DOI: https://doi.org/10.21203/rs.3.rs-222911/v1
Objective: Lung ischemia reperfusion injury (LIRI) is the major cause of primary lung dysfunction after lung transplantation. Lipoxin A4 inhibits the oxidative stress and inflammation. This study aimed to evaluate the potential protective effect of lipoxin A4 on LIRI in rats.
Methods: SD rats were randomized into the sham, LIRI and LA4 groups. Rats in the sham group received anesthesia, thoracotomy and intravenous injection of saline, while those in the LIRI or LA4 group received left lung transplantation and intravenous injection of saline or lipoxin A4, respectively. After 24 hours of reperfusion, the PaO2/FiO2, wet/dry weight ratios and protein levels in lungs were measured to assess the alveolar capillary permeability. The oxidative stress response and inflammation were examined. The histological and apoptosis analyses of lung tissues were performed via HE staining and TUNEL assay, respectively. The effects of lipoxin A4 on the endothelial viability and tube formation of hypoxemia and reoxygenation-challenged rat pulmonary microvascular endothelium cells were determined.
Results: Lipoxin A4 significantly ameliorated the alveolar capillary permeability, reduced the oxidative stress and inflammation in transplanted lungs. The histological injury and apoptosis of lung tissues were also alleviated by lipoxin A4. In vitro lipoxin A4 treatment promoted the endothelial tube formation and improved the endothelial viability .
Conclusion: Lipoxin A4 protects LIRI after lung transplantation in rats, and its therapeutic effect is associated with the properties of anti-inflammation, anti-oxidation, and endothelium protection.
Lung transplantation is a major treatment approach for the patients with end-stage lung disease including cancer and pulmonary fibrosis. However, the lung ischemia reperfusion injury (LIRI), which is characterized by alveolar damage, lung edema and hypoxemia, is the major cause of postoperative primary lung dysfunction1, 2. In addition, LIRI is also the major risk factor for postoperative complications, such as acute graft rejection and obliterative bronchiolitis3. During the lung transplantation, the oxidative stress response, local inflammation, impairment of alveolar capillary permeability and cell apoptosis induced by LIRI significantly deteriorate the function and survival of transplanted lungs4. Although the significant advancement in clinical operation, graft preservation technologies, and pharmacological treatment, LIRI still occurs in about 20-35% patients 5, and had been identified to be the primary cause for the mortality of 14-18% patients in postoperative 90 days6.
Lipoxins A4 is a product of arachidonic acid metabolism that exhibits strong anti-inflammatory properties7. It is characterized by inhibiting the neutrophil migration and accumulation8, reducing the activities of p389, PINK1 signaling10 and inhibiting NF-κB signaling 11 in multiple different models of organ injury. In addition, accumulating studies have demonstrated that lipoxin A4 can ameliorate various acute lung injury by balancing the inflammation and oxidative stress responses 10, 12, 13. Lipoxin A4 has also been suggested to be able to mitigate the renal reperfusion injury14. However, the effect of lipoxin A4 on LIRI after lung transplantation has not been intensively studied so far.
According to the pathology of LIRI and the bioactive effect of lipoxin A4, we postulated that lipoxin A4 can ameliorate the LIRI in vivo and in vitro. In this study, using a lung transplantation model in rats, we investigated the impacts of lipoxin A4 administration on the alveolar capillary permeability, the histological injury, oxidative stress response, and apoptosis status in the grafted lung tissues. In addition, whether lipoxin A4 can affect the in vitro endothelial viability and tube formation of rat pulmonary microvascular endothelium cells was also investigated.
Animals
Male Sprague Dawley rat (6 weeks old, total n=34) were purchased from Charles River Laboratories (Beijing, China), and housed at the specific pathogen-free (SPF) facility at the Animal Center of Harbin Medical University (Harbin, China) at room temperature (22 ± 1 ˚C) with a 12/12 hours light/dark cycle and access to food and water ad libitum. Rats were randomly assigned into the sham group, LIRI group and lipoxin A4 (LA4) group. Rats in the sham group only received the anesthesia and thoracotomy, while rats in the LIRI and LA4 groups received the orthotopic rat left lung transplantation and injection of saline and lipoxin A4, respectively, as our previous studies15, 16. This study was approved by the Secondary Affiliated Hospital of Harbin Medical University. All treatments were carried out in accordance with the Institutional Animal Care and Use Committee of Second Affiliated Hospital of Harbin Medical University and followed national guidelines for the treatment of animals.
Donor graft preparation
A total of 18 donor rats were anesthetized with intraperitoneal injection of 3% pentobarbital sodium (30 mg/kg body weight). After the disappearance of clip tail reflection, the rats were intubated and ventilated with the following parameters: tidal volume 10 ml/kg and 50 breaths per minute (50% O2 +50% N2) with 2 cm H2O positive end-expiratory pressure and inspiratory expiratory ratio of 1:1. Under analgesia with 1% lidocaine, rats were subjected to the thoracotomy. After heparization with 300U/kg heparin via femoral vein, the heart-lungs was collected, and followed by the flushing with 4°C cold saline at 20 cm H2O pressure. Under the microscopy view, the left pulmonary artery, vein, and left bronchus were clipped on the CUFF tube (24 G central vein catheter). The graft was preserved at 4 °C for 60 min with end tidal volume.
Lung transplantation to recipients and intervention
A total of 16 recipient rats (8 rats in the LIRI group and 8 rats in the LA4 group) were anesthetized as the donors and intubated with 12G catheter. The femoral artery and vein were cannulated for blood collection and drug administration. After injection of 0.5 mg/kg atracurium, the recipients were ventilated with the same parameters as described for the donor rats. After left thoracotomy within 3 to 4 rib, the left lung was dislodged, and the pulmonary artery, vein and bronchus were dissociated. After blocking the blood and ventilation with clamps, the artery, vein and bronchus were anastomosed to CUFF tube of the lung graft. During this process, the tidal volume was decreased to 6 ml/kg and returned to 10 ml/kg after reperfusion. After closing the thoracotomy, the recipients were extubated, and followed with spontaneous breath. Rats in the sham and LIRI groups received intravenous injection of saline (1 ml each), while rats in the LA4 group received intravenous injection of lipoxin A4 (Cayman Chemical, Ann Arbor, MI, USA) at the dose of 100 μg/kg (diluted into 1 ml saline) in 30 min after reperfusion, as previously described 12, 14 .
Lung samples collection
After 24 hours of reperfusion, all the rats were anesthetized and cannulated. The arterial blood gas analysis was performed, and the peripheral blood was collected. After sacrificing the rats with overdose of anesthetic, the left lungs were collected and divided into 3 parts. Upper part of the graft (the LIRI and LA4 groups) or control lung (the sham group) was stored at liquid nitrogen for further analysis of protein expression; the middle part was prepared for the histological and apoptotic evaluation; the lower part was homogenized with 0.9% saline (1: 9 weight) for testing the cytokines levels in the 10% homogenate. The peripheral blood and homogenate were centrifuged at 4℃, 1000 g/min for 10 min, and the supernatant was collected for further analysis.
The alveolar capillary permeability
The partial pressure of O2 (PaO2) was analyzed by the Bayer Rapidlab 348 Blood Gas Analyzer (Bayer Diagnostics, Germany). The partial pressure of O2 to fraction inspiratory O2 (PaO2/FiO2) ratio was calculated. The lung tissues were weighed (wet weight) before drying for 72 h at 50°C (dry weight). The wet/dry weight ratio was calculated by dividing the wet weight by the dry weight. The protein concentrations in the homogenate of lung samples were measured by the Bradford method.
Histological estimation
Part of lung samples was preserved in the paraffin, and the lung tissue was prepared for the HE staining to evaluate the histological injury, which was scored by 2 independent investigators. The score of lung injury was based on the Table 1 which included 5 variables such as lung hemorrhage, peri-bronchial infiltration of inflammatory cells, pulmonary interstitial edema, pneumocyte hyperplasia and intra-alveolar infiltration of inflammatory cells. Each criterion was scored on a semiquantitative scale of 0–4, where 0=normal, 1=minimal change, 2=mild change, 3=moderate change and 4=severe change. An overall histological score was calculated by summing the scores for criterion 1 through 5.
|
Parameters |
Score |
|
Hemorrhage |
0 or 1 |
|
Peri-bronchial infiltration |
0 or 1 |
|
Interstitial edema |
0 to 2 |
|
Pneumocyte hyperplasia |
0 to 3 |
|
Intra-alveolar infiltration |
0 to 3 |
Oxidative stress response
The activity of myeloperoxidase (MPO), superoxide dismutase (SOD), xanthine oxidase (XO), and the concentration of malondialdehyde (MDA) in the homogenate samples were measured with the specific kits (Nanjing Jiancheng, Nanjing, China) per the manufacturer’s instructions.
Inflammation assays
The systemic and local inflammation were assessed by testing the cytokines levels in homogenate and serum. The levels of TNF-α, IL-1β and IL-10 in homogenate, as well as the levels of intercellular adhesion molecule-1 (ICAM-1) and monocyte chemotactic protein 1 (MCP-1) in serum, were determined by the Enzyme-Linked Immunosorbent Assays with commercial kits (Wuhan Boster Bio-Engineering Limited Company, Wuhan, China) following the manufacturer’s protocols. The activity of NF-κB in lung tissues was measured using the Transcription Factor Assay Kit (Abcam, Toronto, Canada) according to the manufacturer’s instructions. The expression of NF-κB in lung tissue was determined with Western Blot.
Western blot
Protein samples were prepared from the lung tissues using 1× cell lysis buffer (Cell Signaling Technology, USA). Equivalent amounts of proteins (10-20 µg) were used to assess protein expressions as described previously11, 12. Briefly, protein was denatured by boiling, separated by sodium dodecyl sulfate-polyacrylamide gels (SDS-PAGE, 12%) and transferred to polyvinylidene difluoride (PVDF) membranes (Millipore, USA). The membranes were blocked with 8% non-fat milk/PBS-T (PBS with 0.5% Tween-20) for 2 h and respectively incubated with the following rabbit-derived primary antibodies: NF-κB, Bax, Bcl-xL, cleaved-Caspase-3 and β-actin (all 1:1000 dilution; Sigma Aldrich, St. Louis, MO, USA). After washing, the membranes were probed with horseradish peroxidase-conjugated goat anti-rabbit secondary antibody (1:5000 dilution; Cell Signaling Technology, USA). Proteins of interest were visualized using the enhanced chemiluminescence kit (EMD Millipore, USA), and the band intensities were quantified by densitometry using ImageJ software (National Institutes of Health, Bethesda, MD, USA).
Apoptosis assays
The lung tissue section for TUNEL (Terminal deoxynucleotidyl transferase dUTP nick end labeling) apoptosis assay was prepared according to the instruction of a commercial TUNEL kit (Roche Diagnostics GmbH, Science, Mannheim, Germany). Briefly, the lung tissue sections were treated with proteinase K and incubated in terminal deoxyribonucleotidyl transferase enzyme. And then, the sections were stained with diaminobenzidine–hydrogen peroxidase and Mayer’s hematoxylin. The nuclei with brown staining indicated apoptosis. Ten random fields of each section were selected, and two pathologists counted the apoptotic cells independently. The apoptosis index was calculated as the ratio of positive cells to total cells. In addition, the expressions of apoptosis associated proteins including Bax, Bcl-xL and cleaved-caspase-3 in lung tissues were evaluated by Western blot assays.
Endothelial viability and tube formation assays
Rat pulmonary microvascular endothelium cells were purchased from PriCells (Wuhan, China). The endothelium cells were cultured in normal endothelial cell growth medium supplemented with 10% fetal calf serum, 100 U/mL penicillin, 100 mg/mL streptomycin, and 1% endothelial cell growth factors under standard cell culture conditions (21% O2, 5% CO2, and 74% N2). To mimic hypoxemia and reoxygenation, cells seeded in 96-well plates with a density of 1×104 cells per well were cultured in glucose-deprived medium in a hypoxic chamber (5% CO2, and 95% N2; Biospherix hypoxia chamber, NY, USA) for 1 hour, and then returned to the normal condition for 24 hours. Subsequently, lipoxin A4 (100 ng/ml) was added in the culture medium of the LA4 group as previously described17, and the cells in the LIRI group were treated with the vehicle PBS. Twenty-four hours after reoxygenation, all the cells were collected to test the viability and tube formation capacity.
The endothelial viability was evaluated using the cell counting kit-8 (CCK-8) commercial kit. Briefly, endothelium cells with a density of 1×104 cells/well were plated in the 96-well plates. After incubation with the CCK-8 solution for additional 4 hours, the absorbance of the culture medium was detected at 450nm with a microplate reader (Quant Bio Tek Instruments, Winooski, Vermont, USA). The tube formation activity of endothelium was determined using the commercial assay kit (Abcam, Toronto, Canada) following the manufacture’s instructions. Briefly, 50μl matrigel was added into the 96-well plate, and then the plate was incubated at 37 °C for 30 min. The endothelium cells (104 cells/well) were seeded and cultured for 12 hours. Then, the endothelium was washed with PBS and the tube network was imaged using the IX51 research microscope. Meanwhile, the tube formation was quantitatively measured using Image J software (National Institutes of Health, Bethesda, MD, USA).
Statistical analysis
All the data were presented as mean ± standard deviation (SD). All the variables were analyzed by one-way analysis of variance. Data were analyzed using the IBM SPSS Statistics 19.0 (SPSS, Chicago, IL, USA). A two-tailed p-value of <0.05 was considered statistically significant.
Lipoxin A4 ameliorated the alveolar capillary permeability in rats with lung transplantation
We established the in vivo model of lung transplantation in rats, as our previous reports 15, 16. To evaluate the effects of lipoxin A4 administration on lung ischemia reperfusion injury, we treated the recipients with the vehicle or lipoxin A4 after transplantation, and compared multiple parameters including the alveolar capillary permeability, the histological injury, oxidative stress response, and apoptosis status in the grafted lung tissues.
As shown in Figure 1A, while the control sham group demonstrated neglectable changes in the ratio of PaO2 to FiO2 after reoxygenation, the LIRI group and the LA4 group had significantly reduced PaO2 to FiO2 ratios after reperfusion. Compared with the LIRI group, the LA4 group displayed significantly improved PaO2 to FiO2 ratios. Similarly, after 24 hours of reperfusion, compared with the sham group, the parameters including tissue wet/dry weight ratio (Figure 1B) and protein levels in lung tissues (Figure 1C) were worsened in the LIRI and LA4 groups. However, in comparison to the vehicle administration in the LIRI group, lipoxin A4 administration significantly mitigated the worsening of the wet/dry weight ratio (Figure 1B) and protein levels (Figure 1C).
Lipoxin A4 mitigated the histological injury of grafted lungs in rats
At 24 hours after reperfusion, the typical histological injury was observed in grafted lungs and control lungs. The histological changes of lungs included abnormalities in infiltration of inflammatory cells, severe alveolar and mesenchymal edema, broken alveolar, and even the hemorrhage. Compared with the LIRI group, the treatment with lipoxin A4 significantly reduced the pathological injury, as evidenced by significantly decreased cellular infiltration, ameliorated lung edema, and lessened alveolar injury (Figure 2A). Although the LA4 group still demonstrated significantly higher histological injury scores than the control sham group, lipoxin A4 was able to markedly lower these scores in the rats with lung transplantation (Figure 2B).
Lipoxin A4 suppressed the oxidative stress and inhibited inflammatory responses in grafted rat lungs
We next investigated the impacts of lipoxin A4 on the oxidative and inflammatory responses of grafted lungs. The transplantation caused severe oxidative stress response in the lung tissues, as the lung tissues in the LIRI group and the LA4 group had significantly increased levels of XO (Figure 3A), MPO (Figure 3B), SOD (Figure 3C) and MDA (Figure 3D) in comparison to the lung tissues in the sham group. Compared with the LIRI group, the LA4 group demonstrated remarkably reduced levels of XO, MPO, and MDA. However, the treatment with lipoxin A4 rendered even higher levels of SOD in the grafted lungs (Figure 3).
The systemic and local inflammation was assessed by determining the cytokines levels in homogenate and serum samples, respectively. The lipoxin A4 treatment significantly down-regulated the levels of ICAM-1 and MCP-1 in the serum of rats after lung transplantation and reperfusion, although the lipoxin A4 treated rats still had significantly higher levels of ICAM-1 and MCP-1 than rats in the sham group (Figure 4A). In addition, after reperfusion, the levels of TNF-α, IL-1β and IL-10 in lung homogenate samples were significantly increased, especially for TNF-α and IL-1β, when compared with the sham group. Compared with the LIRI group, the LA4 group had significantly decreased levels of TNF-α and IL-1β, but increased levels of IL-10 (Figure 4B). Furthermore, the activity and expression levels of NF-κB in rat lung tissues were significantly up-regulated by the induction of ischemia and reperfusion. Compared with the LIRI group, the activity and expression levels of NF-κB were significantly down-regulated by the treatment of lipoxin A4 in the LA4 group (Figure 4C).
Lipoxin A4 attenuated the apoptosis of lung tissues in rats after lung transplantation
There were lots of apoptotic cells in the transplanted lung tissue after reperfusion. We next examined how lipoxin A4 administration can affect the apoptosis of grafted lung tissues. Compared with the LIRI group, the LA4 group had significantly reduced number of apoptotic cells as determined by TUNEL assays (Figure 5A). After reperfusion, the expression levels of Bax, Bcl-xL and cleaved-caspase-3 proteins were significantly up-regulated in rats received lung transplantation in the LIRI and LA4 groups. Compared with the LIRI group, the LA4 group had significantly down-regulated expressions of Bax and cleaved-caspase-3 proteins, but up-regulated expression of Bcl-xL protein (Figure 5B).
Lipoxin A4 promoted the endothelial tube formation and improved the endothelial viability
It had been indicated that lipoxin A4 exhibited the anti-inflammation property mainly due to the direct effect on the inflammation status of the endothelium cells in cardiovascular disease18. To investigate the effects of lipoxin A4 on the endothelium function, we established an in vitro cellular hypoxemia and reoxygenation model to study whether lipoxin A4 administration could directly protect the endothelium. After reoxygenation, the tube formation of the endothelium cells was deteriorated in the LIRI and LA4 groups. Compared with the LIRI group, the LA4 group had significantly enhanced capacity of endothelial tube formation (Figure 6A). Moreover, the viability of endothelium after reoxygenation was significantly decreased in the LIRI and LA4 groups in comparison to the sham group. However, the decrease of endothelial viability was partially reversed by the lipoxin A4 administration (Figure 6B).
As a common and severe complication after lung transplantation, the LIRI is still the major cause of death during early period after lung transplantation 1, 2. Although the pathology of LIRI is complex and still not fully elucidated, inflammation, oxidative stress response, and endothelium dysfunction have been indicated to play a pivotal role 3. In this study, we found that lipoxin A4 significantly ameliorated the lung injury after lung transplantation in rats. Lipoxin A4 not only reduced the ischemia reperfusion induced inflammation, oxidative stress response and apoptosis in transplanted lung tissues, but also improved the endothelial function in vitro.
Firstly, we performed assays on capillary permeability and histological injury to estimate the effect of lipoxin A4 on LIRI in rats with lung transplantation. We found that lipoxin A4 significantly reduced the lung histological injury, upregulated the PaO2/FiO2 ratio, and down-regulated the wet/dry weight ratio and protein levels in lung tissue. These indicators suggest that the lipoxin A4 ameliorated the LIRI after lung transplantation. Considering the important role of oxidation in LIRI, we estimated the effect of lipoxin A4 on oxidative stress response. During hypoxemia and reoxygenation, the anaerobic metabolism produces lots of hypoxanthine, which will be degraded to generate the reactive oxygen species under the activation of XO19. XO induced superoxide formation and accumulation plays a major role in oxidative stress during IR injury. Moreover, the neutrophils play an important role in oxidative mechanisms in LIRI via acting on the MPO system. In activated neutrophils, MPO produces the hypochlorite salts through combined H2O2 generation and release of the oxygen free radical. MPO and MPO derived oxidants are important factors in the pathogenesis of organ ischemia reperfusion injury20, 21.
In contrast to XO and MPO, SOD is an important anti-oxidative enzyme and can be activated to eliminate superoxide anion. As the final product of lipid peroxidation, MDA is the final product of oxidative stress, and its expression level represents the severity of oxidative stress response. In this study, we found that lipoxin A4 significantly reduced the concentration of MDA in grafted lung tissue. This result suggests that lipoxin A4 can inhibit the oxidative stress after LIRI. The anti-oxidative effect of lipoxin A4 may be due to its regulation on the levels of XO, MPO and SOD. These results indicate that lipoxin A4 down-regulated the activity of XO and MPO, but increased the activity of SOD, which contributed to the suppression of oxidative stress response induced by the lung reperfusion injury. This result is in agreement with the conclusion of previous studies 14, 22.
Secondly, we evaluated the effect of lipoxin A4 on inflammation of grafted lung tissues in rats after LIRI. During ischemia and reperfusion, the hypoxemia and reoxygenation could lead to endothelial injury, and the NK-κB signaling of damaged endothelium can be activated, which renders the release of the chemoattractant such as ICAM-1 and MCP-1 into serum23, 24. Under activation by the chemoattractant, the inflammatory cells are recruited into the transplanted lung and then secret lots of cytokines. In this study, we found that lipoxin A4 significantly decreased the release of chemoattractant ICAM-1 and MCP-1, and thus inhibited the chemoattraction of inflammatory cells, and further decreased the secretion of TNF-α and IL-1β. The suppressive role of lipoxin A4 on inflammation mainly depended on the inhibition of NF-κB signaling. NF-κB is a key regulator of inflammation25, and the inhibition of NF-κB can alleviate the LIRI26. During LIRI, NF-kB translocates into the nucleus and activates the pro-inflammatory factor genes, and thus promotes the release of inflammatory factors including TNF-α and IL-1β, which finally resultes in organ injury26. In this study, we found that lipoxin A4 significantly down-regulated the expression of NF-κB and lessened the activity of NF-κB, which was consistent with previous study11. Furthermore, the role of lipoxin A4 in regulating inflammation was also associated with the promoted production of IL-1012, which is an important anti-inflammatory factor that can weaken the LIRI27.
Either reactive oxygen species or proinflammatory factors produced by LIRI can lead to apoptosis of transplanted lung tissues, which directly determined the function of transplanted lung 28, 29. In this study, lipoxin A4 significantly reduced the degree of apoptosis in the transplanted lung tissues. To investigate the possible mechanism underlying the anti-apoptotic role of lipoxin A4, we evaluated the effect of lipoxin A4 on apoptosis-associated proteins. We found that lipoxin A4 significantly down-regulated the expressions of Bax and cleaved-caspase-3, but up-regulated the expression of Bcl-xL. Bax is an important pro-apoptotic protein, which can initiate the intrinsic apoptosis pathway30, and further activate the cleavage of caspased-3. Contrast to Bax, Bcl-xL is a pivotal anti-apoptotic protein, which can block the intrinsic apoptosis by inhibiting the release of Bax 31 or extrinsic apoptosis by inhibiting the activation of Bid32. Our results implied that the antiapoptotic effect of lipoxin A4 was associated with the regulation on the expressions of Bax, Bcl-xL and cleaved-caspase-3.
The endothelial injury induced by oxidative stress and inflammation is the key factor in LIRI 33. To further explore the protective role of lipoxin A4 on lung injury after lung transplantation, we examined the effect of lipoxin A4 on endothelial viability and function. In the in vitro cellular experiment, we found the viability and the tube formation capacity of endothelium were significantly deteriorated by hypoxemia and reoxygenation. However, the treatment with lipoxin A4 significantly weakened the worsening of endothelial viability and tube formation capacity. These results suggested that the protective role of lipoxin A4 in LIRI not only depended on the inhibition of oxidative stress, inflammation, and apoptosis, but was also associated with the protection on endothelial viability and function.
Lipoxin A4 can ameliorate the LIRI in rats after lung transplantation, which is associated with the ability of lipoxin A4 in suppressing the oxidative stress, inflammation, and apoptosis of lung tissues, as well as its protection on the endothelial viability and tube formation capacity. Our study sheds new light on the clinical application of lipoxin A4 in the patients with lung transplantation.
ICAM-1 , intercellular adhesion molecule-1 ;
IL , interleukin ;
LA4 , lipoxin A4 ;
LIRI , lung ischemia reperfusion injury ;
MCP-1 , monocyte chemotactic protein 1 ;
MDA , malondialdehyde ;
MPO , myeloperoxidase ;
PaO2 , partial pressure of O2 ;
SOD , superoxide dismutase ;
TNF , tumor necrosis factor ;
XO , xanthine oxidase
Ethics approval and consent to participate
This study was approved by the Secondary Affiliated Hospital of Harbin Medical University. All treatments were carried out in accordance with the Institutional Animal Care and Use Committee of Second Affiliated Hospital of Harbin Medical University and followed national guidelines for the treatment of animals.
Consent for publication
Not applicable.
Availability of data and materials
The datasets used and analysed during the current study are available from the corresponding author on reasonable request.
Competing interests
The authors declare that they have no competing interests.
Funding
This study was funded by the China Postdoctoral Science Foundation (2017T100251), Heilongjiang Natural Science Foundation (YQ2019H009) and Heilongjiang Postdoctoral Science Foundation (LBH-Q9126).
Author’s Contributions
Gao Wei conceived and designed the study. Zhang Lijuan(visiting scholar under Gao Wei’s supervision) and Tai Qihang conducted majority of animal experiments and laboratory assays. Tai Qihang and Xu Guangxiao contributed to analyzed the data and drafted the work. W.G. wrote the manuscript and Tai Qihang reviewed and revised the final draft of the manuscript.
Acknowledgements
Not applicable.