Therapeutic Angiogenesis by Ultrasound-Mediated MicroRNA-126-3p Delivery

Arterioscler Thromb Vasc Biol. 2015 Nov;35(11):2401-11. doi: 10.1161/ATVBAHA.115.306506. Epub 2015 Sep 17.

Abstract

Objective: MicroRNAs are involved in many critical functions, including angiogenesis. Ultrasound-targeted microbubble destruction (UTMD) is a noninvasive technique for targeted vascular transfection of plasmid DNA and may be well suited for proangiogenic microRNA delivery. We aimed to investigate UTMD of miR-126-3p for therapeutic angiogenesis in chronic ischemia.

Approach and results: The angiogenic potential of miR-126-3p was tested in human umbilical vein endothelial cells in vitro. UTMD of miR-126-3p was tested in vivo in Fischer-344 rats before and after chronic left femoral artery ligation, evaluating target knockdown, miR-126-3p and miR-126-5p expression, phosphorylated Tie2 levels, microvascular perfusion, and vessel density. In vitro, miR-126-3p-transfected human umbilical vein endothelial cells showed repression of sprouty-related protein-1 and phosphatidylinositol-3-kinase regulatory subunit 2, negative regulators of vascular endothelial growth factor and angiopoietin-1 signaling, increased phosphorylated Tie2 mediated by knockdown of phosphatidylinositol-3-kinase regulatory subunit 2 and greater angiogenic potential mediated by both vascular endothelial growth factor/vascular endothelial growth factor R2 and angiopoietin-1 /Tie2 effects. UTMD of miR-126-3p resulted in targeted vascular transfection, peaking early after delivery and lasting for >3 days, and resulting in inhibition of sprouty-related protein-1 and phosphatidylinositol-3-kinase regulatory subunit 2, with minimal uptake in remote organs. Finally, UTMD of miR-126-3p to chronic ischemic hindlimb muscle resulted in improved perfusion, vessel density, enhanced arteriolar formation, pericyte coverage, and phosphorylated Tie2 levels, without affecting miR-126-5p or delta-like 1 homolog levels.

Conclusions: UTMD of miR-126 results in improved tissue perfusion and vascular density in the setting of chronic ischemia by repressing sprouty-related protein-1 and phosphatidylinositol-3-kinase regulatory subunit 2 and enhancing vascular endothelial growth factor and angiopoietin-1 signaling, with no effect on miR-126-5p. UTMD is a promising platform for microRNA delivery, with applications for therapeutic angiogenesis.

Keywords: angiogenesis; gene therapy; ischemia; microRNA; ultrasound.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiogenic Proteins / genetics
  • Angiogenic Proteins / metabolism
  • Animals
  • Cells, Cultured
  • Disease Models, Animal
  • Gene Expression Regulation
  • Genetic Therapy / methods*
  • Hindlimb
  • Human Umbilical Vein Endothelial Cells / metabolism*
  • Humans
  • Ischemia / genetics
  • Ischemia / metabolism
  • Ischemia / physiopathology
  • Ischemia / therapy*
  • Male
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Microbubbles
  • Microcirculation
  • Microvessels / physiopathology*
  • Muscle, Skeletal / blood supply*
  • Neovascularization, Physiologic*
  • Rats, Inbred F344
  • Regional Blood Flow
  • Time Factors
  • Transfection / methods*
  • Ultrasonics*

Substances

  • Angiogenic Proteins
  • MIRN126 microRNA, human
  • MicroRNAs