Photoreceptors inhibit pathological retinal angiogenesis through transcriptional regulation of Adam17 via c-Fos
Year: 2024
Type: article
Abstract: Pathological retinal angiogenesis profoundly impacts visual function in vascular eye diseases, such as retinopathy of prematurity (ROP) in preterm infants and age-related macular degeneration in the elderly. While the involvement of photoreceptors in these diseases is recognized, the underlying mechanisms remain unclear. This study delved into the pivotal role of photoreceptors in regulating abnormal retinal blood vessel growth using an oxygen-induced retinopathy (OIR) mouse model through the c-Fos/A disintegrin and metalloprotease 17 (Adam17) axis. Our findings revealed a significant induction of c-Fos expression in rod photoreceptors, and c-Fos depletion in these cells inhibited pathological neovascularization and reduced blood vessel leakage in the OIR mouse model. Mechanistically, c-Fos directly regulated the transcription of Adam17 a shedding protease responsible for the production of bioactive molecules involved in inflammation, angiogenesis, and cell adhesion and migration. Furthermore, we demonstrated the therapeutic potential by using an adeno-associated virus carrying a rod photoreceptor-specific short hairpin RNA against c-fos which effectively mitigated abnormal retinal blood vessel overgrowth, restored retinal thickness, and improved electroretinographic (ERG) responses. In conclusion, this study highlights the significance of photoreceptor c-Fos in ROP pathology, offering a novel perspective for the treatment of this disease.
Source: Angiogenesis
Authors: Xudong Wang, Tianxi Wang, Satoshi Kaneko, Emil Kriukov, Enton Lam, Manon Szczepan, Jasmine Chen, Austin Gregg, Xingyan Wang, Angeles Fernandez-Gonzalez, S. Alex Mitsialis, Stella Kourembanas, Petr Baranov, Ye Sun
Language: English
Subfield: Radiology, Nuclear Medicine and Imaging
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $5,090
Awards: Retinal Ganglion Cell Replacement in Clinically Relevant Models of Optic Neuropathy, The Mechanism of Immune-Vascular Crosstalk in Retinopathy, Photoreceptor Determination of Retinal Blood Vessel Growth in Retinopathy, G5808301577, G5945485887, G9000200862, Boston Children's Hospital/HMS Intellectual and Developmental Disabilities Research Center, UAB Core Grant for Vision Research, MSC Exosome Treatment for BPD: Impact on Immunity and Lung Development
OpenAlex ID: W4392791226
