Hyperoxia-induced acute lung injury (HALI) is a key contributor to the pathogenesis of bronchopulmonary dysplasia (BPD) in neonates, for which no specific preventive or therapeutic agent is available. Here we show that lung micro-RNA (miR)-34a levels are significantly increased in lungs of neonatal mice exposed to hyperoxia. Deletion or inhibition of miR-34a improves the pulmonary phenotype and BPD-associated pulmonary arterial hypertension (PAH) in BPD mouse models, which, conversely, is worsened by miR-34a overexpression. Administration of angiopoietin-1, which is one of the downstream targets of miR34a, is able to ameliorate the BPD pulmonary and PAH phenotypes. Using three independent cohorts of human samples, we show that miR-34a expression is increased in type 2 alveolar epithelial cells in neonates with respiratory distress syndrome and BPD. Our data suggest that pharmacologic miR-34a inhibition may be a therapeutic option to prevent or ameliorate HALI/BPD in neonates.
Hyperoxia is a well-known antecedent of injury to developing lungs and is a major contributor to the pathogenesis of bronchopulmonary dysplasia (BPD) in human preterm neonates1,2,3. BPD is the most common chronic lung disease in infants and the long-term consequences extend well into adulthood, with increasing evidence that it can lead to chronic obstructive pulmonary disease (COPD)4,5. There is currently no specific preventive or therapeutic agent available to alleviate BPD6.
MicroRNAs (miRs) are single stranded and evolutionarily conserved sequences of short non-coding RNAs (~21–25 nucleotides)7 and act as endogenous repressors of gene expression by mRNA degradation and translational repression. They have been shown to have important roles in cell differentiation, development, proliferation, signaling, inflammation, and cell death7,8,9. They have been considered promising candidates for novel targeted therapeutic approaches to lung diseases7. Given the role of hyperoxia in development of BPD, a few studies have evaluated expression profiles of miRs in various animal models and human infants8,10,11,12,13,14.
Angiopoietin-1 (Ang1) is a ligand for receptor tyrosine kinase Tie215 expressed on endothelial and epithelial cells16,17. Ang1-Tie2 signaling has been shown to be mainly involved in angiogenic activity and promoting maturation of blood vessels, regulated by Akt and MAPK signaling18,19,20.
The pulmonary phenotype of BPD is characterized by impaired alveolarization and dysregulated vascularization21. Given the potential role of miRs in the pathogenesis of BPD, in this study, we reveal that lung miR-34a levels are significantly increased in neonatal mice lungs exposed to hyperoxia. Deletion/inhibition of miR-34a globally and locally in type 2 alveolar epithelial cells (T2AECs) limits cell death and inflammation with injury and improves the pulmonary and pulmonary arterial hypertension (PAH) phenotypes in BPD mouse models. Conversely, overexpression of miR-34a in room air (RA) worsened the BPD pulmonary and PAH phenotypes, while the addition of miR-34a in the miR-34a deletion mice model exposed to hyperoxia led to reiteration of the BPD pulmonary phenotype. We also show that administration of recombinant Ang1, one of the downstream targets of miR-34a, ameliorates the BPD pulmonary and PAH phenotypes. Finally, using three independent cohorts of human samples, we show the significant association of increased miR-34a and localization to T2AECs in neonates with respiratory distress syndrome (RDS) and BPD. Collectively, our findings support miR-34a as a novel therapeutic target in regulating hyperoxia-induced acute lung injury (HALI) and BPD.
Hyperoxia upregulates miR-34a in T2AECs in developing lungs
miRs have been recently implicated in the regulation of hyperoxia-induced injury and cell death in developing lungs10,11,22. Hence, to address the role of miR in hyperoxia-induced lung injury in neonates, we exposed newborn (NB) wild-type (WT) mice to 100% O2 from postnatal day (PN)1–4, and ran a comparative miR array analysis for RA vs. hyperoxia-exposed PN4 mouse lungs (Supplementary Fig. 1A). miR-34a was detected in lungs from WT mice breathing RA and increased markedly after exposure to 100% O2 (Supplementary Fig. 1A). Next, we studied the kinetics of miR-34a expression in hyperoxia-exposed lungs at PN2, PN4, PN7, and PN14 (using lung samples from the mouse model of BPD). miR-34a expression was significantly increased with hyperoxia exposure and reached their maximum levels at PN7 (almost 10-fold); even the BPD model showed a significant increase in miR-34a expression as compared to RA control (Fig. 1a; Supplementary Fig. 1B). We next addressed the question whether hyperoxia could increase transcription of miR-34a. Canonically, miRNA genes are transcribed by RNA polymerases into long primary miRNA transcripts (pri-miRNAs). Pri-miRNAs are next cleaved into 60−70 nucleotide-long precursor miRNAs (pre-miRNAs) by the nuclear microprocessor enzymes complex. Pre-miRNAs are next transported to the cytoplasm and processed to mature form of miRNA23,24. In response to hyperoxia, pri-miR-34a was rapidly induced, with the highest expression reaching 15-fold at PN2, after which it began to decline (Fig. 1b), most likely due to the processing of pri-miR-34a into the pre-forms and mature forms. In an effort to localize the specific lung compartment, we checked miR-34a expression in freshly isolated neonatal lung T2AECs, endothelial and macrophage cells. As shown in Fig. 1c, in T2AECs, hyperoxia (95% O2) gradually induced the expression of mature miR-34a at 4 h. We did not find any significant changes in miR-34a expression in hyperoxia-exposed lung endothelial cells or macrophages (Supplementary Fig. 1C, D). To utilize an in vitro model, we used MLE12 cells, and noted that the expression of miR-34a was highest with 95% O2 exposure at 24 h (Fig. 1d) and with 60% O2 exposure at 48 h (Fig. 1e). Since several publications have shown that miR-34a expression is regulated by Trp5325,26, we evaluated and noted that Trp53 was acetylated upon hyperoxia exposure to MLE12 cells (Supplementary Fig. 2A). Next, we transfected Trp53 siRNA in MLE12 cells and neonatal PN4 lungs, but only noted a modest (non-significant) decrease in miR-34a expression (Supplementary Fig. 2B, C). We also evaluated miR34a expression in p53 null mutant and Trp53 siRNA treated mice in room air and our BPD model at PN14. These data are shown in Supplementary Fig. 2D, E, where miR34a expression is significantly increased in RA and BPD, compared to WT controls, in p53 absence/inhibition.
Thus, taken together, our data suggest that miR-34a expression is increased upon hyperoxia exposure in developing lungs, and this appears to be localized to T2AECs, of the three lung cell types investigated, as noted above. In addition, miR-34a expression is also regulated by Trp53 in both our in vitro and in vivo hyperoxia-exposed/BPD models.
miR-34a downregulates Ang1-Tie2 signaling in developing lungs
To identify the molecular targets of miR-34a, we examined the predicted miR-34a targets using bioinformatics tools, focusing our attention on the regulators of lung inflammation and injury. Using three available prediction algorithms (Targetscan, miRANDA, and Pictar), we then produced a comprehensive list of all possible miR-34a targets. We honed onto Ang1 and its receptor, Tie2 (Tek) as potential targets of miR-34a, as they have conserved miR-34a seed sequence in its 3′ UTR (Supplementary Fig. 3A). Ang1 and Tie2 signaling have been consistently demonstrated to be critical players in lung and vascular development27,28,29 and several studies have shown Ang1/Tie2 localization to T2AECs17. We co-localized Ang1 to T2AECs in neonatal lungs (Supplementary Fig. 3B). These data led us to hypothesize that Ang1/Tie2 may be functional downstream targets of miR-34a in the inflammatory/apoptotic response to hyperoxia in lung epithelial cells.
The expression levels of Ang1 and Tie2 were first evaluated in hyperoxia-exposed lungs and epithelial cells. As shown in Fig. 2a, b, Ang1 expression was reduced by roughly 70–80% in PN4 hyperoxia-exposed lungs as compared to RA controls. Additionally, levels of Tie2 protein and its phosphorylation were decreased significantly (Fig. 2a, b). Additional downstream targets of miR-34a (Notch2, Sirt1, c-kit, p-ckit, and SCF) were also decreased upon hyperoxia exposure in PN4 neonatal lungs (Supplementary Fig. 3C−E).
We also observed the same effects on Ang1 and Tie2 proteins expression in MLE12 and neonatal mouse primary (freshly isolated) lung T2AECs (Fig. 2c–e). Hyperoxia caused a decrease in Ang1 and Tie2 proteins after 24 h (Fig. 2c, d) and a concentration dependent decrease at 48 h in MLE12 cells (Fig. 2e, f). As in the neonatal lungs, the expression of miR-34a downstream targets were also decreased in MLE12 cells (Supplementary Fig. 3F, G). Interestingly, Trp53 siRNA increased the expression of miR-34a downstream targets Ang1 and Tie2 in MLE12 cells (Supplementary Fig. 3H). In contrast, hyperoxia-exposure to neonatal T2AECs led to decreased Ang1/Tie2 protein levels (Fig. 2g, h) as well as other downstream targets of miR-34a, Sirt1, and Notch2 (Supplementary Fig. 3I).
Next we transfected MLE12 cells with different concentrations of miR-34a mimic and noted that at 50 nm concentration the expression of Ang1 and Tie2 proteins were markedly decreased (Fig. 3a), as well as other downstream targets of miR-34a (Supplementary Fig. 3J). While this observation that miR-34a modulated Ang1/Tie2 signaling in lung epithelial cells suggested an association, it was important to assess whether miR-34a can directly target Ang1/Tie2 according to the in silico target-prediction analysis. To answer this question, we co-transfected miR-34a mimic/inhibitor with Ang1/Tie2 3′ UTRs in MLE12 cells. Overexpression of miR-34a inhibited the activity of a luciferase reporter construct containing Ang1 and Tie2 3′ UTRs (Fig. 3b, c). Similarly miR-34a inhibitor transfection increased 3′ UTR activity of Ang1 only (Fig. 3D). Furthermore, miR-34a inhibitor increased the expression of the downstream targets of miR-34a (Supplementary Fig. 3K).
miR-34a increases apoptosis in lung epithelial cells
We next evaluated the role of miR-34a in the regulation of hyperoxia-induced cell death in MLE12 cells. We transfected these cells with miR-34a inhibitor, miR-34a mimic and scrambled controls and exposed to 48 h hyperoxia. Cells cultured in 5% CO2 and RA did not show significant cell death (Supplementary Fig. 4, Fig. 4a). In contrast, 95% O2 (with scrambled controls) caused a modest increase in cell death, mostly in Annexin V positive staining after 48 h in hyperoxia (Supplementary Fig. 4, Fig. 4a). This hyperoxia-induced cell death response was significantly increased in the presence of miR-34a mimic (mostly Annexin V+Propidium iodide positive) and decreased with miR-34a inhibitor (mostly Annexin V positive) transfection as compared to scrambled controls (Supplementary Fig. 4, Fig. 4a, b). In addition, miR-34a-inhibitor treatment increased miR-34a targets Ang1 and Tie2 expression in hyperoxia-exposed MLE12 cells as compared to scrambled control (Fig. 4c). Furthermore, cleaved caspase3 expression was also decreased in miR-34a-inhibitor treated group (Fig. 4c, d). Quantification of Tie2 and Ang1 is shown in Fig. 4e, f.
Taken together, these studies show that miR-34a stimulates epithelial cell death and decreases the expression of target proteins Ang1/Tie2; conversely, miR34a-inhibition decreases cell death and enhances the expression of target proteins Ang1/Tie2 upon hyperoxia exposure in vitro.
miR-34a global deletion renders mice resistant to HALI/BPD
To determine the contribution of miR-34a to HALI, we examined WT and miR-34a (−/−) mice exposed to hyperoxia and noted that miR-34a (−/−) NB mice in hyperoxia had better survival than WT mice (Fig. 5a). In the HALI model, as compared to NB WT, hyperoxia exposure to NB miR-34a (−/−) mice lungs at PN7 had improved lung morphometry, as demonstrated by chord length measurements (Fig. 5b, c). The same trend was observed in inflammatory bronchoalveolar lavage fluid (BALF) interleukin (IL)-1β and IL-6 levels, both of which were increased in WT, but not as much in miR-34a (−/−) mice, with IL-6 levels being significantly decreased, at PN7, upon hyperoxia-exposure (Supplementary Figs. 5A, 5B).
We next determined the inflammatory markers, specifically neutrophil influx, and myeloperoxidase (MPO) activity in the BPD model at PN14. Hyperoxia-exposed WT mice had a maximal increase in neutrophils and MPO activity, which were significantly decreased in the miR-34a (−/−) mice lungs (Fig. 5d, e).
In the BPD model, as compared to NB WT, NB miR-34a (−/−) mice BPD lungs had improved lung morphometry, as demonstrated by chord length measurements (Fig. 5f, g) which correlated with TUNEL staining (Fig. 5h). In addition, there was significantly increased Ang1, Tie2, SCF, and Notch2 expression in the miR34a (−/−) BPD mice lungs (Fig. 5i). In contrast, we noted decreased expression of Ang2 in miR34a (−/−) mice lungs upon hyperoxia exposure at PN4 as well as being significantly decreased in BPD mice lungs at PN14, compared to respective controls (Fig. 5j, k).
Collectively, these data demonstrate that miR-34a is a critical component of the neonatal mouse response to hyperoxia and regulates inflammation and alveolarization in HALI and BPD.
Deletion of T2AEC-specific miR-34a reverses the BPD phenotype
To address the role of miR-34a being specifically expressed in T2AECs in mediating alveolarization, we used SPC-CreER/miR-34a fl/fl mouse line to disrupt miR34a specifically in T2AECs. Expression of Cre recombinase is activated in T2AECs by the tamoxifen-inducible system coupled with T2AEC-specific promoter SpC. To determine whether the increased T2AEC expression of miR-34a seen in the above studies is causally related to impairment of lung BPD phenotype, we used mice in which miR-34a deletion was conditionally induced exclusively in T2AECs. We crossed miR-34a-floxed mice (miR-34a fl/fl) with SPC-Cre-ER mice. SPC-Cre-ER mice express Cre recombinase in SP-C positive T2AECs in a tamoxifen-inducible manner. miR-34a deletion was induced by maternal tamoxifen administration (2 mg) from PN1−PN5 in the NB pups, via maternal milk. Tamoxifen-induced Cre recombinase activity markedly decreased miR-34a expression in PN4 lung (Fig. 6a). We confirmed that tamoxifen injection alone had effect on lung morphometry (Supplementary Fig. 5C) in WT, Cre, or miR-34a fl/fl mice.
Importantly, we observed improved chord lengths in T2-miR34a −/− BPD lungs as compared to appropriate controls (Fig. 6b). Additionally, T2AECs miR-34a deletion decreased TUNEL-positive cells (Fig. 6c) and lung inflammation as demonstrated by a decrease in lung neutrophils in the BALF and a significant decrease in tissue MPO activity in T2-miR34a −/− lungs (Fig. 6d, e).
Hence, miR-34a deletion in T2AECs is sufficient to protect the newborn lung to develop the BPD pulmonary phenotype, upon hyperoxia-exposure.
miR-34 overexpression in RA restores the BPD phenotype
To address whether miR-34 expression was required and sufficient for the hyperoxia-induced lung injury and inflammation leading to the BPD pulmonary phenotype, we next asked whether only miR-34a overexpression itself was sufficient, in the absence of hyperoxia i.e., in RA. To test this, we intranasally administered miR-34a mimic in WT and miR-34a (−/−) mice, and confirmed the restoration of miR-34a levels (Supplementary Figs. 6A, 6B). Figures 7a, b show that administration of miR-34a mimic is sufficient to elicit the BPD phenotype in RA.
Furthermore, restoring miR-34a levels by intranasal administration of miR-34a mimic in miR34a (−/−) animals recapitulated the BPD phenotype induced by hyperoxia (Fig. 7c). Mechanistically, we were able to show that miR-34a mimic in RA was able to decrease the expression of the downstream targets (Ang1, Tie2, SCF, c-kit, Notch2, and Sirt1) in MLE12 cells as well as in vivo (Fig. 7d, e).
Taken together, our data show that T2AEC-specific deletion of miR-34a is sufficient to rescue the BPD phenotype in hyperoxia; conversely, increased expression miR-34a in RA is sufficient to re-create the BPD pulmonary phenotype. In addition, provision of miR-34a to the miR34a (−/−) BPD model re-creates the BPD pulmonary phenotype. These effects are associated with differential regulation of downstream targets of miR-34a, impacting on inflammatory and angiogenic pathways.
miR-34a inhibitor treatment improves hyperoxia-induced BPD
Given that genetic deletion of miR-34a was associated with complete protection from hyperoxia-induced changes in lung morphometry and inflammation, we next sought to block miR-34a as a therapeutic strategy in NB WT mice exposed to hyperoxia, using a miR-34a inhibitor via the intranasal route. We administered 5 µl (20 µM concentration) of miR-34a inhibitor (or scrambled control) at PN2 and PN4 intranasally, during hyperoxia exposure. Lung histology showed that, in comparison to the scrambled group, intranasal treatment with miRNA-34a inhibitor in neonatal mice significantly improved the BPD pulmonary phenotype, specifically in terms of chord length and septal thickness (Fig. 8a–c). Administration of miR-34a inhibitor in BPD mice also reduced the TUNEL-positive score (Fig. 8d) and reduced cleaved-caspase3 expression (Fig. 8e). MiR-34a treatment was also effective in reducing lung inflammation as evident by reduced neutrophil infiltration, MPO activity, IL-1β and IL-6 in BALF (Fig. 8f–i). To examine lung regenerative capacity in PN4 mouse lungs, these were stained with PCNA, which revealed increased cell proliferation in the lungs treated with miR-34a inhibitor (Fig. 8j). Finally, in comparison to controls, miR-34a inhibitor treated mice had significantly increased Ang1 and Tie2 as well as Sirt1 and Bcl2 protein expression in hyperoxia-exposed lungs (Fig. 8k).
miR-34a inhibition improved PAH in the mouse BPD model
In addition to impaired alveolarization, dysregulated vascularization is a key component of the pathology of BPD lungs. Hence, to understand the impact on vascular development, we investigated the effects of neonatal hyperoxia on the vessel density in these animals by immunostaining the small non-muscularized vessels with Willebrand Factor (vWF)—a marker for endothelial cells. As previously reported30, we observed decreased vascular growth in BPD animals compared to RA mice lungs, which was improved in miR-34a inhibitor treated animals, confirmed by quantification (Supplementary Fig. 6C, D). Importantly, as was the case with alveolarization (Fig. 7a–c), there was decreased vascular density (equivalent to control and scrambled miR-treated BPD lungs) in the miR34a-mimic treated miR-34a (−/−) mice hyperoxia-exposed BPD lungs (Supplementary Fig. 6C, D).
Another critical element of BPD is the associated PAH, as noted in the mouse model31,32 and human BPD33. miR-34a inhibitor treated animals demonstrated attenuated right ventricular hypertrophy (RVH), as indicated by right ventricle (RV)/left ventricle (LV) ratio and Fulton’s Index (Supplementary Fig. 6E, F). Importantly, the PAH indices worsened upon exposure to miR34a-mimic in the miR34a-mimic treated miR-34a (−/−) hyperoxia-exposed mice (Supplementary Fig. 6E, F). Similar protective responses were noted in the miR-34a (−/−) mice (Supplementary Fig. 6G, H). Using micro-CT, we were able to confirm that the improved PAH indices were secondary to improved numbers of large and medium-sized pulmonary vessels (Supplementary Fig. 6I, J).
Ang1 is protective of the BPD pulmonary and PAH phenotypes
To firmly establish the mechanistic role of miR-34a, given the impact on Ang1 expression, we evaluated the effect of Ang1 administration in the regulation of lung epithelial cell survival pathway and the BPD pulmonary phenotype. In the NB WT murine model of BPD, administration of recombinant Ang1 resulted in a significant decrease in TUNEL-positive cells at PN14 (Fig. 9a). Concomitantly, we noted a significant improvement in alveolarization, as evidenced by decreased chord length (Fig. 9b). In addition, in the PN7 HALI model, Ang1 treatment showed improved Ki67 staining levels similar to that of the miR-34 (−/−) mice lungs (Supplementary Fig. 7).
Furthermore, Ang1 treatment was protective of BPD-associated PAH (Fig. 9c, d). Since Akt and Erk pathways are important for epithelial cell survival and growth in response to hyperoxia34 and Ang1/Tie2 signaling activates Akt and Erk by phosphorylating them, we examined the effect of miR-34a inhibitor in vitro. Phosphorylation of Akt and Erk was increased in miR-34a inhibitor transfected cells treated with recombinant Ang1 (Fig. 9e).
Taken together, our data suggest that miR-34a inhibitor treatment improves the alveolar and vascular development in the hyperoxia-exposed BPD mouse model, at least in part, via the Ang1/Tie signaling pathway.
miR-34a regulates epithelial-mesenchymal transition in BPD
Investigators have reported a role for miR34a in TGF-β1 and drug-induced epithelial-mesenchymal transition (EMT) in alveolar type II cells35. We evaluated 2 EMT markers (N-cadherin and E-cadherin) in lung homogenates of WT and miR-34a null mutant mice upon hyperoxia exposure at PN4 and in the BPD model at PN14 (Supplemental Fig. 8). We noted that the mesenchymal marker (N-cadherin) is decreased in the miR-34a null mutant mice, as compared to WT, in room air, PN4 hyperoxia and BPD lungs at PN14, with no change in the epithelial marker (E-cadherin). Overall, our results would suggest that there is a potential role for miR-34a regulating EMT in the BPD model, but further experiments (beyond the scope of this manuscript) would be required to be definitive.
miR-34a regulation in other models BPD/lung injury
We36,37 and others38 have reported that overexpression of transforming growth factor (TGF)-β1 in the developing lung mimics the BPD pulmonary phenotype. To determine whether the effects of miR-34a are limited to the hyperoxia-induced BPD model or could be dependent on other injury mediators, we tested the expression of miR-34a in lungs of our TGF-β1 doxycycline-inducible overexpressing transgenic mouse model. We noted increased expression of miR-34a at PN10 in the neonatal mouse lungs as compared to transgene negative animals (Supplementary Fig. 9A). Furthermore, we also found miR-34a targets Ang1 and Sirt1 were decreased in TGF-β1 TG mouse lung samples (Supplementary Fig. 9B). Trp53 (p53) expression was also increased in TGF-β1 transgenic neonatal mouse lung tissues (Supplemental Fig. 9B).
We further investigated the role of hypoxia and TGFβ signaling in a newborn mice model39. We obtained lung tissues and noted that miR34a expression was decreased with hypoxia and decreased TGFβ signaling (using inducible dominant-negative mutation of the TGF-beta type II receptor (DNTGFbetaRII) mice) or a combination of the two exposures (Supplementary Fig. 9C). Furthermore, we used antenatal LPS administration (mimicking chorioamnionitis) with/without additional PN hyperoxia exposure in a neonatal rat model, and noted increased expression of miR34a in the lungs, but only when PN hyperoxia exposure was present (Supplemental Fig. 9D).
Taken together, our data would suggest that hyperoxia as well as increased TGFβ signaling is a major contributor to the increased levels of miR34a.
Human BPD infant lungs have increased miR-34a expression
To evaluate the human disease relevance of these findings, we examined whether miR-34a is increased in the TA and/or lungs of babies with RDS/BPD. The expression of miR-34a was significantly higher in TA cell pellets from individuals who went on to develop BPD and/or died, compared to controls (Fig. 10a). Similarly, in situ hybridization showed higher expression of miR-34a in epithelial linings of lungs of neonates with RDS especially with RDS 3-7 and RDS >7 days of PN age, mostly localized to T2AECs (Fig. 10b).
For further validation, we used a third independent collection of human lung samples matched by gestational and/or PN age,40 and conducted an immunoblot analysis. As noted in Fig. 10c–e, there was a marked decrease in the Ang1 and Tie2 proteins, comparing term control infants with no lung disease to those with evolving and established BPD1. Upon densitometry quantification, it was obvious that the Ang1/Tie2 proteins were decreased with increasing severity of disease, with the maximal decrease noted in those with established BPD (Fig. 10c–e).
These data would suggest that hyperoxia and/or ventilation-induced injuries to the developing lung are accompanied by alterations in the miR-34a-Ang1/Tie2 signaling axis in human neonates. A proposed schema for the role of miR-34a in the pathogenesis of BPD is shown in Fig. 10f.
The present study reports on three major novel findings. First, hyperoxia induces miR-34a expression in lung T2AECs of newborn mice and human infants with the clinically relevant diagnoses of RDS, evolving and established BPD suggesting translational significance. Second, using genetic gain-of-function and loss-of-function strategies (including deletion of miR-34a specifically in T2AECs), we comprehensively prove a causal detrimental role of increased miR-34a; conversely, inhibition of miR-34a was protective of the BPD pulmonary and associated PAH phenotypes. Third, we experimentally validate the mechanistic angiogenic, inflammatory, cell death and cell proliferation pathways of miR-34a, focusing on the role of vascular downstream targets, Ang1 and Tie2, and show that Ang1 treatment is protective of the BPD pulmonary and associated PAH phenotypes.
The role of miRNAs in epithelial cells related to inflammatory and immune responses has been demonstrated by various groups22,41,42,43. Recently Narasaraju et al.22 showed decreased miR-150 expression in alveolar epithelium in neonatal mouse upon hyperoxia exposure, which might be responsible for epithelial apoptosis. Similarly overexpression of miR-181b resulted in the induction of an increment in IL-6 levels in bronchial epithelial cells43. The miR-200 family was significantly upregulated during T2AECs differentiation in fetal lung; miR-200 induction was inversely correlated with expression of known targets, transcription factors ZEB1/2, and TGF-β2. miR-200 antagonists inhibited thyroid transcription factor (TTF)-1 and surfactant proteins and upregulated TGF-β2 and ZEB1 expression in T2AECs44.
Several studies have recently examined the role of specific miRNAs in the pathogenesis of lung injury. Accumulating studies have implicated a role of miRNAs in lung diseases such as adult RDS (ARDS), fibrosis, COPD, and BPD45,46,47,48. miR-206 was reduced in BPD mice compared with controls and in BPD patients compared with controls. MiR-206 overexpression significantly induced cell apoptosis, reduced cell proliferation, migration, and adhesion abilities, whereas the inhibition of miR-206 expression had the opposite effect12. Recently, decreased miR-489 has been reported upon hyperoxia exposure in neonatal mice and humans with BPD49. The authors suggest that decreased miR-489 may be inadequate attempts at compensation49. Another group has reported that miR-17∼92 expression is significantly lower in human BPD lungs50. While previous studies have reported the expression of miR-34a in neonatal and adult lung injury11,51, none, to the best of our knowledge, has comprehensively mechanistically defined the role of miR-34a in HALI and BPD in developing lungs.
We provide evidence of the in vivo relevance of miR-34a in hyperoxia-induced neonatal human and murine lung injury. Moreover, we identify the underlying molecular mechanisms by analyzing specific inflammatory/vascular/survival-associated targets of miR-34a. Most importantly, we demonstrate the feasibility and efficacy of in vivo miR-34a inhibition as a protective therapeutic option to ameliorate BPD and associated PAH. Recent direct evidence suggests that miR-34a is correlated with potential inflamed states, including the staphylococcal enterotoxin B-induced acute inflammatory lung injury51, hepatic ischemia/reperfusion injury52, high-fat diet induced hepatic steatosis53, cardiac aging, and myocardial infarction54,55,56 and acute kidney injury57. Therefore, miR-34a may be an indicator of inflammation/injury, especially since its role in cell death and cell cycle is well established58,59,60. Other studies have indicated that miR-34a attenuates cell proliferation, invasion and EMT35,61,62. Consistent with above studies, we also observed that when miR-34a was augmented in neonatal lung, cell proliferation, and angiogenesis levels were notably attenuated, and apoptosis was significantly increased. Furthermore, downregulated miR-34a had the opposite effect suggesting that miR-34a can significantly affect cellular biological function.
To identify the downstream mechanism of miR-34a-regulated protection, we used mRNA databases to identify targets and revealed many apoptosis/inflammation associated genes. We focused on Ang1, Tie2, Sirt1, Notch2, and Bcl2, all of which have established roles in recovery of lung injury and/or apoptosis. Ang1 and Tie2 are protective as regards DNA-damage and oxidative stress and were among the strongest downregulated targets in our profiling approach. Sirt1, Notch2, CDKs, and Bcl2 are predicted targets of miR-34a and these have previously been described as important factors in lung development and injury63,64,65,66. We have previously reported lower levels of Sirt1 to be associated with BPD in human neonates67. Notch2 expression has been reported to be decreased upon hyperoxia exposure to newborn rats68. Interestingly, reconstitution of rAng1 in miR-34a overexpressing epithelial cells underlined their critical importance in miR-34a-mediated effects on cell survival regulation. In vivo, Ang1/Tie2 was significantly upregulated by miR-34a antagonism, and this signaling was able to ameliorate the neonatal BPD phenotype. Ang1 secretion has been shown to be responsible for restoring epithelial protein permeability through suppression of NFκB activity in human T2AECs69. Combined VEGF and Ang1 gene transfer has been reported to mature the new vasculature, reducing the vascular leakage seen in VEGF-induced capillaries70. Our data thus reveal a critical role of miR-34a and the downstream Ang1/Tie2 signaling and the transition between the pro-inflammatory and anti-inflammatory phenotypes, which is believed to be important for the molecular regulation of functional shaping of T2AECs apoptosis and proliferation and the related BPD phenotype. We thus propose Ang1/Tie2 signaling as the major factor in miR-34a-mediated BPD.
In support, using complementary gain-of-function and loss-of-function approaches, we demonstrated that miR-34a inhibits downstream cell survival signaling by directly targeting Ang1/Tie2 in vitro and in vivo, an effect that inhibits apoptosis, neutrophil accumulation, and vascular injury in vivo. Importantly, lung delivery of miR-34a inhibitor repressed activation of the cell death pathway and reduced the lung BPD phenotype in hyperoxia-exposed mice. Moreover, miR-34a overexpression in room air alone was sufficient to produce the BPD phenotype in neonatal mice (Fig. 7a, b).
We identified patients with RDS, evolving and established BPD as having high levels of miR-34a in lung and TA cell pellets compared with “No BPD” term control patients. Ang1/Tie2 signaling was decreased in RDS, evolving and established BPD patient lungs as compared to controls (Fig. 10a–e). These findings coupled with the improved survival observed in miR-34a “knockout” studies in neonatal BPD mice (Figs. 5, 6, 8) suggest that therapies directed at inhibiting miR-34a expression may ameliorate BPD.
Of note, miR-34 family members also have been recognized as tumor suppressor miRNAs. Given that the miR-34 family has been implicated in the p53 tumor suppressor network, and that p53 pathway defects are common features of human cancer25, miR-34 inhibition therapy is considered a promising therapeutic approach26. Recent reports demonstrate that inhibition of the miR-34 family does not promote tumorigenesis, supporting the potential for therapeutic suppression of this family as a treatment for BPD56. It is important to emphasize that future therapeutic approaches using a targeted approach that can restrict inhibition to the lung T2AECs may have the maximal therapeutic potential. Such an approach can be done by utilizing surfactant (which is used routinely in preterm neonates with RDS) as a delivery vehicle for a miR-34a inhibitor. This will not only rapidly and effectively deliver the drug to the alveolar compartment, but will also allow uptake by T2AECs, as surfactant is recycled within the lung.
Another recently described complication of BPD has been BPD-associated PAH33. We found that our BPD model also led to PAH, which was associated with decreased vascular development (Supplementary Fig. 6C−H). Importantly, it should be pointed out that miR-34a deletion/inhibition enhanced pulmonary vascular development and indices of PAH in hyperoxia-exposed neonatal mice. These data suggest that the mechanism of PAH in BPD mice is, to some degree, regulated by the miR-34a/Ang1/Tie2 axis.
In conclusion, we show that miR-34a contributes to neonatal murine BPD by influencing T2AECs apoptosis through regulation of anti-apoptotic Ang1/Tie2 signaling. Silencing of miR-34a ameliorates the apoptotic response in vitro and in vivo, leading to suppressed epithelial apoptosis; this, in turn, is associated with restoration of alveolarization, enhanced angiogenesis and improvement in pulmonary vascular development. Intriguingly, miR-34a is also increased in RDS, evolving and established BPD patients, indicating its potential role in human neonatal lung injury. Pharmacologic miR-34a inhibition has clinical translational potential as a viable therapeutic option in the treatment of neonatal patients to prevent/ameliorate BPD.
All experimental WT mice of the C57BL/6 strain were purchased from The Jackson Laboratory (Bar Harbor, ME) and housed in Yale or Drexel animal care facilities. In addition, miR34a−/− mice71 and conditional miR-34 fl/fl 72 (JAX laboratory) and SPC-CreER (gift from Brigid Hogan, PhD, Duke University, USA) were housed in the Yale and Drexel Universities Animal Care Facilities (New Haven, CT and Philadelphia, PA, respectively). Mice were allowed free access to standard food and water. All animal experiments proceeded in accordance with NIH policies and were approved by the Institutional Animal Care and Use Committees (IACUCs) at Yale and Drexel Universities. Both male and female newborn mice were used for the experiments, at specific postnatal ages, as noted in the figure legends.
T2AECs purification: T2AECs were freshly isolated from fetal mice (E19−E20) by the modified method of Wang et al.73. Briefly, mouse lungs were obtained from timed-pregnant C57B6 mouse (Jax labs, USA). The tissues were transferred into a 50 ml conical tube containing Dulbecco’s modified Eagle’s medium (DMEM) on ice and digested by pipetting up and down with collagenase. The cell suspension was serially filtered through 100, 30, and 20 μm nylon meshes using screen cups (Sigma). Clumped non-filtered cells from the 30 and 20 μm nylon meshes were collected after several washes with DMEM to facilitate the filtration of non-epithelial cells. Cells were next collected and based on epithelial cell morphology and immunostaining for SP-C (marker for type II cells), the purity of the cells was determined to be 90 ± 5% by microscopic analysis. The newly isolated T2AECs were further plated (till 50% confluency) on Bioflex multiwell plates (Flexcell International, Hillsborough, NC, USA) precoated with fibronectin. Monolayers were maintained in serum-free DMEM for further experimental analysis.
MLE12 cells were a gift from Patty J. Lee, MD (Yale University, USA), and were maintained in DMEM supplemented with 2% Fetal Bovine Serum (FBS), 100 U/ml penicillin, 100 µg/ml streptomycin (GIBCO) at 37 °C in 95% air; 5% CO2. Hyperoxia conditions were achieved by placing 70–75% confluent MLE12 cells or freshly isolated T2AECs for specified time points in 95% O2/5% CO2 at 37 °C in a tightly sealed modular chamber (Stem Cell Technologies, Vancouver, Canada).
Exposure to 100% O2 to newborn (NB) mice (along with their mothers) was performed by placing them in cages in airtight Polypropylene chamber (medium size), following standard methods74,75,76,77. For hyperoxia experiments, all NB mice were exposed to 100% O2 along with their mother for different time points. Every alternate day, the mother was changed with a lactating dam between RA and hyperoxia to prevent the mother from hyperoxia-induced death and to ensure sufficient nutrition for the treated pups during the course of hyperoxia exposure. We used two experimental lung injury models. In the HALI (hyperoxia-induced acute lung injury) model, exposure to 100% O2 was initiated on postnatal day 1 (PN1; saccular stage of lung development) and continued till PN7 (alveolar stage). For the BPD model, NB mice were exposed to hyperoxia from PN1 to 4, then allowed to recover in RA for the following 10 days and then killed on PN14, as previously described28,36,78. Oxygen level was constantly monitored to be at 100%. The inside of the chamber was kept at atmospheric pressure, and mice were exposed to a 12 h light-dark cycle. CO2 inhalation was used for euthanasia prior to removing lungs from the NB mice. In all experiments, NB mice were killed at selected time points and lungs were harvested for histology, RNA and protein evaluation. All animal work was approved by Yale and Drexel Universities IACUCs.
Additional rodent models of BPD
Hypoxia Model: Neonatal mice (C57BL/6 background strain) with an inducible dominant-negative mutation of the TGF-beta type II receptor (DNTGFbetaRII) and WT mice controls were exposed to hypoxia (12% O2) or air from birth to 14 days of age following the method of Ambalavanan et al39. The DNTGFβRII mouse is a dominant-negative mutant as it expresses a cytoplasmically truncated TGFβRII receptor that competes with endogenous receptors for heterodimeric complex (TGFβRI and -RII) formation. The DNTGFβRII has no intrinsic activity as it lacks the cytoplasmic kinase domain, and the expression can be induced by administering ZnSO4. This was administered (20 μg/g ip) daily to mice pups kept in air (DT-zinc-air group) or hypoxia (DT-zinc-hypoxia group). Control DNTGFβRII mice were administered saline (vehicle control) and kept in air (DT-saline-air group) or hypoxia (DT-saline-hypoxia group). Also, WT mice were administered saline and ZnSO4 (same dose as mentioned above) as additional controls. RT-PCR was done to detect DNTGFβRII receptor mRNA using the primers: 5′-ATCGTCATCGTCTTTGTAGTC-3′ and 5′-TCCCACCGCACGTTCAGAAG-3′, to confirm induction of DNTGFβRII in the NB mice pups. No differences were noted in mortality of WT or DNTGFβRII mice (administered either vehicle or ZnSO4) over the study duration. Standard techniques were utilized for collecting lungs of the mice pups after PN14 and isolating RNA from them, after completion of the study.
Chorioamnionitis: in a rat model of chorioamnionitis combined with PN hyperoxia exposure, 1 µg of lipopolysaccharide (LPS) was injected into each individual amniotic sac of the pregnant dams on E20 so as to induce chorioamnionitis on E21 and the pups to be normally delivered between E21 and E22. Briefly, a small incision was made in the abdomen of the pregnant dam on gestation day 20 following anesthesia, and carefully the pups were pulled out by lifting the uterine horn. Each individual amniotic sac was injected with 1 µg of LPS and the pups were placed back into the maternal abdominal cavity, the abdomen sutured and the mother was rested to deliver normally the following day. After birth, NB mice were exposed to hyperoxia (100% O2) from PN1-7, and killed thereafter to obtain lung tissue. All animal work was approved by the University of Alabama at Birmingham and Thomas Jefferson University, Philadelphia IACUCs.
Human lung tracheal aspirates
Human lung tracheal aspirates (TA) pellets were obtained from premature infants being mechanically ventilated in the first PN week with an in-dwelling endotracheal tube. These infants had the final outcomes of having the diagnoses of with or without BPD and/or death. Collection and processing of the human lung samples was approved by the institutional review board of Yale University and Cooper University Hospital. Selected clinical details have been shown in Supplementary Table 1.
Real-time reverse transcriptase PCR
For the detection of miRNA expression, RNA was extracted from lungs, MLE12 cells, human tracheal aspirate (TA) pellets and primary T2AECs using miRNeasy mini kit (Qiagen, Valencia, CA). RNA concentration and quality was determined using a Biotek synergy II plate reader (Biotek, Winooski, VT). Across all samples the mean 260/280 ratio was greater than 2.0. cDNA was synthesized using a miScript II RT Kit (Qiagen, Valencia, CA). The StepOnePlus platform (Applied Biosystems) was used for all PCR, done in triplicate using miScript primer assay (Qiagen). Changes in expression were calculated by the change in threshold (ΔΔCT) method with RNU6 as the endogenous control for miRNA analysis and ß-actin (ACTB) for primary miRNA for gene-expression analysis. The miScript primer assay (Qiagen) IDs are mouse MS00001428 (miR-34a), Human MS00003318 (miR-34a), MS00033740 (RNU6), Mouse MP00005614 (Pre-miR-34a) and Mouse QT01136772 (ACTB).
Western blotting was performed as previously described79. Briefly, lung lysate and whole-cells extracts were made in RIPA buffer and protein concentration determined by Bradford method (BioRad Dye). Proteins were separated by SDS-PAGE (4–20%) and transferred to PVDF or nitrocellulose (BioRad) membranes followed by 1 h blocking at room temperature (RT) in either Odyssey blocking Buffer (Licor, Germany) or 5% milk in TBST (Tris buffer saline with 0.1% Tween 20) and incubating with primary antibodies at 4 °C, overnight. The following day membranes were washed three times with either TBST or PBST (Phosphate buffer saline with 0.1% Tween 20), incubated with either HRP-conjugated or fluorescent conjugated secondary antibody, as and when necessary for 2 h at RT, washing and subsequently developing using enhanced chemiluminescence reagent (Amersham, Chalfont St Giles, UK) followed by development with autoradiography or LICOR infrared imaging.
The primary antibodies used were Ang1 (Millipore; AB10516; 1:1000), Ang2 (Millipore; AB10516; 1:1000), N-Cadherin (Millipore; AB10516; 1:1000), b-Catenin (Cell signalling; AB10516; 1:1000), Notch1 (Cell signaling; 3608; 1:1000), Notch2 (Cell signaling; 5732; 1:800), Acetylated P53 (Cell signaling; 2570; 1:500), P53 (Cell signaling; 2524; 1:2000), phospho-Tie2 (R&D; AF2720; 1:500), Tie2 (Abcam; ab24859; 1:1000), Sirt1 (Cell signaling; 2028; 1:800), cyclin D1 (Cell signaling; 2922; 1:800), phospho-c-Kit (Cell signaling; 3391; 1:800), c-Kit (Cell signaling; 3074; 1:1000), Stem cell factor (SCF) (Santa Cruz Biotechnology; SC-9132; 1:1000), Bcl2 (Cell signaling; 3498; 1:1000), CDK4 (Santa Cruz Biotechnology; SC-260; 1:1000), cleaved-caspase 3 (Cell signaling; 9661; 1:500), Caspase 3 (Cell signaling; 9662; 1:1000), phosphor-erk1/2 (Cell signaling; 9101; 1:1000), Total erk1/2 (Cell signaling; 9102; 1:1000), p-Akt (473) (Cell signaling; 9271; 1:1000), Akt (Cell signaling; 9272; 1:1000).
Equality of loading was confirmed by probing for β-actin (Santacruz, Cell signaling Technology, Danvers, MA) or GAPDH (Cell signaling Technology, Danvers, MA). The uncropped raw images of western blot using the above antibodies have been shown in Supplementary Fig. 10.
Luciferase reporter assays
Ang1 and Tie2 3′UTR reporter constructs for mouse were obtained from Genecopoeia along with control construct (Cmi T000001-MT01). All these targets were cloned in miRNA Target clone control vector for pEZX-MT01 (Genecopoeia). For luciferase assays, 5 × 106 MLE12 cells were transfected with endotoxin-free 5× 3′UTR Ang1 and Tie2 reporter luciferase plasmid (Genecopeia, Rockville, MD) and Luc-Pair miR Luciferase Assay Kit (Genecopeia). Cells were allowed to recover for 24 h before being transfected with these constructs as described above. Reporter gene activity was measured with the Dual-Luciferase kit (Promega) 24 h after hyperoxia treatment.
Determination of cytokine and myeloperoxidase levels
The levels of IL-6, and IL-1β in lung homogenates were measured by ELISA (R&D Systems). The lung myeloperoxidase (MPO) levels were determined using lung tissue homogenates using a mouse MPO ELISA kit (Catalog #ab155458; Abcam), according to manufacturer’s instructions.
Alveolar size was estimated from the mean chord length of the airspace and septal thickness, as described previously, using ImageJ76,77. Briefly, hematoxylin-eosin sections (×100 magnification) were analyzed in ImageJ using the plugins and macros for chord length and septal thickness.
TUNEL assay with T2AECs co-localization
TUNEL assay was performed on paraffin lung sections (5 μm) using in situ Cell Death Detection Kit, Fluorescein (Roche) following manufacturer’s instructions. Co-localization for T2AECs marker SP-C (surfactant protein C; Santacruz; 1:50) was done along with the apoptotic cells, as described80. Following TUNEL staining, the sections were incubated with SP-C antibody, overnight at 4 oC, quick washing in 1X PBS and incubated with fluorescent secondary antibody for 2 h at room temperature (Jackson immunoresearch, 1:200), subsequent washing with 1X PBS and mounting with DAPI (Vector labs, California). Quantification of TUNEL-positive cells co-expressing SPC was performed in selected images by an observer masked to the identity of the experimental groups.
PAH-induced right ventricular hypertrophy
Quantitative measurements of PAH-induced right ventricular hypertrophy (RVH) by RV/left ventricle (LV) and RV/(LV + interventricular septum or IVS) ratios were done using the methodology described previously either using ImageJ or Cell Sens Olympus software31. Briefly, the thickness of right and left ventricle was measured on hematoxylin-eosin sections (×40 magnification) and the ratio between the two regions of the heart were calculated.
In situ hybridization for human lung samples
Human lung tissue samples were obtained postmortem from premature infants having the diagnoses of RDS: 1–2 days (RDS 1–2), RDS 3–7 days (RDS 3–7), RDS >7 days (RDS >7), BPD. Collection and processing of the human lung samples was approved by the National Supervisory Authority for Welfare and Health in Finland and the University of Rochester Institutional Review Board. Selected clinical details have been shown in Supplementary Table 2. Whole lungs from humans were isolated and immediately fixed with 10% NBF (neutral-buffered formalin). Briefly, lung sections were subjected to deparaffinization, incubation with 0.5% pepsin solution (20 min at 37 °C in humidified chamber), dehydration, and hybridization with either 40 nM Biotin LNA miR-34a probe, at 55 °C for 3 h. Subsequently sections were washed, blocked and incubated with streptavidin-AP reagent for 20 min and applied with alkaline phosphatase solution containing nitro-blue tetrazolium and 5-bromo-4-chloro-3=indolyphosphate (BCIP/NBT) for 1 h. Finally sections were dehydrated, mounted, and examined under microscope. Counterstaining was omitted for clarity.
Prediction and identification of miRNA gene targets
To identify potential targets for differentially expressed miRNAs, we screened their sequences against the mouse genome database, using the miRNA target identification programs miRBase, PicTar, and TargetScan.
Briefly, after the hyperoxia exposure and treatment, MLE12 cells were trypsinized and washed with cold PBS. Following this, cells were instantly stained using FITC Annexin V Apoptosis Detection Kit (BD Pharmingen) according to the manufacturer’s protocol. Cell density was determined and stained with Annexin V and PI and analyzed by flow cytometry (Becton Dickinson). A worklist was created from the assay and the samples were acquired automatically using the Loader with acquisition criteria of 10,000 events for each tube. The report generated from the apoptosis assay included the following gates and plots:
1. FSC-A vs. SSC-A with a gate for cells.
2. Annexin V FITC-A vs propidium iodide-A (PI-A) with gates for following populations: (1) Annexin V–/PI– (2) Annexin V+/PI– (3) Annexin V+/PI+ (4) Annexin V–/PI+.
A summary of assay results with statistics for untreated and treated samples was automatically calculated.
Values are expressed as mean ± SEM. Groups were compared with the Student’s two-tailed unpaired t-test or 1-way ANOVA (followed by Tukey’s Multiple Comparison post hoc test) or 2-way ANOVA as appropriate (followed by Bonferroni’s Multiple Comparison post hoc test), using GraphPad Prism 7.0 (GraphPad Software, Inc., San Diego, CA). A value of p <0.05 was considered statistically significant.
All relevant data are available from the authors upon reasonable request.
Bhandari, A. & Bhandari, V. Pitfalls, problems, and progress in bronchopulmonary dysplasia. Pediatrics 123, 1562–1573 (2009).
Bhandari, V. Hyperoxia-derived lung damage in preterm infants. Semin. Fetal. Neonatal Med. 15, 223–229 (2010).
Bhandari, A. & Bhandari, V. “New” bronchopulmonary dysplasia-a clinical review. Clin. Pulm. Med. 18, 137–143 (2011).
El Mazloum, D., Moschino, L., Bozzetto, S. & Baraldi, E. Chronic lung disease of prematurity: long-term respiratory outcome. Neonatology 105, 352–356 (2014).
Islam, J. Y., Keller, R. L., Aschner, J. L., Hartert, T. V. & Moore, P. E. Understanding the Short- and Long-Term Respiratory Outcomes of Prematurity and Bronchopulmonary Dysplasia. Am. J. Respir. Crit. Care Med. 192, 134–156 (2015).
Bhandari, V. Drug therapy trials for the prevention of bronchopulmonary dysplasia: current and future targets. Front. Pediatr. 2, 76 (2014).
Ebrahimi, A. & Sadroddiny, E. MicroRNAs in lung diseases: recent findings and their pathophysiological implications. Pulm. Pharmacol. Ther. 34, 55–63 (2015).
Zhang, X. et al. MicroRNA expression profile in hyperoxia-exposed newborn mice during the development of bronchopulmonary dysplasia. Respir. Care 56, 1009–1015 (2011).
Ranjan, R. et al. p47phox and reactive oxygen species production modulate expression of microRNA-451 in macrophages. Free Radic. Res. 49, 25–34 (2015).
Dong, J. et al. MicroRNA-mRNA interactions in a murine model of hyperoxia-induced bronchopulmonary dysplasia. BMC Genom. 13, 204 (2012).
Bhaskaran, M. et al. Identification of microRNAs changed in the neonatal lungs in response to hyperoxia exposure. Physiol. Genom. 44, 970–980 (2012).
Zhang, X. et al. Reduction of microRNA-206 contributes to the development of bronchopulmonary dysplasia through up-regulation of fibronectin 1. PLoS ONE 8, e74750 (2013).
Yang, Y., Qiu, J., Kan, Q., Zhou, X. G. & Zhou, X. Y. MicroRNA expression profiling studies on bronchopulmonary dysplasia: a systematic review and meta-analysis. Genet. Mol. Res. 12, 5195–5206 (2013).
Xing, Y. et al. MicroRNA expression profiles and target prediction in neonatal Wistar rat lungs during the development of bronchopulmonary dysplasia. Int. J. Mol. Med. 36, 1253–1263 (2015).
Saharinen, P. et al. Multiple angiopoietin recombinant proteins activate the Tie1 receptor tyrosine kinase and promote its interaction with Tie2. J. Cell Biol. 169, 239–243 (2005).
Kugathasan, L. et al. The angiopietin-1-Tie2 pathway prevents rather than promotes pulmonary arterial hypertension in transgenic mice. J. Exp. Med. 206, 2221–2234 (2009).
Grzenda, A., Shannon, J., Fisher, J. & Arkovitz, M. S. Timing and expression of the angiopoietin-1-Tie-2 pathway in murine lung development and congenital diaphragmatic hernia. Dis. Models Mech. 6, 106–114 (2013).
Yuan, H. T. et al. Activation of the orphan endothelial receptor Tie1 modifies Tie2-mediated intracellular signaling and cell survival. FASEB J. 21, 3171–3183 (2007).
Kim, S. R. et al. Angiopoietin-1 variant, COMP-Ang1 attenuates hydrogen peroxide-induced acute lung injury. Exp. Mol. Med. 40, 320–331 (2008).
Liu, X. B. et al. Angiopoietin-1 protects mesenchymal stem cells against serum deprivation and hypoxia-induced apoptosis through the PI3K/Akt pathway. Acta Pharmacol. Sin. 29, 815–822 (2008).
Bhandari, V. Postnatal inflammation in the pathogenesis of bronchopulmonary dysplasia. Birth Defects Res. A Clin. Mol. Teratol. 100, 189–201 (2014).
Narasaraju, T. et al. Role of microRNA-150 and glycoprotein nonmetastatic melanoma protein B in angiogenesis during hyperoxia-induced neonatal lung injury. Am. J. Respir. Cell Mol. Biol. 52, 253–261 (2015).
Lund, E., Guttinger, S., Calado, A., Dahlberg, J. E. & Kutay, U. Nuclear export of microRNA precursors. Science 303, 95–98 (2004).
Kawai, S. & Amano, A. BRCA1 regulates microRNA biogenesis via the DROSHA microprocessor complex. J. Cell Biol. 197, 201–208 (2012).
Chang, T. C. et al. Transactivation of miR-34a by p53 broadly influences gene expression and promotes apoptosis. Mol. Cell 26, 745–752 (2007).
Kumamoto, K. et al. Nutlin-3a activates p53 to both down-regulate inhibitor of growth 2 and up-regulate mir-34a, mir-34b, and mir-34c expression, and induce senescence. Cancer Res. 68, 3193–3203 (2008).
Mammoto, T. et al. LRP5 regulates development of lung microvessels and alveoli through the angiopoietin-Tie2 pathway. PLoS ONE 7, e41596 (2012).
Sun, H. et al. Small molecular modulation of macrophage migration inhibitory factor in the hyperoxia-induced mouse model of bronchopulmonary dysplasia. Respir. Res. 14, 27 (2013).
Du, L. et al. Signaling molecules in nonfamilial pulmonary hypertension. N. Engl. J. Med. 348, 500–509 (2003).
Baker, C. D. & Abman, S. H. Impaired pulmonary vascular development in bronchopulmonary dysplasia. Neonatology 107, 344–351 (2015).
Sun, H. et al. A critical regulatory role for macrophage migration inhibitory factor in hyperoxia-induced injury in the developing murine lung. PLoS ONE 8, e60560 (2013).
Berger, J. & Bhandari, V. Animal models of bronchopulmonary dysplasia. The term mouse models. Am. J. Physiol. Lung. Cell Mol. Physiol. 307, L936–L947 (2014).
Ambalavanan, N. & Mourani, P. Pulmonary hypertension in bronchopulmonary dysplasia. Birth Defects Res. A Clin. Mol. Teratol. 100, 240–246 (2014).
Zaher, T. E., Miller, E. J., Morrow, D. M., Javdan, M. & Mantell, L. L. Hyperoxia-induced signal transduction pathways in pulmonary epithelial cells. Free Radic. Biol. Med. 42, 897–908 (2007).
Takano, M., Nekomoto, C., Kawami, M. & Yumoto, R. Role of miR-34a in TGF-beta1- and drug-induced epithelial-mesenchymal transition in alveolar type II epithelial cells. J. Pharm. Sci. 106, 2868–2872 (2017).
Li, Z. et al. A potential role of the JNK pathway in hyperoxia-induced cell death, myofibroblast transdifferentiation and TGF-beta1-mediated injury in the developing murine lung. BMC Cell Biol. 12, 54 (2011).
Sureshbabu, A. et al. Conditional overexpression of TGFbeta1 promotes pulmonary inflammation, apoptosis and mortality via TGFbetaR2 in the developing mouse lung. Respir. Res. 16, 4 (2015).
Gauldie, J. et al. Transfer of the active form of transforming growth factor-beta 1 gene to newborn rat lung induces changes consistent with bronchopulmonary dysplasia. Am. J. Pathol. 163, 2575–2584 (2003).
Ambalavanan, N. et al. Transforming growth factor-beta signaling mediates hypoxia-induced pulmonary arterial remodeling and inhibition of alveolar development in newborn mouse lung. Am. J. Physiol. Lung Cell Mol. Physiol. 295, L86–L95 (2008).
Bhattacharya, S. et al. Genome-wide transcriptional profiling reveals connective tissue mast cell accumulation in bronchopulmonary dysplasia. Am. J. Respir. Crit. Care Med. 186, 349–358 (2012).
Mohan, M., Kumar, V., Lackner, A. A. & Alvarez, X. Dysregulated miR-34a-SIRT1-acetyl p65 axis is a potential mediator of immune activation in the colon during chronic simian immunodeficiency virus infection of rhesus macaques. J. Immunol. 194, 291–306 (2015).
Li, H., Rokavec, M. & Hermeking, H. Soluble IL6R represents a miR-34a target: potential implications for the recently identified IL-6R/STAT3/miR-34a feed-back loop. Oncotarget 6, 14026–14032 (2015).
Wang, Y., Mao, G., Lv, Y., Huang, Q. & Wang, G. MicroRNA-181b stimulates inflammation via the nuclear factor-kappaB signaling pathway. Exp. Ther. Med. 10, 1584–1590 (2015).
Benlhabib, H., Guo, W., Pierce, B. M. & Mendelson, C. R. The miR-200 family and its targets regulate type II cell differentiation in human fetal lung. J. Biol. Chem. 290, 22409–22422 (2015).
Adyshev, D. M. et al. Mechanical stress induces pre-B-cell colony-enhancing factor/NAMPT expression via epigenetic regulation by miR-374a and miR-568 in human lung endothelium. Am. J. Respir. Cell Mol. Biol. 50, 409–418 (2014).
Osei, E. T. et al. Unravelling the complexity of COPD by microRNAs: it’s a small world after all. Eur. Res. J. 46, 807–818 (2015).
Yuan, Z. et al. TREM-1 accentuated lung injury via miR-155 is inhibited by LP17 nanomedicine. Am. J. Physiol. Lung Cell Mol. Physiol. 310, 426–438 (2015).
Ji, X. et al. The anti-fibrotic effects and mechanisms of microRNA-486-5p in pulmonary fibrosis. Sci. Rep. 5, 14131 (2015).
Olave, N., et al. Regulation of alveolar septation by MicroRNA-489. Am. J. Physiol. Lung Cell Mol. Physiol. 310, L476–L487 (2015).
Rogers, L. K. et al. Attenuation of miR-17 approximately 92 Cluster in Bronchopulmonary Dysplasia. Ann. Am. Thor. Soc. 12, 1506–1513 (2015).
Rao, R., Nagarkatti, P. & Nagarkatti, M. Role of miRNA in the regulation of inflammatory genes in staphylococcal enterotoxin B-induced acute inflammatory lung injury and mortality. Toxicol. Sci. 144, 284–297 (2015).
Kim, H. J. et al. Carbon monoxide protects against hepatic ischemia/reperfusion injury by modulating the miR-34a/SIRT1 pathway. Biochim. Biophys. Acta 1852, 1550–1559 (2015).
Li, X., Lian, F., Liu, C., Hu, K. Q. & Wang, X. D. Isocaloric pair-fed high-carbohydrate diet induced more hepatic steatosis and inflammation than high-fat diet mediated by miR-34a/SIRT1 axis in mice. Sci. Rep. 5, 16774 (2015).
Boon, R. A. et al. MicroRNA-34a regulates cardiac ageing and function. Nature 495, 107–110 (2013).
Yang, Y. et al. MicroRNA-34a plays a key role in cardiac repair and regeneration following myocardial infarction. Circ. Res. 117, 450–459 (2015).
Bernardo, B. C. et al. Therapeutic inhibition of the miR-34 family attenuates pathological cardiac remodeling and improves heart function. Proc. Natl Acad. Sci. USA 109, 17615–17620 (2012).
Liu, X. J. et al. MicroRNA-34a suppresses autophagy in tubular epithelial cells in acute kidney injury. Am. J. Nephrol. 42, 168–175 (2015).
Zhang, F. et al. Roles of microRNA-34a targeting SIRT1 in mesenchymal stem cells. Stem Cell Res. Ther. 6, 195 (2015).
Modi, P. K., Jaiswal, S. & Sharma, P. Regulation of neuronal cell cycle and apoptosis by miR-34a. Mol. Cell Biol. 36, 84–94 (2015).
Shan, W. et al. Activation of the SIRT1/p66shc antiapoptosis pathway via carnosic acid-induced inhibition of miR-34a protects rats against nonalcoholic fatty liver disease. Cell Death Dis. 6, e1833 (2015).
Koutsaki, M., Spandidos, D. A. & Zaravinos, A. Epithelial-mesenchymal transition-associated miRNAs in ovarian carcinoma, with highlight on the miR-200 family: prognostic value and prospective role in ovarian cancer therapeutics. Cancer Lett. 351, 173–181 (2014).
Du, R. et al. Hypoxia-induced down-regulation of microRNA-34a promotes EMT by targeting the Notch signaling pathway in tubular epithelial cells. PLoS ONE 7, e30771 (2012).
Bai, X. et al. SIRT1 protects rat lung tissue against severe burn-induced remote ALI by attenuating the apoptosis of PMVECs via p38 MAPK signaling. Sci. Rep. 5, 10277 (2015).
Xu, K., Moghal, N. & Egan, S. E. Notch signaling in lung development and disease. Adv. Exp. Med. Biol. 727, 89–98 (2012).
Nabeyrat, E. et al. Retinoic acid protects against hyperoxia-mediated cell-cycle arrest of lung alveolar epithelial cells by preserving late G1 cyclin activities. Am. J. Respir. Cell Mol. Biol. 25, 507–514 (2001).
Guo, Q. et al. VEGF, Bcl-2 and bad regulated by angiopoietin-1 in oleic acid induced acute lung injury. Biochem. Biophys. Res. Commun. 413, 630–636 (2011).
Mody, K. et al. Sirtuin1 in tracheal aspirate leukocytes: possible role in the development of bronchopulmonary dysplasia in premature infants. J. Matern. Fetal Neonatal Med. 25, 1483–1487 (2012).
Zhang, Q., Chang, L., Liu, H., Rong, Z. & Chen, H. Relationship between Notch receptors and hyperoxia-induced lung injury in newborn rats. J. Huazhong Univ. Sci. Technol. Med. Sci. 25, 155–158 (2005).
Fang, X., Neyrinck, A. P., Matthay, M. A. & Lee, J. W. Allogeneic human mesenchymal stem cells restore epithelial protein permeability in cultured human alveolar type II cells by secretion of angiopoietin-1. J. Biol. Chem. 285, 26211–26222 (2010).
Thebaud, B. et al. Vascular endothelial growth factor gene therapy increases survival, promotes lung angiogenesis, and prevents alveolar damage in hyperoxia-induced lung injury: evidence that angiogenesis participates in alveolarization. Circulation 112, 2477–2486 (2005).
Choi, Y. J. et al. miR-34 miRNAs provide a barrier for somatic cell reprogramming. Nat. Cell Biol. 13, 1353–1360 (2011).
Concepcion, C. P. et al. Intact p53-dependent responses in miR-34-deficient mice. PLoS Genet. 8, e1002797 (2012).
Wang, Y., Huang, Z., Nayak, P. S. & Sanchez-Esteban, J. An experimental system to study mechanotransduction in fetal lung cells. J. Vis. Exp. 60, 3543 (2012).
Syed, M. A. & Bhandari, V. Hyperoxia exacerbates postnatal inflammation-induced lung injury in neonatal BRP-39 null mutant mice promoting the M1 macrophage phenotype. Mediat. Inflamm. 2013, 457189 (2013).
Sureshbabu, A. et al. Conditional overexpression of TGFbeta1 promotes pulmonary inflammation, apoptosis and mortality via TGFbetaR2 in the developing mouse lung. Respir. Res. 16, 4 (2015).
Li, Z. et al. A potential role of the JNK pathway in hyperoxia-induced cell death, myofibroblast transdifferentiation and TGF-beta1-mediated injury in the developing murine lung. BMC Cell. Biol. 12, 54 (2011).
Harijith, A. et al. A role for matrix metalloproteinase 9 in IFNgamma-mediated injury in developing lungs: relevance to bronchopulmonary dysplasia. Am. J. Respir. Cell Mol. Biol. 44, 621–630 (2011).
Choo-Wing, R. et al. Hyperoxia and interferon-gamma-induced injury in developing lungs occur via cyclooxygenase-2 and the endoplasmic reticulum stress-dependent pathway. Am. J. Respir. Cell Mol. Biol. 48, 749–757 (2013).
Yuan, Z. et al. Curcumin mediated epigenetic modulation inhibits TREM-1 expression in response to lipopolysaccharide. Int. J. Biochem. Cell Biol. 44, 2032–2043 (2012).
Bhandari, V. et al. Increased hyperoxia-induced lung injury in nitric oxide synthase 2 null mice is mediated via angiopoietin 2. Am. J. Respir. Cell Mol. Biol. 46, 668–676 (2012).
Supported in part by grants from The Hartwell Foundation (M.S., P.D., and V.B.), HL63039 (G.P.) from the NHLBI of the National Institutes of Health, and Sigrid Jusélius Foundation (S.A.).
The authors declare no competing financial interests.
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Syed, M., Das, P., Pawar, A. et al. Hyperoxia causes miR-34a-mediated injury via angiopoietin-1 in neonatal lungs. Nat Commun 8, 1173 (2017). https://doi.org/10.1038/s41467-017-01349-y
Respiratory Research (2021)
Adiponectin ameliorates hyperoxia-induced lung endothelial dysfunction and promotes angiogenesis in neonatal mice
Pediatric Research (2021)
Hyperoxia-induced S1P1 signaling reduced angiogenesis by suppression of TIE-2 leading to experimental bronchopulmonary dysplasia
Cell Biochemistry and Biophysics (2021)
Knockdown of miR-203a-3p alleviates the development of bronchopulmonary dysplasia partly via the up-regulation of vascular endothelial growth factor A
Journal of Bioenergetics and Biomembranes (2021)
Inhibition of microRNA-29a alleviates hyperoxia-induced bronchopulmonary dysplasia in neonatal mice via upregulation of GAB1
Molecular Medicine (2020)