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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 Article has an altmetric score of 51

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 5

Genetic ablation of amacrine and horizontal cells phenocopies the defects in the intermediate plexus observed in Hif-1α and Vegfa mutants.

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Genetic ablation of amacrine and horizontal cells phenocopies the defect...
(A) DT was injected daily at the time points indicated. (B–E) The reduced number of cells after ablation was examined by comparing cryosectioned retinas from P23 Ptf1a-Cre R26iDTR/+:tdTomato/+ and P23 Ptf1a-Cre R26+/+:tdTomato/+ mice after injecting DT (B), and by measuring the thickness of the GCL/IPL and INL (C; yellow brackets) from images captured in vivo using SD-OCT (D and E) (n = 4–6). (F and G) An attenuated intermediate plexus is observed (F; green) and quantified (G) in P23 Ptf1a-Cre R26iDTR/+ mice (n = 6). (H and I) An attenuated intermediate plexus is also seen when amacrine and horizontal cells are ablated well after intermediate plexus development (H; quantified in I), suggesting that amacrine cells are required for development and maintenance of the intermediate plexus (n = 4). *P < 0.05, **P < 0.01, ***P < 0.001; 2-tailed Student’s t tests. Error bars indicate mean ± SD. Scale bar: 50 μm (B, F, and H).

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

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