Triggering receptor expressed on myeloid cells-1 (TREM-1) is expressed on neutrophils and monocyte/macrophages and amplifies Toll-like receptor-mediated inflammation during infection. TREM-1 also exists in an antagonistic soluble form (sTREM-1) that has been used as a peripheral biomarker in sepsis, though the mechanisms of its release are not entirely clear. The requirement of TREM-1 in single microbial infections is controversial, with some studies showing a protective role and others a contribution to immunopathology. Furthermore, the role of membrane-bound and sTREM-1 in polygenic infections is currently unknown. In a mouse co-infection model where preceding viral infection greatly enhances bacteria co-infection, we now determine a mechanisms for the striking increase in sTREM-1 and the loss of TREM-1 on surface of neutrophils. We identified a matrix metalloproteinase (MMP)-9 cleavage site in TREM-1 and that the increase of MMP-9 in bronchoalveolar lavage fluid mirrors sTREM-1 release. In vitro studies with neutrophils and MMP-9 and the reduction of sTREM-1 in vivo after MMP-9 inhibition verifies that this enzyme cleaves TREM-1. Intriguingly, MMP-9 inhibition significantly reduces bacterial load and ensuing immunopathology in a co-infection model. This highlights MMP-9 inhibition as a potential therapeutic via blocking cleavage of TREM-1.
Bacterial super-infections often follow pulmonary virus infection and are a major cause of excess morbidity and mortality.1 Enhanced disease is due to a combination of excessive host immune responses and an exponential increase in bacterial replication that invades the lung and disseminates to distant organs.2 Membrane-bound pathogen recognition receptors on innate immune cells respond either alone or in combination to allow diversification of the early immune response. Co-operation between receptors draws in a variety of signaling cascades that shape an appropriate response, or in the case of some co-receptors, timely termination of inflammation. The triggering receptors expressed on myeloid cells (TREM) family either amplifies (TREM-1) or dampens (TREM-2) inflammation.3 TREM-1 amplifies the inflammatory response to Toll-like receptor signaling by recruiting the transmembrane adapter molecule DAP12, which recruits the tyrosine kinase Syk and leads to the activation of PI3K and MAPK.4 TREM-1 signaling also enhances NF-κB induced cytokine production in dendritic cells via caspase-recruitment domain protein (CARD)-95 and downregulates suppressor of cytokine signaling-1 (SOCS-1) by inducing the expression of miR-155 in macrophages and lungs of mice treated with LPS.6
Like many membrane bound receptors, TREM-1 also exists in soluble form (sTREM-1). Although the function of sTREM-1 is unknown, it is likely to negatively regulate membrane TREM-1 receptor signaling through competition with the ligand(s). sTREM-1 is under investigation as a biomarker in a variety of infectious and non-infectious inflammatory conditions and is detected in the bronchoalveolar lavage (BAL) fluid in pneumonia7 and in the serum8, 9 and urine10 of septic patients. It is a marker of neonatal sepsis11 and predicts shock and death.12 sTREM-1 and its gene polymorphisms are also associated with sepsis prognosis13 and high sTREM-1 is predictive of Systemic Inflammatory Response Syndrome (SIRS)14 after surgery. TREM-1 and its soluble form are therefore potential diagnostic markers for infectious and chronic inflammatory diseases and also potential future targets for therapeutic manipulation.15, 16 In order for sTREM-1 to be a reliable marker of disease, a greater understanding of the cells relevant to its release and mechanisms of its cleavage are required. Furthermore, the long term impact of reducing TREM-1 cleavage into the soluble form is currently unknown.
Secondary bacterial infections are a consequence of many lung inflammatory diseases and arise due to defective microbicidal responses in the remodeled airspaces.17 We reasoned that the release of sTREM-1 is at least partly responsible for impaired innate immune responses to bacteria following influenza virus infection. We now report a matrix metalloproteinase (MMP)-9 cleavage site within the TREM-1 sequence and demonstrate an in vivo correlation between MMP-9 expression, the appearance of sTREM-1 in airway lavage and neutrophil recruitment during pulmonary influenza infection. This correlation is amplified in influenza virus/bacterial super-infected mice. Inhibition of MMP-2/9 decreases sTREM-1 and restores membrane-bound TREM-1 and anti-bacterial immunity that prevents mortality following bacterial superinfection. Although cleavage of immune stimulatory receptors such as TREM-1 is an efficient means to curtail inflammatory responses, it may have deleterious effects if the pathogen has not been completely cleared. MMP-9 is raised in a variety of pathologies associated with infectious complications. We therefore conclude that inhibition of MMP-9 and TREM-1 cleavage represents novel therapeutic targets for the alleviation of secondary bacterial pneumonia.
Influenza infection increases susceptibility to Streptococcus pneumoniae superinfection
The murine model of bacterial superinfection following influenza virus is well established with high reproducibility.18 Similar to prior studies, we show that uninfected mice gain weight whereas intranasal influenza PR8 (H1N1) virus infection causes substantial weight loss, peaking on day 7 after which they begin to recover (Figure 1a). Phosphate-buffered saline (PBS) mock-infected mice administered 106 colony-forming unit (CFU) S. pneumoniae (Strep) intranasally on day 7 did not lose weight and were similar to PBS alone controls. However, intranasal infection with S. pneumoniae 7 days after influenza infection (PR8+Strep) caused extensive weight loss and the mice had to be killed. Co-infection was accompanied by enhanced total cells in the BAL (Figure 1b) and lung (Figure 1c), enhanced neutrophilia (Figure 1d), elevated levels of tumor necrosis factor (TNF)-α (Figure 1e) and exponentially higher bacterial loads in the BAL (Figure 1f), lung (Figure 1g) and blood (Figure 1h) of co-infected mice.
Excessive release of MMP-9 and sTREM-1 during secondary bacterial superinfection
We next determined the expression of sTREM-1, TREM-1 and MMP-9 in our murine model of bacterial superinfection following influenza virus. sTREM-1 levels in the BAL of PBS control mice were very low, significantly increased in mice infected with influenza alone and S. pneumoniae alone, but were strongly elevated in co-infected mice (Figure 2a). A similar pattern, though at lower concentration, was observed measuring sTREM-1 in the serum (Figure 2b). MMP-9 expression in the BAL followed the same pattern with an average 12- and 9-fold increase in co-infected mice compared with those infected with influenza or S. pneumoniae alone, respectively (Figure 2c). The correlation between MMP-9 and sTREM-1 by Spearman rank test was highly significant (R=0.755, P<0.0001; Figure 2d).
As it has been suggested that sTREM-1 is generated via cleavage of membrane-bound TREM-1 from the cell surface,19 and the co-infection model recruits a large number of neutrophils that express it, we analyzed whether there is a correlation between membrane-anchored TREM-1 on neutrophils and the release of sTREM-1 in the BAL. Both PBS control and influenza infected mice expressed high levels of TREM-1 on lung neutrophils (24% and 22%, respectively) and displayed low levels of sTREM-1 in the BAL (Figure 2e). By contrast bacterial infection alone, and especially following influenza infection, reduced membrane-bound TREM-1 on neutrophils and increased sTREM-1. This result was also obtained applying total neutrophil numbers (Figure 2f). Thus, it is indicated that the balance of membrane bound TREM-1 versus sTREM-1 is altered during inflammation of the lung, which may lead to inefficient clearance of bacteria, resulting in systemic dissemination and mortality.
Trem-1 contributes to neutrophil degranulation
Neutrophils constitute the main cellular defence against S. pneumoniae.20 At the site of infection they phagocytose bacteria that are killed by reactive oxygen species21, 22 and serine proteases cathepsin G, elastase and proteinase 3 released from intracellular granules.23 Neutrophils also express pattern-recognition receptors to sense and respond to pathogens.24 The function of TREM-1, and the impact of sTREM-1, however, is currently unknown. We therefore purified neutrophils from bone marrow and cultured them with LPS in the presence of a TREM-1 agonist antibody or an antagonistic TREM-1 peptide (LP17). Agonism of TREM-1 had no effect on phagocytosis of bacterial particles and ROS production (data not shown), but enhanced degranulation, which is reflected by the upregulation of CD63 (Figure 3a), and CD11b expression (Figure 3b) whereas LP17 had the opposite effect (Figure 3c,d). Thus TREM-1 potentiates certain aspects of neutrophil anti-bacterial immunity.
Inhibition of MMP-2/9 prevents bacterial infiltration and the proinflammatory response during secondary bacterial superinfection
The TREM-1 sequence (MRKAGLWGLL CVFFVSEVKA AIVLEEERTD LVEQTLTVKCPFNIMKYAN SQKAWQRLPD GKEPLTLVVT QRPFTRPSEV HMGKFTLKHD PSEAMLQVQM TDLQVTDSGL YRCVIYHPPN DPVVLFHPVR LVVTKGSSDVFTPVIIPITR ITERPILITT KYSPSDTTTT RSLPKPTAVV SSPGLGVTII NGTDADSVST SSVTISVICG IISKSLVFII LFIVTKRTFG) contains an MMP-9 cleavage site (underlined). The possible sequence for an MMP-9 cleavage site is P-X-X-H-T, where X is any amino acid and H is hydrophobic.
To formally prove that MMP-9 causes the cleavage of membrane-bound TREM-1, we incubated murine bone-marrow-derived neutrophils with unactivated MMP-9 or AMPA activated MMP-9 (as described by Marcy AL et al25). Stimulation of bone-marrow-derived neutrophils with activated MMP-9 reduced the expression of membrane-bound TREM-1 and increased the levels of sTREM-1 compared with unactivated MMP-9 (Figure 4a).
We next infected mice intranasally (i.n.) with influenza virus strain PR8 and with S. pneumoniae on day 7. One co-infected group was treated with an MMP-2/9 inhibitor i.n. on day 6 and day 7, whereas the other group received vehicle only. Mice were sacrificed on day 8 (Figure 4b). The activation status of MMP-9 was assessed by zymography in the BAL of influenza and S. pneumoniae infected mice administered the MMP-2/9 inhibitor and compared with co-infected mice that received vehicle only (Figure 4c). Co-infected mice showed strong activity of MMP-9, which was substantially reduced upon inhibitor treatment. Levels of sTREM-1 in BAL (Figure 4d) and serum (Figure 4e) and MMP-9 protein levels in BAL (Figure 4f) and serum (Figure 4g) were significantly suppressed in the inhibitor treated group. The activity (data not shown) and expression (Figure 4h) of MMP-2 in the BAL was not affected by the MMP-2/9 inhibitor, though this is likely to reflect the very low levels found in this model compared with MMP-9 (data not shown). The correlation of sTREM-1 (Figure 4i) with CFU was significant by Spearman Rank test (R=0.744; P=0.002). However, similar to the correlation between CFU and MMP-9 levels (Figure 4j), a certain threshold of bacteria had to be present in order for sTREM-1 to increase. In both cases this threshold appeared to be above 106 CFU per ml (Figure 4i,j). Our results indicate that inhibition of MMP-2/9 reduces the release of TREM-1 in vivo.
Inhibition of MMP-2/9 increases the expression of TREM-1 on neutrophils in the lung during secondary bacterial superinfection
A decrease in sTREM-1 could reflect a reduction in recruited neutrophils rather than a decrease in sTREM-1 release. During infection neutrophils are the main cellular source of MMP-9.26 As one role of MMP-9 is to cleave IL-8,27 (mouse homolog KC),28 to form a more potent neutrophil chemoattractant we next determined the impact of MMP-2/9 inhibition on cell recruitment. Both vehicle and MMP-2/9 inhibitor treatment of co-infected mice displayed equivalent airway (Figure 5a) and only partially reduced lung (Figure 5b) cellularity. Importantly, expression of TREM-1 on neutrophils was significantly higher in BAL (Figure 5c,d) and lung (Figure 5e,f) of mice treated with the MMP-2/9 inhibitor compared with the control group. Administration of the MMP-2/9 inhibitor increased the expression of TREM-1 on neutrophils in the BAL 4.3-fold and in the lung 4.5-fold. A similar result was obtained for total numbers of lung neutrophils where membrane-bound TREM-1 was restored to pre-infection levels (Figure 5f). Comparison of the release of sTREM-1 with membrane-bound TREM-1 revealed that high amounts of sTREM-1 correlated with low expression of TREM-1 on neutrophils in BAL (Figure 5g) and lung (Figure 5h). Thus, MMP-9 contributes to bacterial super-infection by cleaving membrane-bound TREM-1, preventing the timely removal of the bacterium from the influenza infected lung.
Inhibition of MMP-2/9 reduces the expression of MMP-9 and sTREM-1 during secondary bacterial superinfection
As our results show that secondary bacterial superinfection following influenza results in excessive release of MMP-9 and sTREM-1, we next addressed whether inhibition of MMP-9 in vivo has an impact on disease outcome. As our results show that secondary bacterial superinfection following influenza results in excessive release of MMP-9 and sTREM-1, we next addressed whether inhibition of MMP-9 in vivo has an impact on disease outcome using the MMP-2/9 inhibitor co-infection model infection model described in Figure 4b. No difference in weight loss was observed in the inhibitor treated mice compared with the PR8 influenza and S. pneumoniae infected control mice administered vehicle only (Figure 6a). As demonstrated previously, infection of mice with S. pneumoniae 7 days post influenza leads to a high bacterial load in the airway, lung and blood (Figure 1f and h). However, treatment with the MMP-2/9 inhibitor significantly reduced bacterial titers in the BAL (Figure 6b) and lung (Figure 6c) and, remarkably, completely prevented sepsis (Figure 6d). In contrast to our co-infected control group displaying a high bacterial load (9 × 107 CFU per ml), no bacteria were detected in the blood of mice treated with the inhibitor. We also observed a significant reduction in the airway proinflammatory cytokines interleukin (IL)-6 (Figure 6e), IL-1α (Figure 6f) and TNF-α (Figure 6g) compared with the control group, whereas the expression of interferon-γ remained unchanged (Figure 6h). Noteworthy, although secondary bacterial infection leads to a systemic disease, these results were achieved via intranasal administration of the inhibitor only. Altogether, our data indicate that inhibition of MMP-2/9 strongly reduces the bacterial load in BAL and lung, prevents sepsis and the proinflammatory response.
The resolution of inflammation requires integrated responses that return damaged tissues to homeostasis. The release of soluble ectodomains of immune stimulatory receptors by proteases, which are upregulated during inflammation, is an effective method of producing anti-inflammatory antagonists (as proposed for sTREM-1 (ref. 20)). A classic example is the release of soluble TNF receptor trimers that sequester TNF-α preventing activation of membrane-bound receptors. Other examples include shed L-selectin that binds PSGL1 on endothelial cells curtailing cell adhesion21 and JAM-A that binds LFA-1 on leukocytes impeding transmigration.22 MMP-9 is released during a variety of infections, which we now show is elevated further upon bacterial super-infection. This additional production likely reflects the recruitment of large number of neutrophils containing MMP-9 in pre-formed granules.23, 24 MMP-9 promotes endothelial permeability, assists inflammatory cell migration through the breakdown of vascular basement membranes and extracellular matrix29 and is associated with the release of membrane-anchored signaling molecules in response to different stimuli. For example, MMP-9 activates the inactive form of TGF-β and IL-1β30 via cleavage. Some cleaved ectodomains are inert or have advantageous biological activity.31 Others may, however, contribute to the pathological process. During chronic Staphylococcus aureus lung infection the activation of ADAM10 cleaves epidermal growth factor stimulating mucus production that contributes to airway obstruction. Genome-wide association studies implicate ADAM33 in asthma and airway hyper-reactivity and TGF-β causes ectodomain shedding of ADAM33 that contributes to lung remodeling. Furthermore, MMP-7 increases ectodomain shedding of E-cadherin from epithelia, leading to loss of epithelial coherence.32
We now show TREM-1 cleavage by MMP-9, similar to that reported for peritoneal and RAW macrophages in vitro,33 and that MMP-9 inhibition restores neutrophil membrane TREM-1 expression. Interestingly, MMP-9 also cleaves surfactant protein D decreasing its ability to aggregate bacteria and facilitate phagocytosis by alveolar macrophages.34 This suggests that MMP-9 inhibition would restore a number of neutrophil anti-bacterial mechanisms. Definitive proof of a direct effect of MMP-9 on TREM-1 cleavage is difficult to obtain however, and would require generating a knockin of TREM-1 expressing a mutated MMP-9 cleavage site. Although in vivo MMP-2/9 neutralisation would suggest other mechanisms are not involved with TREM-1 cleavage, we cannot rule out a role for other proteases. Compelling associations combined with in vivo and in vitro studies however indicate a classic feedback loop curtailing neutrophil function that has deleterious effects on subsequent bacterial control.
Although cleavage of activation receptor ectodomains affords resolution, the timing of this cleavage is crucial, since early release will allow remaining pathogens to escape and ultimately lead to prolonged and exaggerated inflammation. Indeed, blockage of TREM-1 signaling causes severe proinflammatory responses to Streptococcus suis, whereas activation has the opposite effect.35 Similarly agonistic TREM-1 antibodies facilitate early clearance of S. pneumoniae single infection.7 We now additionally show that TREM-1 facilitates neutrophil degranulation and hence bactericidal activity. Inflammation can therefore arise in the presence and absence of membrane TREM-1. Intact membrane bound TREM-1 slows the resolution of inflammation, whereas once cleaved bacteria grow exponentially leading to more immune stimulation. The timing of membrane to secreted TREM-1 is therefore critical. Secondary pulmonary bacterial infections are a feature of a wide range of lung inflammatory disorders (including asthma, COPD, cystic fibrosis and IPF) that are also associated with increased MMP-9 production. The link to soluble TREM-1, however, has not previously been investigated. In general the outcome depends on whether TREM-1 is neutralized or the gene deleted. Neutralization of TREM-1 attenuates inflammation, preventing experimentally induced bacterial septic shock36, 37, 38, 39, 40, 41, 42 and attenuating disease severity in mice infected with Leishmania major, influenza virus and Legionella pneumophila.43 However, the situation for Klebsiella pneumoniae appears to be different with TREM-1/3-deficient mice showing impaired host defence,44 similar to that observed for pneumococcal pneumonia45 and Pseudomonas aeruginosa8 in the same mice. These results are not necessarily contradictory since global knockout affects innate immunity from the outset, whereas therapeutic neutralisation does not.
Ectodomain cleavage of membrane-bound TREM-1 via MMP-9 during influenza virus infection associates with secondary bacterial super-infection that is lethal. Cleavage of TREM-1 is likely required to prevent influenza virus-mediated damage, but has the disadvantage of creating a window of susceptibility to bacteria. Respiratory syncytial virus also stimulates MMP-9 release from human airway epithelium and is a biomarker of disease severity in mechanically ventilated children with respiratory syncytial virus lung infection.46 This suggests that common processes may be occurring in respiratory disease, which is important in the absence of knowing the etiological agent(s). We would propose that MMP-9 inhibition in those most severely affected by respiratory viral infection would restore membrane TREM-1 expression and abolish the lethal synergistic viral–bacterial disease. However, additional effects of neutralizing these proteases would need to be taken into consideration.
Considering that MMP-2 and MMP-9 cooperate to cleave chemokines involved in neutrophil migration,47 particularly IL-8,48 we were surprised to see little effect of these metalloproteinases on neutrophil numbers in the airways of bacterial super-infected influenza resolved mice. A partial reduction was, however, observed in lung tissue. A previous study of single influenza virus lung infection in MMP-9 knockout mice reports reduced neutrophil migration and disease pathogenesis.49 We believe the mild effect on airway neutrophilia seen in our study reflects their over-whelming recruitment in this super-infection model that masks any subtle effect. It is also interesting that MMP-2/9 inhibition dramatically reduced the bacterial load, completely prevented sepsis and subsequently reduced many proinflammatory cytokines, except interferon-γ. This suggests beneficial effects on both bacterial clearance and immune-mediated pathology. TNF and IL-6 are dominant innate responses to bacterial infection whereas interferon-γ is likely a remnant from the T-cell response to the previous viral infection and less affected by MMP-2/9 inhibition. The restriction of bacteria from the blood of MMP-2/9 inhibitor treated mice may reflect reduced effects of metalloproteinases on endothelial permeability and the destruction of vascular basement membranes and extracellular matrix.21 Alternatively, our data of TREM-1 modulation of degranulation suggests that bacteria are cleared quickly without becoming invasive.
A TREM-1 genetic polymorphism rs2234246 has recently been described that correlates with susceptibility to septic shock in the Chinese Han population,50 though the implications of this for membrane bound and soluble TREM-1 are currently unclear. Soluble TREM-1 has also been utilized as a biomarker for disease severity, particularly in pneumonia and septic shock. Importantly, we show a relative insensitivity of serum soluble TREM-1 compared with airway lavage, which suggests that sputum may provide better differentiation of disease status. The timing of TREM-1 ectodomain shedding is clearly critical to the outcome of bacterial super-infections. In patients with underlying disease, this shedding may already have occurred by the time bacteria start to expand. Protease imbalance and elevated MMPs are a hallmark of an array of chronic diseases also susceptible to bacterial infection. Inhibition of MMP-2/9 is therefore an interesting and feasible target in order to redress the inability of innate immunity to respond rapidly.
Influenza A Puerto Rico/8/34 H1N1 (PR8), a kind gift from Prof Andreas Wack (National Institute for Medical Research, Mill Hill, UK), was stored at −80 °C in single-use aliquots. Wild type S. pneumoniae (serotype 2) strain D39 (NTCC 7466, National Collection of Type Cultures, London, UK) was a kind gift from Jeremy Brown (Centre for Respiratory Research, UCL, London, UK). Bacterial stocks were cultured at 37 °C in 5% CO2 in Todd-Hewitt broth (Sigma, Dorset, UK) supplemented with 0.5% yeast extract (OXOID, Basingstoke, UK) to an OD600 of 0.4 (∼1 × 108 colony-forming units (CFU)/mL) and stored at −80 °C in 10% glycerol as single-use aliquots.
Secondary bacterial pneumonia model
Six- to 8-week old or 17–19 g female BALB/c mice were purchased from Harlan Olac (Bicester, UK) and maintained in specific pathogen-free conditions at Bio Safety Level 2 in accordance with institutional and UK Home Office guidelines. Mice were anesthetized and i.n. inoculated with 15 plaque-forming units (PFU) influenza A virus PR8 strain in 50 μl PBS or PBS alone as mock control. On day 7 post-viral infection, mice were inoculated i.n. with S. pneumoniae (106 CFU). Disease severity and weight loss were monitored daily. Mice were culled 24 h post-bacterial infection by intraperitoneal injection of 3 mg pentobarbitone (Animal Care, York, UK) and exsanguination by cardiac puncture.
MMP-2/9 inhibitor administration during secondary bacterial pneumonia
Female BALB/c mice were infected i.n. with PR8 influenza (7 PFU in 50 μl PBS) or PBS alone as control. On day 6, mice were treated with MMP-2/9 inhibitor I (Calbiochem/Milipore, Hertfordshire UK,) i.n. (100 μg per mouse in 25 μl) in dimethylsulfoxide (DMSO). On day 7, mice were administered MMP-2/9 inhibitor i.n. (100 μg per mouse in 25 μl) in DMSO or vehicle alone as control and infected i.n. with S. pneumoniae (106 CFU in 25 μl PBS).
Sample recovery and cell isolation
Mice were sacrificed and blood, BAL fluid and lung tissue were harvested. For bacterial CFU analysis, 10 μl of sodium heparin were added to 90 μl of blood to prevent clotting (Leo Pharma, Berkshire, UK). The remaining blood was collected in serum-separating Microtainer tubes (BD Diagnostics, Oxford, UK) tubes, left to clot overnight at 4 °C prior to centrifugation at 8,000 r.p.m. for 5 min and stored at −80 °C for future analysis. BAL was performed by inflation of the lung three times with 0.4 ml ice-cold PBS via an intratracheal cannula. Volume of 100 μl were used for CFU analysis, the remaining BAL fluid was centrifuged at 1,200 r.p.m. for 5 min and the supernatant stored at −80 °C. Lung tissue was chopped, incubated with 0.14 Wunsch units per ml Liberase (Roche, Welwyn Garden City, UK) and 50 μg m−1 DNAse I (Roche) for 30 min at 37 °C and passed through a 70 μM cell strainer. Prior to centrifugation at 1,500 r.p.m. for 5 min, 100 μl of lung cell suspension were used for CFU analysis. Red blood cells in BAL and lung cell suspensions were lysed with ammonium chloride potassium (ACK) buffer (0.15 M ammonium chloride, 1 M potassium hydrogen carbonate and 0.01 mM EDTA, pH 7.2) for 3 mins and washed with RPMI-1640 medium (PAA, Buckinghamshire, UK) containing 10% v/v foetal calf serum (FCS; Sigma). Cell viability was assessed by trypan blue exclusion.
Bacterial titers in BAL, lung and blood were determined by counting CFU from serial ten-fold dilutions of bacterial cell suspensions plated on Columbia blood agar plates supplemented with 5% defibrinated horse blood (TCS Bioscience, Buckingham, UK) and incubated for 24 h at 37 °C.
Neutrophil in vitro assay
Murine bone-marrow-derived neutrophils (2 × 105 cells) were stimulated with Pro-MMP-9 (1 μg ml−1; R&D systems, Abingdon, UK), p-aminophenylmercuric acetate (APMA; 1 mM, Sigma), and APMA-activated MMP-9 (1 μg ml−1) in RPMI-1640 with 5% FCS serum at 37 °C for 15 min. Pro-MMP-9 was activated by pre-incubation with 1 mM APMA for 2 h at 37 °C. Expression of TREM-1 on the neutrophils was determined by FACS. Cell supernatants were collected and frozen at −80 °C prior to detection of sTREM-1 by enzyme-linked immunosorbent assay (ELISA).
In some experiments neutrophils were flushed out of bone marrow with ice-cold PBS and isolated using the neutrophil isolation kit (Miltenyi Biotec, Bisley, UK) as per the manufacturer instructions. Neutrophils (100 000) were incubated with 10 μg ml−1 anti-TREM-1 antibody, 10 μg ml−1 control Goat IgG (both from R&D, Minneapolis, USA), 1 μg ml−1 LP17 (LQVTDSGLYRCVIYHPP) or 1 μg ml−1 LP17 control peptide (TDSRCVIGLYHPPLQVY) (both from Biotrend Chemical, Destin, USA) for 1 h.51 Neutrophils were then stimulated with 10 nM fMLP (Sigma) for 5 and 10 min, stained with anti-CD63 and anti-CD11b antibodies (both from eBioscience, Altrincham, UK) and analyzed by flow cytometry.
Cells isolated from BAL or lung tissue digest were stained with the live/dead marker Zombie Aqua (Biolegend, London, UK), Ly6G (eBioscience, Hatfield, UK) and TREM-1 (R&D systems). Labeled cells were acquired on a BD Fortessa (BD Bioscience) and analyzed using FlowJo (Treestar, Ashland, OR, USA).
Murine sTREM-1, MMP-2 and MMP-9 were measured by Duoset ELISA kits (R&D systems) and murine IL-6, IL-1α, TNF-α and interferon-γ (eBioscience) ELISA kits according to the manufacturer’s instructions. MMP-9 activity was determined using Novex 10% zymogram gelatin gels (Invitrogen, Paisley, UK). Images were captured and analyzed using myECL Imager software (Thermo-Scientific, Cheshire, UK).
Data were analyzed using Prism 5 (GraphPad Software, CA, USA). P-values were determined by the Mann–Whitney test comparing between 2 groups and are indicated on graphs as * P<0.05, **P<0.01, ***P<0.001. Correlations were analyzed using Spearman’s rank test.
G.W. is a Marie Curie Research Fellow (303039). C.L. was funded by a PhD studentship from the M.R.C. & Asthma UK Centre in Allergic Mechanisms of Asthma. R.J.S. is a Wellcome Trust Career Development Fellow (095707/Z/11/Z). T.H., A.M.G. and M.E.F. are supported by a pre-competitive, Open Innovation Centre grant from GlaxoSmithKline and AstraZeneca.
G.W. and C.L. generated all in vivo data presented. C.L. performed the neutrophil MMP-9 in vitro assay. M.E.F. and A.M.G. performed the studies relating to TREM-1 function on neutrophils. G.X. provided the proof of concept for the study. R.J.S and B.T. assessed MMP9 activity. T.H., G.W., C.M.L. and R.J.S. designed the research, generated the funds to perform the work and wrote the manuscript.
About this article
Inflammation Research (2018)