Autophagy plays a major role in defending against oxidative stress in respiratory epithelial cells. The complement regulatory protein CD46 can enhance autophagy and decrease local complement activation at sites of inflammation. This study investigated the mechanism by which CD46 protects against oxidative stress-mediated apoptosis in respiratory epithelium in asthmatic patients. Nasal mucosa samples were obtained from 60 adults with mild asthma who received turbinectomy and 30 controls. A decreased expression of CD46 and increased apoptosis were noted in the damaged nasal epithelium from the asthmatic patients. Primary epithelial cells cultured with Dermatophagoides pteronyssinus 2 showed decreased CD46 and increased cleaved CASPASE-3A expressions. Crosslinking CD46 mAb could induce the formation of autophagosomes and LC3-II expression in primary epithelial cells. CD46 engagement could induce autophagy against hydrogen peroxide-induced epithelial cell death, whereas the autophagy inhibitor 3-methyladenine decreased this effect. In addition, CD46 engagement decreased the expressions of PRO-IL-1β and NLRP3, enhanced the expression of scaffold protein GOPC, and diminished hydrogen peroxide-induced 8-OHdG, IL-1β and IL-6 production. Silencing ATG5 in human lung epithelial A549 cells decreased CD46-activated autophagy with LC3-II. CD46 induced autophagy and decreased the oxidative stress-mediated apoptosis of respiratory epithelium, and this may offer a new therapeutic strategy to treat asthma.
The bronchial epithelium plays an important role in chronic airway inflammation, bronchial hyperreactivity and airway wall remodeling in allergic asthma1,2. The respiratory epithelium forms an interface with the external environment and can be damaged by oxidative stress3,4. Numerous studies have reported increased levels of reactive oxygen species (ROS) and decreased levels of antioxidants in asthmatic patients5,6,7. The susceptibility of airway epithelial cells to oxidative stress has been shown to increases with allergic sensitization, and exposure to allergens or environmental pollutant has been shown to increase airway inflammation8,9,10. Bronchial epithelial cells that produce proinflammatory signals in response to ROS may worsen the airway response and have been associated to the severity of asthma11,12,13.
Normal bronchial epithelial cells are relatively refractory to apoptotic stimulation when exposed to ROS and death receptor ligands secreted by inflammatory cells14. However, abnormal apoptotic mechanisms which disrupt the bronchial epithelial barrier have been associated with the pathogenesis of asthma. Moreover, excess oxidative stress has been reported to result in chromatin dysfunction, apoptosis and necrosis with loss of columnar epithelial cells in asthma14,15,16.
Autophagy is an intracellular degradation mechanism that eliminates damaged organelles and promotes survival during starvation17,18. Accumulating evidence suggests that autophagy can modulate cellular death, inflammation and immune function17,18,19, and that impaired autophagy may lead to accelerated senescence, neurodegenerative diseases, cancer and inflammatory bowel disease20,21,22,23. The integrity of the epithelial barrier depends on homeostatic regulatory mechanisms, and autophagy may protect against oxidative stress in respiratory diseases24,25,26,27,28.
The complement system has been reported to be locally and systemically activated to amplify inflammatory responses in allergic asthma29,30. The complement regulatory protein CD46 is widely distributed in human leukocytes, epithelial cells and fibroblasts, and it has been shown to have a protective effect against autologous complement-mediated lysis at sites of inflammation31,32. Complement regulatory proteins may interfere with oxidative stress-programmed apoptosis to avoid triggering inflammation. In addition, surface CD46 has been shown to be rapidly lost from apoptotic T cells to facilitate their rapid complement-mediated removal33. Crosslinking CD46 during T-cell receptor activation has been shown to lead to the development of inducible T regulatory cells34,35,36, which may assist in maintaining immune tolerance in autoimmune diseases37 and allergic asthma35,36.
A high expressions of CD46 in chronic obstructive pulmonary diseases has been reported to protect against lung inflammation by T regulatory cells and restraining complement cascade-induced apoptosis38. Autophagy is important for innate cellular defense against viral and bacterial pathogens. Two CD46-binding pathogens, measles virus and group A Streptococcus, have been shown to induce autophagy pathways39,40. Targeting autophagy and apoptosis manipulating factors in inflamed respiratory epithelium is important to decrease ongoing damage in respiratory epithelium and consequent airway remodeling. In this study, we assessed the functional role of CD46 in respiratory epithelium with regards to autophagy and apoptosis in asthmatic patients. Our findings may provide further evidence regarding the practical application of CD46 in clinical practice to protect respiratory epithelium in patients with asthma.
Decreased Expression of CD46 and Increased Apoptosis in the Damaged Nasal Epithelium of the Asthmatic Patients
The patient characteristics are shown in Table 1. To examine the relationship between CD46 and apoptosis in the respiratory epithelium, we analyzed the expression of CD46 and apoptosis in nasal epithelium samples from the normal controls and asthmatic patients who received nasal polypectomy. The area of intact epithelium of nasal biopsy samples taken from the normal controls showed mild immunoreactivity for CD46 (Fig. 1A). However, intact epithelium from the asthmatic patients showed strong immunostaining for CD46 (red arrow), and a decreased CD46 expression in desquamated nasal epithelium (Fig. 1A). Representative confocal microscopic analysis of the nasal mucosa biopsies between intact nasal epithelium (Fig. 1B) and fragile epithelium (Fig. 1C) from the asthmatic patients were shown. Confocal microscopic analysis of the nasal mucosa biopsies from the asthmatic patients revealed increased immunoreactivity for CD46 without TUNEL staining in intact epithelium (Fig. 1B). TUNEL-positive epithelial cells (yellow arrow) were detected with decreased immunoreactivity for CD46 in fragile epithelium in the asthmatic patients (Fig. 1C). Experiments were performed with 10 paired samples, and the results showed significant statistical differences (p < 0.05) (Fig. 1D,E).
Decreased CD46 and Increased Dermatophagoides pteronyssinus 2-mediated Cell Death of the Primary Epithelial Cells from the Asthmatic Patients
To evaluate the role of CD46 in the pathogenesis of respiratory epithelium apoptosis, we evaluated the CD46 expression with mite allergen-induced epithelial cell death in the asthmatic patients. Dermatophagoides pteronyssinus 2 (Der p 2) is the major allergen in Taiwan. It contains a cysteine protease which may cause proteolysis of CD46 with a subsequent increase in the apoptosis of respiratory epithelial cells35. After Der p 2 stimulation, the expressions of the apoptosis markers with cleaved CASPASE-3A and CD46 were analyzed in primary nasal epithelial cells from the asthmatic patients. A decrease in the expression of CD46 was noted in the epithelial cells (Fig. 2A), with an increase in the expression of cleaved CASPASE-3A (as shown by Western blotting; Fig. 2B) in the asthmatic patients (p < 0.05). Experiments were performed with 30 paired samples, and the statistical results are shown in Fig. 2C,D.
Autophagy Induced by CD46 Antibody Activation in Normal and Asthmatic Epithelial Cells
Engagement of CD46, a ubiquitous human surface receptor able to bind several different pathogens, can induce autophagy to control infection39. To further investigate the role of CD46 in the autophagy of respiratory epithelium, we examined whether antibody-driven CD46 crosslinking could induce the formation of autophagosomes. Crosslinking CD46 mAb at the surface of primary nasal airway epithelial cells induced macropinocytosis-like internalization, and led to the degradation of the cell surface of CD46 via the same molecular mechanism as the CD46 ligand (Supplement Fig. 1). CD46 mAb crosslinking increased the number of GFP-LC3 (autophagosomes) puncta per cell (Fig. 3A) in epithelial cells from the asthmatic patients and controls. Quantification of GFP-LC3 puncta per cell was assayed, and the statistical data are shown in Fig. 3B. We monitored autophagy following the conversion of LC3-I to LC3-II by Western blot of the epithelial cell lysates. The presence of CD46 resulted in an increase in LC3-II in cell lysates compared to IgG control cells (Fig. 3C). The statistical data of experiments with 30 paired samples are shown in Fig. 3D (p < 0.05). To determine whether autophagosome detection subsequent to CD46 engagement was the result of an increase in autophagic flux or an accumulation of basal autophagosomes, we analyzed autophagy in the presence of lysosomal inhibitors with bafilomycin. We found that crosslinking CD46 mAb induced autophagy marker with LC3-II (p < 0.05) during bafilomycin clamp in primary nasal epithelial cells from the asthmatic patients as shown in Fig. 3E,F.
Crosslinking CD46 Antibody Mediated Autophagy Against Hydrogen Peroxide-induced Apoptosis in Normal and Asthmatic Epithelial Cells
To evaluate the protective role of CD46-induced autophagy in the prevention of respiratory epithelium apoptosis in asthma, we evaluated hydrogen peroxide-induced epithelial cell death from CD46 mAb co-cultured with the autophagy inhibitor 3-methyladenine (3-MA). In analysis of the hydrogen peroxide-mediated cells with annexin V expression, the percentage of apoptosis of CD46 mAb-pretreated primary nasal epithelium cells from the asthmatic patients was decreased compared with the IgG control group in asthmatic patients (3.3 ± 1.8% vs. 7.3 ± 2.2%, p < 0.05) (Fig. 4A,B). The extent of cell death was further increased when CD46-induced autophagy was inhibited with 3-MA treatment (3.3 ± 1.8% vs. 6.4 ± 2.0%, p < 0.05). Experiments were performed with 30 paired samples, and the statistical data are shown in Fig. 4B.
CD46 Antibody Inhibited 8-OHdG, IL-1β and IL-6 from Hydrogen Peroxide-induced Epithelial Cells
The levels of 8-OHdG, IL-1β and IL-6 in the supernatant from CD46 mAb-pretreated primary nasal epithelium cells from the asthmatic patients after exposure to H2O2 were analyzed using ELISA. The results showed decreased levels of 8-OHdG (Fig. 5A), IL-1β (Fig. 5B) and IL-6 (Fig. 5C) compared with the IgG control group (p < 0.05).
Silencing ATG5 Decreased CD46-activated Autophagy in A549 Cells
A549 cells were transfected with siRNA targeting human ATG5 or control siRNA and incubated with anti-CD46 mAb, isotype control antibody (IgG), or in nutrient-deprived media (starvation). Proteins were extracted from the A549 human lung epithelial cells and analyzed by Western blotting (Fig. 6). The reduced expression of the ATG5 gene for autophagy using short siRNA prevented CD46-induced and starvation-induced autophagy with LC3-II (Fig. 6).
Crosslinking CD46 Antibody Enhanced GOPC and Inhibited PRO-IL-1β and NLRP3 Expressions from H2O2-activated A549 Cells
To evaluate the mechanism of CD46-induced autophagy in the respiratory epithelium, we examined whether CD46 crosslinking by mAb could induce induction of the scaffold protein GOPC. We demonstrated that crosslinking of CD46 by the specific mAb could induce the expression of GOPC in human lung epithelial A549 cells (p < 0.05) (Fig. 7A). To investigate the mechanism by which CD46-induced autophagy reduced IL-1β, we evaluated the expressions of pro-IL-1β and NLRP3 inflammasome in an H2O2-induced epithelial cell model in the presence of anti-CD46 mAb and/or the autophagy inhibitor 3-MA. The expressions of PRO-IL1β and NLRP3 in the H2O2-activated A549 cells were reduced in the presence of anti-CD46 mAb, and 3-MA treatment reversed this effect (p < 0.05) as shown in Fig. 7B.
The results of the present study showed a significantly increased surface expression of the complement regulatory protein CD46 in nasal epithelium from asthmatic patients compared to healthy subjects. In addition, there was an increase in apoptosis with a decrease in CD46 expression in fragile epithelium from the asthmatic patients, and a decrease in the expression of CD46 and increase in the expression of cleaved CASPASE-3A in Der p 2-cultured primary epithelial cells. CD46 crosslinking could induce the formation of autophagosomes and LC3-II expression in primary respiratory epithelium cells. Furthermore, CD46 mAb suppressed hydrogen peroxide-induced epithelial cell apoptosis, and treatment with the autophagy inhibitor 3-MA reversed this effect. CD46 also decreased the hydrogen peroxide-induced production of 8-OHdG, IL-1β and IL-6 from the epithelial cells. In addition, silencing ATG5 in A549 cells decreased CD46-activated autophagy with LC3-II expressions. Taken together, these results suggest that CD46 could induce autophagy and decrease oxidative stress-mediated apoptosis in respiratory epithelium, and this may offer a new potential therapeutic strategy to treat allergic asthma.
Numerous studies have reported that ROS can increase airway inflammation, and that modification of airway oxidative stress may affect the pathological features of asthma3,4,5,6,7,8,9,10,11,12,13. It has also been reported that asthmatic airway epithelial cells are susceptible to oxidative stress, and that cumulative oxidative damage contributes to apoptosis in epithelium lining asthmatic airways16. Complement has emerged as an important factor in the pathophysiology of asthma, and the identification of complement split products at the airway surface has been shown to be a common pathway for the induction of Th2-mediated inflammatory responses29,30. CD46 acts as ‘don’t-eat me’ signal and is down-regulated during apoptosis, and this leaves cells less protected against complement activation by oxidative stress33,41,42,43. It is known that respiratory epithelial cells express membrane-bound complement regulatory protein (CD46) to prevent complement-mediated autologous tissue damage. Mahtout et al. reported that Porphyromonas gingivalis, a major etiological agent of chronic periodontitis, causes shedding of CD46 expressed by epithelial cells44. The allergen Dermatophagoides pteronyssinus 2 contains a cysteine protease, and it may cause proteolysis of CD46 with a subsequent increase in the apoptosis of respiratory epithelial cells.
Studies on bronchial epithelial cells in asthmatic patients are hampered by difficulties in obtaining suitable human samples. The concept of a “united airway disease” has been proposed between allergic rhinitis and asthma. Nasal epithelial cells have been used as surrogates for lower airway cells in which nasal and bronchial cells have a similar morphological appearance and uniform cytokine expressions45. Varsano et al. demonstrated that the normal human respiratory tract from the nose to the alveoli expresses CD46, and that this expression was increased during inflammation and retained under cell culture conditions46. We also found that the expression of CD46 increased in asthmatic respiratory epithelium. In addition, we also detected apoptosis of the fragile respiratory epithelium concurrently with a decrease in CD46 expression. Furthermore, primary nasal epithelial cells were susceptible to mite allergen-induced apoptosis following a decrease in CD46 expression. This suggests that CD46-inhibited oxidant-induced apoptosis may offer a new strategy to treat lung injuries linked to oxidative stress in asthma.
Many studies have established an important crosslink between oxidative stress and autophagy in the pathogenic processes of asthma26,27. Poon et al. reported an increase in autophagy in human bronchial tissues of patients with asthma, and suggested an association between autophagy and reduced lung function in patients with moderately severe asthma47. In addition, an experimental mice model showed that autophagy protein-deficient bronchial epithelial cells were hyperresponsive to methacholine exposure, and that this contributed to smooth muscle hyperreactivity48. However, to date, no studies have documented the autophagy regulation of respiratory epithelium cells by CD46 stimulation. Importantly, we found that CD46 mAb could induce the formation of autophagosomes and LC3-II expression in primary respiratory epithelium cells. It is therefore reasonable to assume that increased autophagy would be necessary for epithelial apoptosis. Our results showed that hydrogen peroxide promoted epithelial apoptosis and that this was blocked by anti-CD46 mAb. In addition, we showed that treatment with the autophagy inhibitor 3-MA decreased the anti-apoptosis effects. These findings may help to explain the survival mechanisms by which CD46-activated autophagy plays a key role in the respiratory homeostatic mechanism that facilitates immune tolerance and establishment of respiratory tract integrity.
Several studies have reported that ATG5 gene polymorphisms are associated with childhood asthma28,49, and that the expression of the ATG5 gene is increased during acute asthma exacerbations in nasal epithelial cells49. Joubert et al. first demonstrated that crosslinking CD46 agonist antibodies (mAb) can directly trigger autophagy through ATG539. The molecular pathway by which CD46 induces de novo formation of autophagosomes relies on the scaffold protein GOPC39. We further demonstrated that CD46 crosslinking by agonist antibodies induced the expression of GOPC in human lung epithelial A549 cells. Furthermore, we found that silencing ATG5 in human lung epithelial A549 cells decreased CD46-activated autophagy with LC3-II. Therefore, we suggest that ATG5 plays an important role in the ability of respiratory epithelium to increase autophagy and protect against asthma.
During epithelial injury caused by oxidative stress in asthma, the epithelium becomes an important source of inflammatory cytokines that contribute to ongoing inflammation and airway remodeling13,50. Autophagy can directly regulate the secretion of cytokines, and disruption of normal autophagy pathways by ROS has been linked with increased secretion of the proinflammatory cytokine IL-1β51,52. Harris et al. demonstrated that autophagy controls IL-1β production through at least two separate mechanisms: by decreasing activation of the NLRP3 inflammasome, and by regulating PRO-IL-1β for lysosomal degradation50. We found that CD46 could decrease H2O2-induced oxidative stress through 8-OHdG and the production of the inflammatory cytokines IL-1β and IL-6 from epithelial cells. We further demonstrated that CD46-induced autophagy inhibited IL-1β by H2O2-activated airway epithelial cells due to a decrease in the expressions of PRO-IL-1β and NLRP3. Therefore, CD46 may be effective in ameliorating asthmatic airway diseases through modulating the autophagy signaling pathway.
In conclusion, we found that CD46 was a target antagonizing the apoptosis of oxidative stress-associated respiratory epithelial cells through autophagy. Further studies are needed to clarify the effect of autophagy in asthma and the effect of modulating CD46 on lower airway inflammation. These findings may provide further evidence regarding the practical application of CD46 in clinical practice as a treatment for asthma.
Materials and Methods
A total of 60 adult patients with mild intermittent asthma with concomitant rhinitis and sensitivity to house dust mites (Der p) as proven by an IgE specific test result greater than third grade (>3.5 kU/L) using a CAP system (Pharmacia, Uppsala, Sweden) who were referred for turbinectomy were enrolled in this study. The asthmatic patients in our study were initially diagnosed at the study hospital. Definition of mild asthma was based on symptoms and a forced expiratory volume in 1 s (FEV1) of ≥80% according to the Global Initiative for Asthma guidelines. Surgery was performed under strict clinical indications, and all patients had difficulty in nose breathing. The samples obtained from the asthmatic patients were randomly subdivided into different treatment groups for immunohistochemistry, confocal immunofluorescence, flow cytometry and Western blot analysis. Healthy controls (n = 30) with normal serum IgE levels who visited the hospital for reasons unrelated to the study were enrolled as controls. Patients with either congenital or acquired immune deficiency and who were receiving systemic immune suppressive therapy were excluded. Nasal and inhaled corticosteroid treatment was stopped 4 weeks before surgery. Informed consent was obtained from each subject before participating in the study. The study was approved by the Institutional Review Board (No:101103) of Changhua Christian Hospital, and all methods were performed in accordance with the relevant guidelines and regulations.
Tissue Sample, Cells, Antibodies and Reagents
Nasal biopsy specimens were cut into small pieces and placed in trypsin (0.025%)/EDTA (0.01%; Gibco, Grand Island, NY) for 3 hours at 37 °C and 5% CO2. Cells were strained through 70-mm nylon mesh (Becton Dickinson Labware, Franklin Lakes, NJ), washed, seeded at a density of 4 × 103 cells/cm2 in T-75 cell culture flasks (Hyclone, GE Healthcare, USA), and cultured in bronchial epithelial cell medium (Hyclone) supplemented with 100 U/mL penicillin, 100 mg/mL streptomycin, and 0.25 mg/mL amphotericin B (Gibco) in a humidified atmosphere containing 5% CO2 at 37 °C. Confluent monolayer primary nasal epithelial cells or A549 cells (human bronchial epithelial cell line, American Type Culture Collection, Rockville, MD) were cultured with or without anti-human CD46 mAb (5 ug/ml) (Clone: MEM-258) (GeneTex, San Antonio, Texas, USA) in RPMI-1640 medium containing 10% fetal bovine serum (Gibco). Recombinant Dermatophagoides pteronyssinus 2 (Der p 2) (Indoor Biotechnologies, Cardiff, UK) served as the allergen. The following antibodies were used for Western blot analysis: anti-human CD46 mAb (Genetex), anti-cleaved CASPASE 3 A (Genetex), anti-ATG5 mAb (Genetex), anti-LCB3-I mAb (Genetex), anti-LCB3-II mAb (Novus Biologicals, Littleton, CO), anti-GOPC mAb (Genetex), anti-IL-1β mAb (Abcam, Cambridge, MA), anti-NLRP3 mAb (Genetex), IgG (Abcam) and β-ACTIN (Abcam).
Histology and Immunohistochemistry
Paraffin-embedded nasal tissue samples were soaked in xylene and then sequentially in solutions of 100%, 95%, and 70% ethanol to remove the paraffin wax and for rehydration. Antigen unmasking was performed by heating the slides in retrieval buffer, and then cooled to room temperature. H2O2 block (Lab Vision, Fremont, CA) and protein block (Lab Vision, Fremont, CA) were then applied to the tissues to prevent non-specific protein binding and to block endogenous peroxidases. Rabbit monoclonal anti-human CD46 antibody (GeneTex) was diluted 1:500 with antibody diluent (Lab Vision, Fremont, CA) and applied to the tissues for 30 minutes at room temperature. Immunohistochemical staining was performed using an UltraVision Quanto Detection System HRP (Thermo Fisher Scientific, Waltham, MA). Visualization was achieved using the diaminobenzidine (DAB) method. Slides were counterstained with hematoxylin.
Cells were incubated with diluted Autophagy Reagent A according to the manufacturer’s recommendations in a FlowCellect™ Autophagy LC3 Antibody-based Assay Kit (Millipore, Billerica, MA). This kit contains two key detection reagents to help facilitate the monitoring of lipidated LC3-II in a given cell system. Briefly, the use of selective permeabilization solution discriminates between cytosolic LC3 from autophagic LC3 by extracting the soluble cytosolic proteins, while protecting LC3 which has been sequestered into the autophagosome. Primary nasal epithelial cells were incubated with Reagent A at 37 °C and 5% CO2 for 60 min. Cells were washed and resuspended in 100 μL of Reagent B, centrifuged immediately, and resuspended in 100 μL of Assay buffer with 1:20 diluted FITC-conjugated anti-LC3 antibody. LC3-II was photographed live on a Confocal Olympus FV1200 fluorescent microscope. The number of GFP-LC3 vesicles in primary nasal epithelial cells was calculated from 200 cells for each experiment. Quantification of GFP-LC3 puncta per cell was assayed. For terminal nucleotidyl transferase-mediated nick end labeling (TUNEL) assay, we used an ApopTag Plus Peroxidase In Situ Apoptosis Detection Kit (Takara, Shiga, Japan) according to the manufacturer’s instructions. In order to detect apoptosis of CD46-expressing cells, confocal microscopic analyses between intact and fragile primary nasal epithelium with TUNEL (FITC), CD46 (PE), and 4′,6-diamidino-2-phenylindole (DAPI) (nuclear stain) were performed. To evaluate whether CD46 crosslinking could induce autophagy in primary upper airway epithelial cells, epithelial cells were incubated for 4 hours in complete medium either in the presence of anti-CD46 mAb (5 μg/ml), isotype control antibody (IgG), or in nutrient-deprived media (starvation), and quantification of GFP-LC3 puncta (autophagosomes) in the nasal epithelial cells was performed using confocal microscopy.
Flow Cytometry and Annexin V/Propidium Iodide Double Staining
To detect the role of CD46-induced autophagy in primary upper respiratory epithelial cells after exposure to hydrogen peroxide, an FITC Annexin V/propidium iodide Apoptosis Detection Kit I (BD Pharmingen, USA) was used. Anti-CD46 mAb (5 μg/ml) and/or autophagy inhibitor 3-methyladenine (3-MA) (10 mmol/L) (Sigma-Aldrich, St. Louis, MO) was co-incubated with primary nasal epithelial cells (1 × 105 cells) and then cultured with H2O2 (0.5 mM) for 1 hour, followed by 8 hours recovery. The treated cells were then stained with propidium iodide and Annexin V-FITC for 15 minutes according to the manufacturer’s instructions, and then subjected to flow cytometry analysis (FC500, Beckman Coulter, Fullerton, CA).
Enzyme-Linked Immunosorbent Assay (ELISA)
The concentrations of IL-1β and IL-6 in cell supernatants were determined using a commercially available ELISA-based assay system (R&D Systems, London, UK). The expression of the oxidative stress marker 8-hydroxy-2′-deoxyguanosine (8-OHdG) induced by oxygen radicals was measured using a highly sensitive 8-OHdG ELISA kit (JalCA, Fukuroi, Shizuoka, Japan). Supernatant from anti-CD46 mAb (5 μg/ml) pretreated primary nasal epithelium cells from the asthmatic patients after exposure to H2O2 (0.5 mM) were analyzed with 8-OHdG and IL-1β and IL-6 ELISA-based systems.
The mechanism of the CD46 mAb-mediated de-novo formation of autophagosomes has been shown to be regulated by ATG5 gene-induced autophagy39. Small interfering RNAs (siRNAs) targeting human ATG5 (Sense: (5′->3′) GAACCAUACUAUUUGCUUUtt; and Antisense: AAAGCAAAUAGUAUGGUUCtg) or control siRNA (GeneDirex) were purchased from Cell Signaling Technology. Cells were transfected using the siRNA transfection reagent Lipofectamine™ RNAiMAX according to the manufacturer’s instructions (Invitrogen, Carlsbad, CA). Diluted siRNA (final = 20 nM) added in 2 ml Opti-MEM I Medium (Invitrogen, Carlsbad, CA) without serum in the 100 mm culture plate. Mixed gently (30 µl Lipofectamine™ RNAiMAX to each well containing the diluted siRNA molecules) and incubate for 20 minutes at room temperature. A549 cells (1 × 105 cells/mL) solution in antibiotic-free complete medium and mixed with siRNA- Lipofectamine™ RNAiMAX complexes after 24 hours, replace the transfection medium with complete medium and continue incubation 72 hours for assay.
Western Blot Analysis
Protein levels of CD46, cleaved CASPASE 3A, ATG5, LCB3-I and LCB3-II, GOPC, PRO-IL-1β and NLRP3 were determined by Western blot analysis. Equal amounts of proteins in each study groups were ascertained using a Bio-Rad protein assay kit (Bio-Rad, Hercules, CA). Cellular proteins were resolved by 10% SDS-polyacrylamide gel. After electrophoresis, protein levels were determined by Western blot analysis.
All data were presented as mean ± SD. As the continuous variables were not in normal distribution, nonparametric statistics including the Wilcoxon rank-sum test was used for comparisons. Groups of datasets in each treatment group were compared using the Kruskal-Wallis test, followed by the Duncan test. A p value less than 0.05 was considered to be statistically significant.
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This work was supported in part by grants from the Ministry of Science and Technology, Taiwan, ROC (MOST 103-2314-B-371-006 and 106-2314-B-371-008 and MOST 107-2314-B-371-011-MY2) and Changhua Christian Hospital(Y_104_0252 and Y_104_0127 and Y_105_0246 and Y_105_0023 and Y_105_0050).
The authors declare no competing interests.
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