key: cord-0686920-w4j8zq7d
authors: Niemiec, Stephen M.; Hilton, Sarah A.; Wallbank, Alison; Louiselle, Amanda E.; Elajaili, Hanan; Hu, Junyi; Singh, Sushant; Seal, Sudipta; Nozik, Eva; Smith, Bradford; Zgheib, Carlos; Liechty, Kenneth W.
title: Lung function improves after delayed treatment with CNP-miR146a following acute lung injury()
date: 2021-11-26
journal: Nanomedicine
DOI: 10.1016/j.nano.2021.102498
sha: cc6fa69381cd08bc43917ea94dd3f892e4ff804a
doc_id: 686920
cord_uid: w4j8zq7d

Acute respiratory distress syndrome (ARDS) is a highly morbid pulmonary disease characterized by hypoxic respiratory failure. Its pathogenesis is characterized by unrestrained oxidative stress and inflammation, with long-term sequelae of pulmonary fibrosis and diminished lung function. Unfortunately, prior therapeutic ARDS trials have failed and therapy is limited to supportive measures. Free radical scavenging cerium oxide nanoparticles (CNP) conjugated to the anti-inflammatory microRNA-146a (miR146a), termed CNP-miR146a, have been shown to prevent acute lung injury in a pre-clinical model. In this study, we evaluated the potential of delayed treatment with CNP-miR146a at three or seven days after injury to rescue the lung from acute injury. We found that intratracheal CNP-miR146a administered three days after injury lowers pulmonary leukocyte infiltration, reduces inflammation and oxidative stress, lowers pro-fibrotic gene expression and collagen deposition in the lung, and ultimately improves pulmonary function.

in the past year secondary to the global pandemic (1-4). Mortality with moderate to severe ARDS is nearly 40%, and patients who survive their initial hospitalization are at increased risk of long-term pulmonary disease secondary to fibrotic changes in the lung (5, 6). Unfortunately, therapies are largely limited to supportive strategies such as mechanical ventilation and prone positioning (3, 7). ARDS can be triggered by a range of etiologies, such as pneumonia or trauma, but all share the common pathways of an unrestrained inflammatory response and profound oxidative stress. These inflammatory pathways have been shown to be key mediators in the pathogenesis of ALI and ARDS (8-10). Studies have shown that higher levels of interleukin (IL)-6 and tissue necrosis factor (TNF) α in patients with ARDS are associated with increased morbidity and mortality (11, 12) . The inflammatory response results in pulmonary edema and worsening hypoxia, and promotes downstream fibrotic changes in the lung (13) . Therefore, therapeutics that inhibit the inflammatory cascade could offer a promising avenue for the treatment of ALI/ARDS.

One class of small molecules being studied for the treatment of acute lung injury are microRNAs (miRNA, miR) (14) . One such miRNA, miR146a, is an anti-inflammatory miRNA that inhibits the nuclear factor kappa B (NFκB) pathway through upstream inhibition of tumor necrosis factor receptor associate factor (TRAF) 6 and IL-1 receptor associated kinase (IRAK) 1 (15, 16) . NFκB activation normally upregulates pro-inflammatory IL-6, IL-8, and TNFα, so inhibition of the NFκB pathway with miR146a is able to lower pro-inflammatory signaling in lung disease (17, 18) . Because miRNAs are quickly degraded, nanoparticle technology is often used to improve miRNA stability and improve therapeutic delivery to the target organ. miR146a delivery with liposomal nanoparticles has been shown to decrease ventilator-induced lung injury (19) . Cerium oxide nanoparticles (CNP) are a divalent metal oxide that can conjugate to and stabilize miRNAs for therapeutic use (20) . Unlike some other nanoparticle delivery systems, the divalent nature of CNP offers the synergistic therapeutic benefit of lowering reactive oxygen J o u r n a l P r e -p r o o f Journal Pre-proof species levels by acting as a free radical scavenger (8, [21] [22] [23] [24] [25] [26] . CNP has had recent implications as a potential treatment for coronavirus-associated ARDS (27) . Furthermore, CNP has been shown to inhibit transforming growth factor (TGF)-β, which is an important mediator of ARDS-associated pulmonary fibrosis (28, 29) .

Previous research has shown that a single intratracheal (IT) dose of CNP-miR146a is able to prevent ALI in a murine bleomycin injury model (20) . The IT drug delivery route allows for localized therapeutic delivery to the lung while minimizing systemic absorption and avoiding first-pass drug degradation common with intravenous and gastrointestinal administration (20, 30) . Treatment at the time of injury provides a mechanistic understanding of ALI pathophysiology and the role of CNP-miR146a in decreasing the injury cascade. Preventative treatment could be applied to patients who have an observed aspiration event or are placed on the ventilator for surgery, however, the majority of patients with ALI will present hours to days after onset of injury, after which the inflammatory cascade has already been initiated and lung function has deteriorated. Therefore, it is critical to examine the efficacy of delayed treatment with novel therapeutics like CNP-miR146a after the onset of oxidative stress and inflammatory signaling. We hypothesized that delayed treatment with CNP-miR146a three or seven days following acute injury with bleomycin would rescue pulmonary function by decreasing oxidative stress, inflammation, and fibrosis in the lung.

The synthesis of CNP, also named nanoceria, has previously been described in detail (31, 32) . Briefly, Ce(NO) 3 , 6H 2 O was mixed and dissolved in deionized water. Excess hydrogen peroxide was then added to oxidize the cerium (III) ions to cerium (IV) oxide at a pH below 3.5.

The acidic pH maintains nanoparticle suspension. Oxidized nanoparticles precipitate into crystalline structures, which are then isolated with centrifugation. Nanoceria is resuspended in RNase-free water to a final concentration of 10 µM. To conjugate miR146a to CNP, 1,1-J o u r n a l P r e -p r o o f Journal Pre-proof carbonyldiimidazole (CDI) is activated and chemically couples the miR146a amino group to the CNP hydroxyl group.

C57BL/6 male mice, aged eight-to 10-weeks (strain No. 000642, Jackson Laboratory), were used for this study. All mice were maintained one week in standard housing to allow for acclimation to Denver ambient atmosphere (1600m altitude) prior to use in the experiment. Remaining mice were given an equivalent volume of phosphate buffered saline (PBS) for the uninjured control group (Control). Treatment of injured mice with CNP-miR146a was performed at three or seven days (Bleo + CNP-miR146a D3; Bleo + CNP-miR146a D7), as described below.

CNP-miR146a toxicity studies have been previously described including a 3-(4,5dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) toxicity assay, comparative pathology, and systemic distribution analyses (20) . For this study, conjugated 100ng CNP-miR146a was diluted in 50µL phosphate buffered solution (PBS) for intratracheal dosing. A subset of mice injured with bleomycin were treated with 100ng/50µL CNP-miR146a three days after injury or seven days after injury to evaluate for delayed treatment effect on reactive oxygen species (ROS) production, inflammation, fibrosis, and lung function. Previous study identified that the conjugate treatment performed better than individual component dosing (using CNP or miR146a mimetic alone), and therefore rescue treatment was only tested with CNP-miR146a to optimize animal use (20) . We utilized the control data initially published in our original J o u r n a l P r e -p r o o f prevention manuscript (20) in our comparison analysis with the delayed day three and seven treatment groups in an effort to ethically reduce animal numbers given the same endpoint in experiments. All measurements described below were taken from distinct samples.

Whole lung tissue was harvested 14 days following injury (n = 5, 10, 12, 5 for Control, Bleo, Bleo + CNP-miR146a D3, and Bleo + CNP-miR146a D7, respectively) following pulmonary flushing with five mL of chilled PBS via right cardiac puncture. Tissue was homogenized using sucrose buffer (0.25M sucrose, 10mM TRIS-HCl, 1mM EDTA, pH 7.4).

Lung homogenate was mixed with Krebs-HEPES buffer (KHB), 100µM DTPA (metal chelator), and 0.2mM 1-hydroxy-3-methoxycarbonyl-2, 2, 5, 5-tetramethylpyrrolidine (CMH). CMH is a superoxide selective spin probe that reacts with superoxide to form the more stable CM• radical. CM• can then be detected by EPR and its concentration reflects ROS production. Samples were incubated for 60 minutes at 37 o C prior to loading 150µL into rubber-top sealed PTFE tubing (33). EPR acquisition was performed using the Bruker EMX nano-X-band spectrometer and CM• concentration was detected in the Bruker liquid nitrogen Finger Dewar at 77 K. CMH in KHB without the lung homogenate was used as a blank sample to determine the background signal, which was subtracted from the CM• signal. Double integration followed by Spin count using the Bruker software was used to measure CM• nitroxide radical concentration for each sample. The acquisition parameters used were: microwave frequency = 9.65 GHz; center field = 3438 G; modulation amplitude = 4.0 G; sweep width = 150 G; microwave power = 0.316 mW; total number of scans = 10; sweep time = 60 s; and time constant = 1.28 ms, as described previously (20) .

Whole lung tissue was collected at seven-and 14n-days following injury for real-time quantitative polymerase chain reaction (RT-qPCR) analysis of pro-inflammatory and pro-fibrotic gene expression. Three groups were evaluated at the seven-day timepoint (n = 6, 6, 7 for the J o u r n a l P r e -p r o o f Journal Pre-proof Control, Bleo, and Bleo + CNP-miR146a D3 groups, respectively), while all four groups were evaluated at the fourteen-day timepoint (n = 6, 6, 6, 5 for Control, Bleo, Bleo + CNP-miR146a D3, and Bleo + CNP-miR146a D7, respectively). Collected lung tissue was flash frozen prior to homogenizing in Qiazol (Qiagen) per manufacturer instructions. RNA was isolated and converted to cDNA (Applied Biosystems RT kit). Amplification of cDNA was performed by reverse transcriptase amplification with the BioRad CFX-9600 thermal cycler. RT-qPCR was done for IL-6, IL-8, and TNFα for pro-inflammatory genes and collagen (Col) 1α2, Col3α1, and transforming growth factor (TGF)-β1 for pro-fibrotic genes, with glyyceraldehyde 3-phosphate dehydrogenase (GAPDH) used as the housekeeper gene for normalization. Each sample was analyzed in triplicate with the average of each triplicate used for normalization.

Histologic analysis of inflammatory cell infiltrate and collagen deposition was performed on lung tissue collected fourteen days after injury (n = 7, 7, 6, 7 for Control, Bleo, Bleo + CNP-miR146a D3, and Bleo + CNP-miR146a D7, respectively). Lungs were inflated with melted agarose solution and removed into 4% paraformaldehyde (PFA). The lung was immersion fixed in 4% PFA for 24 hours at room temperature prior to dehydrating in 70% ethyl alcohol (EtOH).

Dehydrated tissue was embedded into paraffin blocks and sectioned at four µm. Sectioned slides were stained with Mason's trichrome, which is a general collagen stain turning collagen fibers blue under bright field microscopy. Twenty high-powered fields (HPF) at 400x total magnification were randomly imaged for each sample. An automated counting algorithm on NIS Elements -Advanced Research imaging software was used by a blinded researcher to quantify the area of blue staining per HPF, which quantifies the area of collagen per HPF. The 20 random fields were averaged for each sample for comparison between groups.

Additional slides were deparaffinized for immunohistochemistry with CD45 staining.

CD45 is a common leukocyte antigen that stains all leukocytes brown under bright field microscopy. The heat-induced epitope was acquired using the Biocare Medical Decloaker prior J o u r n a l P r e -p r o o f Journal Pre-proof to slide staining with Leica's Bond Rx instrument. Slides were then treated with primary CD45 antibodies (1:50 solution, BD Biosciences) and developed with Vectastain Elite ABC kit (Vector laboratories). As above, 20 random 400x magnification HPFs were imaged and the number of CD45-positive cells per HPF were quantified. Average counts per HPF for each sample were used for analysis.

Mice underwent mechanical ventilation testing 14 days after injury to assess pulmonary function (n = 11, 8, 9, 9 for Control, Bleo, Bleo + CNP-miR146a D3, and Bleo + CNP-miR146a D7). For the ventilatory procedure, mice were anesthetized with acepromazine (2.5 mg/kg), ketamine (100 mg/kg), and xylazine (8 mg/kg) via intraperitoneal (IP) injection. A tracheostomy was performed using an 18-gauge canula through which mice were ventilated using a computer-controlled small animal ventilator (SCIREQ flexiVent). Once on the ventilator, mice were given 0.8mg/kg IP pancuronium bromide to suppress respiratory efforts that would invalidate the measurements of lung mechanics. All subjects underwent a 10-minute stabilization period of baseline ventilation of 10mL/kg tidal volume at 200 breaths per minute with positive end expiratory pressure (PEEP) = 3 cmH 2 0. Every two minutes the mice received a recruitment maneuver (RM) consisting of a 3-second ramp to 30 cmH 2 0 with a 3-second breath hold.

The lung mechanics assessment included an RM followed by a 16-second step-wise pressure-volume loop with a maximal pressure of 30 cmH 2 0, which was then used to calculate quasi-static compliance at 5 cmH 2 0 during expiration and the delivered volume, which we refer to as the inspiratory capacity. To measure pulmonary system impedance, an RM was performed and the baseline ventilation was applied at PEEP = 0 cmH 2 O. Four 3-second multi-frequency forced oscillations (delivered volume 3mL/kg, PEEP=0 cmH 2 O, 13 mutually prime frequencies from 1 to 20.5 Hz) were then applied at 10 second intervals. This impedance data was then J o u r n a l P r e -p r o o f Journal Pre-proof used to determine pulmonary system elastance, tissue resistance, and airway resistance by fitting to the constant phase model (34) .

Quantitative variables were compared between groups using One-Way ANOVA for a significance value of α = 0.05. Statistical analysis was performed with GraphPad Prism 9 (San Diego, CA).

Immunohistochemical analysis of leukocyte infiltrate into pulmonary tissue was performed on samples collected 14 days after injury. Representative images at 100X magnification of CD45+ stained slides are shown in Figure 1A -D. Qualitatively, control lungs had less alveolar collapse and debris than bleomycin-injured lungs. There were significantly more CD45+ cells per HPF in bleomycin-injured lungs than controls (p = 0.0004, 95% CI: [-131 .5, -35.49]). The alveolar structure subjectively appeared more preserved in the bleomycin lungs treated with CNP-miR146a 3 days after injury ( Figure 1C) . Quantitative analysis of CD45+ cells per HPF showed that treatment with CNP-miR146a on day 3 significantly lowered leukocyte infiltrate compared to untreated lungs (p = 0.0003, 95% CI: [38.94, 138 .9]), however treatment with CNP-miR146a seven days after injury did not significantly lower CD45+ cell counts (p = 0.1499).

Whole lung tissue was collected at seven and 14-days following injury and processed for RT-qPCR to evaluate for relative gene expression of pro-inflammatory genes IL-6, IL-8, and

TNFα. As depicted in Figure 2A 

Quantitative PCR analyzing the relative gene expression of Col1α2, Col3α1, and TGFβ-1 was performed on days seven and fourteen after initial injury. Pro-fibrotic gene expression in lungs treated with CNP-miR146a three days after injury returned to control levels, with significantly lower expression levels of Col1α2, Col3α1, and TGFβ-1 compared to untreated, bleomycin-injured lungs on day seven (Figure 4A 

Quantitative analysis of trichrome stained slides was performed for samples collected 14 days after injury as an assessment of collagen levels in the lung. Representative images at 100X total magnification (10x objective lens) of trichrome stained samples are shown in 

Pulmonary mechanics were measured 14 days after injury during invasive mechanical ventilation. Multi-frequency forced oscillation measurements at PEEP=0 cmH 2 O show that bleomycin-injured mice had significantly higher pulmonary system elastance and tissue 

In this study, we have demonstrated that a single dose of CNP-miR146a three days after the onset of ALI due to bleomycin is able to improve pulmonary mechanics. Previously shown to prevent inflammation, oxidative stress, and fibrosis with co-treatment at the time of injury, this study highlights that IT delivery of CNP-miR146a in a delayed fashion after ALI onset is able to still inhibit the inflammatory and fibrotic processes, ultimately improving lung mechanics.

CNP-miR146a attenuated the increase seen in bleomycin-induced pro-inflammatory gene expression when delivered as a rescue therapy, as depicted in Figure 2 . Human ARDS is associated with increased circulating levels of TNFα, IL-6, and IL-8, important mediators and markers of inflammation (35, 36) . Patients with novel coronavirus-associated ARDS have higher IL-6 and TNFα levels and have increased risk of requiring mechanical ventilation and mortality (11, 12). MiR146a inhibits IRAK1 and TRAF6, upstream promotors of NFκB, which in turn inhibit IL-6, IL-8, and TNFα (15) (16) (17) (18) . CNP-miR146a increases miR146a levels in the lung following IT delivery (20) , and this activation of intrinsic anti-inflammatory pathways may protect the lung from ongoing tissue damage and therefore improve function.

A possible pathway by which CNP-miR146a lowers inflammation is through reduction in pro-inflammatory signaling, as described above, but it may additionally contribute to a decrease in leukocyte recruitment to the site of injury. Leukocyte response to acute lung injury is complex, but involves rapid recruitment of circulating neutrophils and activation of alveolar macrophages (37, 38) . These cell lines increase signaling cytokines and chemokines such as TNFα, TGFβ-1, J o u r n a l P r e -p r o o f and monocyte chemoattractant protein-1 (MCP-1) to recruit additional monocytes to the area.

CD45 is a common leukocyte marker, so it reflects total leukocyte infiltration rather than specific cell lines, and we saw significantly lower CD45 cells in the lung with CNP-miR146a treatment 3 days after injury. Future investigation of whether the reduction in pro-inflammatory gene signaling and ROS could be secondary to a decrease in overall leukocyte infiltration, a change in leukocyte plasticity, or a combination of these conditions will help better elucidate the mechanisms of ARDS pathophysiology and the potential cell-level implications of CNP-miR146a as a therapy. Cellular level studies looking at the specific cell lines recruited to the site of injury, as well as the effect of CNP-miR146a on alveolar and interstitial macrophage recruitment and polarization, will better identify the direct mechanism by which CNP-miR146a decreases inflammatory signaling.

CNP is a divalent metal oxide with ROS scavenging properties, offering a potential benefit in reducing oxidative stress in ALI and ARDS, which is characterized by excess ROS (23, 24, 39) . CNP and CNP-miR146a have been more fully characterized in our previous work with diabetic wounds (40) . Briefly, CNP and CNP-miR146a have a size of 20nm and 190nm, respectively, and conjugation of CNP to miR-146a significantly alters surface zeta charge while maintaining redox potential. High doses of CNP, up to 2000µg/mL, which is over 1000 times the dose tested in this experiment, have been shown to have no toxicity to cell lines after 24 hours of high-dose exposure (41, 42) . We have previously shown similar data showing no cellular toxicity with CNP or CNP-miR146a. Additionally, IT CNP-miR146a does not increase plasma or lung CNP concentration 72 to 168 hours after exposure, suggesting these lower doses may be adequately cleared with lower potential for toxicity (20) . The conjugation of CNP to miR146a could synergistically lower ROS, as miR146a modulates ROS production through the inhibition of cytokine signaling. We have previously shown that both CNP and miR146a alone can prevent ROS elevations in a bleomycin lung injury model (20, 43) . Increased production of ROS J o u r n a l P r e -p r o o f promotes collagen formation and fibroblast proliferation, and ROS activates TGFβ-1, further increasing the pro-fibrotic response (44) (45) (46) .

Delayed treatment with CNP-miR146a attenuated pro-fibrotic gene expression and lowered collagen levels in the lung, as seen in Figures 4 and 5 . The long-term effects of ARDS in survivors often manifest as fibrotic changes in the lung (5, 6). Survivors of ARDS have an exercise capacity at 66% of predicted and a mere 49% of patients return to work in the first year following hospitalization (47) . Extracellular matrix (ECM) remodeling in ARDS is multifactorial, however pathways known to induce ARDS-associated fibrosis include TGFβ signaling and alterations in collagen types I and III (13) . The lung parenchyma is largely composed of type I and type III collagen fibers, and fibrotic remodeling is characterized by increased Col1α2 gene expression and higher collagen I-to-III protein ratios (48) . Trichrome is a general collagen marker, and therefore, we are unable to differentiate whether the histologic changes seen two weeks following injury with bleomycin is due to increases in collagen 1 or collagen 3 protein; however, CNP-miR146a lowers Col1α2, Col3α1, and TGFβ-1 signaling, potentially through alterations in ROS activation of ECM pathways. By lowering pro-fibrotic gene signaling and overall collagen levels, CNP-miR146a could have the potential to improve long-term clinical effects while also improving lung function.

Ultimately, the goal of treatment is preservation of pulmonary function, and CNP-miR146a improved lung function at two weeks when given three days after injury, as depicted in Figure 6 . Human ARDS is characterized by significant reductions in pulmonary system compliance due to inflammatory cell induction of alveolar collapse and pulmonary edema, and lower available lung volume is reflected in higher elastance (49, 50) . While delaying treatment to seven days did not improve mechanical lung function following ALI, there were improvements in ROS and pro-inflammatory signaling. It is possible that our end-point of 14 days did not provide enough time for any functional improvement to be identified secondary to CNP-miR146a instillation seven days after injury. Future study to evaluate later timepoints and if higher doses J o u r n a l P r e -p r o o f of CNP-miR146a at later timepoints may improve lung function will be important for determining the optimal treatment window for ALI with CNP-miR146a. CNP-miR146a could therefore have implications clinically in reducing the need for mechanical ventilation or duration of mechanical ventilation through rescuing of pulmonary mechanics even after inflammatory and oxidative stress pathways have been activated.

ALI and ARDS pathophysiology in humans is multi-factorial in etiology and pathogenesis, so a wide range of pre-clinical models, such as lipopolysaccharide (LPS)-induced lung injury, are used. We chose to use the bleomycin-induced lung injury as it is a wellestablished lung injury model secondary to its long-term fibrotic effects and well accepted mechanism of injury, and it is a continuation of our previous work with CNP-miR146a cotreatment at the time of injury (20) . Future study utilizing different models, such as LPS-induced lung injury and ventilator-induced lung injury, will help to generalize the utility of CNP-miR146a as a rescue treatment for ALI. The dose chosen for this study was based on work performed in both diabetic wounds and bleomycin-induced lung injury (20, 51) . In our work with diabetic wounds, higher doses of CNP-miR146a delayed wound healing, which we hypothesized was secondary to the need for some inflammation to promote healing. We therefore wished to look at this established dose in treating ALI in a delayed fashion, and future evaluation of a doseresponse will be undertaken specifically looking at the effect on pulmonary function, toxicity, and cellular uptake. CNP and miR146a have been shown to have potential applications in treating acute lung injury (14, 18, 19, 27, 52) . We have previously shown that IT delivery of CNP-miR146a has low toxicity with local delivery and no systemic uptake, and that the conjugate treatment of CNP-miR146a is able to prevent ALI better than the individual component doses (20) . While there have been advancements in understanding the pathogenesis of ARDS, mortality remains high and therapeutic innovation is of critical importance. This study is the first to look at the potential of CNP-miR146a in treating ALI/ARDS using a delayed treatment strategy, which has greater J o u r n a l P r e -p r o o f shown for n = 6, 6, 7 samples at day seven for the Control, Bleo, and Bleo + CNP-miR146a D3 J o u r n a l P r e -p r o o f groups, respectively, and for n = 6, 6, 6, 5 samples at day fourteen for Control, Bleo, Bleo + CNP-miR146a D3, and Bleo + CNP-miR146a D7, respectively.

Fourteen days after injury, CM• concentration is significantly lower in control, day 3-treated, and day 7-treated lungs compared to untreated, bleomycin-injured lungs. Bars indicate statistical significance with p < 0.05. Mean and standard deviation values are shown for n = 5, 10, 12, 5 samples for Control, Bleo, Bleo + CNP-miR146a D3, and Bleo + CNP-miR146a D7, respectively. gene expression seven and fourteen days after injury. Treatment with CNP-miR146a 3 days after injury significantly lowered Col1α2 and Col3α1 gene expression at seven days, also lowering TGFβ-1 at this timepoint. Treatment with CNP-miR146a seven days after injury lowered Col3α1 gene expression compared to untreated, bleomycin-injured lungs 14 days after injury. Bars indicate statistical significance with p < 0.05. Mean and standard deviation values are shown for n = 6, 6, 7 samples at day seven for the Control, Bleo, and Bleo + CNP-miR146a D3 groups, respectively, and for n = 6, 6, 6, 5 samples at day fourteen for Control, Bleo, Bleo + CNP-miR146a D3, and Bleo + CNP-miR146a D7, respectively. 

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Figure 6: Treatment with CNP-miR146a three days after injury rescues lung function (A) Pulmonary elastance and (D) tissue resistance are increased, and (B) quasi-static compliance and (C) inspiratory capacity are lowered, with bleomycin injury. CNP-miR146a treatment three days after injury significantly improves elastance, quasi-static compliance, and inspiratory capacity to control levels. Bars indicate statistical significance with p < 0.05. Mean and standard deviation are shown for n = 11, 8, 9, 9 samples for Control, Bleo, Bleo + CNP-miR146a D3, and Bleo + CNP-miR146a D7, respectively

clinical implications than a preventative therapy. In this study, we have shown that treatment with CNP-miR146a three days after injury improves pulmonary function by lowering proinflammatory gene expression and oxidative stress, reducing leukocyte infiltration, and decreasing pro-fibrotic gene expression and collagen levels in the lung.

The authors would like to thank the University of Colorado Denver Histology Shared Resource Center for their contribution to this work.