Dendritic cell-endothelial cell cross-talk in angiogenesis

被引:102
|
作者
Sozzani, Silvano [1 ]
Rusnati, Marco [1 ]
Riboldi, Elena [1 ]
Mitola, Stefania [1 ]
Presta, Marco [1 ]
机构
[1] Univ Brescia, Dept Biomed Sci & Biotechnol, Unit Gen Pathol & Immunol, I-25123 Brescia, Italy
关键词
FIBROBLAST GROWTH FACTOR-2; CUTTING EDGE; OSTEOPONTIN EXPRESSION; CHEMOKINE PRODUCTION; INTERFERON-ALPHA; INNATE IMMUNITY; HUMAN MONOCYTES; FACTOR VEGF; IN-VITRO; DIFFERENTIATION;
D O I
10.1016/j.it.2007.07.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dendritic cells (DCs) are professional antigen-presenting cells that have a pivotal role in the onset and regulation of adaptive immune responses. DCs have the ability to regulate inflammation through their capacity to release cytokines and chemokines and kill pathogens, which they share with other phagocytes. Recent observations have shown that different DC subsets produce and release various pro- and anti-angiogenic mediators depending on their activation status and cytokine milieu. In particular, alternatively activated DCs exert a potent pro-angiogenic activity that is mediated by the prototypic angiogenic growth factor vascular endothelial growth factor-A (VEGF-A). In turn, pro- and anti-angiogenic mediators can affect the biology of DCs, modulating their differentiation and maturation. Finally, DCs can trans-differentiate into endothelial-like cells, possibly contributing to vasculogenesis in the adult. Thus, DCs might exert an important impact on the neovascularization process in different physiopathological conditions.
引用
收藏
页码:385 / 392
页数:8
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