Macrophage Notch Ligand Delta-Like 4 Promotes Vein Graft Lesion Development: Implications for the Treatment of Vein Graft Failure

Research output: Contribution to journalArticle

Authors

External Institution(s)

  • Harvard University
  • David H. Koch Institute for Integrative Cancer Research
  • Institutes for Medical Engineering and Science
  • Center for Interdisciplinary Cardiovascular Sciences
  • Juntendo University
  • Massachusetts Institute of Technology

Details

Original languageEnglish (US)
Pages (from-to)2343-2353
Number of pages11
JournalArteriosclerosis, thrombosis, and vascular biology
Volume35
Issue number11
StatusPublished - Nov 1 2015
Peer-reviewedYes

Abstract

Objective-Despite its large clinical impact, the underlying mechanisms for vein graft failure remain obscure and no effective therapeutic solutions are available. We tested the hypothesis that Notch signaling promotes vein graft disease. Approach and Results-We used 2 biotherapeutics for Delta-like ligand 4 (Dll4), a Notch ligand: (1) blocking antibody and (2) macrophage-or endothelial cell (EC)-targeted small-interfering RNA. Dll4 antibody administration for 28 days inhibited vein graft lesion development in low-density lipoprotein (LDL) receptor-deficient (Ldlr-/-) mice, and suppressed macrophage accumulation and macrophage expression of proinflammatory M1 genes. Dll4 antibody treatment for 7 days after grafting also reduced macrophage burden at day 28. Dll4 silencing via macrophage-targeted lipid nanoparticles reduced lesion development and macrophage accumulation, whereas EC-targeted Dll4 small-interfering RNA produced no effects. Gain-of-function and loss-of-function studies suggested in vitro that Dll4 induces proinflammatory molecules in macrophages. Macrophage Dll4 also stimulated smooth muscle cell proliferation and migration and suppressed their differentiation. Conclusions-These results suggest that macrophage Dll4 promotes lesion development in vein grafts via macrophage activation and crosstalk between macrophages and smooth muscle cells, supporting the Dll4-Notch axis as a novel therapeutic target.

    Research areas

  • endothelial cells, inflammation, lipid, macrophage, nanoparticles

Citation formats

APA

Koga, J. I., Nakano, T., Dahlman, J. E., Figueiredo, J. L., Zhang, H., Decano, J., ... Aikawa, M. (2015). Macrophage Notch Ligand Delta-Like 4 Promotes Vein Graft Lesion Development: Implications for the Treatment of Vein Graft Failure. Arteriosclerosis, thrombosis, and vascular biology, 35(11), 2343-2353. https://doi.org/10.1161/ATVBAHA.115.305516

Harvard

Koga, JI, Nakano, T, Dahlman, JE, Figueiredo, JL, Zhang, H, Decano, J, Khan, OF, Niida, T, Iwata, H, Aster, JC, Yagita, H, Anderson, DG, Keith Ozaki, C & Aikawa, M 2015, 'Macrophage Notch Ligand Delta-Like 4 Promotes Vein Graft Lesion Development: Implications for the Treatment of Vein Graft Failure', Arteriosclerosis, thrombosis, and vascular biology, vol. 35, no. 11, pp. 2343-2353. https://doi.org/10.1161/ATVBAHA.115.305516