Quercetin prevents necroptosis of oligodendrocytes by inhibiting macrophages/microglia polarization to M1 phenotype after spinal cord injury in rats
Oligodendrocytes (OLs) death after spinal cord injury (SCI) contributes to demyelination, even leading to a permanent neurological deficit. Besides apoptosis, our previous study demonstrated that OLs underwent receptor-interacting serine-threonine kinase 3(RIP3)/mixed lineage kinase domain-like protein (MLKL)-mediated necroptosis. Considering that necroptosis is always accompanied with pro-inflammatory response and quercetin has long been used as anti-inflammatory agent, in the present study we investigated whether quercetin could inhibit necroptosis of OLs and suppress the M1 macrophages/microglia-mediated immune response after SCI as well as the possible mechanism.
In this study, we applied quercetin, an important flavonoid component of various herbs, to treat rats with SCI and rats injected with saline were employed as the control group. Locomotor functional recovery was evaluated using Basso-Beattie-Bresnahan (BBB) scoring and rump-height Index (RHI) assay. In vivo, the necroptosis, apoptosis, and regeneration of OLs were detected by immunohistochemistry, 5′-bromo-2′-deoxyuridine (BrdU) incorporation. The loss of myelin and axons after SCI were evaluated by Luxol fast blue (LFB) staining, immunohistochemistry, and electron microscopic study. The polarization of macrophages/microglia after SCI and the underlying mechanisms were detected by quantitative reverse transcription-polymerase chain reaction (qRT-PCR) and immunohistochemistry. In vitro, the ATP and reactive oxygen species (ROS) level examination, propidium iodide (PI) labeling, and Western blotting were used to analyze the necroptosis of cultured OLs, while the signaling pathways-mediated polarization of cultured macrophages/microglia was detected by qRT-PCR and Western blotting.
We demonstrated that quercetin treatment improved functional recovery in rats after SCI. We then found that quercetin significantly reduced necroptosis of OLs after SCI without influencing apoptosis and regeneration of OLs. Meanwhile, myelin loss and axon loss were also significantly reduced in quercetin-treated rats, as compared to SCI + saline control. Further, we revealed that quercetin could suppress macrophages/microglia polarized to M1 phenotype through inhibition of STAT1 and NF-κB pathway in vivo and in vitro, which contributes to the decreased necroptosis of OLs.
Quercetin treatment alleviated necroptosis of OLs partially by inhibiting M1 macrophages/microglia polarization after SCI. Our findings suggest that necroptosis of OLs may be a potential therapeutic target for clinical SCI.
KeywordsSpinal cord injury Oligodendrocyte Necroptosis Macrophages/microglia Quercetin
Glial fibrillary acidic protein
Luxol fast blue
Mixed lineage kinase domain-like protein
Oligodendrocyte precursor cells
Quantitative reverse transcription polymerase chain reaction
Receptor-interacting serine-threonine kinase 3
Reactive oxygen species
Spinal cord injury
The secondary injury after spinal cord injury (SCI), more tightly related to severity of neurological deficit, includes cell death, demyelination, axonal degeneration, and inflammatory response [1, 2, 3]. Among these, oligodendrocytes (OLs) death after SCI contributes to demyelination of spared axons, even leading to a permanent neurological deficit .
Given that the survival of OLs is crucial for functional recovery after SCI, in the present study we focused on death and regeneration of OLs. Apoptosis of OLs occurs mainly in the first several hours after SCI, and the injury is accompanied by chronic inflammatory demyelination [5, 6, 7], indicating other types of cell death accounted for the delayed loss of OLs. It has been reported that necroptosis of OLs mediates axonal degeneration in ALS . Our previous study demonstrated that some OLs were receptor-interacting serine-threonine kinase 3(RIP3)/mixed lineage kinase domain-like protein (MLKL)-positive after SCI, indicating that necroptosis occurred in OLs . The chronic, detrimental, M1 macrophages/microglia-mediated inflammatory response contributed to necroptosis of astrocytes after SCI [10, 11]. Likewise, the dominance of M1 sub-population might play a role in necroptosis of OLs. Thus, there is an urgent need for new treatment strategies to prevent OLs death and to ameliorate the M1 macrophages/microglia-mediated immune response after SCI.
Quercetin, an important flavonoid component of various herbs, has long been used as antioxidant and anti-inflammatory agent in traditional Chinese medicine [12, 13, 14]. It was confirmed to have neuroprotective effects on SCI by reducing death of neurons, decreasing neural tissue damage, and inhibiting inflammatory responses [15, 16, 17, 18]. However, the effects of quercetin on survival of OLs and polarization of macrophages/microglia after SCI still remain unclear.
In this study, we investigated whether quercetin promoted OLs survival and suppressed the detrimental M1-type immune response after SCI, and explored the possible mechanism. We first showed that quercetin improved functional recovery after SCI. We then demonstrated that quercetin significantly reduced necroptosis of OLs after SCI without affecting apoptosis and regeneration of OLs. Meanwhile, quercetin significantly reduced myelin and axon loss after SCI. We further revealed that quercetin suppressed macrophages/microglia polarized to M1 phenotype through inhibition of STAT1 and NF-κB pathway, which contributes to the ameliorated necroptosis of OLs. Taken together, our study demonstrated that quercetin alleviated necroptosis of OLs in part by suppressing M1 macrophages/microglia polarization through inhibition of STAT1 and NF-κB pathway after SCI.
Male Sprague-Dawley rats (200–250 g) were purchased from the Laboratory Animal Center of Xi’an Jiaotong University. This study was carried out in accordance with the recommendations of ‘Animal Care and Use, Committee of Xi’an Jiaotong University.’ The protocol was approved by the ‘Committee of Xi’an Jiaotong University.’ A total of 120 rats were equally randomized into three groups: Sham group, SCI + saline group, and SCI + quercetin group. The sham group received only laminectomy, and the vehicle (1 ml sterile saline plus 1% DMSO) was administrated via intraperitoneal injection (i.p.) after SCI as SCI + saline group. According to the previous finding that functional recovery correlates treatment duration of quercetin after SCI , 7.5 mg/kg quercetin (Sigma-Aldrich, St. Louis, MO, USA) in 1 ml vehicle was administered i.p. twice daily for 10 days after SCI.
Animal model of spinal cord injury
Rats were anesthetized with 1% sodium pentobarbital (60 mg/kg), and bilateral laminectomy of vertebrae T8 was performed to expose the spinal cord. The spinal cord crush model was made by a mechanical device . Briefly, we used the forceps (53327T, 66 Vision-Tech Co., Ltd., China) mounted onto the device to clamp the cord, with the forceps tips of 0.5-mm width when fully closed, and the duration of the injury remained for 20 s. After crush, manual bladder expression was performed once a day, until reestablishment of micturition reflex. Depending on the following experiments, rats were sacrificed at 10 and 21 days post injury (dpi).
The Basso-Beattie-Bresnahan (BBB) scores were used to test rat open-field locomotion at 1 day before, and 1, 3, 7, 10, 14, and 21 days after spinal cord injury (SCI) following methodology of BBB . Functional scores ranges from 0 to 21 points in terms of the ankle, hip, knee, and trunk movement, as well as the coordination of each rat. The locomotion scores was observed and recorded by two independent observers blinded to the experiments.
Rump-height Index assay
The rats were video-recorded during walking through the left to right side on a runway bar (160 cm long, 10 cm wide, and 8 cm thick) at 1 day prior to and 1, 3, 7, 10, 14, and 21 days post-SCI. The rump-height Index (RHI) is defined as the height of the rump, normalized to the thickness of the beam measured along the same vertical line . To minimize the variations of pre-surgery RHI of each animal, the standardized RHI (dividing post-injury value by pre-injury value) was applied for comparisons.
Seven days after SCI or at the end of the 21-day observation period, rats were anesthetized and trans-cardially perfused with 200 ml of saline, followed by 400 ml of 4% PFA. Subsequently, 2-cm spinal cord segments encompassing the lesion site were obtained and cryoprotected in sucrose (30% in 0.1 M phosphate buffer, pH 7.4) until the blocks sank.
Both serial transverse sections (12-μm-thick) and serial sagittal sections (12-μm-thick) were cut on a cryostat and prepared for immunostaining.
After blocking in 0.01 M PBS containing 3% BSA and 0.3% Triton X-100 for 30 min, sections were incubated with primary antibodies in humidified boxes overnight at 4 °C. The primary antibodies used in the experiment included rabbit anti-RIP3 (1:500, ENZO, New York, NY, USA), rat anti-MLKL (1:200, Millipore, Billerica, MA, USA), rabbit anti-phosphorylated MLKL (pMLKL) (1:300, Abcam, Cambridge, Cambridgeshire, UK), mouse anti-CC1 (1:600, Milipore, Billerica, MA, USA), rabbit anti-iNOS (1:200, Abcam, Cambridge, Cambridgeshire, UK), goat anti-Arginase1(1:200, Santa Cruz Biotechnology, Dallas, Texas, USA), mouse anti-glial fibrillary acidic protein (GFAP,1:2000, Sigma-Aldrich, St. Louis, MO, USA), rabbit anti-MBP(1:200, Abcam, Cambridge, Cambridgeshire, UK), mouse anti-NF200 (1:200,Abcam, Cambridge, Cambridgeshire, UK), rabbit anti-Cleaved Caspase-3(1:200, Cell Signaling, Danvers, MA, USA), goat anti-Iba-1(1:200,Abcam, Cambridge, Cambridgeshire, UK), mouse anti-PDGFRα (1:200, Cell Signaling, Danvers, MA, USA), rat anti-BrdU (1:300,Abcam, Cambridge, Cambridgeshire, UK), and rabbit anti-Olig2 (1:200, Abcam, Cambridge, Cambridgeshire, UK). The sections were then incubated with the corresponding secondary antibodies conjugated with Alexa Fluor 594 (donkey anti-rabbit IgG or donkey anti-mouse IgG, 1:1000, Jackson ImmunoResearch, West Grove, PA, USA), Alexa Fluor 488 (donkey anti-rat IgG or donkey anti-mouse IgG, 1:1000, Jackson mmunoResearch, West Grove, PA, USA) in a dark environment for at RT 1 h. The sections were counterstained with Hoechst 33342 to identify all nuclei. Sections were examined and photographed under a confocal microscope (LSM 800, Zeiss, Oberkochen, Germany).
BrdU incorporation and detection
For detection of regeneration of OLs, BrdU (100 mg/kg, Sigma, St. Louis, MO, USA) injection was initiated at 24 h after injury, once a day for 9 days. Rats were sacrificed at 10 days after injury. HCl treatment (2 N HCl, 30 min at 37 °C) was performed for BrdU staining.
Luxol fast blue staining
For Luxol fast blue (LFB) staining, serial transverse cryosections (12 μm thickness) were stained as previously described. Briefly, slides were incubated in 0.1% LFB (Sigma, St. Louis, MO, USA) in acidified 95% ethanol overnight at 60 °C. The slides were then differentiated and counterstained with 0.05% lithium carbonate and cresyl violet solution. LFB-stained sections at 2000 μm rostral and caudal to the injury site, as well as at the lesion epicenter, were analyzed for myelin sparing. The spared myelin in white matter was quantified by Image pro-plus (Media Cybernetics, Silver Spring, USA).
Electron microscopic study
Rats were deeply anesthetized with 1% sodium pentobarbital intraperitoneally (60 mg/kg body weight) and perfused with 200 ml saline, followed by 500 ml 4% PFA containing 0.05% glutaraldehyde. Then the injured cord was removed and postfixed in the same fixative solution for 4 h at 4 °C. Serial coronal sections of 50 μm thickness were prepared with a vibratome (VT 1000S, Leica, Wetzlar, Hesse, Germany), then placed in 0.01 M PBS containing 25% sucrose and 10% glycerol for 2 h for cryoprotection. The sections were then immersed in 0.5% osmium tetroxide for 1 h, dehydrated with graded ethanol series, then in propylene oxide, and finally flat-embedded in Epon812 (SPI-CHEM). After trimming under a stereomicroscope, the sections were glued onto blank resin stubs. Serial ultrathin sections were cut with an ultramicrotome (Leica EM UC6, Leica, Wetzlar, Hesse, Germany) and mounted on mesh grids. They were then counterstained with uranyl acetate and lead citrate, observed, and photographed under an electron microscope (JEM-1230, JEOL Ltd., Akishima, Tokyo, Japan) equipped with CCD camera and its application software (832 SC1000, Gatan, Pleasanton, CA, USA).
Axonal diameter and G ratio determination
Axonal diameter was determined from counting of about 200 axons in white matter of the injured segments of three rats at 21 dpi using Image J software. G-ratio was determined as the ratio of inner axonal diameter to the total outer diameter of each axon fiber of about the same 200 axons of three rats at 21 dpi.
Primary microglial culture and polarization
Microglia were isolated from P2 Sprague-Dawley rat pups as described. Briefly, the spinal cord was dissected, mechanically dissociated, and then digested with 0.125% trypsin/0.02% EDTA. Cells were plated onto poly-d-lysine-coated culture flasks and cultured in DMEM (Gibco, Waltham, USA) containing 10% FCS at 37 °C with 5% CO2. The medium was exchanged every 3 days and at about 8th day when cells became confluent, the flasks were shaken with a shaker at 260 rpm for 0.5 h to obtain microglia. The quality of microglia was analyzed by immunostaining of Iba1 (> 90% Iba1+).
After about 7 days culture, microglial cells were treated with LPS (100 ng/ml, Sigma, Santa Clara, USA) and IFN-γ (20 ng/ml, Peprotech, Rocky Hill, USA) for M1 polarization, or quercetin plus LPS and IFN-γ, followed by medium replacement. Twenty-four hours later, the conditioned medium (M1 CM and Q-M1 CM) was obtained.
Primary oligodendrocytes culture
After microglia was harvested, with another overnight shaking at 280 rpm, cell suspension was harvested and seeded on tissue culture dishes (Corning, NY, USA) for 40 min. The dishes were then gently swirled every 6 min to remove contaminating astrocytes and microglia. The non-adherent cells were seeded onto poly-d-lysine-coated culture dishes in DMEM containing 10% FCS at density of 5 × 105 cells/cm2 for 3 h, and the medium was then changed by oligodendrocyte precursor cells (OPCs) proliferation medium (chemically defined medium with 10 ng/ml PDGF-AA and 10 ng/ml bFGF). Three days later, OPCs were isolated with DMEM/F12 containing 0.01% EDTA, 0.2 mg/ml DNase I, and 5 mg/ml insulin, and seeded in differentiation medium (chemically defined medium with 30 nM triiodothyronine and 5 mg/ml N-acetyl-l-cysteine). Mature oligodendrocytes (OLs) were obtained 5 days later. Chemically defined medium contains high glucose DMEM/F12 supplemented with 4 mM l-glutamine, 50 mg/ml transferrin, 1 mM sodium pyruvate, 5 mg/ml insulin, and 10 ng/ml d-biotin. The mature OLs were identified by MBP staining.
About 1.5 cm length of injured cord segments or primary cultured microglia were harvested and homogenized with ice-cold radio-immunoprecipitation assay (RIPA) lysis buffer. Proteins were separated in 10% SDS–PAGE gel, and transferred onto polyvinylidene difluoride (PVDF) membrane. The membranes were first blocked with 5% non-fat milk in TBST for 1 h at RT, and incubated with primary antibodies for RIP3 (1:800, ENZO, New York, NY, USA), MLKL (1:500, Millipore, Billerica, MA, USA), pMLKL (1:500, Abcam, Cambridge, Cambridgeshire, UK), iNOS(1:500, Abcam, Cambridge, Cambridgeshire, UK), p-STAT1 (1:1000, Cell Signaling, Danvers, MA, USA), nuclear factor-kappa B (NF-κB) (P65,1:1000, Cell Signaling, Danvers, MA, USA), phospho-NF-κB p65/p-P65 (1:1000, Cell Signaling, Danvers, MA, USA), or beta-actin (1:5000, Sigma, Santa Clara, USA) at 4 °C overnight. The membranes were then incubated with corresponding horseradish peroxidase-conjugated secondary antibodies (1:5000, Jackson ImmunoResearch, West Grove, PA, USA) at RT for 1 h. The immunoreactive bands were scanned with the Bio-Rad Image Lab system. The expression level was measured by ImageJ software (NIH, USA) corresponding to the band intensities.
Quantitative reverse transcription polymerase chain reaction
PCR primer sequences
Reverse primer (5′-3′)
Propidium iodide staining
After the cells were treated with M1 CM and Q-M1 CM, propidium iodide (PI) (5 μg/ml, Sigma, Santa Clara, USA) and Hoechst 33342 (3 μg/ml, Sigma, Santa Clara, USA) were added into the culture medium and incubated for 20 min at 37 °C. After washing with 0.01 M PBS three times, cells were fixed with 4% PFA for 10 min at RT. Cells were then imaged and counted under inverted fluorescence microscope (IX71, Olympus, Tokyo, Japan).
DCFH-DA probe (Sigma, St. Louis, MO, USA) was used to detect reactive oxygen species (ROS) levels. DCFH-DA (10 μM) was added to 96-well plates seeded with OLs incubated for 30 min at 37 °C. ROS levels were then examined by a multimode microplate reader (TECAN, Infinite M200, Mannedorf, Switzerland).
ATP levels were measured using the Cell Titer-Glo assay kit (Promega, Madison, USA). Equivalent Cell Titer-Glo Reagent was added into medium for 5 min to induce cell lysis, followed by incubating for 15 min to stabilize luminescent signal. Luminescence was detected by multimode microplate reader (TECAN, infinite M200, Mannedorf, Switzerland).
Quantification of cells
In our study, the method of profile counts followed by calibration with the empirical method was adopted for unbiased data [23, 24].The 12-μm thickness of the section ensures that the plane of central canal is cut through on every slide, making random selection of the slide possible. For cells quantification, all of the positive cells in the defined area in all sections of the randomly chosen slide were counted. Then calibration of the profile numbers was made by empirical method. Cell counting was performed by an observer who was blinded to the experiment design.
For quantitative analysis of density of MBP and NF200, serial transverse cryosections (12-μm thickness) were collected every millimeter section rostral and caudal 2000 μm to the lesion site. The longitudinal sections were also performed to confirm the density of MBP. The data were presented as a percentage relative to that in sham control (100%).
Quantification was performed by researchers who were blinded to the group allocation. No data were excluded from the analysis, except for five rats evaluated by BBB scores. In the present study, data are expressed as the mean ± standard error of the mean (SEM). Comparisons between two groups were evaluated by the Student’s t test . For multiple comparisons with the three or four groups, we performed one-way analysis of variance (ANOVA), followed by Tukey post-hoc tests, except for BBB scoring and RHI assay which were further analyzed by the Bonferroni post hoc test as recommended [26, 27]. Differences were considered statistically significant if *p < 0.05, **p < 0.01, or ***p < 0.001.
Quercetin improved functional recovery after SCI
Quercetin prevented necroptosis of OLs without affecting apoptosis and regeneration of OLs after SCI
Moreover, we showed that just a small proportion of OLs(about 2.3%) died through apoptosis in the first 5 days after SCI, and from 5 dpi to 10 dpi, more OLs were eliminated by necroptosis (about 13%) rather than apoptosis (about 3.1%) (Additional file 1: Figure S1a–c), indicating that necroptosis was the main way of OLs loss in our model of SCI. In addition, no significant effect of quercetin on apoptosis of OLs was found (Additional file 1: Figure S1d-e).
Quercetin reduced myelin and axonal loss after SCI
Quercetin influenced the macrophages/microglia M1-M2 polarization balance after SCI
The mechanism of effect of quercetin on M1 macrophages/microglia-induced necroptosis of OLs
Further, we explored the possible mechanism of the above effect by examining the STAT1 and NF-κB signaling pathway, which was reported to be involved in transcriptional regulation of M1polarization of macrophages/microglia. In vitro, the expression of iNOS, pSTAT1, NF-κB, and p-NF-κB was decreased by 56.94 ± 2.49%, 58.31 ± 5.86%, 56.6 ± 3.46%, and 53.33 ± 9.58% respectively when quercetin was added to M1 microglia (n = 3, **p < 0.01, *p < 0.05, Fig. 8c, d). In vivo, SCI dramatically induced the expression of iNOS, pSTAT1, NF-κB, and p-NF-κB, and quercetin treatment significantly reduced their expressions by 42.86 ± 4.01%, 51.28 ± 2.41%, 30.43 ± 3.46%, and 57.37 ± 6.16% respectively (n = 3, **p < 0.01, *p < 0.05, Fig. 8e, f).
In this study, we demonstrated that quercetin treatment improved functional recovery after SCI. Quercetin also attenuated RIP3/MLKL-mediated necroptosis of OLs after injury, while suppressed myelin and axon loss in the white matter after SCI. We then explored the reason and mechanism of increased number of rescued OLs after SCI, and we found that quercetin alleviated macrophages/microglia polarized to M1 phenotype, while promoted M2 polarization after SCI. The new balance of M1-M2 polarization of macrophages/microglia may form a permissive environment allowing for OL survival. Our in vitro study provided direct evidence that quercetin prevented necroptosis of OLs induced by M1 macrophages/microglia.
As numerous intact demyelinated axons are observed after SCI , there is an urgent need to rescue myelin sheath. It was reported that p75NTR-mediated apoptosis of OLs can be induced by proNGF produced in activated macrophages/microglia after SCI [40, 41]. However, this acute apoptosis of OLs could not explain the chronic, delayed demyelination after SCI , suggesting that other types of OLs death accounted for the delayed demyelination. In our previous studies, we demonstrated that necroptosis is a chronic process and necroptosis can occur in OLs after SCI [9, 10]; we thus focused on the effects of quercetin on necroptosis of OLs in the present study. We found that quercetin inhibited necroptosis of OLs and reduced myelin and axonal loss. Further, we examined that whether quercetin could improve OL preservation only or enhance both OL preservation and OL regeneration after SCI. In the previous study, quercetin has been found to promote proliferation and differentiation of OPCs after oxygen/glucose deprivation-induced injury in vitro , which is a direct effect of quercetin on OPCs. However, in this study, no significant difference of OL regeneration between control and quercetin-treated rats was found, and we speculated that the microenvironment is one of the possible reasons for the different results between in vitro and in vivo. Moreover, no significant effect of quercetin on apoptosis of OLs was observed. Thus, in the present study, we concluded that quercetin inhibited necroptosis of OLs without influencing regeneration and apoptosis of OLs.
Spinal cord injury can activate quiescent microglia polarized to M1/M2 phenotypes as well as the recruited macrophages. The distinct phenotype may exert their respective roles in pathological event of SCI. The inflammatory response in SCI is characterized by predominant and prolonged M1 macrophages/microglia polarization , which forms a detrimental environment for OL survival. Quercetin, a compound acting as anti-oxidative and anti-inflammatory, has been shown to have neuroprotective effects partially by inhibiting inflammatory response after SCI . In our study, we mainly focused on the effect of quercetin on polarization of macrophage/microglia and the data revealed that quercetin suppressed macrophages/microglia polarization to M1 phenotype, while promoted M2 polarization without affecting the total amount of macrophage/microglia.
After hemorrhagic brain injury, reduced M1polarization of microglia was reported by inhibiting TLR4 , and we speculated that the difference between our study and the previous research is that we combined LPS and IFNγ to treat cells. It is also known that activation of STAT1 and NF-κB signaling pathways can skew macrophages/microglia toward the M1 phenotype . In this study, we found that quercetin suppressed macrophages/microglia polarized to M1 phenotype through inhibition of STAT1 and NF-κB pathway, which was consistent with the previous results from BV2 cell lines . Nevertheless, the specific mechanism for inhibition of M1 polarization by quercetin requires further study.
Time window for administration of agents is pivotal to therapeutic effect . Although the previous study showed that neuroprotection can be found when quercetin was administered twice daily for a period of either 3 or 10 days , we selected the latter because the M1 macrophages/microglia-mediated inflammatory response is a chronic and long-lasting period . In addition, in our preliminary experiment, quercetin alone was administrated to normal rats without SCI, and no effect was found.
Since the functions of microglia and macrophages are similar but not exactly the same [48, 49], a major challenge after SCI is to distinguish microglia and recruited macrophages to determine their phenotype and function. In the present study, we investigated the effects of quercetin on polarization of microglia/macrophages, and one general limitation of our research is that these two distinct cells had not been distinguished. It was reported that application of genetic reporter mice and flow cytometry are the commonly used method to distinguish host microglia and recruited macrophages after injury [50, 51, 52]. In the present study, we applied Sprague-Dawley rats instead of genetic mice. Data of cytometry analysis from previous studies showed that CD11b+, CD45low, Ly6G−, and Ly6C− represent the vast majority (> 95%) of microglia after SCI [52, 53]. Therefore, we tried our best to differentiate the host microglia and recruited macrophages by flow cytometry, but we failed to get data due to our technical restrictions. However, this important issue is worthy to be studied in future.
This study demonstrated that quercetin treatment alleviated necroptosis of OLs at least in part by inhibiting M1 macrophages/microglia polarization after SCI. Its beneficial effects can be potentially useful as a therapeutic agent for clinical SCI.
We thank the support from Translational Medicine Center and Department of Spine Surgery, Hong Hui Hospital, Xi’an Jiaotong University. All experiments were conducted in compliance with the ARRIVE guidelines.
HF and HBT wrote the paper and performed the most of experiments. LQS, SCL, DGH, XC, ZC, MY, and XHY contributed morphological study and analyzed the data. HY and DJH designed the research and revised the manuscript. All authors read and approved the final manuscript.
This work was supported by grants from the National Natural Science Foundation of China (NSFC, Grant code: 81701204) and Project funded by China Postdoctoral Science Foundation (Grant code: 2018 M643703) to Hong Fan, NSFC (Grant code: 81830077, 81472098) to Ding-Jun Hao, NSFC (Grant code: 81571208) to Hao Yang, NSFC (Grant code: 81802690) to Shi-Chang Liu, and Research Project of Xi’an Health Commission (Grant code: J201902019) to Hai-Bin Tang.
Ethics approval and consent to participate
All protocols were approved by the Animal Care and Use Committee of Xi’an Jiaotong University, and conformed to the Guide for the Care and Use of Laboratory Animals by the National Institutes of Health.
Consent for publication
The authors declare that they have no competing interests.
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