Pharmacological depletion of retinal neurons prevents vertical angiogenic sprouting without affecting the superficial vascular plexus

다국어 초록 (Multilingual Abstract)

In mice, a tri‐layered (superficial, intermediate, and deep) vascular structure is formed in the retina during the third postnatal week. Short‐term treatment of newborn mice with vascular endothelial growth factor (VEGF) receptor inhibitors delays the formation of superficial vascular plexus and this allows us to investigate the developmental process of superficial and deep vascular plexuses at the same time. Using this model, we examined the effect of pharmacological depletion of retinal neurons on the formation of superficial and deep vascular plexuses.
Neuronal cell loss induced by an intravitreal injection of N‐methyl‐d‐aspartic acid on postnatal day (P) 8 delayed vascular development in the deep layer but not in the superficial layer in mice treated with KRN633, a VEGF receptor inhibitor, on P0 and P1. In KRN633‐treated mice, neuronal cell loss decreased the number of vertical sprouts originating from the superficial plexus without affecting the number of angiogenic sprouts growing in front. Neuronal cell loss did not impair networks of fibronectin and astrocytes in the superficial layer.
Our results suggest that inner retinal neurons play a crucial role in forming the deep vascular plexus by directing the sprouts from the superficial blood vessels to the deep layer.

By interrupting the retinal superficial vascular growth in neonatal mice, it is possible to investigate the developmental process of superficial and deep vascular plexuses simultaneously.
Neuronal cell loss decreases the number of vertical sprouts originating from the superficial plexus without affecting the number of angiogenic sprouts growing in front.
Neuronal cells play a crucial role in forming the deep vascular plexus by directing the sprouts from the superficial blood vessels to the deep layer in the mouse retina.