIRT1 agonist (15 mg/kg) 15 min before SNI surgery for consecutive 10 days alleviated the mechanical allodynia. (B) The time courses of the changes in the expression of SIRT1 after SNI surgery. *p < 0.05, ***p < 0.001 compared with sham group, $p < 0.05, $$p < 0.01 compared with SNI+DMSO group.
SIRT1 Is Expressed in DRG Neurons
It has been reported that SIRT1 is only expressed in neurons in the spinal cord; however, the distribution of SIRT1 in DRG remains unclear. To further verify the distribution of SIRT1 in the DRG of rats, double immunofluorescent staining was performed. As shown in Figure 4, SIRT1 was primarily expressed in NF200-positive cells (large-diameter neurons), IB4-positive cells, and CGRP-positive cells (small- and medium-diameter neurons).
Figure 4. SIRT1 in DRG mainly expressed in neurons of rats. Double immunofluorescence staining showed that SIRT1 expressed in peptidergic neurons (CGRP marked) and non-peptidergic (IB-4 and NF-200 marked) neurons in DRG. Scale bar 200 μm.
Activation of SIRT1 Downregulated IL-33/ ST2, TNF-α, and IL-1β
Several recent studies have presented evidence that SIRT1 mediates chronic pain through modulation of inflammation in the spinal cord. Thus, we determined whether SIRT1 regulated the DRG IL-33/ST2 signaling in rats with SNI-induced neuropathic pain. The double immunofluorescence staining showed that SIRT1 colocalized with IL-33 and ST2 (Supplementary Figure S1). As shown in Figures 5A,B, DRG IL-33 and its receptor ST2 were remarkably downregulated on day 7 following intrathecal injection of the SIRT1 agonist SRT1720. Similarly, the expression of the inflammatory cytokines TNF-α and IL-1β was reduced on day 7 after the injection of SRT1720 (Figures 5C,D). Furthermore, the enhanced acetylation of NF-κB was significantly alleviated by SRT1720 but have no effects on p-ERK (Supplementary Figure S2).
Figure 5. The increased expression of IL-33, ST2, TNF-α, and IL-1β were retarded by intrathecal injection of SIRT1 agonist SRT1720. (A,B) Application of SRT1720(i.t.) reduced the expression of IL-33 and its receptor ST2 after SNI surgery on day 7. (C,D) Inflammatory cytokines TNF-α and IL-1β were significantly downregulated by delivery of SRT1720(i.t.) on day 7, n = 4/group, ***p < 0.001 compared with the sham group, ###p < 0.001 compared with SNI+DMSO group.
SIRT1 Antagonist EX527 Induced Mechanical Allodynia in Naïve Rats
To further define the effects of SIRT1 in DRG on pain behavior, the rats were intrathecally administered the SIRT1 antagonist EX-527 at a dose of 10 mg/kg for five consecutive days. A mechanical allodynia behavior test using von Frey filaments demonstrated that the paw withdrawal threshold was decreased in naïve rats from day 2 and lasted until day 8 after EX-527 treatment. However, the naïve rats that were administered saline exhibited no significant mechanical allodynia compared with naïve rats. Therefore, the EX-527 treatment in naïve rats induced mechanical allodynia (Figure 6).
Figure 6. Continuous intrathecal injection of SIRT1 agonist EX527 at a dose of 10 mg/kg for successive 5 days induced mechanical allodynia in naïve rats. n = 6/group, *p < 0.05, **p < 0.01,***p < 0.001 compared with sham group.
Inactivation of SIRT1 Can Enhance the Expression of IL-33 and ST2 in Naïve Rats
Having observed that the SIRT1 antagonist contributed to mechanical allodynia in naïve rats, we tested whether the inactivation of SIRT1 modulated the expression of IL-33 and ST2. The results of the western blot analysis demonstrated that both IL-33 and ST2 proteins were upregulated on day 5 after intrathecal administration of EX-527 compared with saline treatment in naïve rats (Figures 7A,B).
Figure 7. Continuous intrathecal injection of SIRT1 antagonist EX-527 upregulated DRG IL-33 and ST2. (A,B) The expression of IL-33 and ST2 significantly upregulated on day 5 after continuous delivery EX-527 in naïve rats. n = 4/group, ***p < 0.001 compared with the sham group.
Discussion
In the present study, we found that the expression of IL-33 and its receptor ST2 in DRG increased after SNI surgery. Intrathecal administration of both IL-33 and ST2 antibodies alleviated mechanical allodynia induced by SNI. Intrathecal injection of IL-33 antibody and rat recombinant IL-33 decreased the enhanced expression of TNF-α and IL-β in SNI rats and induced the expression of TNF-α and IL-β in naïve rats, respectively. In addition, SNI surgery reduced the expression of SIRT1 in DRG neurons, and intrathecal injection of the SIRT1 agonist SRT1720 ameliorated mechanical allodynia and reversed the upregulation of IL-33 induced by SNI. Collectively, our results revealed a new mechanism in which reduction of SIRT1 activates IL-33/ST2 signaling and subsequently triggers the TNF-α and IL-1β inflammatory cascade, thus contributing to the mechanical allodynia induced by SNI.
The Role of IL-33 in Triggering Inflammatory Cascade in Neuropathic Pain Following SNI
IL-33 is a cytokine in human endothelial cells that was discovered in 2003 (Baekkevold et al., 2003), it exerts its biological effects through the ST2/IL-1RAcP (IL-1 receptor accessory protein) receptor complex. Recent evidence has shown that IL-33 deficiency results in reduced innate papain-induced lung inflammation (Oboki et al., 2010). More recent studies have suggested that IL-33/ST2 contributes to the development of pain. For example, the expression of spinal IL-33 and ST2 was enhanced in mice with formalin-induced inflammatory pain (Zarpelon et al., 2013). Furthermore, activation of spinal IL-33 and ST2 has been reported to contribute to bone cancer pain (Zhao et al., 2013). In this study, we first found that the expression of DRG IL-33 and ST2 increased in a rat model of neuropathic pain induced by SNI. Intrathecal administration of IL-33 and ST2 antibodies alleviated mechanical allodynia. It has been firmly established that inflammatory cytokines are involved in the development and maintenance of neuropathic pain (Old et al., 2015; Ronchetti et al., 2017). Both TNF-α and IL-β have been reported to be cytokines that trigger the inflammatory cascade (Rider et al., 2011; Zelová and Hošek, 2013). In our study, we found that intrathecal administration of IL-33 and ST2 antibodies in SNI-treated rats could reduce the enhanced expression of TNF-α and IL-β. These results demonstrated that SNI could activate the IL-33/ST2 signaling pathway in DRG, subsequently trigger the inflammatory cascade, and contribute to the mechanism of allodynia.
SIRT1 in DRG Contributes to the Activation of IL-33/ST2 Signaling Following SNI
Accumulating evidence has demonstrated that SIRT1 modulates the expression of inflammatory cytokines via targeting nuclear factor (NF)-κB (Yeung et al., 2004; Kauppinen et al., 2013). A recent study revealed that SRT1720 ameliorated chronic pain induced by chronic CCI through the regulation of spinal cord inflammation (Lv et al., 2015). Similarly, we found that intrathecal injection of the SIRT1 agonist SRT1720 suppressed the upregulation of TNF-α and IL-1β in the DRG and alleviated mechanical allodynia in SNI-treated rats. We also observed that the reduction of SIRT1 in DRG neurons contributed to the activation of the IL-33/ST2 signaling pathway. SIRT1 is an important deacetylase that directly deacetylates NF-κB (Deng et al., 2017). In addition, IL-33 can activate NF-κB through binding to ST2 (Numata et al., 2016). In our study, we observed that SRT1720 dramatically reduced the acetylation of NF-κB p65 induced by SNI. It is possible that the reduction of SIRT1 in the DRG increased acetylated NF-κB, upregulated IL-33, and triggered the inflammatory cascade, which may have played a vital role in the development of mechanical allodynia induced by SNI surgery.
Collectively, our results demonstrate that IL-33 in DRG and its receptor ST2 upregulated and modulated the expression of TNF-α and IL-1β in neuropathic pain induced by SNI. In addition, we observed that the reduction of DRG SIRT1 activated IL-33/ST2 signaling and contributed to mechanical allodynia in SNI rats. These results may suggest a new potential therapeutic target for neuropathic pain.
Data Availability Statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation, to any qualified researcher.
Ethics Statement
The animal study was reviewed and approved by Southern medical university animal protection and use committee.
Author Contributions
YZ conceived and designed the experiments. YZ, YS, HZha, WL, GC, HZho, YW, and SH performed the experiments. YZ and YS collected and analyzed the data and wrote the article. HZha and WL contributed the reagents, materials and analysis tools. WW and SC provided the financial support. The first communication author in this article is WW, and the second communication author is SC.
Funding
This work was supported by: (1) National Natural Science Foundation of China (NNSFC), China; Contract grant number: 81772430; (2) Clinical Research Foundation of Southern Medical University, China; Contract grant number: LC2016PY037; (3) Guangzhou Science and Technology Project, China; Contract grant number: 201607010288; and (4) Science and Technology Planning Project of Guangdong Province, China; Contract grant number: 2015A030401070; (5) China Postdoctoral Science Foundation, China; Contract grant number: 2019M662995.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We would like to thank Hui Deng for excellent technical support of intrathecal injection, Huifang Shi for guiding animal injection, Wenchao Liu for the guidance of modeling and the extraction of nerve tissue, Luying Lai for guiding basic experiment related skills, Cuicui Liu for guiding the animal behavior test, Zhengnan Zhou and Xiaolan Wang for their suggestions on the experimental scheme, and Mengyu Yao for critical comments on a previous version of the manuscript.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnmol.2020.00017/full#supplementary-material.
FIGURE S1 | The colocalization of SIRT1/IL-33 and SIRT1/ST2. Double immunofluorescence staining showed that SIRT1 colocalized with IL-33 (A–C) and ST2 in DRG (D–F). Scale bar 100 μm.
FIGURE S2 | SIRT1 agonist reduced the acetylation of NF-κB p65 but had no effects on p-ERK. (A) The enhanced acetylation of NF-κB p65 in DRG was significantly alleviated in SNI rats by intrathecal administration SIRT1 agonist SRT1720 (n = 4/group). (B) SIRT1 agonist SRT1720 showed no effects on the increased p-ERK in DRG of SNI rats (n = 4/group). ***p < 0.001 compared with the sham group, ##p < 0.01 compared with the SNI+DMSO group.
References
Alford, D. P., Liebschutz, J., Chen, I. A., Nicolaidis, C., Panda, M., Berg, K. M., et al. (2008). Update in pain medicine. J. Gen. Intern. Med. 23, 841–845. doi: 10.1007/s11606-008-0570-8
Baekkevold, E. S., Roussigne, M., Yamanaka, T., Johansen, F. E., Jahnsen, F. L., Amalric, F., et al. (2003). Molecular characterization of NF-HEV, a nuclear factor preferentially expressed in human high endothelial venules. Am. J. Pathol. 163, 69–79. doi: 10.1016/s0002-9440(10)63631-0
Boccella, S., Guida, F., Palazzo, E., Marabese, I., Novellis de, V., Maione, S., et al. (2018). Spared nerve injury as a long-lasting model of neuropathic pain. Methods Mol. Biol. 1727, 373–378. doi: 10.1007/978-1-4939-7571-6_28
Brunet, A., Sweeney, L. B., Sturgill, J. F., Chua, K. F., Greer, P. L., Lin, Y., et al. (2004). Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase. Science 303, 2011–2015. doi: 10.1126/science.1094637
Buckley, M. L., Williams, J. O., Chan, Y. H., Laubertova, L., Gallagher, H., Moss, J. W. E., et al. (2019). The interleukin-33-mediated inhibition of expression of two key genes implicated in atherosclerosis in human macrophages requires MAP kinase, phosphoinositide 3-kinase and nuclear factor-κB signaling pathways. Sci. Rep. 9:11317. doi: 10.1038/s41598-019-47620-8
Cavaillon, J. M., Adib-Conquy, M., Fitting, C., Adrie, C., and Payen, D. (2003). Cytokine cascade in sepsis. Scand. J. Infect. Dis. 35, 535–544. doi: 10.1080/00365540310015935
Chaplan, S. R., Bach, F. W., Pogrel, J. W., Chung, J. M., and Yaksh, T. L. (1994). Quantitative assessment of tactile allodynia in the rat paw. J. Neurosci. Methods 53, 55–63. doi: 10.1016/0165-0270(94)90144-9
Chen, K., Fan, J., Luo, Z. F., Yang, Y., Xin, W. J., and Liu, C. C. (2018). Reduction of SIRT1 epigenetically upregulates NALP1 expression and contributes to neuropathic pain induced by chemotherapeutic drug bortezomib. J. Neuroinflammation 15:292. doi: 10.1186/s12974-018-1327-x
Decosterd, I., and Woolf, C. J. (2000). Spared nerve injury: an animal model of persistent peripheral neuropathic pain. Pain 87, 149–158. doi: 10.1016/s0304-3959(00)00276-1
Deng, Z., Jin, J., Wang, Z., Wang, Y., Gao, Q., and Zhao, J. (2017). The metal nanoparticle-induced inflammatory response is regulated by SIRT1 through NF-κB deacetylation in aseptic loosening. Int. J. Nanomedicine 12, 3617–3636. doi: 10.2147/ijn.s124661
Ding, X., Jin, S., Shao, Z., Xu, L., Yu, Z., Tong, Y., et al. (2019). The IL-33-ST2 pathway contributes to ventilator-induced lung injury in septic mice in a tidal volume-dependent manner. Shock 52, e1–e11. doi: 10.1097/shk.0000000000001260
Gomes, B. A. Q., Silva, J. P. B., Romeiro, C. F. R., Dos Santos, S. M., Rodrigues, C. A., Goncalves, P. R., et al. (2018). Neuroprotective mechanisms of resveratrol in Alzheimer’s disease: role of SIRT1. Oxid. Med. Cell. Longev. 2018:8152373. doi: 10.1155/2018/8152373
Han, Y., Luo, H., Wang, H., Cai, J., and Zhang, Y. (2017). SIRT1 induces resistance to apoptosis in human granulosa cells by activating the ERK pathway and inhibiting NF-κB signaling with anti-inflammatory functions. Apoptosis 22, 1260–1272. doi: 10.1007/s10495-017-1386-y
Hnasko, T. S., and Hnasko, R. M. (2015). The Western Blot. Methods Mol. Biol. 1318, 87–96. doi: 10.1007/978-1-4939-2742-5_9
Hirai, T., Enomoto, M., Kaburagi, H., Sotome, S., Yoshida-Tanaka, K., Ukegawa, M., et al. (2014). Intrathecal AAV serotype 9-mediated delivery of shRNA against TRPV1 attenuates thermal hyperalgesia in a mouse model of peripheral nerve injury. Mol. Ther. 22, 409–419. doi: 10.1038/mt.2013.247
Iwawaki, T. (2017). [From property of IL-1β to imaging of inflammation]. Nihon Rinsho Meneki Gakkai Kaishi 40, 329–336. doi: 10.2177/jsci.40.329
Jablonska, B., Gierdalski, M., Chew, L. J., Hawley, T., Catron, M., Lichauco, A., et al. (2016). Sirt1 regulates glial progenitor proliferation and regeneration in white matter after neonatal brain injury. Nat. Commun. 7:13866. doi: 10.1038/ncomms13866
Ji, R. R., Nackley, A., Huh, Y., Terrando, N., and Maixner, W. (2018). Neuroinflammation and central sensitization in chronic and widespread pain. Anesthesiology 129, 343–366. doi: 10.1097/ALN.0000000000002130
Kauppinen, A., Suuronen, T., Ojala, J., Kaarniranta, K., and Salminen, A. (2013). Antagonistic crosstalk between NF-κB and SIRT1 in the regulation of inflammation and metabolic disorders. Cell. Signal. 25, 1939–1948. doi: 10.1016/j.cellsig.2013.06.007
Ling, L., Gu, S., and Cheng, Y. (2017). Resveratrol inhibits adventitial fibroblast proliferation and induces cell apoptosis through the SIRT1 pathway. Mol. Med. Rep. 15, 567–572. doi: 10.3892/mmr.2016.6098
Ling, H., Peng, L., Wang, J., Rahhal, R., and Seto, E. (2018). Histone deacetylase SIRT1 targets Plk2 to regulate centriole duplication. Cell Rep. 25, 2851.e3–2865.e3. doi: 10.1016/j.celrep.2018.11.025
Lv, C., Hu, H. Y., Zhao, L., Zheng, H., Luo, X. Z., and Zhang, J. (2015). Intrathecal SRT1720, a SIRT1 agonist, exerts anti-hyperalgesic and anti-inflammatory effects on chronic constriction injury-induced neuropathic pain in rats. Int. J. Clin. Exp. Med. 8, 7152–7159.
Meacham, K., Shepherd, A., Mohapatra, D. P., and Haroutounian, S. (2017). Neuropathic pain: central vs. peripheral mechanisms. Curr. Pain Headache Rep. 21:28. doi: 10.1007/s11916-017-0629-5
Nakamura, K., Zhang, M., Kageyama, S., Ke, B., Fujii, T., Sosa, R. A., et al. (2017). Macrophage heme oxygenase-1-SIRT1–p53 axis regulates sterile inflammation in liver ischemia-reperfusion injury. J. Hepatol. 67, 1232–1242. doi: 10.1016/j.jhep.2017.08.010
Numata, T., Ito, T., Maeda, T., Egusa, C., and Tsuboi, R. (2016). IL-33 promotes ICAM-1 expression via NF-κB in murine mast cells. Allergol. Int. 65, 158–165. doi: 10.1016/j.alit.2015.10.004
Oboki, K., Ohno, T., Kajiwara, N., Arae, K., Morita, H., Ishii, A., et al. (2010). IL-33 is a crucial amplifier of innate rather than acquired immunity. Proc. Natl. Acad. Sci. U S A 107, 18581–18586. doi: 10.1073/pnas.1003059107
Old, E. A., Clark, A. K., and Malcangio, M. (2015). The role of glia in the spinal cord in neuropathic and inflammatory pain. Handb. Exp. Pharmacol. 227, 145–170. doi: 10.1007/978-3-662-46450-2_8
Pinto, M. R. C., Kakehasi, A. M., Souza, A. J., Tavares, W. C. Jr., Rocha, M. A., Trant, C., et al. (2019). Methotrexate use, not interleukin 33, is associated with lower carotid intima-media thickness in patients with rheumatoid arthritis. Adv. Rheumatol. 59:15. doi: 10.1186/s42358-019-0060-1
Pizzo, P. A., and Clark, N. M. (2012). Alleviating suffering 101—pain relief in the United States. N. Engl. J. Med. 366, 197–199. doi: 10.1056/nejmp1109084
Rider, P., Carmi, Y., Guttman, O., Braiman, A., Cohen, I., Voronov, E., et al. (2011). IL-1α and IL-1β recruit different myeloid cells and promote different stages of sterile inflammation. J. Immunol. 187, 4835–4843. doi: 10.4049/jimmunol.1102048
Ronchetti, S., Migliorati, G., and Delfino, D. V. (2017). Association of inflammatory mediators with pain perception. Biomed. Pharmacother. 96, 1445–1452. doi: 10.1016/j.biopha.2017.12.001
Shao, H., Xue, Q., Zhang, F., Luo, Y., Zhu, H., Zhang, X., et al. (2014). Spinal SIRT1 activation attenuates neuropathic pain in mice. PLoS One 9:e100938. doi: 10.1371/journal.pone.0100938
Singh, P., Hanson, P. S., and Morris, C. M. (2017). SIRT1 ameliorates oxidative stress induced neural cell death and is down-regulated in Parkinson’s disease. BMC Neurosci. 18:46. doi: 10.1186/s12868-017-0364-1
Verri, W. A. Jr., Guerrero, A. T., Fukada, S. Y., Valerio, D. A., Cunha, T. M., Xu, D., et al. (2008). IL-33 mediates antigen-induced cutaneous and articular hypernociception in mice. Proc. Natl. Acad. Sci. U S A 105, 2723–2728. doi: 10.1073/pnas.0712116105
Xu, D., Barbour, M., Jiang, H. R., and Mu, R. (2019). Role of IL-33/ST2 signaling pathway in systemic sclerosis and other fibrotic diseases. Clin. Exp. Rheumatol. 119, 141–146.
Yeung, F., Hoberg, J. E., Ramsey, C. S., Keller, M. D., Jones, D. R., Frye, R. A., et al. (2004). Modulation of NF-κB-dependent transcription and cell survival by the SIRT1 deacetylase. EMBO J. 23, 2369–2380. doi: 10.1038/sj.emboj.7600244
Zarpelon, A. C., Cunha, T. M., Alves-Filho, J. C., Pinto, L. G., Ferreira, S. H., McInnes, I. B., et al. (2013). IL-33/ST2 signalling contributes to carrageenin-induced innate inflammation and inflammatory pain: role of cytokines, endothelin-1 and prostaglandin E2. Br. J. Pharmacol. 169, 90–101. doi: 10.1111/bph.12110
Zelová, H., and Hošek, J. (2013). TNF-α signalling and inflammation: interactions between old acquaintances. Inflamm. Res. 62, 641–651. doi: 10.1007/s00011-013-0633-0
Zhang, H., Shan, Y., Wu, Y., Xu, C., Yu, X., Zhao, J., et al. (2017). Berberine suppresses LPS-induced inflammation through modulating Sirt1/NF-κB signaling pathway in RAW264.7 cells. Int. Immunopharmacol. 52, 93–100. doi: 10.1016/j.intimp.2017.08.032
Keywords: neuropathic pain, IL-33, ST2, SIRT1, inflammation
Citation: Zeng Y, Shi Y, Zhan H, Liu W, Cai G, Zhong H, Wang Y, Chen S, Huang S and Wu W (2020) Reduction of Silent Information Regulator 1 Activates Interleukin-33/ST2 Signaling and Contributes to Neuropathic Pain Induced by Spared Nerve Injury in Rats. Front. Mol. Neurosci. 13:17. doi: 10.3389/fnmol.2020.00017
Received: 24 September 2019; Accepted: 20 January 2020;
Published: 12 February 2020.
Edited by:
John Martin, City College of New York (CUNY), United StatesReviewed by:
Vicente Barrios, Niño Jesús University Children’s Hospital, SpainSun Kwang Kim, Kyung Hee University, South Korea
Copyright © 2020 Zeng, Shi, Zhan, Liu, Cai, Zhong, Wang, Chen, Huang and Wu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Wen Wu, wuwen66@163.com; Shangjie Chen, csjme@163.com
† These authors have contributed equally to this work and share first authorship