Proinflammatory Cytokines Increase Vascular Endothelial Growth Factor Expression in Alveolar Epithelial Cells

被引:57
|
作者
Maloney, James P. [1 ]
Gao, Li [2 ]
机构
[1] Univ Colorado Denver, Div Pulm & Crit Care Med, Aurora, CO 80045 USA
[2] Johns Hopkins Univ, Dept Med, Div Allergy & Clin Immunol, Baltimore, MD 21224 USA
关键词
RESPIRATORY-DISTRESS-SYNDROME; PULMONARY-EDEMA; GENE-EXPRESSION; UP-REGULATION; A549; CELLS; IN-VITRO; VEGF; INFLAMMATION; LUNG; ANGIOGENESIS;
D O I
10.1155/2015/387842
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Vascular endothelial growth factor (VEGF) is an endothelial permeability mediator that is highly expressed in lung epithelium. In nonlung cells proinflammatory cytokines have been shown to increase VEGF expression, but their effects on lung epithelium remain unclear. We hypothesized that increases in alveolar epithelial cell VEGF RNA and protein expression occur after exposure to proinflammatory cytokines. We tested this using human alveolar epithelial cells (A549) stimulated with 5 proinflammatory cytokines. VEGF RNA expression was increased 1.4-2.7-fold in response to IL-1, IL-6, IL-8, TNF-alpha, or TGF-beta over 6 hours, with TGF-beta. having the largest response. TNF-alpha increased VEGF RNA as early as 1 hour. A mix of IL-1, IL-6, and IL-8 had effects similar to IL-1. TNF-alpha increased protein expression as early as 4 hours and had a sustained effect at 16 hours, whereas IL-1 did not increase protein expression. Only VEGF 165 was present in cultured A549 cells, yet other isoforms were seen in human lung tissue. Increased expression of VEGF in alveolar epithelial cells occurs in response to proinflammatory cytokines. Increased VEGF expression likely contributes to the pathogenesis of inflammatory lung diseases and to the angiogenic phenotype of lung cancer, a disease typically preceded by chronic inflammation.
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页数:7
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