I-309 binds to and activates endothelial cell functions and acts as an angiogenic molecule in vivo

Male 0301 basic medicine Neovascularization, Physiologic Chick Embryo Cornea Chemokine CCL1 03 medical and health sciences Allantois Animals Humans RNA, Messenger Cells, Cultured 0303 health sciences Chemotaxis Cell Differentiation Chorion 3. Good health Drug Combinations Gene Expression Regulation Chemokines, CC Proteoglycans Collagen Endothelium, Vascular Laminin
DOI: 10.1182/blood.v96.13.4039 Publication Date: 2019-10-14T05:13:26Z
ABSTRACT
AbstractSeveral chemokines have been shown to act as angiogenic molecules or to modulate the activity of growth factors such as fibroblast growth factor 2 (FGF-2) and vascular endothelial growth factor (VEGF). The detection of the CC chemokine receptor (CCR) 8 message in human umbilical vein endothelial cells (HUVECs) by reverse transcription– polymerase chain reaction (RT-PCR) and RNase protection assay (RPA), prompted us to investigate the potential role exerted by the CC chemokine I-309, a known ligand of such receptor, in both in vitro and in vivo angiogenesis assays. We show here that I-309 binds to endothelial cells, stimulates chemotaxis and invasion of these cells, and enhances HUVEC differentiation into capillary-like structures in an in vitro Matrigel assay. Furthermore, I-309 is an inducer of angiogenesis in vivo in both the rabbit cornea and the chick chorioallantoic membrane assay (CAM).
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