Pharmacologic inhibition of MEK1/2 reduces lung inflammation without impairing bacterial clearance in experimental Pseudomonas aeruginosa pneumonia
© The Author(s) 2017
Received: 11 April 2017
Accepted: 3 August 2017
Published: 5 September 2017
This study was designed to test the therapeutic potential of a MEK1/2 inhibitor (MEKi) in an experimental model of Pseudomonas aeruginosa pneumonia. The study found that treatment with MEKi reduced alveolar neutrophilic inflammation and led to faster recovery of weight compared to carrier-treated mice, without impairing bacterial clearance. Alveolar macrophages isolated from MEKi-treated mice also had increased M2 gene and protein expression, supporting the concept that MEKi modulates in vivo macrophage inflammatory responses. In summary, this report demonstrates the potential of MEKi to promote the resolution of inflammation in vivo during a primary lung infection without impairing bacterial clearance.
KeywordsMacrophage MEK1/2 Pseudomonas aeruginosa Lung
Pseudomonas aeruginosa pulmonary infections are common in hospitalized patients and are one of the drivers of progressive lung decline in patients with cystic fibrosis . Recurrent or chronic P. aeruginosa infections result in increased lung inflammation, subjecting the lung to host-mediated tissue damage. Immune modulating strategies to reduce deleterious lung inflammation without compromising host-defense mechanisms may be therapeutically beneficial in this situation, and new strategies to reduce lung injury are needed.
The mitogen-activated protein kinases MEK1 (Map2k1) and MEK2 (Map2k2) participate in intracellular signaling networks and exert control on the downstream effector molecules ERK1 and ERK2, via MEK1/2-dependent serine and tyrosine phosphorylation . Several recent studies, including this one, have investigated the potential therapeutic use of MEKi compounds as immune modulating agents [3–9]. Given that a MEKi is now FDA-approved for use in certain cancer chemotherapeutic regimens , the potential for application of these pharmaceuticals to fulfill unmet clinical needs in infectious diseases is intriguing.
We recently reported  that MEKi delivery to mice, starting 1 day post- lipopolysaccharide (LPS) acute lung injury (ALI), reduced lung neutrophilia and led to faster resolution of lung injury and greater macrophage M2 polarization. These findings suggest that MEK pathways may be important therapeutic targets; however, information on the therapeutic use of MEKi in bacterial pneumonia models is lacking. The goals of the current study were to determine if MEKi promotes the resolution of inflammation in vivo during experimental P. aeruginosa pneumonia in mice without increasing susceptibility to infection or compromising bacterial clearance.
This study used age (8–12 weeks) and sex-matched C57BL/6J mice that included both male and female groups. The University of Washington Institutional Animal Care and Use Committee reviewed and approved all animal procedures prior to initiation of these studies.
Bacterial strain and culture conditions
P. aeruginosa strain K (PAK) was grown overnight in lysogeny broth (LB-Miller) at 37°C. Bacteria were pelleted at 13,000 x g, washed twice in phosphate buffer saline (PBS), and re-suspended in PBS so that a target inoculum of 5 × 106 colony-forming units (CFU) in 50 μl was delivered via oropharyngeal aspiration.
Infection, drug treatment, and sample processing
C57BL/6J mice were anesthetized using isoflurane and positioned for oropharyngeal PAK infection. After instillation, mice were monitored daily for weight change and activity. MEKi PD0325901 (20 mg/kg, InvivoGen, San Diego, California [CA], United States of America [USA]) or carrier control (10% dimethylsulfoxide [DMSO] in PBS) was delivered by intraperitoneal (IP) injection on days 2 and 3 after infection. Animals were sacrificed on day 4 after infection. Alveolar immune cells were collected by three serial bronchoalveolar lavage (BAL) with PBS + 5 mM EDTA. BAL cells were centrifuged for 10 min at 350 x g and re-suspended in sterile PBS. Total BAL cells were enumerated on a Cellometer Auto 2000 (Nexcelom Bioscience, Lawrence, Massachusetts [MA], USA) and 50,000 cells were used for slide cytospin preparations and stained using Diff-Quik (Siemens, Newark, Delaware, USA). Random fields of view from slides at a magnification of 40× were observed to determine the percentage of neutrophils and mononuclear cells in each sample. A minimum of 200 total cells from each slide was counted.
Quantitative real-time polymerase chain reaction
The remaining cells from day 4 BAL were plated in 24-well tissue culture plates and incubated for 60 min at 37 °C, 5% CO2, to allow for alveolar macrophage adherence. Wells were rinsed 3 times with PBS to remove non-adherent cells and total macrophage ribonucleic acid (RNA) was isolated with a NucleoSpin RNA isolation kit (Clontech Laboratories, Mountain View, CA, USA). A cDNA template was created from RNA by the High-Capacity cDNA Reverse Transcription kit (Applied Biosystems, Foster City, CA, USA) that was then used in quantitative real-time PCR (qPCR) reactions with validated TaqMan FAM-labeled primer probes for Hprt, Retnla, Ccl17, Arg1, and Tgfb1 (Life Technologies, Carlsbad, CA, USA) using the SensiMix II Probe Hi-ROX Kit (Bioline, Taunton, MA, USA). Reactions were performed on an ABI 7900HT Fast Real-Time PCR System. Duplicate replicates from each sample were used to obtain the average cycle threshold (Ct) and the ΔCt for each primer probe relative to Hprt was calculated as previously described . Samples were normalized to the average of carrier-treated mice from an individual experiment.
BAL fluid total protein, immunoglobulin M, and CXCL1/KC measurements
Cell free BAL fluid (BALF) was obtained from mice at day 4 post-infection and stored at −80 °C. Aliquots were used to measure total protein by a bicinchoninic acid (BCA) assay (Pierce, Rockford, Illinois, USA), IgM (Bethyl Laboratories, Inc., Montgomery, Texas, USA), and CXCL1/KC (R&D Systems, Minneapolis, Minnesota, USA) by enzyme-linked immunosorbent assay (ELISA). Standard manufacturer’s protocols were followed for each assay.
Multicolor flow cytometry on lung homogenates prepared from the right lobe were used to measure surface expression of transferrin receptor (CD71) on alveolar macrophages. Alveolar macrophages were identified as CD45+/Ly6G−/CD11c+/SigF+ cells. The median fluorescence intensity (MFI) for CD71-PerCP/Cy5.5 was determined using Flowjo software (TreeStar, Ashland, Oregon, USA) The ΔMFI was calculated by subtracting the MFI of isotype-stained from the MFI of CD71-stained samples, as previously described [3, 11]. A Canto RUO (BD Biosciences) was used for acquisition of data.
Quantification of bacterial burden
After sacrifice and lavage, the left lung and the spleen were removed and each tissue sample placed in 1 ml of sterile PBS. A sterile sonicator tip was immersed into the PBS and tissues were homogenized by sonication for 30 s. Tissue homogenates were subjected to serial dilution and spots were plated on Pseudomonas isolation agar (Sigma-Aldrich, St. Louis, Missouri, USA). Plates were incubated at 37 °C for 1–2 days and colonies were enumerated when visible. Organs from uninfected mice and from aliquots of sterile PBS used in making dilutions were plated to confirm that procedures were performed under sterile conditions.
Statistical analyses were performed using GraphPad Prism 6 software. Normal Gaussian distribution was assessed by the D’Agostino–Pearson normality test using an alpha = 0.05. Samples in which Gaussian distribution were assumed were analyzed by the unpaired t test to compare groups, while samples in which a Gaussian distribution was not assumed were analyzed using the nonparametric Mann-Whitney t test. Two-way analysis of variance (ANOVA) with Bonferroni’s multiple comparisons was used where appropriate. Statistical significance was considered as p < 0.05.
MEKi reduces inflammation without inhibiting bacterial clearance during experimental Pseudomonas aeruginosa pneumonia
The study also measured the total number of cells in the BAL from mice on day 4 post-infection and found that MEKi-treated groups had reduced BAL cell counts compared to carrier-treated controls (Fig. 1c). Differential analyses revealed that MEKi significantly reduced neutrophils compared to carrier-treatment, but did not alter macrophage numbers (Fig. 1c), similar to findings during LPS ALI . Uninfected groups treated with carrier control or MEKi demonstrated no effect of MEKi on weight (Fig. 1a), BAL cell counts (Fig. 1c), or BAL cell differential (data not shown). As additional characterization of MEKi-treatment, total protein and IgM levels in BALF were measured as indicators of lung injury and vascular leak. While the three uninfected groups were near the lower limits of detection for both total protein and IgM (Fig. 1d), infected mice had elevated levels of both total protein and IgM, although MEKi-treatment had no effect on these levels at this time point. In summary, MEKi delivery after infection was able to reduce some parameters of inflammation, such as neutrophil levels, and improve weight recovery without inhibiting bacterial clearance.
MEKi alters macrophage responses in vivo during resolution of inflammation
P. aeruginosa is an opportunistic pathogen that can induce significant lung inflammation and tissue damage, for which new immune modulating therapeutic strategies are needed . One concern of anti-inflammatory therapeutics is the potential for impairment of host–defense mechanisms involved in pathogen clearance, resulting in increased susceptibility to infection. This study examined the ability of MEKi to promote the resolution of inflammation during an experimental model of P. aeruginosa pneumonia. Importantly, the data indicate that MEKi did not impair clearance of pulmonary P. aeruginosa infection. No difference in lung CFUs was observed, and no bacterial dissemination to the spleen was detected 4 days after infection. MEKi treatment decreased alveolar neutrophilic inflammation and led to faster recovery of weight, which we interpreted as beneficial effects. Given reduced BAL neutrophils in infected MEKi-treated mice, our study looked at whether MEKi treatment reduced the level of the neutrophil chemokine, CXCL1/KC, in the alveolar compartment. The levels of CXCL1/KC in the BALF at day 4 in uninfected and infected mice treated with MEKi or carrier control were measured. At this time point, CXCL1/KC were near the lower limit of detection for this assay and were approximately 100-fold lower at this time point compared to what has previously been observed within 4 h of P. aeruginosa infection . However, despite these low levels, our study did not find a decrease in CXCL1/KC levels in MEKi-treated mice compared to carrier-control mice to explain reduced BAL neutrophil numbers (not shown). In addition, although MEKi did not alter BAL total protein or IgM levels at the time point examined, it is unknown if MEKi reduces these indicators of lung injury at earlier times after treatment. For example, the levels of BAL IgM peak within the first 24 h after infection and then decline [14, 17]. Hence, it is possible that delivery of MEKi may need to be initiated earlier to effect a change in markers of vascular leak or to detect differences in CXCL1/KC.
In summary from the data presented here, MEKi-treatment appears to modulate some, but not all, indicators of ALI. Macrophage M2 programming is increased during the resolution of ALI and it has recently been identified that MEKi increases macrophage M2 polarization in vitro and in vivo [3, 13]. Here, further data that support this notion is presented, showing that MEKi increased several markers of alveolar macrophage M2 polarization after P. aeruginosa infection, which may contribute to, or be a marker of, more rapid resolution of lung inflammation in MEKi-treated mice. These results contribute additional evidence that MEK1/2 inhibition has the potential to dampen pro-inflammatory responses and increase anti-inflammatory responses in murine models of infection and inflammation [3, 5, 6, 9].
As with all potential anti-inflammatory agents, there are concerns about increasing susceptibility to infection due to impaired host-defense mechanisms. Several experimental studies have evaluated the use of MEKi-treatment in the rat and mouse cecal-ligation and puncture (CLP) models of sepsis, demonstrating therapeutic anti-inflammatory effects without altering bacterial burdens [5, 8]. However, these models are limited in their scope of evaluation for several reasons. First, utilizing a pre-treatment regimen does not fully capture the clinical utility of MEKi as an anti-inflammatory in patients who present with inflammatory lung disease/infection. Second, the limited duration of time (< 24 h) and anatomical location of the CLP model does not allow for evaluation of a primary lung infection and potential alterations in lung host–defense mechanisms. A study examining both pre- and post-infection treatment with a MEKi during primary lung infection was recently reported . However, this study utilized a lethal F. tularensis murine infection model, which results in rapid and extensive dissemination of infection from lung to the liver and spleen , therefore not allowing examination of whether MEKi has detrimental effects on pulmonary host defense mechanisms.
Although prophylactic pre-treatment drug strategies are utilized in many pre-clinical studies to maximize potential beneficial results, therapeutic strategies employed post-infection are most likely to simulate clinical applications of a potential drug, which is a strength of this study design. Under this premise, these data indicate that MEKi is capable of promoting the resolution of inflammation and increasing macrophage M2 polarization, similar to what was previously observed during experimental LPS-induced lung injury . Additionally, recent findings have demonstrated that MEK1/2 inhibitor treatment can dampen the inflammatory response and provide a beneficial outcome when applied in a mouse model of cerebral malaria, in part by increasing IgM production by B1 cells and increasing the phagocytic activity of macrophages and neutrophils .
There are several limitations to the current study. First, based on published studies that demonstrate peak injury and inflammation occurring at days 2–3 after infection [11, 14, 17], we chose to model the effect of MEKi during this period with assessment of inflammation on day 4 after infection. However, it is recognized that examination of MEKi-treatment at both earlier and later time points are necessary to gain a more meaningful understanding of MEKi effects on inflammation and resolution. A primary goal of the current study was to determine if MEKi-treatment acutely impaired the ability of mice to control infection; however, whether MEKi alters susceptibility to recurrent or polymicrobial infections remains to be examined. Future studies will examine the mechanism by which MEKi reduces neutrophil levels in the lung. While the current data did not support a role for reduced CXCL1/KC at day 4, it is possible that CXCL1/KC, or additional neutrophil chemokines, may be altered by MEKi at earlier time points after treatment. Alternatively, previous studies found that MEKi enhances expression of receptors involved in efferocytosis and increases clearance of apoptotic polymorphonuclear cells (PMNs). Whether MEKi enhances macrophage efferocytosis in the lung or alters intrinsic properties of neutrophil migration should be investigated [3, 9]. While all of the effects of MEKi treatment are not fully understood, this study demonstrates that MEKi delivery did not impair bacterial clearance during acute infection. It is anticipated that further investigations into the use of MEKi as an anti-inflammatory therapeutic during recurrent or chronic P. aeruginosa infection models will yield additional insights into the potential beneficial effects and mechanisms of immune modulation.
This work was supported by the National Heart, Lung, and Blood Institute, National Institutes of Health Grants R01 HL 116514 (to A.M.M) and T32 HL007828 (to M.E.L.) and by University of Washington Cystic Fibrosis Foundation Research Development Program SINGH15R0 (to M.E.L.). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Heart, Lung, and Blood Institute, the National Institutes of Health, or the Cystic Fibrosis Foundation.
Availability of data and materials
All data generated or analyzed during this study are included in this published article.
MEL, KQG, and WEE performed experiments and collected all data, MEL, KQG, WEE, WCL, and AMM analyzed and interpreted data and contributed to writing and reviewing of manuscript. All authors read and approved the final manuscript.
Ethics approval and consent to participate
The University of Washington Institutional Animal Care and Use Committee reviewed and approved all animal procedures prior to initiation of this study. This study did not involve human participants.
Consent for publication
The authors declare that they have no competing interests.
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