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Impact of vegf on astrocytes: Analysis of gap junctional intercellular communication, proliferation, and motility
Author(s) -
Wuestefeld Ricarda,
Chen Jingchen,
Meller Karl,
BrandSaberi Beate,
Theiss Carsten
Publication year - 2012
Publication title -
glia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.954
H-Index - 164
eISSN - 1098-1136
pISSN - 0894-1491
DOI - 10.1002/glia.22325
Subject(s) - biology , angiogenesis , microbiology and biotechnology , vascular endothelial growth factor , cell growth , gap junction , vascular endothelial growth factor a , intracellular , cell , motility , astrocyte , cancer research , neuroscience , vegf receptors , central nervous system , biochemistry
The purpose of the present study was to investigate the effects of vascular endothelial growth factor (VEGF) on gap junctional intercellular communication (GJIC), cell proliferation, and cell dynamics in primary astrocytes. VEGF is known as a dimeric polypeptide that potentially binds to two receptors, VEGFR‐1 and VEGFR‐2, however many effects are mediated by VEGFR‐2, for example, actin polymerization, forced cell migration, angiogenesis, and cell proliferation. Recently it has been shown that in case of hypoxia, ischemia or injury VEGF is upregulated to stimulate angiogenesis and cell proliferation. Besides this, VEGF reveals a potent therapeutical target for averting tumor vascularization, emerging in bevacizumab, the first humanized anti‐VEGF‐A antibody for treating recurrent Glioblastoma multiforme. To expand our knowledge about VEGF effects in glial cells, we cultivated rat astrocytes in medium containing VEGF for 1 and 2 days. To investigate the effects of VEGF on GJIC, we microinjected neurobiotin into a single cell and monitored dye‐spreading into adjacent cells. These experiments showed that VEGF significantly enhances astrocytic GJIC compared with controls. Cell proliferation measured by BrdU‐labeling also revealed a significant increase of astrocytic mitose rates subsequent to 1 day of VEGF exposure, whereas longer VEGF treatment for 2 days did not have additive effects. To study cell‐dynamics of astrocytes subsequent to VEGF treatment, we additionally transfected astrocytes with LifeAct‐RFP. Live‐cell imaging and quantitative analysis of these cells with aid of confocal laser scanning microscopy revealed higher process movement of VEGF‐treated astrocytes. In conclusion, VEGF strongly affects cell proliferation, GJIC, and motility in astrocytes. © 2012 Wiley Periodicals, Inc.