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. 2015 Feb 2;13(2):170–179. doi: 10.1038/cmi.2015.02

IRG1 induced by heme oxygenase-1/carbon monoxide inhibits LPS-mediated sepsis and pro-inflammatory cytokine production

Md Jamal Uddin 1, Yeonsoo Joe 1, Seul-Ki Kim 1, Sun Oh Jeong 2, Stefan W Ryter 3, Hyun-Ock Pae 2, Hun Taeg Chung 1
PMCID: PMC4786624  PMID: 25640654

Abstract

The immunoresponsive gene 1 (IRG1) protein has crucial functions in embryonic implantation and neurodegeneration. IRG1 promotes endotoxin tolerance by increasing A20 expression in macrophages through reactive oxygen species (ROS). The cytoprotective protein heme oxygenase-1 (HO-1), which generates endogenous carbon monoxide (CO), is expressed in the lung during Lipopolysaccharide (LPS) tolerance and cross tolerance. However, the detailed molecular mechanisms and functional links between IRG1 and HO-1 in the innate immune system remain unknown. In the present study, we found that the CO releasing molecule-2 (CORM-2) and chemical inducers of HO-1 increased IRG1 expression in a time- and dose-dependent fashion in RAW264.7 cells. Furthermore, inhibition of HO-1 activity by zinc protoporphyrin IX (ZnPP) and HO-1 siRNA significantly reduced expression of IRG1 under these conditions. In addition, treatment with CO and HO-1 induction significantly increased A20 expression, which was reversed by ZnPP and HO-1 siRNA. LPS-stimulated TNF-α was significantly decreased, whereas IRG1 and A20 were increased by CORM-2 application and HO-1 induction, which in turn were abrogated by ZnPP. Interestingly, siRNA against IRG1 and A20 reversed the effects of CO and HO-1 on LPS-stimulated TNF-α production. Additionally, CO and HO-1 inducers significantly increased IRG1 and A20 expression and downregulated TNF-α production in a LPS-stimulated sepsis mice model. Furthermore, the effects of CO and HO-1 on TNF-α production were significantly reversed when ZnPP was administered. In conclusion, CO and HO-1 induction regulates IRG1 and A20 expression, leading to inhibition of inflammation in vitro and in an in vivo mice model.

Keywords: A20, anti-inflammatory effects, carbon monoxide, HO-1, IRG1

Introduction

Sepsis is a systemic inflammatory response to microbial infection. During sepsis, excessive activation of the innate immune response as the result of bacteremia or hyper-inflammation may cause organ dysfunction and death.1,2 During inflammation, pro-inflammatory cytokines and reactive oxygen species (ROS) responsible for antimicrobial activity are produced by activated peripheral macrophages, microglial cells and the resident immune cells of the central nervous system.3 However, during endotoxin-tolerance, a hypo-inflammatory state of the innate immune system can also result in secondary infections with organisms not typically pathogenic in the immunocompetent host.1

The immunoresponsive gene 1 (IRG1), of which protein is known as cis-aconitate decarboxylase (CAD) in human, was first recognized as a 2.3-kb cDNA from a murine macrophage cell line stimulated with lipopolysaccharide (LPS).4 Gene expression profiling studies of murine macrophages and microglial cells have revealed that IRG1 is highly expressed under pro-inflammatory conditions.5,6 Avian spleen macrophages displayed significantly increased expression of IRG1 after Salmonella enterica infection.7 Furthermore, IRG1 is highly expressed in the pregnant uterus during the early events leading to implantation,8 the specific phase of pregnancy in which high levels of inflammatory cytokines are secreted.9 IRG1 expression is also deregulated in autoimmune or inflammatory diseases.6 Furthermore, IRG1 localizes to the mitochondria and may represent a key link between immunological and metabolic processes.6 IRG1 has crucial functions in embryonic implantation and neurodegeneration.10 Also, IRG1 promotes endotoxin tolerance by increasing A20 expression in macrophages via increased ROS production.11 In addition, knockdown of IRG1 increased the activation of NF-κB and IRF3, which was accompanied by decreased A20 expression and ROS production. Despite these observations, the precise molecular and biological functions of IRG1 in the innate immune response remain unknown.

Heme oxygenase-1 (HO-1), a stress-inducible protein, catalyzes the oxidative degradation of heme to generate carbon monoxide (CO), iron and biliverdin-IXα and promotes cellular protection.12 In addition, anti-inflammatory, anti-apoptotic and cytoprotective properties of CO have been described.13 The anti-inflammatory effects of HO-1 may have therapeutic potential in inflammatory conditions such as arthritis14 and inflammatory bowel disease.15 In sepsis, HO-1 is involved in the induction of IL-10 and the suppression of pro-inflammatory factors such as TNF-α and nitric oxide synthase-2 in macrophages,16 and also mediates the anti-inflammatory effects of adiponectin in Kupffer cells.17 Furthermore, increased HO-1 expression was observed in the lung during LPS tolerance and cross tolerance.18 In addition, overexpression of hepatic HO-1 has been observed during endotoxin tolerance.19 Currently, there are no reports regarding the effects of HO-1 on the regulation of IRG1 expression under pro-inflammatory conditions.

Since both HO-1 and IRG1 proteins are simultaneously expressed during endotoxin tolerance and regulate anti-inflammatory functions, we examined the functional link between HO-1 and IRG1 expression with respect to inhibition of inflammation in a murine model in vivo and in vitro.

Methods and materials

Reagents and antibodies

Antibodies against HO-1 and A20 were purchased from Cell Signaling Technology (Danvers, MA, USA). Antibodies against IRG1, β-actin and anti-mouse and anti-goat antibodies conjugated to horseradish peroxidase were obtained from Santa Cruz Biotechnology (Santa Cruz, CA, USA). CO-releasing molecule-2 (CORM-2, tricarbonyl dichlororuthenium dimer), ruthenium chloride (RuCl3), LPS, cobalt protoporphyrin IX (CoPP), hemin and protease inhibitor cocktail sets were purchased from Sigma-Aldrich (St Louis, MO, USA). Zinc protoporphyrin IX (ZnPP) was from Frontier Scientific Inc. (Logan, UT, USA). Dulbecco's modified Eagle medium, fetal bovine serum, penicillin–streptomycin and sodium pyruvate were purchased from Invitrogen (Grand Island, NY, USA). All other chemicals were obtained from Sigma-Aldrich.

Cell culture

RAW264.7 cells were cultured in Dulbecco's modified Eagle medium with 10% heat-inactivated fetal bovine serum and 1% penicillin-streptomycin at 37 °C in 5% CO2. Cells were cultured to 75%–80% confluence and then split at a density of 5×105 cells/ml in six-well plates. The cells were incubated overnight and then treated with or without LPS (100 ng/ml) for 8 h, 16 h or 24 h. After incubation, cells were harvested for reverse transcription-polymerase chain reaction (RT-PCR), real-time RT-PCR and western blotting. Cell supernatants were collected for ELISA assays (R&D Systems, Inc., Minneapolis, MN, USA) for measuring the level of TNF-α production.

Animal model of endotoxemia

Seven-week-old male C57BL/6 wild-type mice were exposed to inhalation of CO gas (250 ppm) 4 h/day for 6 days or treated with CORM-2 (30 mg/kg, i.p.) and hemin (10 mg/kg, i.p.) for 2 h; with or without ZnPP (5 mg/kg, i.p.), respectively (Tsoyi et al., 2011). After 2 h or 6 days, the mice were injected with LPS (12.5 mg/kg, i.p.) to induce endotoxemia. At 16 h post-injection, mice were sacrificed, and blood serum and liver tissues were collected and stored at −80 °C for protein and RNA analysis. All experiments with mice were approved by the Animal Care Committee of the University of Ulsan, Ulsan, Korea.

Transfection

Predesigned siRNAs were purchased from Santa Cruz Biotechnology. RAW264.7 cells (5×105/ml) were cultured in six-well plates for 3 h and then transfected with IRG1 siRNA (100 nM) or A20 siRNA (100 nM) or HO-1 siRNA (100 nM), using lipofectamine 2000 according to the manufacturer's instructions. After transfection, cells were treated with CORM-2 (20 µM) or hemin (10 µM) with or without LPS (100 ng/ml).

Western blotting

After harvesting of the cells, protein extracts were prepared using lysis buffer containing RIPA buffer, with protease and phosphatase inhibitors. Protein concentration in the cell lysate was measured by the bicinchoninic protein assay (Pierce Biotechnology Inc., Rockford, IL, USA). An equal amount of protein for all samples was subjected to electrophoresis and then transferred to polyvinylidene difluoride membranes. The membranes were blocked with 5% non-fat milk in PBS containing 0.1% Tween 20 for 20 min and incubated at 4 °C overnight with primary antibodies for HO-1, IRG1, A20 and β-actin, followed by secondary antibodies conjugated with horseradish peroxidase. Immunocomplexes were visualized using the enhanced chemiluminescence western blotting detection system (GE Healthcare Life Sciences, Buckinghamshire, UK).

RT-PCR

Total RNA was extracted using the TRIzol reagent (Invitrogen, CA, USA) according to the manufacturer's instructions. In short, 2 µg of total RNA was used to make cDNA by using M-MLV reverse transcriptase (Promega Corporation, WI, USA) and oligo (dT) 15 primer (Promega Corporation, Madison, WI, USA). The resulting cDNA was subjected to PCR for mouse GAPDH (forward (f)-aggccggtgctgagtatgtc, reverse (r)-tgcctgcttcaccttct, 530 bp), HO-1 (f-tcccagacaccgctcctccag, r-ggatttggggctggtttc, 313 bp), IRG1 (f-ggtatcattcggaggagaa, r-acagagggagggtggaatct, 440 bp) and TNF-α (f-agcccacgtcgtagcaaaccaccaa, r-acacccattcccttcacagagcaat, 421 bp). PCR was performed with the following conditions: denaturation temperature 94 °C for 0.5 min, annealing temperature (according to respective primer) for 0.5 min and extension temperature 72 °C for 1 min, and the PCR cycle was determined according to a kinetic profile. GAPDH was used as an internal loading control. PCR products were observed on 2% agarose gels containing ethidium bromide using a digital gel documentation set.

Real-time RT-PCR

Total RNA was extracted from RAW264.7 cells or mouse liver tissues using the TRIzol reagent (Invitrogen, Carlsbad CA, USA) according to the manufacturer's instructions. In brief, 2 µg of total RNA was used to make cDNA by using M-MLV reverse transcriptase (Promega Corporation, Madison, WI, USA) and oligo (dT) 15 primer (Promega Corporation, Madison, WI, USA). The resulted cDNA was subjected to real-time RT-PCR using SYBR Green qPCR Master Mix (Applied Biosystem Warrington, WA1, UK) on an ABI 7500 Fast Real-Time PCR System (Applied Biosystem Warrington, WA1, UK) for mouse GAPDH (f-gggaagcccatcaccatct, r-cggcctfcaccccatttg), IRG1 (f-gctgtgcaggtgttgagcc, r-cataactgtgttcccgaggtgtc), A20 (f-gcctgtgcaaaagagatttcagat, r-tgattcacagagcatgtaggcc), HO-1 (f-tcagtcccaaacctcgcggt, r-gctgtgcaggtgttgagcc) and TNF-α (f-agaccctcacactcagatca, r-ttgctacgacgtgggctaca). GAPDH was used as an internal loading control to normalize all PCR products.

Enzyme-linked immunosorbent assay (ELISA)

RAW264.7 macrophages on six-well plates were incubated overnight and then pre-treated with CORM-2 or hemin with or without ZnPP for 30 min followed by stimulation with LPS for 24 h. In addition, mice were administrated with CO gas or CORM-2 or hemin with or without ZnPP for 2 h and sepsis was induced by LPS injection. The TNF-α levels of supernatant collected from different samples or blood serum collected from different mice were assayed by using mouse ELISA kit (R&D systems, Minneapolis, MN, USA).

Statistical analysis

Results are expressed as the means±s.d. Statistical differences between groups were evaluated by one-way ANOVA or Student's t-test when multiple groups were compared. Differences were considered to be significant when P<0.05.

Results

CO and HO-1 induction increases IRG1 expression in macrophages

CO is produced as an end product of HO-1 activity. CO-releasing molecules (i.e., CORM-2) can release CO in a controllable manner under physiological conditions.20 IRG1, which is highly conserved in vertebrates, exerts crucial functions during the immune response,4 whereas HO-1, a stress-inducible enzyme, can confer protection in inflammation. Both HO-119 and IRG111 were found to be increased during endotoxin tolerance, suggesting a potential regulatory link between HO-1 and IRG1. To examine this hypothesis, we treated the murine macrophage cell line RAW264.7 with CORM-2 (20 µM) for varying time periods. Following CORM-2 treatment, IRG1 expression increased at 16 h, whereas HO-1 expression began to increase at 4 h (Figure 1a). Therefore, in subsequent experiments, we measured IRG1 expression at 16 h. In addition, CORM-2 treatment dose-dependently increased activity of HO-1 (Supplemenatry Figure 1c) at 16 h, and the levels of IRG1 and HO-1 mRNA (Figure 1b and Supplementary Figure 1a and b) and protein (Figure 1c) at 8 h and 16 h, respectively. CoPP is a potent and well-known inducer of HO-1.21 Hemin, a constituent of hemoglobin, may have therapeutic potential for the treatment of acute porphyrias.22 The anti-inflammatory or host defense functions of hemin may be mediated via stimulation of HO-1 expression.23 We therefore examined the effects of CoPP and hemin on HO-1 and IRG1 expression. RAW264.7 cells were treated with CoPP or hemin (0–20 µM). CoPP increased the levels of IRG1 and HO-1 mRNA (Figure 1d) and protein (Figure. 1e) in a dose-dependent fashion. Similarly, hemin increased IRG1 and HO-1 mRNA (Figure 1f and Supplementary Figure 1d and e) and protein (Figrue 1g) levels.

Figure 1.

Figure 1

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CORM-2, CoPP and hemin increase IRG1 expression in RAW264.7 macrophages. (a) RAW264.7 cells were treated with 20 µM CORM-2 for 0, 2, 4, 8, 16 and 24 h and protein level of IRG1 and HO-1 were detected by western blot analysis. (b and c) RAW264.7 cells were treated with CORM-2 (0, 5, 10, 20 and 40 µM) for 8 or 16 h. IRG1 and HO-1 mRNA and protein were measured, by RT-PCR analysis. (d–g) RAW264.7 cells were treated with CoPP or hemin (0, 1, 5, 10 and 20 µM) for 8 or 16 h. (d) After CoPP treatment at the indicated concentrations (0–20 µM) for 8 h, mRNA expression of IRG1 and HO-1 were detected. (e) After CoPP treatment (0–20 µM) for 16 h, IRG1 and HO-1 protein level were detected. (f) After hemin treatment at the indicated concentrations (0–20 µM) for 8 h, mRNA expression of IRG1 and HO-1 were detected. (g) After hemin treatment (0–20 µM) for 16 h, IRG1 and HO-1 protein level were detected. Protein level was detected by western blot analysis and mRNA levels were measured by RT-PCR analysis. Representative bands are shown.

To confirm the effect of CO on HO-1 and IRG1 expression, we used RuCl3 as a negative control for CORM-2 to rule out the effect of the ligand ruthenium of CORM-2. RuCl3 contains the metal ruthenium as ligand and the non-metal chloride as substitute group, and the ligand ruthenium of CORM-2 itself may influence HO-1 expression. RuCl3 (10–20 µM) had no effect on HO-1 and IRG1 expression (Figure 2a), confirming the involvement of CO (but not ruthenium) in the effects of CORM-2. To further confirm the effects of CO, CO gas (250 ppm) was used. We found that treatment of CO gas significantly increased mRNA levels of HO-1 and IRG1 in a time dependent manner (Supplementary Figure 2a). Furthermore, to evaluate the role of CORM-2-induced HO-1 on IRG1 expression, the HO-1 inhibitor ZnPP was used. ZnPP treatment (10–20 µM) inhibited the expression of IRG1 mRNA (Figure 2b and Supplementary Figure 2b) and protein (Figure 2d and Supplementary Figure 2c) induced by CORM-2 in RAW264.7 cells with no significant effect on HO-1 mRNA (Figure 2c and Supplementary Figure 2b). In loss function experiment of HO-1 using HO-1 siRNA, we found that HO-1 gene silencing significantly inhibited CORM-2 induced protein (Figure 2e) and mRNA (Supplementary Figure 2d) levels of IRG1. This result suggests that CO-induced HO-1 activity may regulate IRG1 expression in macrophages. In support of this hypothesis, we found that the HO-1 inducing compounds CoPP and hemin (10 µM) induced IRG1 mRNA (Figure 2f and Supplementary Figure 2e) and protein (Figure 2g and Supplementary Figure 2f); whereas expression induced by these agents was significantly (P<0.01) inhibited by ZnPP treatment (20 µM). In addition, basal expression of IRG1 mRNA was significantly inhibited in the liver tissue from HO-1 KO mice (Supplementary Figure 2g). These data suggest that HO-1 is an upstream regulatory protein for IRG1 expression.

Figure 2.

Figure 2

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CORM-2 and CoPP/hemin-induced expression of IRG1 is dependent on HO-1 in RAW264.7 macrophages. (a) RAW264.7 cells were treated with CORM-2 (0, 5, 10 and 20 µM) or its negative control, RuCl3 (10 and 20 µM) for 8 h and the levels of IRG1 and HO-1 mRNA were detected by using RT-PCR analysis. (b–d) Cells were pre-treated with ZnPP (10 and 20 µM) for 0.5 h and treated with CORM-2 for 8 or 16 h. The levels of IRG1 (b) and HO-1 (c) mRNA were measured at 8 h by real-time RT-PCR and (d) IRG1 protein levels were determined at 16 h by western blot analysis. (e) Cells were transfected with HO-1 siRNA or control siRNA (Con siRNA). After treatment with 20 µM CORM-2 for 16 h, cells were harvested and protein levels of HO-1 and IRG1 were performed by western blotting. (f and g) Cells were pre-treated with ZnPP (20 µM) for 0.5 h and treated with CoPP (10 µM) and hemin (10 µM) for 8 or 16 h. (f) IRG1 mRNA was measured at 8 h by real-time RT-PCR and (g) IRG1 protein levels were determined at 16 h by western blot analysis. The representative bands or blots are shown. Data represent mean±s.e.m., * P<0.05 and ** P<0.001 as compared with control and ## P<0.001 as compared with the cells exposed to only CORM-2, hemin or CoPP.

NO increases IRG1 expression in a HO-1-dependent manner in macrophages

The free radical gas NO can exert a variety of physiological functions, including the promotion of cell survival during conditions of serum starvation and oxidative stress.24,25 Furthermore, NO is involved in HO-1 upregulation.26 To further elucidate the involvement of HO-1 in IRG1 regulation, we used the NO donor SNAP. Treatment of RAW264.7 cells with SNAP (0–40 µM) significantly increased both IRG1 and HO-1 expression (Supplementary Figure 3a and b). To further confirm the role of HO-1 in NO-dependent IRG1 expression, we pre-treated RAW264.7 cells with ZnPP (20 µM) and then incubated the cells with SNAP for 8 h or 16 h. ZnPP treatment significantly inhibited IRG1 mRNA and protein level induced by SNAP (Supplementary Figure 3c and d). These data further support the regulatory link between HO-1 and IRG1 in anti-inflammatory processes.

HO-1 regulates A20 in macrophages

The zinc-finger protein A20 (also known as TNFAIP3) is a key negative regulator of NF-κB signaling downstream of innate immune receptors such as tumors necrosis factor receptor and Toll-like receptors.27 Furthermore, IRG1 is known to promote endotoxin tolerance by increasing A20 expression.11 Therefore, we measured the effects of CO and HO-1 on A20 regulation. CORM-2 time-dependently increased A20 protein level beginning at 16 h (Figure 3a). Treatment of RAW264.7 macrophages with CORM-2 also increased A20 expression in a dose-dependent manner (Figure 3b and c). To evaluate the effect of CORM-2-induced HO-1 on A20 expression, we pre-treated RAW264.7 macrophages with ZnPP (20 µM), and the cells were incubated with CORM-2. Interestingly, ZnPP (20 µM) pre-treatment reduced A20 mRNA (Figure 3d) and protein (Figure 3e and Supplementary Figure 4a) expression in response to CORM-2 stimulation. In loss function experiment using HO-1 siRNA, we found that HO-1 gene silencing dramatically diminished CORM-2 induced protein levels of A20 (Figure 2f). In addition, to confirm the direct effect of HO-1 on A20 expression, macrophages were treated with hemin, which caused increased A20 expression (Figure 3g and 3h). ZnPP pre-treatment (20 µM), significantly decreased A20 protein level in response to hemin (Figure 3h and Supplementary Figure 4b), suggesting a role for HO-1 in A20 regulation.

Figure 3.

Figure 3

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CORM-2 and hemin increases A20 expression via HO-1 activation in RAW264.7 macrophages. (a) RAW264.7 cells were incubated with CORM-2 (20 µM) for 0, 2, 4, 8, 16 and 24 h, and western blot analysis was performed to detect A20 expression. (b and c) Cells were treated with CORM-2 (0, 5, 10, 20 and 40 µM) for 8 and 24 h and then, the levels of (b) A20 protein and (c) A20 mRNA were measured by western blot analysis and real-time RT-PCR analysis, respectively. (d and e) Cells were pre-treated with ZnPP (20 µM) for 0.5 h and further incubated with CORM-2 (10 and 20 µM) for 8 or 24 h. (d) The levels of A20 mRNA were analyzed at 8 h by real-time RT-PCR. (e) A20 protein level was carried out at 24 h by western blot analysis. (f) Cells were transfected with HO-1 siRNA or control siRNA (Con siRNA). Cells were treated with 20 µM CORM-2 for 24 h, and cells were harvested and protein levels of HO-1 and A20 were performed by western blotting. (g) Cells were treated with hemin at various doses for 8 h, and the levels of A20 mRNA were analyzed by real-time RT-PCR. (h) Cells were pre-treated with ZnPP (20 µM) for 0.5 h and hemin (10 and 20 µM) was treated for 24 h, and then A20 protein level was analyzed by western blot analysis. The representative bands or blots are shown. Data represent mean±s.e.m., ** P<0.001 as compared with control; and ## P<0.001 as compared with the cells exposed only to CORM-2, respectively.

CO and HO-1 mediated IRG1 expression decreases inflammation via A20 expression in macrophages

A20 is widely known to regulate inflammation and immunity, and confers cellular protection from TNF-α-induced cytotoxicity.28 RAW264.7 macrophages were pre-treated with CORM-2 or hemin in the presence of ZnPP and then stimulated with LPS for 24 h. CORM-2 or hemin treatment induced the upregulation of IRG1 and A20 protein (Figure 4b and f) and mRNA (Supplementary Figure 5) which were dramatically inhibited by ZnPP. Additionally, CORM-2 or hemin treatment significantly decreased LPS-induced TNF-α protein (Figure 4a and e) and mRNA (Supplementary Figure 5), and this effect was abrogated by ZnPP treatment. These results indicate a role of IRG1 and A20 expression induced by CO/HO-1 in the inhibition of inflammation. To confirm the function of IRG1 expression by CO/HO-1 in terms of inflammation regulation by A20, macrophages were transfected with IRG1 siRNA and treated with CORM-2 or hemin and stimulated with LPS. We found that CORM-2 or hemin-induced A20 expression was significantly downregulated whereas TNF-α mRNA was significantly increased by IRG1 siRNA transfection compared to control siRNA transfection (Figure 4c and g). Furthermore, when cells were transfected with A20 siRNA, we detected increased expression of TNF-α in LPS-stimulated cells while CORM-2 or hemin treatment did not reverse TNF-α production (Figure 4d and h). Based on these results, we conclude that CO and HO-1 mediates anti-inflammatory effects through the IRG1-A20 axis.

Figure 4.

Figure 4

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CORM-2/hemin-induced IRG1 decreases inflammation via A20 expression in RAW264.7 macrophages. (a and b) RAW264.7 cells were pre-treated with ZnPP (20 µM) for 0.5 h and then administrated with CORM-2 (20 µM) for 1 h and further incubated with LPS (100 ng/ml) for 24 h. (a) Cell supernatants were analyzed by ELISA to measure TNF-α. (b) Cell lysates were subjected western blot analysis for protein level of IRG1 and A20. (c) Cells were transiently transfected with IRG1 siRNA or control siRNA (Con siRNA). After treatment with CORM-2 (20 µM) for 1 h, the cells were stimulated with LPS (100 ng/ml) for 24 h, and the levels of TNF-α, A20 and IRG1 mRNA were analyzed by real-time RT-PCR. (d) Cells were transfected with A20 siRNA or control siRNA (Con siRNA). Following treatment with 20 µM CORM-2 for 1 h, the cells were stimulated with 100 ng/mL LPS for 24 h, the levels of TNF-α and A20 mRNA were analyzed by real-time RT-PCR. (e and f) Cells were pre-treated with ZnPP (20 µM) for 0.5 h and then administrated with hemin (10 µM) for 1 h and incubated with LPS (100 ng/mL) for 24 h. (e) Cell supernatants were subjected for ELISA to measure TNF-α. (f) Cell lysates were subjected to western blot analysis to determine the protein level of IRG1 and A20. (g) Cells were transfected with IRG1 siRNA or control siRNA (Con siRNA). After treatment with 10 µM hemin for 1 h, the cells were stimulated with 100 ng/ml LPS for 24 h, and the levels of TNF-α, A20 and IRG1 mRNA were analyzed by real-time RT-PCR. (h) Cells were transfected with A20 siRNA or control siRNA (Con siRNA). After treatment with 10 µM hemin for 1 h, the cells were stimulated with 100 ng/ml LPS for 24 h, and the levels of TNF-α and A20 mRNA were analyzed by real-time RT-PCR. Data represent mean±s.e.m., * P<0.05 and ** P<0.001 as compared with control; and # P<0.05, ## P<0.001 as compared with the cells exposed to only LPS (normal condition or IRG1/A20 siRNA, compared separately) and ns, non-significant as compared with only LPS (IRG siRNA or A20 siRNA).

CO and HO-1 inhibits inflammation via IRG1 and A20 expression in an in vivo mouse model

HO-1 was reported to improve animal survival in lethal endotoxemia.29,30 Furthermore, HO-1,18 IRG1 and A2011 were found to be expressed under conditions of endotoxin tolerance. We also demonstrated that IRG1 and A20 increased in endotoxin tolerance (Supplementary Figure 6b–d) where TNF-α was decreased (Supplementary Figure 6a, b and d). However, no reports have previously examined the effects of HO-1 in relation to the regulation of IRG1 and A20 expression in the septic mouse model. In our study, we investigated the effect of CO/HO-1-induced IRG1 and A20 expression on LPS-induced TNF-α production as an indicator of lethal endotoxemia. To examine the in vivo effects of CO on LPS-induced endotoxemia and expression of IRG1 and A20, mice were subjected to inhalation CO (250 ppm) for 4 h/day for 6 days in the absence or presence of ZnPP (5 mg/kg, i.p.) on a daily basis for 6 days and then LPS was injected (12.5 mg/kg, i.p.). At 16 h post LPS injection, CO inhalation significantly decreased LPS-induced TNF-α levels in blood serum (Figure 5a) and liver tissues (Figure 5b) of endotoxemic mice, which were reversed by ZnPP treatment. In addition, CO inhalation significantly increased IRG1 and A20 mRNA levels in liver tissues, which were reversed by ZnPP treatment (Figure 5c). Furthermore, to confirm the effects of CO and HO-1 on LPS-induced endotoxemia, we pre-treated mice with CORM-2 (30 mg/kg, i.p.), hemin (10 mg/kg, i.p.) and ZnPP (5 mg/kg, i.p.) for 2 h, and then the mice were administrated with LPS (12.5 mg/kg, i.p.) for 16 h. Interestingly, treatment with CORM-2 or hemin significantly increased the expression of HO-1, IRG1 and A20 mRNA (Figure 5f), and simultaneously decreased the levels of TNF-α protein (Figure 5d) and mRNA (Figrue 5e) in liver tissue and blood serum from LPS-induced endotoxemic mice. Therefore, the results from in vivo experiments suggest that CO and HO-1 mediate anti-inflammatory activities through IRG1 and A20 expression in the septic mice model.

Figure 5.

Figure 5

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Inhalation of CO gas and administration of CORM-2 and hemin increase IRG1 and A20 expression via HO-1 expression and decrease inflammation in a sepsis mouse model in vivo. (a–c) Wild-type 7-week-old male C57BL/6 mice were inhaled with CO gas (250 ppm) for 6 days (4 h daily basis) and some of them were administrated with ZnPP (5 mg/kg; i.p.). After 6 days, the mice were administrated with LPS (12.5 mg/kg; i.p.) for 16 h. (a) Blood serum was analyzed for the TNF-α level by ELISA. (b) Liver tissues were analyzed for the levels of TNF-α by real-time RT-PCR. (c) Liver tissues were analyzed for the levels of IRG1, A20 and HO-1 mRNA by real-time RT-PCR. (d–f) Wild-type 7-week-old male C57BL/6 mice were pre-treated with CORM-2 (30 mg/kg; i.p.), hemin (10 mg/kg; i.p.) and ZnPP (5 mg/kg; i.p.) for 2 h and, then, the mice were administrated with LPS (12.5 mg/kg; i.p.) for 16 h. (d) Blood serum was analyzed for the TNF-α level by ELISA. (e) Liver tissues were analyzed for the levels of TNF-α by real-time RT-PCR. (f) Liver tissues were analyzed for the levels of IRG1, A20 and HO-1 mRNA by real-time RT-PCR. Data represents mean±s.e.m., * P<0.05 and ** P<0.001 as compared with control; and # P<0.05 and ## P<0.001 as compared with the cells exposed to LPS+CO/CORM-2/hemin (in case TNF-α, ## P<0.001 as compared with the cells exposed to only LPS).

Discussion

Macrophages can exert pro- or anti-inflammatory functions depending on the type of stimuli.31 Anti-microbial activity has been observed in activated peripheral macrophages and microglial cells during inflammation.3 Previously, it has been reported that HO-1 induction through the PI3K/Akt/Nrf2 signaling pathway is associated with protection against oxidative stress.32,33 In murine cerebral endothelium, inhibition of NF-κB and COX2 by CoPP, a HO-1 inducing compound, suggests protective functions of HO-1.34 Mitochondrial injury is experimentally and clinically well recognized in sepsis.35 HO-1 activates mitochondrial biogenesis,36 and thus, may limit inflammatory damage and improve cell survival during bacterial sepsis.37

IRG1 is highly upregulated in murine macrophages and microglial cells under pro-inflammatory conditions.6 Furthermore, reduced antimicrobial activity was evident in IRG1-deficient macrophages during bacterial infection.38 IRG1 can regulate mitochondrial β-oxidation and mitochondrial ROS production.38 Mitochondrial localization of IRG16 is involved in mitochondrial ROS production which governs macrophage bactericidal activity,38 and altered production of pro-inflammatory cytokines.39 In addition, IRG1 exerts anti-microbial activity on pathogens through synthesizing itaconic acid.40 Thus, IRG1 plays a crucial role in macrophage function and inflammation.38 Interestingly, HO-1 and IRG1 are both expressed during LPS tolerance and provide protection against inflammation, suggesting a possible relationship between HO-1 and IRG1. IRG1 is highly expressed during inflammation and proven to have anti-inflammatory as well as anti-microbial activity in macrophages, yet the underlying molecular mechanisms have not yet been elucidated. In this study, we demonstrate that HO-1 mediates its anti-inflammatory effects through IRG1 expression under septic conditions.

To investigate a possible interaction between HO-1 and IRG1, we treated macrophages with ZnPP, a selective inhibitor of HO-1 activity.41 Inhibition of HO-1 activity resulted in the inhibition of IRG1 expression that was upregulated by treatment of macrophages with CORM-2 or HO-1 inducers. Our results suggest that the stimulatory effect of CORM-2, a CO donor, on IRG1 expression depends on the subsequent stimulation of HO activity, which generates CO and other end products. Thus, our results suggest a regulatory role for HO-1 activity in IRG1 expression. Furthermore, genetic deletion of HO-1 in mice resulted in significant reduction of IRG1 mRNA expression, confirming regulation of IRG1 by HO-1. The endogenous free radical gaseous mediator NO can also induce HO-1 expression in a variety of cells, including macrophages and vascular smooth muscle cells.26,42 To confirm HO-1 involvement in IRG1 expression, we used the NO donor SNAP. We found that IRG1 was significantly upregulated by SNAP, which was reversed by ZnPP-dependent inhibition of HO-1 activity, which further supports a regulatory role of HO-1 in IRG1 expression.

A20 was at first identified as a TNF-inducible gene in HUVECs.43 A20 protein can protect cells from TNF-α-induced cytotoxicity.28 The significance of A20 in downregulating NF-κB and inflammation was found in A20-knockdown mice that underwent severe and multiorgan inflammation and cachexia just after birth.44 Furthermore, TNF-α-induced apoptosis and NF-κB activation were inhibited by A20 over-expression.45 Thus, it is clear that A20 is involved in the inhibition of NF-κB signaling and inflammation. Recently, IRG1 has been reported to promote endotoxin tolerance by increasing A20 expression in macrophages through ROS production.11 Therefore, to examine the anti-inflammatory, interactive and mechanistic effects of both CO treatment and HO-1 induction on IRG1 and A20 expression, we treated macrophages with CORM-2 and hemin. Based on our observations that CORM-2 treatment and HO-1 induction by hemin significantly increased IRG1 and A20 expression, which were reversed by ZnPP, we conclude that the HO-1/CO system increases both IRG1 and A20 expression. These results prompted us to examine whether CO treatment and HO-1 induction would mediate anti-inflammatory effects via IRG1 and A20 expression. To support the anti-inflammatory effects of HO-1/CO -mediated IRG1 and A20, we incubated macrophages with CO or hemin in the absence and presence of ZnPP, followed by LPS stimulation. Interestingly, ZnPP significantly reversed HO-1/CO-mediated inhibition of TNF-α expression, along with a decrease in IRG1 and A20 expression. Our findings thus suggest that CO and HO-1 inhibit inflammation by increasing IRG1 and A20 expression. Furthermore our results were confirmed by observations that siRNA targeting IRG1 and A20 reversed the inhibitory effect of HO-1/CO on LPS-stimulated TNF-α production.

Sepsis, a systemic inflammatory response, results from excessive stimulation of the host immune system by pathogen components to produce various pro-inflammatory cytokines, and the excessive secretion of these cytokines cause systemic inflammation leading to the lethal multiple organ damage.46 In our study, we demonstrated that CO treatment and HO-1 induction significantly increased IRG1 and A20 expression and decreased TNF-α production in an LPS-stimulated sepsis mice model. In addition, the effect of CO/HO-1 on TNF-α production was significantly reversed with intraperitoneal administration of ZnPP, confirming a role for HO-1 activity.

In summary, we have identified that CO treatment with exogenous donor compounds and chemically induced HO-1 induction can regulate IRG1 and A20 expression, thereby inhibiting inflammation in vitro and in a mouse model of sepsis, as illustrated in Fig. 6. This study identifies a novel CO/HO-1/IRG1/A20 signaling pathway responsible for the inhibition of LPS-driven inflammation and potentially provides the rationale for novel therapeutic strategies for the treatment of inflammatory diseases.

Figure 6.

Figure 6

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Regulation of LPS-induced inflammation by CO in RAW264.7 macrophages and in mice. CO, in addition to HO-1 inducers including hemin, CoPP and NO, induces HO-1 expression that in turn induces IRG1 and A20 expression, thereby regulating LPS-induced inflammation.

Acknowledgments

This study was supported by the Bio & Medical Technology Development Program of the National Research Foundation (NRF) funded by the Ministry of Science, ICT & Future Planning (2012M3A9C3048687) and NRF-2014R1A6A1030318.

There is no conflict of interest.

Footnotes

Supplementary information accompanies the paper on Cellular & Molecular Immunology's website(http://www.nature.com/cmi/).

Supplementary Information

Supplementary information
Click here for additional data file. (515.3KB, pdf)

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