Targeted delivery of bone marrow mononuclear cells by ultrasound destruction of microbubbles induces both angiogenesis and arteriogenesis response

Arterioscler Thromb Vasc Biol. 2005 Oct;25(10):2128-34. doi: 10.1161/01.ATV.0000179768.06206.cb. Epub 2005 Jul 28.

Abstract

Objective: Ultrasound (US)-mediated destruction of contrast microbubbles causes capillary rupturing that stimulates arteriogenesis, whereas intramuscular implantation (im) of bone marrow mononuclear cells (BM-MNCs) induces angiogenesis. We therefore studied whether US-targeted microbubble destruction combined with transplantation of BM-MNCs can enhance blood flow restoration by stimulating both angiogenesis and arteriogenesis.

Methods and results: US-mediated destruction of phospholipid-coated microbubbles was applied onto ischemic hindlimb muscle and subsequently BM-MNCs were transfused. A significant enhancement in blood flow recovery after Bubble+US+BM-MNC infusion (34% increase, P<0.05) was observed compared with Bubble+US (25%). The ratio of capillary/muscle fiber increased by Bubble+US+BM-MNC-i.v (260%, P<0.01) than that in the Bubble+US group (172%), into which BM-MNCs were incorporated (angiogenesis). Smooth muscle alpha-actin-positive arterioles were also increased, and angiography showed augmented collateral vessel formation (arteriogenesis). Platelet-derived proinflammatory factors activated by Bubble+US induces the expression of adhesion molecules (P-selectin and ICAM-1), leading to the attachment of transplanted BM-MNCs on the endothelium. Flow assay confirmed that the platelet-derived factors cause the adhesion of BM-MNCs onto endothelium under laminar flow.

Conclusions: This study demonstrates that the targeted delivery of BM-MNCs by US destruction of microbubbles enhances regional angiogenesis and arteriogenesis response, in which the release of platelet-derived proinflammatory factors activated by Bubble+US play a key role in the attachment of transplanted BM-MNCs onto the endothelial layer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiography
  • Animals
  • Arterioles / cytology
  • Arterioles / diagnostic imaging
  • Bone Marrow Cells / cytology
  • Bone Marrow Transplantation / methods*
  • Capillaries / cytology
  • Capillaries / diagnostic imaging
  • Cell Adhesion
  • Cell Adhesion Molecules / metabolism
  • Cell Lineage
  • Cells, Cultured
  • Endothelium, Vascular / diagnostic imaging
  • Endothelium, Vascular / ultrastructure
  • Femoral Artery / cytology
  • Femoral Artery / diagnostic imaging
  • Femur / blood supply
  • Femur / cytology
  • Ischemia / diagnostic imaging
  • Ischemia / therapy*
  • Microbubbles*
  • Microscopy, Electron
  • Muscle, Skeletal / blood supply
  • Neovascularization, Physiologic / physiology*
  • Rats
  • Regional Blood Flow / physiology
  • Ultrasonography, Interventional / methods*

Substances

  • Cell Adhesion Molecules