Cortical and retinal defects caused by dosage-dependent reductions in VEGF-A paracrine signaling

Item Type:	Article
Title:	Cortical and retinal defects caused by dosage-dependent reductions in VEGF-A paracrine signaling
Creators Name:	Haigh, J.J. and Morelli, P.I. and Gerhardt, H. and Haigh, K. and Tsien, J. and Damert, A. and Miquerol, L. and Muhlner, U. and Klein, R. and Ferrara, N. and Wagner, E.F. and Betsholtz, C. and Nagy, A.
Abstract:	To determine the function of VEGF-A in nervous system development, we have utilized the Nestin promoter-driven Cre recombinase transgene, in conjunction with a conditional and hypomorphic VEGF-A allele, to lower VEGF-A activity in neural progenitor cells. Mice with intermediate levels of VEGF-A activity showed decreased blood vessel branching and density in the cortex and retina, resulting in a thinner retina and aberrant structural organization of the cortex. Severe reductions in VEGF-A led to decreases in vascularity and subsequent hypoxia, resulting in the specific degeneration of the cerebral cortex and neonatal lethality. Decreased neuronal proliferation and hypoxia was evident at E11.5, leading to increased neuronal apoptosis in the cortex by E15.5. In order to address whether the observed changes in the structural organization of the nervous system were due to a direct and autocrine role of VEGF-A on the neural population, we conditionally inactivated the main VEGF-A receptor, Flk1, specifically in neuronal lineages, by using the Nestin Cre transgene. The normality of these mice ruled out the possibility that VEGF-A/Flk1 signaling has a significant autocrine role in CNS development. VEGF-A dosage is therefore a critical parameter regulating the density of the vascular plexus in the developing CNS that is in turn a key determinant in the development and architectural organization of the nervous system.
Keywords:	VEGF-A, Cre Recombinase, Conditional Gene Inactivation, Blood Vessel, Endothelum, Nervous System, Cortex, Retina, Animals, Mice
Source:	Developmental Biology
ISSN:	0012-1606
Publisher:	Academic Press
Volume:	262
Number:	2
Page Range:	225-241
Date:	15 October 2003
Official Publication:	https://doi.org/10.1016/S0012-1606(03)00356-7
PubMed:	View item in PubMed

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