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Inhibitors of IFN gene stimulators (STING) improve intestinal ischemia–reperfusion-induced acute lung injury by activating AMPK signaling

European Journal of Medical Research volume 27, Article number: 79 (2022) Cite this article

Abstract

Background

Acute lung injury (ALI) caused by intestinal ischemia–reperfusion is a life-threatening disease. Interferon gene stimulator (STING) is a cytoplasmic DNA sensor that participates in the initiation of the inflammatory response. This study aims to establish whether C-176 (STING inhibitor) improves ALI under intestinal ischemia–reperfusion conditions.

Methods

To induce ALI, 72 male C57BL/6 mice were subjected to intestinal ischemia for 60 min and reperfusion for 3 h. Through intraperitoneal injection, C-176, a selective STING inhibitor, was injected 30 min before surgical treatment; meanwhile, compound C, an antagonist of adenosine monophosphate-activated protein kinase (AMPK), was administered 30 min after surgery. Based on immunofluorescence and Western blot assays, post-ALI assessments included lung water content (TLW), bronchoalveolar lavage fluid (BALF) protein, H&E staining, Masson staining, pulmonary pyroptosis [Gasdermin-D (GSDMD), cleaved caspase-1], and apoptosis (TUNEL, cleaved caspase-3).

Results

C-176 administration significantly attenuated intestinal ischemia–reperfusion-mediated ALI; this effect was reflected by exacerbated TLW and BALF protein, aggravated lung injury score, elevated degree of pulmonary fibrosis, increased TUNEL- and GSDMD-positive cells, and upregulated phospho-AMPK, cleaved caspase-1, cleaved caspase-3 and IFNβ mRNA expression. Moreover, C-176 increased phospho-AMPK under ALI conditions. Nonetheless, compound C partially reversed these beneficial effects.

Conclusion

C-176, a selective STING inhibitor, improves intestinal ischemia–reperfusion-mediated ALI, and its underlying mechanism may be associated with AMPK signal activation.

Introduction

Acute lung injury (ALI) is a severe respiratory disease causing high global mortality. It is characterized by dyspnea, interstitial edema, accumulation of activated inflammatory cells, mass migration of neutrophils, and diffuse alveolar damage [1, 2]. A growing body of recent evidence indicates that distant lung organ injuries, including abdominal ischemia–reperfusion, infection, and surgery, can cause ALI [3,4,5]. Moreover, reports indicate that the inflammatory response after intestinal ischemia–reperfusion injury promotes ALI [6]. To date, potential treatments or drugs against intestinal ischemia–reperfusion injury-induced ALI are unavailable in clinical therapy.

Interferon gene stimulator (STING) is an important mediator of the innate immune response; it detects double-stranded DNA (dsDNA) in the cytoplasm of immune cells, including DCs, T cells, and macrophages [7]. After catalyzing endogenous dsDNA leaking from mitochondria and exogenous dsDNA from pathogens by cyclic GMP-AMP synthase (cGAS), STING translocates from the endoplasmic reticulum to perinuclear microsomes via the Golgi apparatus [8]. Notably, STING activation controls mitochondrial DNA-mediated lung injury by evoking an inflammatory storm [9]. Several studies indicate that lipopolysaccharide (LPS)-induced ALI is associated with upregulation of STING expression [10, 11]. To date, limited studies have explored STING function in intestinal ischemia–reperfusion injury-induced ALI.

Although STING is essential in the process of ALI [12, 13], its downstream proteins remain underexplored. Notably, adenosine monophosphate-activated protein kinase (AMPK) promotes various anabolic and catabolic signals, hence maintaining suitable levels of adenosine triphosphate under energetic and/or cellular stress [14]. Interestingly, the STING–AMPK signal is implicated in high-fat diet-induced cardiac anomalies [15]. Moreover, compound C, which is annotated as a reversible inhibitor of AMPK, inhibits dsDNA-dependent type I interferon induction [16]. However, the role of STING–AMPK signaling in the ALI model should be further investigated.

This study hypothesizes that surgical intervention induces intestinal ischemia–reperfusion followed by ALI. Using a selective inhibitor of STING and an AMPK inhibitor, we aimed to determine the role of STING–AMPK signaling in the pathogenesis of ALI after intestinal ischemia–reperfusion injury.

Materials and methods

Adult male C57/BL mice (7–9 weeks old; weight, 27.1 ± 2.3 g) were purchased from Changsheng Biotechnology Co., Ltd. (Benxi, Liaoning, China). All the mice had free access to food and water; they were kept in a 12-h alternating light and dark facility at 25 °C ± 1 °C (humidity 50–70%). The tests involving animals were performed following the guidelines of the Animal Ethics Committee of Cangzhou Central Hospital.

Grouping and intestinal ischemia–reperfusion (IR)-induced ALI

In the first stage, animals were randomly grouped into five groups: sham (n = 24); intestinal ischemia–reperfusion (IR) + vehicle (n = 24); IR + C-176 (350 nmol, 4.7 mg/kg) (n = 18); IR + C-176 (550 nmol, 7.3 mg/kg) (n = 24) and IR + C-176 (750 nmol, 10 mg/kg) (n = 18). In the second stage, animals were randomly divided into two groups: IR + C176 + compound C (n = 12) and IR + C176 + Vehicle (n = 12).

Mice were anesthetized with pentobarbital (10 mg/kg) via intraperitoneal injection. An oral endotracheal tube for the mouse was established and then connected with a ventilator (model: volume-controlled; tidal volume: 8 mL/kg; frequency: 120 beats/min). Throughout the experiment, the animals were kept on a warm blanket to maintain their body temperature within 37–38 °C. Based on previous studies [17], the IR model was established as follows: (1) a lower midline laparotomy was performed; (2) the superior mesenteric artery was identified and occluded below the celiac trunk with an arterial microclamp, and intestinal ischemia was confirmed by the paleness of the jejunum and ileum; (3) the clamp was removed after 60 min; (4) 0.5 mL of sterile saline at 37 °C was injected into the peritoneal cavity; and (5) the incision was sutured and blocked using ropivacaine. In the first stage, a selective STING inhibitor, three dosages of C-176 (4.7 mg/kg, 7.3 mg/kg, and 10 mg/kg) (HY-112906, MedChemExpress, NJ, USA) were administered 30 min before surgical exposure via intraperitoneal injection. In the pd stage, a selective antagonist of AMPK, compound C (25 mg/kg) (HY-13418A, MedChemExpress), was administered via subcutaneous injection 30 min after initiation of IR. Both C-176 and compound C were dissolved with 10% DMSO (HY-Y0320, MedChemExpress) and 90% corn oil (HY-Y1888, MedChemExpress). The mice in the sham, IR + Vehicle, and IR + C176 + Vehicle groups were only administered solvent containing 10% DMSO and 90% corn oil using intraperitoneal or subcutaneous injection. Notably, the sham animals underwent a similar procedure without clamps (Fig. 1).

Fig. 1
figure 1

Experimental schematic diagram. Mice with intestinal ischemia–reperfusion injury (IR) and C-176 treatment. IR: mice received an occlusion of the superior mesenteric artery below the celiac trunk with an arterial microclamp for 60 min and reperfusion for 3 h. C-176: C-176 administered via intraperitoneal injection 30 min before surgical exposure. Compound C: compound C was administered via subcutaneous injection 30 min after the initiation of IR. Vehicle: 10% DMSO and 90% corn oil were administered via intraperitoneal or subcutaneous injection as a control. Sham: mice subjected to identical surgery and vehicle injection except for the occlusion of the superior mesenteric artery

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Assessment of lung injury

Three hours after reperfusion, mice (n = 6) were euthanized through cervical dislocation under 8% sevoflurane. The surface of the left lungs was wiped after rinsing with saline. The weight was recorded as wet weight (W). After drying at 70 °C for 24 h, the dry weight (D) was recorded. Total lung water content (TLW) was calculated using the equation TLW = (W − D)/D × 100%.

Mice (n = 6) were anesthetized under 3–4% sevoflurane and injected with 0.5 mL of normal saline via the trachea. Then, the liquid of bronchoalveolar lavage was gently aspirated, and bronchoalveolar lavage was performed twice. After centrifugation at 4000×g at 4 ℃ for 10 min, the supernatant from the lavage solution was obtained as bronchoalveolar lavage fluid (BALF). The content of BALF protein was measured using the BCA assay based on the manufacturers’ instructions (P0012, Beyotime, Shanghai, China).

Measurement of diamine oxidase (DAO) and IL-1β in serum

After 3 h of reperfusion, mice (n = 6) were anesthetized under 3–4% sevoflurane. Blood was collected from a ventriculus sinister. Then, the mice were perfused with cold saline via the ventriculus sinister–aorta until clear fluid flowed out from the right atrial appendage. Lung tissues were quickly kept on ice. The lung tissues for RNA and protein were removed and homogenized on ice. Based on DAO synthesized primarily in gastrointestinal mucosal cells, the integrity and functional mass of the intestinal mucosa can be reflected by the level of serum DAO [18]. IL-1β, a marker of the inflammatory response in the serum, was also used to validate the distant organ injury primarily caused by circulating mediators in blood. After centrifugation at 1200×g for 10 min, the serum from the blood sample was used to evaluate DAO and IL-1β levels. According to the manufacturer’s protocol, we detected the level of serum DAO via a chemical assay kit (Cat# A088-1-1, Nanjing Jiancheng Bioengineering Institute, Nanjing, China) with a spectrophotometer. The results were expressed as units per liter serum. Serum IL-1β levels were evaluated by ELISA according to the manufacturer's protocol (Cat# PI301, Beyotime).

Real-time PCR

Total RNA was extracted with a TRIeasy™ Plus Total RNA Kit (Cat# 19211ES60, Yeasen, China) according to the manufacturer's protocol. The extracted RNA (400 ng) was treated with DNase I and then reverse-transcribed into cDNA by a BeyoRT™ Q First Strand cDNA Synthesis Kit (Beyotime) according to the manufacturer’s protocol. Real-time PCR was performed using the Step One Real-Time PCR system (ABI). The expression levels of RNA were normalized to β-actin. The sequences of the primers used for real-time PCR were:

β-actin: 5′-TTTGCAGCTCCTTCGTTGC-3′ (F).

5′-TCGTCATCCATGGCGAACT-3′ (R).

IFNβ: 5′-CCAGCTCCAAGAAAGGACGA(F).

5′-CGCCCTGTAGGTGAGGTTGAT-3′ (R).

Hematoxylin and eosin (H&E) staining and Masson staining

Three hours after reperfusion, mice (n = 6) were anesthetized under 3–4% sevoflurane and perfused with cold saline via the ventriculus sinister–aorta. Mice were perfused with 10% paraformaldehyde after clear saline was released from the right auricle. After fixing with 10% paraformaldehyde for 48 h, the left lungs were cut into 5-μm paraffin coronal sections for hematoxylin and eosin (H&E) and Masson staining as previously published [19, 20]. The slides were observed under a light microscope (BX51; Olympus, Tokyo, Japan). Three fields (magnification,  × 200) in one slice (3 slices in one group) were randomly selected. Lung injury was analyzed by an experienced investigator blinded to the group and recorded as normal (0), mild (1), moderate (2), or severe (3) based on histological parameters, including alveolar edema, diffuse alveolar hemorrhage, congestion, and intra-alveolar infiltration of inflammatory cells. Additionally, the percentage of Masson-stained collagen was measured using ImageJ (1.37v, Wayne Rasband, available through the National Institutes of Health).

Immunofluorescence staining

The slices (thickness: 5 μm) mentioned above were used for immunofluorescence staining. After boiling with sodium citrate at 100 °C for 20 min, the cooled sections were incubated with 1% Triton X-100 for 20 min and blocked with QuickBlock™ Blocking Buffer (P0260, Beyotime) at 25 °C for 1 h. After washing with PBS three times, the sections were incubated overnight with rabbit anti-gasdermin-D (GSDMD) (K009328P, Solarbio, Beijing, China) at 4 °C. After rising with PBS, the slices were incubated with goat anti-rabbit secondary antibodies (P0208, Beyotime) at room temperature for 1 h, coated with anti-fluorescence quenching sealing solution with DAPI (P0131, Beyotime) for 5 min and sealed. Terminal deoxynucleotide transferase deoxyuridine triphosphate (dUTP) nick end labeling (TUNEL) (C1062, Beyotime) assays were performed according to the manufacturer’s protocol to detect pulmonary apoptosis. Six fields with a magnification of × 200 in 3 slices were randomly selected from each group. Under a fluorescence microscope (BX53, Olympus, Tokyo, Japan), the percentage of GSDMD-positive cells and TUNEL-positive cells was calculated using ImageJ (1.37v, Wayne Rasband, available through the National Institutes of Health).

Western blot

Total protein was extracted from lung tissue and quantified through the BCA assay. Each sample containing 40 μg of mixed loading buffer was boiled at 100 °C for 15 min. The sample was separated by 10% SDS-PAGE and transferred to a PVDF membrane. The membrane was incubated with QuickBlock™ blocking buffer (P0235, Beyotime) at 25 °C for 10 min and then rinsed with Western wash buffer (P0023C, Beyotime) for 5 min 3 times. Anti-rabbit p-AMPK (dilution: 1:500, ab133448, Abcam, Cambridge, UK), anti-rabbit AMPK (dilution: 1:1000, ab32047, Abcam, Cambridge, UK), anti-rabbit cleaved-caspase-1 (dilution: 1:500, ab179515, Abcam, Cambridge, UK), anti-rabbit cleaved-caspase-3 (dilution: 1:500, ab32351, Abcam, Cambridge, UK) and GAPDH (dilution 1:1000, K106389P, Solarbio) were used for overnight incubation of PVDF membranes at 4 ℃. After rising with Western washing buffer 3 times, the membranes were incubated with goat anti-rabbit secondary antibody (dilution 1:1000, A0562, Beyotime) at 25 ℃ for 1 h. After washing 3 times with Western washing buffer, protein bands were detected using BeyoECL Moon (P0018, Beyotime). The ratio between the gray value of the target protein and the GAPDH bands (internal reference) was calculated using ImageJ.

Statistical analysis

All results are expressed as the means ± standard deviation (SD). Statistical analysis was performed using Student’s t-test or one-way analysis of variance (ANOVA) with a Tukey post hoc test for multiple comparisons. Differences with P values of less than 0.05 (P < 0.05) were considered statistically significant.

Results

C-176 mitigates lung injury after intestinal ischemia–reperfusion injury

C-176 (a selective inhibitor of STING) was introduced to explore the potential role of STING in intestinal ischemia–reperfusion-induced ALI. Both TLW and BALF protein were used to measure pulmonary edema and exudation. Serum DAO and IL-1β were used to assess intestinal mucosa damage and circulation mediators, respectively. In addition, H&E and Masson staining were used to evaluate pulmonary structure damage and fibrosis, respectively. In contrast with the sham group, both the lung injury score (F4, 25 = 195.7, P < 0.0001; Fig. 2A, B) indicated by H&E staining and the percentage of collagen volume fraction (F4, 25 = 278.8, P < 0.0001; Fig. 2A, C) revealed by Masson staining were increased in the IR + vehicle group. Similarly, TLW (F4, 25 = 215.9, P < 0.0001; Fig. 2D), BALF protein (F4, 25 = 523.3, P < 0.0001; Fig. 2E) were significantly increased in the IR + vehicle group, and serum DAO contents (F4, 25 = 123.5, P < 0.0001; Fig. 2F) and IL-1β levels (F4, 25 = 54.83, P < 0.0001; Fig. 2G) were increased in the IR + vehicle group. Nonetheless, pathological score, the percentage of collagen volume fraction, TLW, BALF protein, serum DAO contents, and IL-1β levels were significantly decreased with increasing doses of C-176 (Fig. 2B–G). No remarkable difference in the index mentioned above was noted between the mice exposed to intestinal ischemia–reperfusion injury with 550 nmol and 750 nmol. Thus, 550 nmol of C-176 was applied in the follow-up study.

Fig. 2
figure 2

Pathological effects of STING on lung injury induced by IR. A Representative photomicrographs of H&E- and Masson trichrome-stained sections. Scale bar = 50 μm. Arrows indicate lung injury and lung collagen, respectively. B Lung injury score and C the percentage of lung collagen content caused by the indicated stimuli 3 h after IR. D Total lung water content (TLW); E content of bronchoalveolar lavage fluid (BALF) protein; F diamine oxidase (DAO) content in serum; and G IL-1β levels in the serum caused by the indicated stimuli 3 h after IR. Data are presented as the mean ± SD (n = 6). Sham, IR, C-176, and vehicle are described above. ****P < 0.0001, ***P < 0.001, **P < 0.01, *P < 0.05

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C-176 mitigates pulmonary pyroptosis and apoptosis induced by intestinal ischemia–reperfusion injury

Immunofluorescence assays for GDSMD (pyroptosis) and TUNEL (apoptosis) were used to evaluate the effects of STING on pulmonary pyroptosis and apoptosis induced by intestinal ischemia–reperfusion injury. As a pyroptosis execution protein, GSDMD is usually used to explore the classical pyroptosis activated by cleaved caspase-1 [21]. During the late stages of apoptosis, DNA degradation in the nuclei can be detected by the TUNEL assay [22]. Immunofluorescence showed an increased number of GSDMD-positive (F2, 15 = 162.4, P < 0.0001; Fig. 3A, B) and TUNEL-positive (F2, 15 = 217.1, P < 0.0001; Fig. 3C, D) cells in the IR + Vehicle group compared to the sham group. Nonetheless, unlike the IR + Vehicle group, both GSDMD-positive cells (F2, 15 = 217.1, P < 0.0001; Fig. 3A, B) and TUNEL (F2, 15 = 162.4, P < 0.0001; Fig. 3C, D) were significantly decreased in the IR + C-176 group. Western blot results showed that the expression levels of the apoptosis-associated factor cleaved caspase-3 (F2, 15 = 1082, P < 0.0001; Fig. 4A, B) and the pyroptosis-associated factor cleaved caspase-1 (F2, 15 = 148.3, P < 0.0001; Fig. 4A, C) were significantly upregulated in the IR + vehicle group compared to the sham group; on the other hand, C-176 partially reversed this upregulation in the IR + C-176 group (F2, 15 = 1082, P < 0.0001 for cleaved caspase-3; F2, 15 = 148.3, P < 0.0001 for cleaved caspase-1; Fig. 4A–C). Additionally, our data also showed that IFNβ mRNA expression was heavily elevated in the IR + Vehicle group compared to that in the sham group, while C-176 partially reversed this elevation in the IR + C-176 group (F2, 15 = 239.5, P < 0.0001; Fig. 4D). The above results indicate that the STING inhibitor C-176 mitigates pyroptosis, apoptosis and IFNβ expression in the lung after intestinal ischemia–reperfusion injury.

Fig. 3
figure 3

C-176 mitigates pulmonary apoptosis and pyroptosis in mice exposed to IR. A Representative photomicrographs of GSDMD-positive cells; C TUNEL-positive cells in the lung; B the number of GSDMD-positive cells; and D the percentage of TUNEL-positive cells in the lung caused by the indicated stimuli 3 h after IR. Scale bar = 50 μm. Arrows indicate GSDMD- and TUNEL-positive cells. Data are presented as the mean ± SD (n = 6). Sham, IR, C-176, and vehicle are described above. ****P < 0.0001, ***P < 0.001, **P < 0.01

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Fig. 4
figure 4

C-176 mitigates pulmonary pyroptosis- and apoptosis-associated factors in mice exposed to IR. A Representative Western blot of cleaved caspase-1 (a marker for pyroptosis) and cleaved caspase-3 (a marker for apoptosis) in the lung caused by the indicated stimuli; B the ratio between the optical density value of cleaved caspase-1 and GAPDH in the lung, as evaluated by Western blot; C the ratio between the optical density value of cleaved caspase-3 and GAPDH in the lung, as evaluated by Western blot. D The expression of IFNβ mRNA in the lung caused by the indicated stimuli. Sham, IR, C-176, and vehicle are described above. ****P < 0.0001

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AMPK signal is involved in the protective effects of C-176 against lung injury induced by intestinal ischemia–reperfusion injury

AMPK signaling is a downstream factor of STING in several processes of inflammatory injury [23, 24]. The ratio of phospho-AMPK to total AMPK was slightly increased in mice exposed to IR compared to those under sham treatment (IR + Vehicle vs. sham, F2, 15 = 348.6, P < 0.0001; Fig. 5A, B). Interestingly, the ratio of phospho-AMPK to total AMPK was further upregulated in mice exposed to IR plus C-176 treatment compared to those exposed to IR plus vehicle (IR + C-176 vs. IR + Vehicle, F2, 15 = 348.6, P < 0.0001; Fig. 5A, B). These findings show that AMPK signaling may regulate the protective effects of C-176 against lung injury induced by IR.

Fig. 5
figure 5

C-176 upregulated phospho-AMPK expression in mice exposed to IR. A Representative Western blot of phospho-AMPK and total AMPK in the lung caused by the indicated stimuli; B the ratio between the optical density value of phospho-AMPK and total AMPK in the lung, as evaluated by Western blot. Sham, IR, C-176, and vehicle are described above. ****P < 0.0001

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Compound C, an AMPK inhibitor, reversed the protective effect of C-176 on ALI

Compound C (a selective inhibitor of AMPK) was introduced to further detect the role of STING–AMPK signaling in lung injury induced by intestinal ischemia–reperfusion injury. Unlike the IR + C-176 + vehicle group, mice in the IR + C-176 + compound C group showed a significant increase in TLW (t = 10.85, P < 0.0001; Fig. 6A); an elevation of BALF protein content (t = 11.86, P < 0.0001; Fig. 6B); an aggravation of lung injury score (t = 6.167, P < 0.001; Fig. 6C, D); an upregulation in the percentage of collagen volume (t = 6.005, P < 0.001; Fig. 6C, E); an increase in serum DAO content (t = 15.56, P < 0.0001; Fig. 6F); and an elevation of IL-1β in serum (t = 9.926, P < 0.0001; Fig. 6G). Additionally, GSDMD- and TUNEL-positive cells in the lung were both increased in the IR + C-176 + compound C group relative to the IR + C-176 + vehicle group (t = 3.543, P < 0.01 for GSDMD; t = 5.478, P < 0.001 for TUNEL; Fig. 7A–D). Based on the Western blot results, compound C significantly decreased the ratio of phospho-AMPK/total AMPK in the IR + C-176 + compound C group relative to the IR + C-176 + vehicle group (t = 11.52, P < 0.0001; Fig. 7E, F). Moreover, the mRNA expression levels of the pyroptosis-associated factor cleaved caspase-1 (t = 8.959, P < 0.0001; Fig. 7E, G), apoptosis-associated factor cleaved caspase-3 (t = 6.078, P < 0.001; Fig. 7E, H), and IFNβ (t = 4.814, P < 0.001; Fig. 7I) were significantly upregulated in the IR + Vehicle group compared to the sham group.

Fig. 6
figure 6

Compound C reverses the protective effects against ALI in mice exposed to IR. A Total lung water content (TLW). B Content of BALF protein caused by the indicated stimuli 3 h after IR. C Representative photomicrographs of H&E and Masson trichrome-stained sections. Scale bar = 50 μm; arrows indicate lung injury and lung collagen, respectively. D Lung injury score; E the percentage of lung collagen content; F diamine oxidase (DAO) content in serum; and G IL-1β levels in the serum caused by the indicated stimuli 3 h after IR. Data are presented as the mean ± SD (n = 6). IR, C-176, compound C and vehicle are described above. ****P < 0.0001, ***P < 0.001

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Fig. 7
figure 7

Compound C reverses the anti-pyroptotic and anti-apoptotic effects of C-176 against ALI in mice exposed to IR. A Representative photomicrographs of GSDMD-positive cells and C TUNEL-positive cells in the lung. B The number of GSDMD-positive cells and D the percentage of TUNEL-positive cells in the lung caused by the indicated stimuli 3 h after IR. Scale bar = 50 μm. E Representative Western blot of phospho-AMPK, total AMPK, cleaved caspase-1 and cleaved caspase-3 in the lung caused by the indicated stimuli. F The ratio between the optical density value of phospho-AMPK and total AMPK in the lung, as evaluated by Western blot. G The ratio between the optical density value of cleaved caspase-1 and GAPDH in the lung, as evaluated by Western blot; H the ratio between the optical density value of cleaved caspase-3 and GAPDH in the lung, as evaluated by Western blot. I The expression of IFNβ mRNA in the lung caused by the indicated stimuli. Data are presented as the mean ± SD (n = 6). Sham, IR, C-176, and vehicle are described above. ****P < 0.0001, ***P < 0.001, **P < 0.01

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Discussion

The present report details STING–AMPK signaling in the pathological process of ALI after intestinal ischemia–reperfusion injury. The main findings included the following: (1) the STING C-176 inhibitor significantly reduced lung injury and pulmonary fibrosis after intestinal ischemia–reperfusion injury; (2) the STING C-176 inhibitor significantly ameliorated pulmonary apoptosis and pyroptosis; and (3) the protective effects of C-176 against ALI after intestinal ischemia–reperfusion injury may be associated with STING–AMPK signaling.

Endogenous toxins released from intestinal bacteria can shift to the circulatory system after intestinal ischemia–reperfusion injury, resulting in systemic inflammation, including lung injury [25]. In addition to endogenous toxins, inflammatory factors, including IL-1 and IL-6, produced during ischemia enter the circulatory system [26]. In the current study, we showed that serum DAO and IL-1β were significantly increased after reperfusion, which indicates that circulation mediators were released from intestinal tissue. Relevant studies revealed that distant lung injury occurs during the process of reperfusion after intestinal ischemia; however, the mechanism of lung injury after intestinal ischemia–reperfusion injury remains unclear [27, 28]. The data showed that lung injury indicated by TLW, BALF protein content, pathological score, and collagen volume fraction were significantly aggravated after intestinal ischemia–reperfusion injury. This implies that this rodent model of intestinal ischemia–reperfusion injury potentially triggers distant lung injury, which can destroy the alveolar membrane.

The formation and activation of the inflammasome are facilitated by the cGAS–STING pathway, subsequently causing pyroptosis and apoptosis [29, 30]. Recent studies have reported that the inflammasome response after bacterial and viral infections is ameliorated by inhibiting the cGAS–STING–NLRP3 axis in human myeloid cells [10]. Benmerzoug et al. reported that STING-mediated self-dsDNA sensing regulates the process of silica-induced lung inflammation [31]. The cGAS–STING–NLRP3 axis in the cytoplasm is a potential therapeutic target against ALI [32]. C-176, which is different from another inhibitor of STING, such as C-178 binding to Cys91, can block palmitoylation induced by STING activation [8]. STING assembly into polymer complexes in the Golgi apparatus is inhibited, subsequently blocking downstream signal transduction [33]. C-176, an effective STING covalent inhibitor, has been suggested to inhibit the activation of the STING downstream pathway and exert a robust anti‐inflammatory effect in previous studies [16, 34]. Interestingly, STING inhibition through a selective inhibitor (C-176) significantly attenuated pulmonary inflammation and fibrosis in mice induced by graphitized multiwalled carbon nanotubes [35]. As previously described, ALI is suggested to be induced by intestinal ischemia–reperfusion injury within 3 h after reperfusion [36, 37]. Mitochondrial injury-induced activation of inflammatory factors and calcium overload can reportedly contribute to cleavages of the caspase family, including caspase-1 and caspase-3, at the early stage of reperfusion, which are indicators of pyroptosis and apoptosis [38, 39]. We showed that C-176 effectively reduced pulmonary pyroptosis and apoptosis caused by intestinal ischemia–reperfusion injury and mitigated ALI at 3 h after reperfusion. Considering the role of C-176, our results confirm the activation of STING signaling in ALI after intestinal ischemia–reperfusion injury.

A recent publication reported that the STING–TBK1 complex inhibits phosphorylation of AMPK, thereby enhancing the inflammatory response in vivo and in vitro [40]. There is overwhelming evidence that STING can downregulate AMPK phosphorylation, but pharmacological inhibition of STING alleviates inflammatory injury via phosphorylated AMPK-related anti-inflammatory signaling [16]. Additionally, AMPK/SIRT1 activation protects ALI induced by LPS by inhibiting pulmonary apoptosis, as indicated by a reduction in cleaved caspase-3 [41]. Endotoxin-induced ALI correlates with pyroptosis via the AMPK/NLRC4 pathways [42]. Moreover, it was suggested that activation of AMPK phosphorylation ameliorates the alleviation of caspase-1-associated pyroptosis in in vivo and in vitro models of diabetic cardiomyopathy [43]. Notably, caspase-1-associated pyroptosis and caspase-3-associated apoptosis can reportedly contribute to the process of ALI after intestinal ischemia–reperfusion injury [6, 17]. We found a slight increase in AMPK phosphorylation, as indicated by the ratio of phosphorylated AMPK to total AMPK, in pulmonary tissue after intestinal ischemia–reperfusion injury; however, C-176 further increased phospho-AMPK. Intriguingly, compound C, an inhibitor of AMPK phosphorylation, significantly decreased phospho-AMPK, partially eliminating the protective effects of C-176. These data indicate that STING–AMPK signaling is implicated in the process of ALI after intestinal ischemia–reperfusion injury.

In conclusion, we evaluated the role of STING–AMPK signaling in the pathophysiological process after ALI induced by intestinal ischemia–reperfusion injury. The findings support the fact that STING–AMPK signaling is a potentially novel therapeutic approach for the treatment of intestinal ischemia–reperfusion injury-induced ALI.

Availability of data and materials

All datasets generated for this study are included in the article. The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.

References

  1. Butt Y, Kurdowska A, Allen TC. Acute lung injury: a clinical and molecular review. Arch Pathol Lab Med. 2016;140(4):345–50.

    Article  CAS  Google Scholar 

  2. Hughes KT, Beasley MB. Pulmonary manifestations of acute lung injury: more than just diffuse alveolar damage. Arch Pathol Lab Med. 2017;141(7):916–22.

    Article  Google Scholar 

  3. Li Y, Cao Y, Xiao J, Shang J, Tan Q, Ping F, Huang W, Wu F, Zhang H, Zhang X. Inhibitor of apoptosis-stimulating protein of p53 inhibits ferroptosis and alleviates intestinal ischemia/reperfusion-induced acute lung injury. Cell Death Differ. 2020;27(9):2635–50.

    Article  CAS  Google Scholar 

  4. Islam D, Huang Y, Fanelli V, Delsedime L, Wu S, Khang J, Han B, Grassi A, Li M, Xu Y, et al. Identification and modulation of microenvironment is crucial for effective mesenchymal stromal cell therapy in acute lung injury. Am J Respir Crit Care Med. 2019;199(10):1214–24.

    Article  CAS  Google Scholar 

  5. Deshpande R, Zou C. Pseudomonas aeruginosa induced cell death in acute lung injury and acute respiratory distress syndrome. Int J Mol Sci. 2020. https://doi.org/10.3390/ijms21155356.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Tan Y, Zuo W, Huang L, Zhou B, Liang H, Zheng S, Jia W, Chen S, Liu J, Yang X, et al. Nervilifordin F alleviates intestinal ischemia/reperfusion-induced acute lung injury via inhibiting inflammasome and mTOR pathway. Int Immunopharmacol. 2020;89(Pt A): 107014.

    Article  CAS  Google Scholar 

  7. Wu J, Dobbs N, Yang K, Yan N. Interferon-independent activities of mammalian STING mediate antiviral response and tumor immune evasion. Immunity. 2020;53(1):115-126.e115.

    Article  CAS  Google Scholar 

  8. Haag SM, Gulen MF, Reymond L, Gibelin A, Abrami L, Decout A, Heymann M, van der Goot FG, Turcatti G, Behrendt R, et al. Targeting STING with covalent small-molecule inhibitors. Nature. 2018;559(7713):269–73.

    Article  CAS  Google Scholar 

  9. Liu Q, Wu J, Zhang X, Li X, Wu X, Zhao Y, Ren J. Circulating mitochondrial DNA-triggered autophagy dysfunction via STING underlies sepsis-related acute lung injury. Cell Death Dis. 2021;12(7):673.

    Article  Google Scholar 

  10. Ning L, Wei W, Wenyang J, Rui X, Qing G. Cytosolic DNA-STING-NLRP3 axis is involved in murine acute lung injury induced by lipopolysaccharide. Clin Transl Med. 2020;10(7): e228.

    Article  Google Scholar 

  11. Comish PB, Liu MM, Huebinger R, Carlson D, Kang R, Tang D. The cGAS-STING pathway connects mitochondrial damage to inflammation in burn-induced acute lung injury in rat. Burns. 2021. https://doi.org/10.1016/j.burns.2021.04.007.

    Article  PubMed  Google Scholar 

  12. Balka KR, Louis C, Saunders TL, Smith AM, Calleja DJ, D’Silva DB, Moghaddas F, Tailler M, Lawlor KE, Zhan Y, et al. TBK1 and IKKε act redundantly to mediate STING-induced NF-κB responses in myeloid cells. Cell Rep. 2020;31(1): 107492.

    Article  CAS  Google Scholar 

  13. Balka KR, De Nardo D. Molecular and spatial mechanisms governing STING signalling. FEBS J. 2021;288(19):5504–29.

    Article  CAS  Google Scholar 

  14. Carling D. AMPK signalling in health and disease. Curr Opin Cell Biol. 2017;45:31–7.

    Article  CAS  Google Scholar 

  15. Gong Y, Li G, Tao J, Wu NN, Kandadi MR, Bi Y, Wang S, Pei Z, Ren J. Double knockout of Akt2 and AMPK accentuates high fat diet-induced cardiac anomalies through a cGAS-STING-mediated mechanism. Biochim Biophys Acta Mol Basis Dis. 2020;1866(10): 165855.

    Article  CAS  Google Scholar 

  16. Peng Y, Zhuang J, Ying G, Zeng H, Zhou H, Cao Y, Chen H, Xu C, Fu X, Xu H, et al. Stimulator of IFN genes mediates neuroinflammatory injury by suppressing AMPK signal in experimental subarachnoid hemorrhage. J Neuroinflammation. 2020;17(1):165.

    Article  CAS  Google Scholar 

  17. Kim JH, Kim J, Chun J, Lee C, Im JP, Kim JS. Role of iRhom2 in intestinal ischemia-reperfusion-mediated acute lung injury. Sci Rep. 2018;8(1):3797.

    Article  Google Scholar 

  18. Zhang XY, Liu ZM, Wen SH, Li YS, Li Y, Yao X, Huang WQ, Liu KX. Dexmedetomidine administration before, but not after, ischemia attenuates intestinal injury induced by intestinal ischemia-reperfusion in rats. Anesthesiology. 2012;116(5):1035–46.

    Article  CAS  Google Scholar 

  19. Tang J, Xu L, Zeng Y, Gong F. Effect of gut microbiota on LPS-induced acute lung injury by regulating the TLR4/NF-kB signaling pathway. Int Immunopharmacol. 2021;91: 107272.

    Article  CAS  Google Scholar 

  20. Song C, He L, Zhang J, Ma H, Yuan X, Hu G, Tao L, Zhang J, Meng J. Fluorofenidone attenuates pulmonary inflammation and fibrosis via inhibiting the activation of NALP3 inflammasome and IL-1β/IL-1R1/MyD88/NF-κB pathway. J Cell Mol Med. 2016;20(11):2064–77.

    Article  CAS  Google Scholar 

  21. Karmakar M, Minns M, Greenberg EN, Diaz-Aponte J, Pestonjamasp K, Johnson JL, Rathkey JK, Abbott DW, Wang K, Shao F, et al. N-GSDMD trafficking to neutrophil organelles facilitates IL-1β release independently of plasma membrane pores and pyroptosis. Nat Commun. 2020;11(1):2212.

    Article  CAS  Google Scholar 

  22. Kyrylkova K, Kyryachenko S, Leid M, Kioussi C. Detection of apoptosis by TUNEL assay. Methods Mol Biol. 2012;887:41–7.

    Article  CAS  Google Scholar 

  23. Peng Y, Zhuang J, Ying G, Zeng H, Zhou H, Cao Y, Chen H, Xu C, Fu X, Xu H. Stimulator of IFN genes mediates neuroinflammatory injury by suppressing AMPK signal in experimental subarachnoid hemorrhage. J Neuroinflammation. 2020. https://doi.org/10.1186/s12974-020-01830-4.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Prantner D, Perkins DJ, Vogel SN. AMP-activated kinase (AMPK) promotes innate immunity and antiviral defense through modulation of stimulator of interferon genes (STING) signaling. J Biol Chem. 2016. https://doi.org/10.1074/jbc.M116.763268.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Qian J, Li G, Jin X, Ma C, Cai W, Jiang N, Zheng J. Emodin protects against intestinal and lung injury induced by acute intestinal injury by modulating SP-A and TLR4/NF-κB pathway. Biosci Rep. 2020. https://doi.org/10.1042/BSR20201605.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Yuan B, Xiong LL, Wen MD, Zhang P, Ma HY, Wang TH, Zhang YH. Interleukin-6 RNA knockdown ameliorates acute lung injury induced by intestinal ischemia reperfusion in rats by upregulating interleukin-10 expression. Mol Med Rep. 2017;16(3):2529–37.

    Article  CAS  Google Scholar 

  27. Wu D, Wang J, Li H, Xue M, Ji A, Li Y. Role of hydrogen sulfide in ischemia-reperfusion injury. Oxid Med Cell Longev. 2015;2015: 186908.

    PubMed  PubMed Central  Google Scholar 

  28. Jin C, Chen J, Gu J, Zhang W. Gut-lymph-lung pathway mediates sepsis-induced acute lung injury. Chin Med J. 2020;133(18):2212–8.

    Article  Google Scholar 

  29. Gaidt MM, Ebert TS, Chauhan D, Ramshorn K, Pinci F, Zuber S, O’Duill F, Schmid-Burgk JL, Hoss F, Buhmann R, et al. The DNA inflammasome in human myeloid cells is initiated by a STING-cell death program upstream of NLRP3. Cell. 2017;171(5):1110-1124.e1118.

    Article  CAS  Google Scholar 

  30. McArthur K, Whitehead LW, Heddleston JM, Li L, Padman BS, Oorschot V, Geoghegan ND, Chappaz S, Davidson S, San Chin H, et al. BAK/BAX macropores facilitate mitochondrial herniation and mtDNA efflux during apoptosis. Science. 2018. https://doi.org/10.1126/science.aao6047.

    Article  PubMed  Google Scholar 

  31. Benmerzoug S, Rose S, Bounab B, Gosset D, Duneau L, Chenuet P, Mollet L, Le Bert M, Lambers C, Geleff S, et al. STING-dependent sensing of self-DNA drives silica-induced lung inflammation. Nat Commun. 2018;9(1):5226.

    Article  CAS  Google Scholar 

  32. Wang W, Hu D, Wu C, Feng Y, Li A, Liu W, Wang Y, Chen K, Tian M, Xiao F, et al. STING promotes NLRP3 localization in ER and facilitates NLRP3 deubiquitination to activate the inflammasome upon HSV-1 infection. PLoS Pathog. 2020;16(3): e1008335.

    Article  CAS  Google Scholar 

  33. Xiaohong L, Zhenting Z, Yunjie Y, Wei C, Xiangjin X, Kun X, Xin L, Lu L, Jun L, Pin C. Activation of the STING-IRF3 pathway involved in psoriasis with diabetes mellitus. J Cell Mol Med. 2022;26(8):2139–51.

    Article  Google Scholar 

  34. Pham PT, Fukuda D, Nishimoto S, Kim-Kaneyama JR, Lei XF, Takahashi Y, Sato T, Tanaka K, Suto K, Kawabata Y, et al. STING, a cytosolic DNA sensor, plays a critical role in atherogenesis: a link between innate immunity and chronic inflammation caused by lifestyle-related diseases. Eur Heart J. 2021;42(42):4336–48.

    Article  CAS  Google Scholar 

  35. Han B, Wang X, Wu P, Jiang H, Yang Q, Li S, Li J, Zhang Z. Pulmonary inflammatory and fibrogenic response induced by graphitized multi-walled carbon nanotube involved in cGAS-STING signaling pathway. J Hazard Mater. 2021;417: 125984.

    Article  CAS  Google Scholar 

  36. Dong H, Qiang Z, Chai D, Peng J, Xia Y, Hu R, Jiang H. Nrf2 inhibits ferroptosis and protects against acute lung injury due to intestinal ischemia reperfusion via regulating SLC7A11 and HO-1. Aging. 2020;12(13):12943–59.

    Article  CAS  Google Scholar 

  37. Chen Y, Bian W, Xu B. Pretreatment with dexmedetomidine alleviates lung injury in a rat model of intestinal ischemia reperfusion. Mol Med Rep. 2020;21(3):1233–41.

    CAS  PubMed  PubMed Central  Google Scholar 

  38. Namura S, Zhu J, Fink K, Endres M, Srinivasan A, Tomaselli KJ, Yuan J, Moskowitz MA. Activation and cleavage of caspase-3 in apoptosis induced by experimental cerebral ischemia. J Neurosci. 1998;18(10):3659–68.

    Article  CAS  Google Scholar 

  39. Zheng GY, Zhang C, Li ZG. Early activation of caspase-1 after retinal ischemia and reperfusion injury in mice. Chin Med J. 2004;117(5):717–21.

    CAS  PubMed  Google Scholar 

  40. Konno H, Konno K, Barber GN. Cyclic dinucleotides trigger ULK1 (ATG1) phosphorylation of STING to prevent sustained innate immune signaling. Cell. 2013;155(3):688–98.

    Article  CAS  Google Scholar 

  41. Li X, Jamal M, Guo P, Jin Z, Zheng F, Song X, Zhan J, Wu H. Irisin alleviates pulmonary epithelial barrier dysfunction in sepsis-induced acute lung injury via activation of AMPK/SIRT1 pathways. Biomed Pharmacother. 2019;118: 109363.

    Article  CAS  Google Scholar 

  42. He Y, Xu K, Wang Y, Chao X, Xu B, Wu J, Shen J, Ren W, Hu Y. AMPK as a potential pharmacological target for alleviating LPS-induced acute lung injury partly via NLRC4 inflammasome pathway inhibition. Exp Gerontol. 2019;125: 110661.

    Article  CAS  Google Scholar 

  43. Yang F, Qin Y, Wang Y, Meng S, Xian H, Che H, Lv J, Li Y, Yu Y, Bai Y, et al. Metformin inhibits the nlrp3 inflammasome via AMPK/mTOR-dependent effects in diabetic cardiomyopathy. Int J Biol Sci. 2019;15(5):1010–9.

    Article  CAS  Google Scholar 

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Acknowledgements

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Funding

The present study was supported by the Science and Technology Plan of Cangzhou (Grant No. 1213056ZD).

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Authors and Affiliations

  1. Department of Gerontology, Cangzhou Central Hospital, Hebei Medical University, No. 16, Xinhua West Road, Cangzhou, China

    Mei Yang, Yu-Xia Ma, Ying Zhi, Hai-Bin Wang, Li Zhao, Peng-Sheng Wang & Jie-Ting Niu

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  1. Mei Yang
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Contributions

MY and JTN performed the study and drafted the manuscript; YXM, HBW, LZ and YZ helped to design the study and acquire the data; MY and PSW performed the statistical analyses; JTN conceived the study and revised the manuscript. All authors have read and approved the final manuscript.

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Correspondence to Mei Yang.

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All animal testing was conducted in accordance with the National Institutes of Health Guidelines for the Care and Use of Laboratory Animals and approved by the Animal Review Board of Cangzhou Central Hospital.

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Yang, M., Ma, YX., Zhi, Y. et al. Inhibitors of IFN gene stimulators (STING) improve intestinal ischemia–reperfusion-induced acute lung injury by activating AMPK signaling. Eur J Med Res 27, 79 (2022). https://doi.org/10.1186/s40001-022-00703-1

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European Journal of Medical Research

ISSN: 2047-783X

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