Abstract
Background
Inhalation of dust containing silica particles is associated with severe pulmonary inflammation and lung injury leading to chronic silicosis including fibrotic remodeling of the lung. Silicosis represents a major global health problem causing more than 45.000 deaths per year. The inflammasome-caspase-1 pathway contributes to the development of silica-induced inflammation and fibrosis via IL-1β and IL-18 production. Recent studies indicate that tetracycline can be used to treat inflammatory diseases mediated by IL-1β and IL-18. Therefore, we hypothesized that tetracycline reduces silica-induced lung injury and lung fibrosis resulting from chronic silicosis via limiting IL-1β and IL-18 driven inflammation.
Methods
To investigate whether tetracycline is a therapeutic option to block inflammasome-caspase-1 driven inflammation in silicosis, we incubated macrophages with silica alone or combined with tetracycline. The in vivo effect of tetracycline was determined after intratracheal administration of silica into the mouse lung.
Results
Tetracycline selectively blocks IL-1β production and pyroptotic cell death via inhibition of caspase-1 in macrophages exposed to silica particles. Consistent, treatment of silica-instilled mice with tetracycline significantly reduced pulmonary caspase-1 activation as well as IL-1β and IL-18 production, thereby ameliorating pulmonary inflammation and lung injury. Furthermore, prolonged tetracycline administration in a model of chronic silicosis reduced lung damage and fibrotic remodeling.
Conclusions
These findings suggest that tetracycline inhibits caspase-1-dependent production of IL-1β in response to silica in vitro and in vivo. The results were consistent with tetracycline reducing silica-induced pulmonary inflammation and chronic silicosis in terms of lung injury and fibrosis. Thus, tetracycline could be effective in the treatment of patients with silicosis as well as other diseases involving silicotic inflammation.
Similar content being viewed by others
Background
Silicosis is a pulmonary disease caused by inhalation of silica particles in occupational or environmental settings. With more than 45.000 deaths per year globally, silicosis represents one of the major occupational diseases worldwide [1, 2]. Inhaled silica particles, encountered in occupations including mining and construction, accumulate in small airways and alveoli inaccessible for mucocilial clearance [3, 4]. Ingestion of silica particles by alveolar macrophages leads to acute pulmonary inflammation hallmarked by excessive production of inflammatory mediators and cell death [4]. Subsequently, ingested silica particles are released and re-ingested by other macrophages, amplifying a vicious circle of inflammation and cell death [4]. Dependent on the time being exposed to silica particles, silicosis can be subdivided into an acute, inflammatory form marked by silicoproteinosis and a chronic form characterized by pulmonic collagen deposition and fibrotic remodeling of the lung [2, 5, 6]. To embank morbidity and mortality associated with irreversible progressive and incurable silicosis, there is an urgent need for new therapies preventing prolonged inflammation and collagen deposition in silicosis [2].
Increasing evidence highlights the proinflammatory cytokines IL-1β and IL-18 as key drivers in the development of silicosis [3,4,5]. IL-1β and IL-18 production is regulated via the inflammasome-caspase-1 pathway. Inflammasomes are multiprotein complexes consisting of a sensor e.g. the nucleotide-binding oligomerization domain–like receptor (NLR) family, e.g. pyrin domain–containing 3 (NLRP3), the adapter protein apoptosis-associated speck-like protein containing a CARD domain (ASC) and caspase-1 [7]. Assembly of the inflammasome complex and subsequent caspase-1 activation requires two signals. Signal 1 comprises the activation of pattern-recognition receptors (PRR) including Toll-like receptors (TLRs) by pathogen-associated molecular patterns (PAMPs) such as lipopolysaccharides (LPS). Subsequently nuclear factor kappa-light-chain-enhancer of activated B cells (NF-ƙB) initiates transcription of inflammasome components including pro-caspase-1, pro–IL-1β and pro-IL-18 [7]. The source of signal 1 in macrophages during silicosis is not conclusively identified and may be mediated by locally produced cytokines or respiratory infections [3]. Silica particles function as signal 2 leading to the activation of the sensor such as NLRP3 and subsequent assembly of the inflammasome complex [3, 4]. This activates caspase-1 that results in proteolytic activation of pro-IL-1β and pro-IL-18 into bio-active IL-1β and IL-18. Further caspase-1 facilitates pyroptosis, a highly inflammatory form of cell death characterized by rupture of the cell membrane and distinct LDH release [3, 4, 7].
Tetracycline and its derivatives have been evaluated in studies of inflammatory diseases where they are reported to be both safe and have immunomodulatory activity [8,9,10,11,12]. Several experimental and clinical studies highlighted anti-inflammatory and lung protective effects of tetracycline derivatives in inflammatory lung diseases including idiopathic pulmonary fibrosis and cystic fibrosis [13,14,15,16,17,18,19]. Recent evidence suggests that tetracycline limits both cytokine production of IL-1β and IL-18 as well as pyroptosis via selective inhibition of caspase-1, thereby reducing acute lung injury [20]. Therefore, we hypothesized that tetracycline reduces silica-induced lung injury via limiting caspase-1 driven inflammation. As silicosis is a chronic disease, we further explored the long-term effects of tetracycline following repeated exposure to silica.
Material and methods
Mice
Wild type (wt) mice C57BL/6 J, 8–10 weeks, male, (Charles River Laboratories, Sulzfeld, Germany) were kept in a pathogen-free facility. The animals were handled according to the principles of laboratory animal care (NIH publication No. 85–23, revised 1996). The animal procedures were in accordance with German legal guidelines and were approved by the responsible local authority for animal care (animal protocols: AZ 81-02.04.2018.A110).
Silica preparation
Silica crystals (MIN-U-SIL-15) (mean particle length 5 μm) were purchased from US Silica (Berkeley Springs, WV) and used in all experiments. To avoid potential endotoxin contamination silica crystals were prepared as described previously [6].
In vivo model
Mice were anesthetized by isoflurane (Pirmal, Mumbai, India) inhalation and intubated with a 20-gauge catheter. Silica (0.33 mg/mouse in 50 μl sterile PBS) or 50 μl sterile PBS (Thermo Fisher Scientific, Darmstadt, Germany) was instilled intratrachealy (i.t.) on days 0, 7, 14 and 21. Instantaneous mice were treated by intraperitoneal (i.p.) injection (75 μg/g mouse in 200 μl sterile PBS) of tetracycline (Sigma-Aldrich, St. Louis, MO, USA) or 200 μl sterile PBS and thereafter every 24 h for 10d. Afterwards i.p. injections were performed 3 times a week. Mice were sacrificed 24 h and 12 weeks after instillation. Bronchoalveolar lavage fluid (BALF) was collected from mice by twice instilling and removing 1 ml of PBS using a 20-gauge catheter. IL-1ß, IL-18 and albumin levels were analyzed by ELISA (R&D Systems, Minneapolis, MN, USA and Bethyl, Montgomery, TX, USA) and total protein concentration by BCA (Thermo Fisher Scientific). Single cell suspension was prepared and blocked with CD16/CD32 antibody (Ab) (2.4G2, BD Bioscience, Franklin Lakes, NJ, USA) to avoid non-specific binding of immunoglobulin to the Fc receptors. Dead cells were excluded by using LIVE/DEAD Fixable Dead Cell Stain kit (Thermo Fisher). Absolute cell numbers were determined by adding CaliBRITE APC-beads (BD Bioscience). FACS Canto II (BD Bioscience, Franklin Lakes, NJ, USA) (FACSDiva software 6.1.2), FlowJo software 10.6.1 (TreeStar, Ashland, OR, USA) and antibodies (Abs) against, CD45 (30-E11, eFluor450), Ly-6C (HK1.4, PE), F4/80 (BM8, PE-Cy7) (Thermo Fisher Scientific), CD3 (17A2 FITC eBiosience) and Ly-6G (148, APC) (BioLegend) were used for neutrophil, macrophage and lymphocyte characterization.
Histopathologic analyses
Lungs were inflated (with a pressure of 15 cm H2O) and fixed with zinc-formalin (Z-fix; Anatech, Battle Creek, MI, USA). Lungs were embedded in paraffin, sectioned at 3 µm and stained with hematoxylin and eosin (H&E) (Sigma-Aldrich) or sirius red (Sigma-Aldrich) as described previously [5]. Two blinded investigators evaluated the samples according to a semi quantitative lung injury score [21].
In vitro analyses
Bone marrow from wt mice was harvested. Bone marrow derived macrophages (BMDM) were differentiated for 4d in DMEM (Thermo Fisher Scientific) supplemented with 10% heat inactivated FCS (Biochrom, Berlin, Germany) and 10 ng/ml mouse macrophage colony-stimulating factor (m-CSF) (ImmunoTools, Friesoythe, Germany). Afterwards medium was removed, cells were scraped and seeded at 1 × 106/ml in 24-well plates for 24 h before replacing medium and conducting experiments. Cells were primed with LPS for 1 h and afterwards stimulated with silica and co-incubated with tetracycline or VX765 (25 µM, specific caspase-1 inhibitor) (Invivogen) for 3 h. Supernatants were analyzed for, IL-1ß and TNF-α secretion by ELISA (R&D Systems). Pyroptosis was measured in cell supernatants via determination of LDH release by the CytoTox 96 assay (Promega, Madison, WI, USA).
Immunoblotting
Cells were lysed in RIPA buffer (R&D Systems) containing protease inhibitors (Sigma-Aldrich) and total protein was determined by BCA (Thermo Fisher Scientific). Lysates or supernatants were separated by SDS-PAGE (NuPAGE, Thermo Fisher Scientific) and blotted onto nitrocellulose, nytrane membranes (GE healthcare, Chicago, IL, USA). Anti-mouse caspase-1, full-length and activated p20 fragment (mAb Casper-1, Adipogen Life Sciences, Liestal, Switzerland), ASC (anti-Asc, pAb (AL177), Adipogen Life Sciences), NLRP3 (mAB Cryo-2, Adipogen Life Sciences), IL-1 ß (anti-mIL-1β R&D Systems) were used as primary and horseradish-peroxidase-conjugated anti-rabbit and anti-mouse IgG (both Cell Signaling Technology, Beverly, MA, USA) as secondary antibodies. Chemiluminescent substrate (Biozym Scientific GmbH, Hessisch Oldendorf, Germany) was used for visualization.
RT-PCR
Total RNA was extracted by TRIzol reagent (Invitrogen), as specified by the manufacturer; cDNA was synthesized with the cDNA Reverse Transcription kit (Applied Biosystems) and Real-Time (RT) PCR was performed as previously described [22]. Gene expression levels (normalized to 18 s) were calculated using the 2 (-DeltaDeltaC(T)) method. All reagents and probes used were purchased from Applied Biosystems (Darmstadt, Germany).
SIRCOL assay
The level of collagen in the lung tissue was determined using the SIRCOL collagen assay (Biocolor LTD., UK) according to manufacturer’s instructions. Briefly, right lung lobes were removed, homogenized and collagen was solved in 0.5 M acetic acid and incubated with Sirius red dye. The absorbance was analyzed at 540 nm using a spectrophotometer revealing the amount of collagen in the lung.
Statistics
Statistical analysis was performed using GraphPad Prism 8 Software (La Jolla, CA, USA). In nonparametric data variables were compared by Mann–Whitney U test. For more than two groups, overall group differences were assessed by Kruskal–Wallis test and intergroup-differences were assessed by ranksum-testing adjusting for multiple comparison by false discovery rate (Benjamini, Krieger and Yekutieli). Values of p < 0.05 were considered significant. All data are expressed as median with interquartile range.
Results
Tetracycline selectively inhibits silica induced IL-1ß production and pyroptosis
To investigate the inhibitory effect of tetracycline on silica-induced activation of the inflammasome-caspase-1 pathway, we primed murine BMDM with LPS and stimulated the cells with silica in the presence or absence of tetracycline. As expected, silica exposure led to a significant release of IL-1ß in LPS primed BMDM (Fig. 1A). Tetracycline dose-dependently inhibited this IL-1ß production (p ≤ 0.0121) and pyroptosis associated LDH release (p ≤ 0.0011) (Fig. 1A, B). Consistent with previous results [20], inflammasome-caspase-1 independent TNF-α production was not affected by tetracycline (Fig. 1C). These results indicate that tetracycline selectively blocks silica-induced IL-1ß production and pyroptosis of BMDM.
Tetracycline inhibits silica-induced activation of caspase-1
Since tetracycline decreased both silica-induced IL-1ß production and pyroptosis, we conducted immunoblot analysis to examine whether tetracycline inhibits caspase-1 activation in BMDM in response to silica. Tetracycline dose-dependently reduced caspase-1 activation, indicated by less cleavage of the p45 caspase-1 precursor into its p20 subunit while expression of NLRP3 and ASC, which is upstream of caspase-1, was not affected (Fig. 2A, B). Consistent with the previous findings (Fig. 1A), active IL-1ß but not pro- IL-1ß was dose-dependently reduced by tetracycline (Fig. 2A, C). Of note, VX765, a selective caspase-1 inhibitor, served as a control in these experiments. To further evaluate potential effects of tetracycline on upstream TLR4-NF-ƙB signaling, expression of NF-ƙB-dependent genes encoding components of the inflammasome-caspase-1 pathway were investigated. Tetracycline had no effect on the expression of mRNA levels of NLRP3, ASC, pro-caspase-1 or pro-IL-1ß after stimulation with LPS and silica (Fig. 2D–G). These data suggest that tetracycline reduces silica-induced IL-1ß production by direct inhibition of caspase-1.
Tetracycline inhibits pulmonary inflammation and caspase-1 in acute silicosis
To test whether tetracycline ameliorates caspase-1 dependent pulmonary inflammation in acute silicosis, we challenged C57Bl/6 J mice i.t. with silica particles and treated them with tetracycline. 24 h after silica instillation, IL-1ß and IL-18 concentrations were analyzed in BALF. As shown in Fig. 3A, B, silica exposure markedly induced pulmonary IL-1ß and IL-18 levels. Treatment with tetracycline significantly inhibited IL-1ß (p = 0.0260) and IL-18 (p = 0.0159) production (Fig. 3A, B). We next examined activation of caspase-1 in lung homogenates by immunoblotting. In comparison to PBS treated controls, silica induced the activation of caspase-1, which was indicated by increased p20 fragment. In contrast, tetracycline inhibited caspase-1 activation in this model and cleavage of the caspase-1 precursor was reduced (Fig. 3C). Consistent with the in vitro experiments (Fig. 2C), upstream expression of ASC was not affected by tetracycline (Fig. 3C). These results indicate that tetracycline reduces silica-induced caspase-1 dependent cytokine production in the lungs.
Tetracycline ameliorates lung injury in acute silicosis
We next examined whether inhibition of caspase-1 could ameliorate disease related lung injury. Therefore, the accumulation of total protein, albumin and neutrophils, macrophages and lymphocytes in BALF was quantified 24 h after silica administration. Silica challenge induced the accumulation of all injury markers (Fig. 4A–D). Treatment with tetracycline significantly reduced silicoproteinosis, indicated by reduced levels of protein (p = 0.0002) and albumin (p = 0.0012) as well as lower numbers of neutrophils (p = 0.0317) and Macrophages (0.0496) in the BALF in comparison to PBS controls. The number of lymphocytes was not affected by the treatment with tetracycline (Fig. 4E). Consistent with reduced neutrophil, macrophage and protein levels in the BALF, the histology of silica exposed lungs revealed that treatment with tetracycline significantly decreases lung injury (Fig. 4F). This series of findings demonstrates that tetracycline can reduce the severity of lung injury in acute silicosis.
Tetracycline treatment reduces silica-induced chronic lung pathology
Present data reveals that tetracycline effectively reduces silica-induced acute pulmonary inflammation and lung injury (Figs. 3 and 4). Since chronic silicosis results in fibrotic remodeling of the lungs, we investigated the effect of tetracycline in a murine model of long-term silica exposure. Therefore, C57Bl/6 J mice were repetitively i.t. challenged with silica and subsequently treated with tetracycline. Silica exposure led to pronounced lung injury including proteinaceous debris, invasion of leucocytes and alveolar septal thickening (Fig. 5A, B). Treatment with tetracycline significantly ameliorated lung injury (p = 0.0303) (Fig. 5B). Furthermore, substantial collagen deposition was detectable in lungs of silica challenged mice, whereas tetracycline-treated mice possessed significantly reduced collagen levels (p = 0.04) (Fig. 5A, C). In conclusion, these data show protective long-term effects of tetracycline following repeated exposure to silica.
Discussion
Exposure to silica particles can lead to inflammation of the lung with development of silicosis [23]. Evidence suggests that silica dependent inflammation and lung injury is mediated by excessive production of caspase-1 dependent cytokines and pyroptotic cell death [3,4,5, 24, 25]. To our knowledge the present report shows for the first time that tetracycline selectively inhibits caspase-1-dependent IL-1β but not NF-ƙB dependent TNF-α production and pyroptosis in response to silica in vitro (Figs. 1 and 2). The results were consistent with tetracycline reducing silica-induced IL-1β and IL-18 production as well as activation of caspase-1 in the lungs (Fig. 3), thereby ameliorating pulmonary inflammation, lung injury (Fig. 4) and subsequent fibrosis (Fig. 5).
Controversies exist whether tetracycline or its derivates selectively inhibit inflammasome-dependent signaling. Lu et al. showed that using minocycline in an oxygen–glucose deprivation / reoxygenation model inhibited both TNF-α (signal 1) and IL-1β (signal 2) in microglia concluding that the effect is unspecific [26]. However, the findings were inconsistent as signal-1 dependent NLRP3 and pro-IL-1β but not pro-caspase-1 production was inhibited by minocycline [26]. Reduced gene expression of NLRP3 and caspase-1 (signal 1) by minocycline has also been described in mouse models of diabetic nephropathy or Huntington disease [10, 27]. Yet, those studies evaluated the effect of minocycline on inflammasome signaling at very late time points [10, 27]. Since IL-1β production is a very early step in the inflammatory response to silica [3, 4], it is likely that secondary effects (such as feedback loops via IL-1R-NF-ƙB) explain the findings of these studies. Current study found no effect of tetracycline on NF-ƙB dependent gene expression of caspase-1 or other inflammasome components in macrophages. Furthermore, tetracycline did not block NLRP3 or ASC production in silica-exposed macrophages, suggesting a tetracycline-mediated blockade of inflammasome-signaling downstream of ASC. Furthermore, there was no effect of tetracycline on pro-IL-1β. Consistent with this, our group recently showed that tetracycline had neither an effect on NF-ƙB dependent gene expression nor on ASC-specking, but rather selectively inhibits activation of caspase-1 in LPS and nigericin activated macrophages [20]. In summary present report suggests that inhibition of IL-1β production and pyroptosis by tetracycline in silica exposed macrophages is mediated via inhibition of caspase-1.
Silica particles cause progressive, inflammasome-associated inflammation and lung injury [3,4,5]. Increased pulmonary IL-1ß concentrations associated with progressive fibrosis are found in patients with silicosis [28, 29]. Consistent with this, previous studies revealed that IL-1β-, ASC- and NLRP-3-deficient mice were protected from pulmonary inflammation in response to inhaled silica particles [3, 19]. Furthermore, pharmacological intervention by using anti-IL-1β antibody reduced inflammation and lung injury in silica exposed mice [14]. Thus, we questioned whether tetracycline would be a therapeutic option against silica induced inflammation and fibrotic lung remodeling. Therefore, we used a widely accepted murine model featuring i.t. instillation of silica particles [3,4,5]. For the first time we showed that tetracycline was effective in decreasing silica-induced IL-1β and IL-18 production in silica exposed mice. This was due to tetracycline-mediated inhibition of caspase-1, resulting in significantly reduced lung injury. Comparable effects of tetracycline in reducing pulmonary inflammation have been shown recently in two models of acute lung injury. Here, tetracycline reduced IL-1β and IL-18 levels, pulmonary inflammation and lung injury in mice that were challenged with either LPS or influenza virus [20]. Furthermore, lung injury and inflammation in response to LPS was significantly lower in caspase-1 deficient mice compared to wild-type animals. Of note, tetracycline had no effect on pulmonary inflammation and damage in caspase-1 deficient mice [20].
In summary, current study suggests that tetracycline ameliorates silica-induced inflammation and lung injury via inhibition of caspase-1.
This study has several limitations. First, animal models are limited to mimic the long period of silica exposure (at least 10 years of exposure to low concentrations of silica particles) necessary to induce chronic silicosis in humans [2]. Yet, we evaluated the long-term effects of tetracycline in an established model of chronic silicosis featuring repetitive i.t. instillation of silica particles provoking constitutive pulmonary inflammation [5]. In accordance with others showing amelioration of bleomycin-induced lung fibrosis by doxycycline [13, 14], we found that tetracycline clearly reduced progression of fibrotic lung remodeling and significantly reduced collagen deposition in the lungs of silica challenged mice. This was in line with a chronic silicosis model showing that blocking of IL-1ß reduces pulmonary fibrosis [5].
Second, since BMDM are commonly used to examine silica-induced inflammasome activation [4], we also demonstrate the molecular effects of tetracycline on inflammsasome-caspase-1 pathway in BMDM in vitro. This cannot fully reflect the complex interplay between different cell types orchestrating silica-induced inflammation and lung injury in vivo. Pulmonary inflammation in the context of silicosis is also maintained by non-immune cells and silica exposure leads also to upregulation of NLRP3 inflammasome-caspase-1 activation in lung epithelium [30].
In summary, current study suggests that tetracycline inhibits caspase-1 activation in response to silica and ameliorates silica-induced pulmonary inflammation including IL-1ß production, thereby reducing lung injury and fibrotic lung remodeling.
Conclusions
Tetracycline reduced caspase-1-dependent production of IL-1β in response to silica in vitro and in vivo. These results were consistent with tetracycline reducing silica-induced pulmonary inflammation and subsequent lung injury and fibrosis in a murine model. Tetracycline and derivates have been shown to provide beneficial immunomodulatory effects in experimental and clinical studies of inflammatory and lung fibrosing diseases including acute lung injury [9, 10, 20]. Since tetracycline is an approved antibiotic drug with a good safety profile and there is a growing number of chemically modified tetracyclines which have been attributed to lack anti-bacterial but retain anti-inflammatory activities [31, 32], tetracycline and its derivates could be repurposed as a protective agent for silica-induced pulmonary inflammation and subsequent disease progression.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Abbreviations
- ASC:
-
Adapter protein apoptosis-associated speck-like protein containing a CARD domain
- ABS:
-
Antibodies
- BALF:
-
Bronchoalveolar lavage fluid
- BMDM:
-
Bone marrow derived macrophages
- H&E:
-
Hematoxylin and eosin
- LPS:
-
Lipopolysaccharides
- m-CSF:
-
Mouse macrophage colony-stimulating factor
- NF-ƙB:
-
Nuclear factor kappa-light-chain-enhancer of activated B cells
- NLR:
-
Nucleotide-binding oligomerization domain–like receptor
- NLRP3:
-
NLR family pyrin domain–containing 3
- PAMP:
-
Pathogen-associated molecular pattern
- PRR:
-
Pattern-recognition receptors
- TLR:
-
Toll-like receptor
References
GBD 2013 Mortality and Causes of Death Collaborators. Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990–2013: a systematic analysis for the Global Burden of Disease Study 2013. Lancet. 2015;385:117–71.
Leung CC, Yu ITS, Chen W. Silicosis Lancet. 2012;379:2008–18.
Cassel SL, Eisenbarth SC, Iyer SS, Sadler JJ, Colegio OR, Tephly LA, et al. The Nalp3 inflammasome is essential for the development of silicosis. Proc Natl Acad Sci U S A. 2008;105:9035–40.
Hornung V, Bauernfeind F, Halle A, Samstad EO, Kono H, Rock KL, et al. Silica crystals and aluminum salts activate the NALP3 inflammasome through phagosomal destabilization. Nat Immunol. 2008;9:847–56.
Biswas R, Trout KL, Jessop F, Harkema JR, Holian A. Imipramine blocks acute silicosis in a mouse model. Part Fibre Toxicol. 2017;14:36.
Bode C, Kinjo T, Alvord WG, Klinman DM. Suppressive oligodeoxynucleotides reduce lung cancer susceptibility in mice with silicosis. Carcinogenesis. 2014;35:1078–83.
Latz E, Xiao TS, Stutz A. Activation and regulation of the inflammasomes. Nat Rev Immunol. 2013;13:397–411.
Garrido-Mesa J, Algieri F, Rodríguez-Nogales A, Vezza T, Utrilla MP, Garcia F, et al. Immunomodulatory tetracyclines ameliorate DNBS-colitis: Impact on microRNA expression and microbiota composition. Biochem Pharmacol. 2018;155:524–36.
Metz LM, Li DKB, Traboulsee AL, Duquette P, Eliasziw M, Cerchiaro G, et al. Trial of Minocycline in a Clinically Isolated Syndrome of Multiple Sclerosis. N Engl J Med. 2017;376:2122–33.
Shahzad K, Bock F, Al-Dabet MM, Gadi I, Nazir S, Wang H, et al. Stabilization of endogenous Nrf2 by minocycline protects against Nlrp3-inflammasome induced diabetic nephropathy. Sci Rep. 2016;6:34228.
Krakauer T, Buckley M. Doxycycline is anti-inflammatory and inhibits staphylococcal exotoxin-induced cytokines and chemokines. Antimicrob Agents Chemother. 2003;47:3630–3.
Bode C, Diedrich B, Muenster S, Hentschel V, Weisheit C, Rommelsheim K, et al. Antibiotics regulate the immune response in both presence and absence of lipopolysaccharide through modulation of Toll-like receptors, cytokine production and phagocytosis in vitro. Int Immunopharmacol. 2014;18:27–34.
Fujita M, Ye Q, Ouchi H, Harada E, Inoshima I, Kuwano K, et al. Doxycycline attenuated pulmonary fibrosis induced by bleomycin in mice. Antimicrob Agents Chemother. 2006;50:739–43.
Fujita H, Sakamoto N, Ishimatsu Y, Kakugawa T, Hara S, Hara A, et al. Effects of doxycycline on production of growth factors and matrix metalloproteinases in pulmonary fibrosis. Respiration. 2011;81:420–30.
Guo J, Gu N, Chen J, Shi T, Zhou Y, Rong Y, et al. Neutralization of interleukin-1 beta attenuates silica-induced lung inflammation and fibrosis in C57BL/6 mice. Arch Toxicol. 2013;87:1963–73.
Bhattacharyya P, Nag S, Bardhan S, Acharya D, Paul R, Dey R, et al. The role of long-term doxycycline in patients of idiopathic pulmonaryfibrosis: The results of an open prospective trial. Lung India. 2009;26:81–5.
Mishra A, Bhattacharya P, Paul S, Paul R, Swarnakar S. An alternative therapy for idiopathic pulmonary fibrosis by doxycycline through matrix metalloproteinase inhibition. Lung India. 2011;28:174–9.
Xu X, Abdalla T, Bratcher PE, Jackson PL, Sabbatini G, Wells JM, et al. Doxycycline improves clinical outcomes during cystic fibrosis exacerbations. Eur Respir J. 2017. https://doi.org/10.1183/13993003.01102-2016.
Sauer A, Peukert K, Putensen C, Bode C. Antibiotics as immunomodulators: a potential pharmacologic approach for ARDS treatment. Eur Res Rev. 2021. https://doi.org/10.1183/16000617.0093-2021.
Peukert K, Fox M, Schulz S, Feuerborn C, Frede S, Putensen C, et al. Inhibition of caspase-1 with tetracycline ameliorates acute lung injury. Am J Respir Crit Care Med. 2021. https://doi.org/10.1164/rccm.202005-1916OC.
Matute-Bello G, Downey G, Moore BB, Groshong SD, Matthay MA, Slutsky AS, et al. An official American Thoracic Society workshop report: features and measurements of experimental acute lung injury in animals. Am J Respir Cell Mol Biol. 2011;44:725–38.
Steinhagen F, Zillinger T, Peukert K, Fox M, Thudium M, Barchet W, et al. Suppressive oligodeoxynucleotides containing TTAGGG motifs inhibit cGAS activation in human monocytes. Eur J Immunol. 2018;48:605–11.
Ding M, Chen F, Shi X, Yucesoy B, Mossman B, Vallyathan V. Diseases caused by silica: mechanisms of injury and disease development. Int Immunopharmacol. 2002;2:173–82.
Srivastava KD, Rom WN, Jagirdar J, Yie T-A, Gordon T, Tchou-Wong K-M. Crucial role of interleukin-1beta and nitric oxide synthase in silica-induced inflammation and apoptosis in mice. Am J Respir Crit Care Med. 2002;165:527–33.
Dostert C, Pétrilli V, Van Bruggen R, Steele C, Mossman BT, Tschopp J. Innate immune activation through Nalp3 inflammasome sensing of asbestos and silica. Science. 2008;320:674–7.
Lu Y, Xiao G, Luo W. Minocycline suppresses NLRP3 inflammasome activation in experimental ischemic stroke. NeuroImmunoModulation. 2016;23:230–8.
Chen M, Ona VO, Li M, Ferrante RJ, Fink KB, Zhu S, et al. Minocycline inhibits caspase-1 and caspase-3 expression and delays mortality in a transgenic mouse model of Huntington disease. Nat Med. 2000;6:797–801.
Yucesoy B, Vallyathan V, Landsittel DP, Simeonova P, Luster MI. Cytokine polymorphisms in silicosis and other pneumoconioses. Mol Cell Biochem. 2002;234–235:219–24.
Zhai R, Ge X, Li H, Tang Z, Liao R, Kleinjans J. Differences in cellular and inflammatory cytokine profiles in the bronchoalveolar lavage fluid in bagassosis and silicosis. Am J Ind Med. 2004;46:338–44.
Peeters PM, Eurlings IMJ, Perkins TN, Wouters EF, Schins RPF, Borm PJA, et al. Silica-induced NLRP3 inflammasome activation in vitro and in rat lungs. Part Fibre Toxicol. 2014;11:58.
González-Lizárraga F, Ploper D, Ávila CL, Socías SB, Dos-Santos-Pereira M, Machín B, et al. CMT-3 targets different α-synuclein aggregates mitigating their toxic and inflammogenic effects. Sci Rep. 2020;10:20258.
He B, Garmire L. Prediction of repurposed drugs for treating lung injury in COVID-19. F1000Res. 2020;9:609.
Acknowledgements
Not applicable.
Funding
Open Access funding enabled and organized by Projekt DEAL. This research was funded by grants and fellowships from the University of Bonn (BONFOR), and the B. Braun Foundation.
Author information
Authors and Affiliations
Contributions
KP and FS contributed equally to the work. KP, FS, CW, EL and CB designed the work. KP, MF, SS, CF, PS and MS conducted experiments. KP, BS and CB interpreted data and prepared figures. KP, FS, and CB drafted the work and CP, AS and SF substantively revised it. All authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate
The animal procedures were in accordance with German legal guidelines and were approved by the responsible local authority for animal care (animal protocols: AZ 81-02.04.2018.A110).
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Peukert, K., Steinhagen, F., Fox, M. et al. Tetracycline ameliorates silica-induced pulmonary inflammation and fibrosis via inhibition of caspase-1. Respir Res 23, 21 (2022). https://doi.org/10.1186/s12931-022-01937-7
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s12931-022-01937-7