Abstract
Objective- To characterize the expression and function of interleukin (IL) 19, a recently described T-helper 2 anti-inflammatory IL, on endothelial cell (EC) pathophysiological features. Methods and results- The expression and effects of anti-inflammatory ILs on EC activation and development of angiogenesis are uncharacterized. We demonstrate by immunohistochemistry and immunoblot that IL-19 is expressed in inflamed, but not normal, human coronary endothelium and can be induced in cultured human ECs by serum and basic fibroblast growth factor. IL-19 is mitogenic and chemotactic, and it promotes EC spreading. IL-19 activates the signaling proteins STAT3, p44/42, and Rac1. In functional ex vivo studies, IL-19 promotes cordlike structure formation of cultured ECs and enhances microvessel sprouting in the mouse aortic ring assay. IL-19 induces tube formation in gelatinous protein (Matrigel) plugs in vivo. Conclusion- To our knowledge, these data are the first to report expression of the anti-inflammatory agent, IL-19, in ECs; and the first to indicate that IL-19 is mitogenic and chemotactic for ECs and can induce the angiogenic potential of ECs.
Original language | English |
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Pages (from-to) | 167-175 |
Number of pages | 9 |
Journal | Arteriosclerosis, Thrombosis, and Vascular Biology |
Volume | 31 |
Issue number | 1 |
DOIs | |
State | Published - Jan 2011 |
Keywords
- Animals
- Blotting, Western
- Cell Proliferation
- Cell Shape
- Cells, Cultured
- Chemotaxis
- Endothelial Cells/immunology
- Fibroblast Growth Factor 2/metabolism
- Humans
- Immunohistochemistry
- Inflammation/immunology
- Interleukins/metabolism
- Mice
- Mice, Inbred C57BL
- Microvessels/metabolism
- Mitogen-Activated Protein Kinase 1/metabolism
- Mitogen-Activated Protein Kinase 3/metabolism
- Neovascularization, Physiologic
- Phosphorylation
- STAT3 Transcription Factor/metabolism
- Signal Transduction
- Time Factors
- rac1 GTP-Binding Protein/metabolism