Affiliations 1 Qingdao Medical College, Qingdao University, Qingdao, China. 2 Eye Institute of Shandong First Medical University, Qingdao Eye Hospital of Shandong First Medical University, Qingdao, China. 3 School of Ophthalmology, Shandong First Medical University, Qingdao, China. 4 State Key Laboratory Cultivation Base, Shandong Provincial Key Laboratory of Ophthalmology, Qingdao, China.
刊名
Investigative ophthalmology & visual science
年份
2025
卷号
Vol.66 No.4
页码
48
ISSN
1552-5783
摘要
Purpose: The purpose of this study was to evaluate the neuroprotective effects of delivering nerve growth factor to retinal ganglion cells through adeno-associated virus serotype 2 carrying a neuronal-specific human synapsin promoter. Methods: AAV2-hSyn-NGF was injected intravitreally in three glaucoma models: optic nerve crush , microbead-induced ocular hypertension , and genetic glaucoma model . Quantitative polymerase chain reaction and enzyme-linked immunosorbent assay determined the o...更多
Purpose: The purpose of this study was to evaluate the neuroprotective effects of delivering nerve growth factor to retinal ganglion cells through adeno-associated virus serotype 2 carrying a neuronal-specific human synapsin promoter. Methods: AAV2-hSyn-NGF was injected intravitreally in three glaucoma models: optic nerve crush , microbead-induced ocular hypertension , and genetic glaucoma model . Quantitative polymerase chain reaction and enzyme-linked immunosorbent assay determined the optimal injection concentration of AAV vector. Flow cytometry monitored immune responses. Transduction efficiency was quantified using green fluorescent protein co-localization with RGC-specific marker RNA-binding protein with multiple splicing . The RGCs' density, retinal nerve fiber density, ganglion cell complex thickness, and positive scotopic threshold response were measured to assess structural and functional outcomes of the RGCs. Non-parametric Mann-Whitney U tests or Kruskal-Wallis tests were utilized to ascertain the statistical significance . Results: The optimal concentration of AAV vector for intravitreal injection was determined to be 1 × 1010 vector particles per eye. The use of the hSyn promoter significantly enhanced targeting specificity to RGCs, resulting in a transduction efficiency of 46.64% ± 2.18%. Administration of AAV2-hSyn-NGF effectively preserved the RGCs' density, nerve fiber layer integrity, and the thickness of ganglion cell complex, while maintaining the RGCs' function across three glaucoma models. Furthermore, this gene delivery system did not elicit detectable immune responses or structural damage to the retina. Conclusions: The AAV2-hSyn-NGF gene therapy offers a safe and effective neuroprotective strategy for RGCs across multiple glaucoma models, making it a promising candidate for future clinical trials in patients with glaucoma.收起
