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HIF-1α and HIF-2α redundantly promote retinal neovascularization in patients with ischemic retinal disease
Jing Zhang, … , Silvia Montaner, Akrit Sodhi
Jing Zhang, … , Silvia Montaner, Akrit Sodhi
Published June 15, 2021
Citation Information: J Clin Invest. 2021;131(12):e139202. https://doi.org/10.1172/JCI139202.
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Research Article Angiogenesis Ophthalmology

HIF-1α and HIF-2α redundantly promote retinal neovascularization in patients with ischemic retinal disease

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Abstract

Therapies targeting VEGF have proven only modestly effective for the treatment of proliferative sickle cell retinopathy (PSR), the leading cause of blindness in patients with sickle cell disease. Here, we shift our attention upstream from the genes that promote retinal neovascularization (NV) to the transcription factors that regulate their expression. We demonstrated increased expression of HIF-1α and HIF-2α in the ischemic inner retina of PSR eyes. Although both HIFs participated in promoting VEGF expression by hypoxic retinal Müller cells, HIF-1 alone was sufficient to promote retinal NV in mice, suggesting that therapies targeting only HIF-2 would not be adequate to prevent PSR. Nonetheless, administration of a HIF-2–specific inhibitor currently in clinical trials (PT2385) inhibited NV in the oxygen-induced retinopathy (OIR) mouse model. To unravel these discordant observations, we examined the expression of HIFs in OIR mice and demonstrated rapid but transient accumulation of HIF-1α but delayed and sustained accumulation of HIF-2α; simultaneous expression of HIF-1α and HIF-2α was not observed. Staggered HIF expression was corroborated in hypoxic adult mouse retinal explants but not in human retinal organoids, suggesting that this phenomenon may be unique to mice. Using pharmacological inhibition or an in vivo nanoparticle-mediated RNAi approach, we demonstrated that inhibiting either HIF was effective for preventing NV in OIR mice. Collectively, these results explain why inhibition of either HIF-1α or HIF-2α is equally effective for preventing retinal NV in mice but suggest that therapies targeting both HIFs will be necessary to prevent NV in patients with PSR.

Authors

Jing Zhang, Yaowu Qin, Mireya Martinez, Miguel Flores-Bellver, Murilo Rodrigues, Aumreetam Dinabandhu, Xuan Cao, Monika Deshpande, Yu Qin, Silvia Aparicio-Domingo, Yuan Rui, Stephany Y. Tzeng, Shaima Salman, Jin Yuan, Adrienne W. Scott, Jordan J. Green, M. Valeria Canto-Soler, Gregg L. Semenza, Silvia Montaner, Akrit Sodhi

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Figure 1

Peripheral ischemia in patients with sickle cell disease is not sufficient to promote the development of NV.

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Peripheral ischemia in patients with sickle cell disease is not sufficie...
(A) Retinal ischemic index in all patients with sickle cell disease without PSR (no PSR) and with PSR (PSR). Blue and red dotted lines identify mean retinal ischemic index in patients with and without PSR, respectively. (B) Retinal ischemic index in patients with sickle cell disease divided by hemoglobin status (SS, SC, and Sβthal) without (–) and with (+) PSR. Blue arrows identify patients without PSR with a retinal ischemic index greater than the average for patients with PSR. Red arrows identify patients with PSR with retinal ischemic index less than the average for patients without PSR. The ischemic indices of patients without PSR and with PSR were compared using a 2-tailed Student’s t test. *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001.

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

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