Suppression of cAMP/PKA/CREB signaling ameliorates retinal injury in diabetic retinopathy

Bibliographic Details
Title: Suppression of cAMP/PKA/CREB signaling ameliorates retinal injury in diabetic retinopathy
Authors: Xiao‐Ling Fang, Qin Zhang, Wen‐Wen Xue, Jin‐Hua Tao, Hai‐Dong Zou, Qiu‐Rong Lin, Yu‐Lan Wang
Source: Kaohsiung Journal of Medical Sciences, Vol 39, Iss 9, Pp 916-926 (2023)
Publisher Information: Wiley, 2023.
Publication Year: 2023
Collection: LCC:Medicine (General)
Subject Terms: cAMP/PKA/CREB signaling, diabetic retinopathy, Müller cells, Medicine (General), R5-920
More Details: Abstract The blood‐retinal barrier (BRB), homeostasis, neuronal integrity, and metabolic processes are all directly influenced by Müller cells, the most important retinal glial cells. We isolated primary Müller cells from Sprague–Dawley (SD) neonatal rats and treated them with glucose at varying doses. CCK‐8 was used to quantify cellular viability, and a TUNEL assay was performed to detect cell apoptosis. ELISA, immunofluorescence, and western blotting were used to assess cAMP/PKA/CREB signaling, Kir4.1, AQP4, GFAP, and VEGF levels, respectively. H&E staining was used to examine histopathological alterations in diabetic retinopathy (DR)‐affected retinal tissue in rats. As glucose concentration increases, gliosis of Müller cells became apparent, as evidenced by a decline in cell activity, an increase in apoptosis, downregulation of Kir4.1 level, and overexpression of GFAP, AQP4, and VEGF. Treatments with low, intermediate, and high glucose levels led to aberrant activation of cAMP/PKA/CREB signaling. Interestingly, blocking cAMP and PKA reduced high glucose‐induced Müller cell damage and gliosis by a significant amount. Further in vivo results suggested that cAMP or PKA inhibition significantly improved edema, bleeding, and retinal disorders. Our findings showed that high glucose exacerbated Müller cell damage and gliosis via a mechanism involving cAMP/PKA/CREB signaling.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2410-8650
1607-551X
Relation: https://doaj.org/toc/1607-551X; https://doaj.org/toc/2410-8650
DOI: 10.1002/kjm2.12722
Access URL: https://doaj.org/article/d5f0ce8a0b694bfb8d6ff5f9788b6d38
Accession Number: edsdoj.5f0ce8a0b694bfb8d6ff5f9788b6d38
Database: Directory of Open Access Journals
More Details
ISSN:24108650
1607551X
DOI:10.1002/kjm2.12722
Published in:Kaohsiung Journal of Medical Sciences
Language:English