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MicroRNA 139-5p coordinates APLNR-CXCR4 crosstalk during vascular maturation.

Irinna PapangeliJongmin KimInna MaierSaejeong ParkAram LeeYujung KangKeiichiro TanakaOmar F KhanHyekyung JuYoko KojimaKristy Red-HorseDaniel G AndersonArndt F SiekmannHyung J Chun
Published in: Nature communications (2016)
G protein-coupled receptor (GPCR) signalling, including that involving apelin (APLN) and its receptor APLNR, is known to be important in vascular development. How this ligand-receptor pair regulates the downstream signalling cascades in this context remains poorly understood. Here, we show that mice with Apln, Aplnr or endothelial-specific Aplnr deletion develop profound retinal vascular defects, which are at least in part due to dysregulated increase in endothelial CXCR4 expression. Endothelial CXCR4 is negatively regulated by miR-139-5p, whose transcription is in turn induced by laminar flow and APLN/APLNR signalling. Inhibition of miR-139-5p in vivo partially phenocopies the retinal vascular defects of APLN/APLNR deficiency. Pharmacological inhibition of CXCR4 signalling or augmentation of the miR-139-5p-CXCR4 axis can ameliorate the vascular phenotype of APLN/APLNR deficient state. Overall, we identify an important microRNA-mediated GPCR crosstalk, which plays a key role in vascular development.
Keyphrases
  • endothelial cells
  • cell migration
  • optical coherence tomography
  • type diabetes
  • diabetic retinopathy
  • adipose tissue
  • high fat diet induced
  • long non coding rna
  • soft tissue
  • fluorescent probe
  • optic nerve