TY - JOUR
T1 - Astrocyte-derived vascular endothelial growth factor stabilizes vessels in the developing retinal vasculature
AU - Scott, Andrew
AU - Powner, Michael B.
AU - Gandhi, Pranita
AU - Clarkin, Claire
AU - Gutmann, David H.
AU - Johnson, Randall S.
AU - Ferrara, Napoleone
AU - Fruttiger, Marcus
PY - 2010
Y1 - 2010
N2 - Vascular endothelial growth factor (VEGF) plays a critical role in normal development as well as retinal vasculature disease.During retinal vascularization, VEGF is most strongly expressed by not yet vascularized retinal astrocytes, but also by retinal astrocytes within the developing vascular plexus, suggesting a role for retinal astrocyte-derived VEGF in angiogenesis and vessel network maturation. To test the role of astrocyte-derived VEGF, we used Cre-lox technology in mice to delete VEGF in retinal astrocytes during development. Surprisingly, this only had a minor impact on retinal vasculature development, with only small decreases in plexus spreading, endothelial cell proliferation and survival observed. In contrast, astrocyte VEGF deletion had more pronounced effects on hyperoxia-induced vaso-obliteration and led to the regression of smooth muscle cell-coated radial arteries and veins, which are usually resistant to the vessel-collapsing effects of hyperoxia. These results suggest that VEGF production from retinal astrocytes is relatively dispensable during development, but performs vessel stabilizing functions in the retinal vasculature and might be relevant for retinopathy of prematurity in humans.
AB - Vascular endothelial growth factor (VEGF) plays a critical role in normal development as well as retinal vasculature disease.During retinal vascularization, VEGF is most strongly expressed by not yet vascularized retinal astrocytes, but also by retinal astrocytes within the developing vascular plexus, suggesting a role for retinal astrocyte-derived VEGF in angiogenesis and vessel network maturation. To test the role of astrocyte-derived VEGF, we used Cre-lox technology in mice to delete VEGF in retinal astrocytes during development. Surprisingly, this only had a minor impact on retinal vasculature development, with only small decreases in plexus spreading, endothelial cell proliferation and survival observed. In contrast, astrocyte VEGF deletion had more pronounced effects on hyperoxia-induced vaso-obliteration and led to the regression of smooth muscle cell-coated radial arteries and veins, which are usually resistant to the vessel-collapsing effects of hyperoxia. These results suggest that VEGF production from retinal astrocytes is relatively dispensable during development, but performs vessel stabilizing functions in the retinal vasculature and might be relevant for retinopathy of prematurity in humans.
UR - http://www.scopus.com/inward/record.url?scp=77955619335&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0011863
DO - 10.1371/journal.pone.0011863
M3 - Article
C2 - 20686684
AN - SCOPUS:77955619335
SN - 1932-6203
VL - 5
JO - PloS one
JF - PloS one
IS - 7
M1 - e11863
ER -