Adeno-associated virus vector-mediated interleukin-10 gene transfer inhibits atherosclerosis in apolipoprotein E-deficient mice View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2004-10-21

AUTHORS

T Yoshioka, T Okada, Y Maeda, U Ikeda, M Shimpo, T Nomoto, K Takeuchi, M Nonaka-Sarukawa, T Ito, M Takahashi, T Matsushita, H Mizukami, Y Hanazono, A Kume, S Ookawara, M Kawano, S Ishibashi, K Shimada, K Ozawa

ABSTRACT

Inflammation is a major contributor to atherosclerosis by its effects on arterial wall biology and lipoprotein metabolism. Interleukin-10 (IL-10) is an anti-inflammatory cytokine that may modulate the atherosclerotic disease process. We investigated the effects of adeno-associated virus (AAV) vector-mediated gene transfer of IL-10 on atherogenesis in apolipoprotein E (ApoE)-deficient mice. A murine myoblast cell line, C2C12, transduced with AAV encoding murine IL-10 (AAV2-mIL10) secreted substantial amounts of IL-10 into conditioned medium. The production of monocyte chemoattractant protein-1 (MCP-1) by the murine macrophage cell line, J774, was significantly inhibited by conditioned medium from AAV2-mIL10-transduced C2C12 cells. ApoE-deficient mice were injected with AAV5-mIL10 into their anterior tibial muscle at 8 weeks of age. The expression of MCP-1 in the vascular wall of the ascending aorta and serum MCP-1 concentration were decreased in AAV5-mIL10-transduced mice compared with AAV5-LacZ-transduced mice. Oil red-O staining of the ascending aorta revealed that IL-10 gene transfer resulted in a 31% reduction in plaque surface area. Serum cholesterol concentrations were also significantly reduced in AAV5-mIL10-transduced mice. To understand the cholesterol-lowering mechanism of IL-10, we measured the cellular cholesterol level in HepG2 cells, resulting in its significant decrease by the addition of IL-10 in a dose-dependent manner. Furthermore, IL-10 suppressed HMG-CoA reductase expression in the HepG2 cells. These observations suggest that intramuscular injection of AAV5-mIL10 into ApoE-deficient mice inhibits atherogenesis through anti-inflammatory and cholesterol-lowering effects. More... »

PAGES

1772-1779

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/sj.gt.3302348

DOI

http://dx.doi.org/10.1038/sj.gt.3302348

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1033088671

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/15496963


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