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Neurovascular crosstalk between interneurons and capillaries is required for vision
Yoshihiko Usui, … , Michael I. Dorrell, Martin Friedlander
Yoshihiko Usui, … , Michael I. Dorrell, Martin Friedlander
Published April 27, 2015
Citation Information: J Clin Invest. 2015;125(6):2335-2346. https://doi.org/10.1172/JCI80297.
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Research Article Vascular biology

Neurovascular crosstalk between interneurons and capillaries is required for vision

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Abstract

Functional interactions between neurons, vasculature, and glia within neurovascular units are critical for maintenance of the retina and other CNS tissues. For example, the architecture of the neurosensory retina is a highly organized structure with alternating layers of neurons and blood vessels that match the metabolic demand of neuronal activity with an appropriate supply of oxygen within perfused blood. Here, using murine genetic models and cell ablation strategies, we have demonstrated that a subset of retinal interneurons, the amacrine and horizontal cells, form neurovascular units with capillaries in 2 of the 3 retinal vascular plexuses. Moreover, we determined that these cells are required for generating and maintaining the intraretinal vasculature through precise regulation of hypoxia-inducible and proangiogenic factors, and that amacrine and horizontal cell dysfunction induces alterations to the intraretinal vasculature and substantial visual deficits. These findings demonstrate that specific retinal interneurons and the intraretinal vasculature are highly interdependent, and loss of either or both elicits profound effects on photoreceptor survival and function.

Authors

Yoshihiko Usui, Peter D. Westenskow, Toshihide Kurihara, Edith Aguilar, Susumu Sakimoto, Liliana P. Paris, Carli Wittgrove, Daniel Feitelberg, Mollie S.H. Friedlander, Stacey K. Moreno, Michael I. Dorrell, Martin Friedlander

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Figure 3

Vhl deletion in amacrine and horizontal cells induces formation of a dense and convoluted intermediate plexus at the expense of the deep plexus.

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Vhl deletion in amacrine and horizontal cells induces formation of a de...
(A and B) Schematic of angiogenesis in Vhlf/f (control) or Ptf1a-Cre Vhlf/f retinas at P13. Note dramatic alterations in the intermediate plexus (green) and deep plexus (red) at P13 (A) and P23 (B) in flat-mounted retinas. (C) 100 μm sections from P23 Ptf1a-Cre Vhlf/f mice were stained with GS-lectin to highlight the extent of the neovascularization in the VHL mutants. Counterstained with DAPI. (D) The number of branching events in P13 Vhlf/f or Ptf1a-Cre Vhlf/f retinas was plotted (n = 4). (E) Three-dimensional reconstruction of 3 retinal plexuses in P23 Ptf1a-Cre Vhlf/f retina (superficial, blue; intermediate, green; deep plexus, red) highlighted the abnormally dense intermediate plexus. (F) qPCR analyses revealed that nondiffusible Vegf188 was the most abundant isoform expressed in Ptf1a-Cre Vhlf/f mice at P15 (n = 4). *P < 0.05, **P < 0.01, ***P < 0.001; 2-tailed Student’s t tests. Error bars indicate mean ± SD. Scale bars: 50 μm (A–C and E).

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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