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Retinal organoids: current status of development and new avenues for application in disease modeling, drug discovery and therapeutics

神经科学 诱导多能干细胞 视网膜 色素性视网膜炎 生物 药物发现 视网膜 视网膜变性 黄斑变性 疾病 基因组编辑 药物开发 斯塔加德特病 电池类型 生物信息学 计算生物学 视网膜病变 医学 视网膜色素上皮 干细胞 细胞 模式生物 祖细胞
作者
Renu Agarwal,Igor Nikolayevich Iezhitsa,José R. Hombrebueno,Puneet Agarwal
出处
期刊:International journal of retina and vitreous [BioMed Central]
卷期号:12 (1) 被引量:2
标识
DOI:10.1186/s40942-026-00846-x
摘要

Visual impairment affects over 2.2 billion people worldwide and the major causes include age-related macular degeneration (AMD), glaucoma, and diabetic retinopathy. For research in these areas, although animal models offer a more physiologically complex system than in vitro approaches, their use raises ethical considerations, and species-specific differences such as variations in protein sequences and signaling pathways. This can limit the direct translatability of the outcomes. Traditional 2-D cell cultures, in contrast, lack the multicellular organization and dynamic microenvironment necessary to replicate human retinal complexity. Retinal organoids (ROs), three-dimensional tissue constructs derived from pluripotent stem cells, have emerged as a promising model due to their human origin and complex cellular interactions that cannot be achieved in conventional 2-D/3-D co-culture models. In this review, we provide a brief overview of the evolution from 2-D to 3-D retinal models, highlight the structural and functional features of ROs including the presence of layered retinal architecture, photoreceptor outer segment formation, and light-responsive electrophysiological activity and summarize their applications in disease modeling, drug discovery, and gene and cell therapy. ROs represent a significant advancement over traditional models by enabling the recapitulation of human-specific retinal development, facilitating the study of patient-derived disease phenotypes, and providing a platform for personalized therapeutic screening. Their development has deepened understanding of pathological mechanisms in conditions such as retinitis pigmentosa and AMD, while enabling preclinical testing of targeted interventions like CRISPR-based gene editing and photoreceptor cell replacement. Nonetheless, challenges remain in fully replicating retinal vascularization, long-term functional maturation, and synaptic connectivity, underscoring the need for continued refinement and integration with complementary model systems.
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