Pulmonary arterial hypertension (PAH) is a disease characterized by the vascular remodeling of the pulmonary arterioles, including formation of plexiform and concentric lesions comprised of proliferative endothelial cells. We recently found that disruption of the G protein-coupled receptor signaling axis comprised of the ligand apelin and the receptor APJ leads to significant worsening of hypoxia induced pulmonary hypertension (PH) in mice, and found that the pathway is also perturbed in clinical PAH. To further characterize the downstream endothelial targets which may be utilized by apelin-APJ signaling to protect against the remodeling processes in PAH, we carried out a microRNA (miRNA) array analysis of pulmonary artery endothelial cells (PAECs) subjected to knockdown of apelin, APJ, or both. We identified two miRNAs (miR-424 and miR-503) that are highly expressed in PAECs, but are significantly downregulated in the context of apelin/APJ knockdown. Remarkably, these miRNAs are also markedly decreased in the experimental monocrotaline rat model of PH, as well as in PAECs isolated from patients with clinically diagnosed PAH. Our in vitro functional studies demonstrated that both miR-424 and miR-503 exert anti-proliferative, anti-angiogenic effects, via a mechanism that at least in part involves targeting of the FGF signaling pathway. We found that restoration of miR-424/503 expression in the monocrotaline induced model of PH by intranasal lentiviral delivery can significantly ameliorate the severity of the disease. Based o these preliminary data, we hypothesize that miR-424/503 play a critical role in maintaining pulmonary vascular homeostasis, and that disruption of their expression serves a critical contribution to the aberrant endothelial proliferation which is a hallmark of PAH. We propose the following aims to further evaluate the role of miR-424/503 in PAH: 1) Determine the transcriptional regulatory mechanisms of miR-424/503 in PAECs that involves targeting of the myocyte-specific enhancer factor 2 (MEF2) by apelin-APJ signaling, 2) Evaluate the efficacy of endothelial specific expression of miR-424/503 in experimental models of PH, and 3) Further validate the role for miR-424/503 in clinical PAH.
Pulmonary arterial hypertension (PAH) is a syndrome in which remodeling of the pulmonary arteries and increased pulmonary vascular resistance result in right ventricular failure, and if untreated ultimately leads to death. The limited existing therapies have improved outcome but mortality remains exceedingly high (up to 45% mortality at 3 years after diagnosis). We seek to define a novel microRNA based molecular mechanism that may be a key determinant of the disease process that will lead to better understanding of the mechanism of PAH and may ultimately identify novel pathways that can serve as therapeutic targets.
|Papangeli, Irinna; Chun, Hyung J (2017) A Tale of Two Elabela Null Mice. Trends Endocrinol Metab 28:759-760|
|Chun, Hyung J; Bonnet, Sebastien; Chan, Stephen Y (2017) Reply: Transforming Growth Factor ?1- and Bone Morphogenetic Protein 2/PPAR?-regulated MicroRNAs in Pulmonary Arterial Hypertension. Am J Respir Crit Care Med 196:1228-1229|
|Hwangbo, Cheol; Wu, Jingxia; Papangeli, Irinna et al. (2017) Endothelial APLNR regulates tissue fatty acid uptake and is essential for apelin's glucose-lowering effects. Sci Transl Med 9:|
|Ceneri, Nicolle; Zhao, Lina; Young, Bryan D et al. (2017) Rac2 Modulates Atherosclerotic Calcification by Regulating Macrophage Interleukin-1? Production. Arterioscler Thromb Vasc Biol 37:328-340|
|Hwangbo, Cheol; Lee, Heon-Woo; Kang, Hyeseon et al. (2017) Modulation of Endothelial Bone Morphogenetic Protein Receptor Type 2 Activity by Vascular Endothelial Growth Factor Receptor 3 in Pulmonary Arterial Hypertension. Circulation 135:2288-2298|
|Chun, Hyung J; Bonnet, Sébastien; Chan, Stephen Y (2017) Translational Advances in the Field of Pulmonary Hypertension. Translating MicroRNA Biology in Pulmonary Hypertension. It Will Take More Than ""miR"" Words. Am J Respir Crit Care Med 195:167-178|
|Li, Na; Hwangbo, Cheol; Jaba, Irina M et al. (2016) miR-182 Modulates Myocardial Hypertrophic Response Induced by Angiogenesis in Heart. Sci Rep 6:21228|
|Papangeli, Irinna; Kim, Jongmin; Maier, Inna et al. (2016) MicroRNA 139-5p coordinates APLNR-CXCR4 crosstalk during vascular maturation. Nat Commun 7:11268|
|Chun, Hyung J; Yu, Paul B (2015) Elafin in pulmonary arterial hypertension. Beyond targeting elastases. Am J Respir Crit Care Med 191:1217-9|
|Papangeli, Irinna; Sharma, Bikram; Chun, Hyung J (2015) Letter by Papangeli et al Regarding Article, ""The ERG-APLNR Axis Controls Pulmonary Venule Endothelial Proliferation in Pulmonary Veno-Occlusive Disease"". Circulation 132:e16|
Showing the most recent 10 out of 15 publications