Abstract

Pulmonary hypertension (PH) is a complex disorder, spanning several known vascular cell types. Recently, we identified the microRNA-130/301 (miR-130/301) family as a regulator of multiple pro-proliferative pathways in PH, but the true breadth of influence of the miR-130/301 family across cell types in PH may be even more extensive. Here, we employed targeted network theory to identify additional pathogenic pathways regulated by miR-130/301, including those involving vasomotor tone. Guided by these predictions, we demonstrated, via gain- and loss-of-function experimentation in vitro and in vivo, that miR-130/301-specific control of the peroxisome proliferator-activated receptor γ regulates a panel of vasoactive factors communicating between diseased pulmonary vascular endothelial and smooth muscle cells. Of these, the vasoconstrictive factor endothelin-1 serves as an integral point of communication between the miR-130/301-peroxisome proliferator-activated receptor γ axis in endothelial cells and contractile function in smooth muscle cells. Thus, resulting from an in silico analysis of the architecture of the PH disease gene network coupled with molecular experimentation in vivo, these findings clarify the expanded role of the miR-130/301 family in the global regulation of PH. They further emphasize the importance of molecular cross-talk among the diverse cellular populations involved in PH.

Highlights

  • The microRNA-130/301 family regulates pulmonary hypertension (PH), but its breadth of activity remains undefined

  • We demonstrated, via gainand loss-of-function experimentation in vitro and in vivo, that miR-130/301-specific control of the peroxisome proliferator-activated receptor ␥ regulates a panel of vasoactive factors communicating between diseased pulmonary vascular endothelial and smooth muscle cells

  • We demonstrated that the miR-130/301-PPAR␥ axis regulates a panel of vasoactive factors, most notably EDN1, serving as central mediators of vascular communication between diseased pulmonary artery endothelial cells (PAECs) and pulmonary artery smooth muscle cells (PASMCs), vasomotor tone, and Pulmonary hypertension (PH) manifestation in vivo

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Summary

Background

The microRNA-130/301 family regulates pulmonary hypertension (PH), but its breadth of activity remains undefined. We employed targeted network theory to identify additional pathogenic pathways regulated by miR-130/301, including those involving vasomotor tone Guided by these predictions, we demonstrated, via gainand loss-of-function experimentation in vitro and in vivo, that miR-130/301-specific control of the peroxisome proliferator-activated receptor ␥ regulates a panel of vasoactive factors communicating between diseased pulmonary vascular endothelial and smooth muscle cells. To identify additional pathogenic pathways that may be regulated by these miRNAs, we performed targeted networkbased analyses of PH-relevant targets of the miR-130/301 family and their closest interactors Guided by these predictions, we demonstrated that the miR-130/301-PPAR␥ axis regulates a panel of vasoactive factors, most notably EDN1, serving as central mediators of vascular communication between diseased PAECs and PASMCs, vasomotor tone, and PH manifestation in vivo

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