Nguyen Linda, Vallejos Catalina A, Mill Pleasantine, Megaw Roly
MRC Human Genetics Unit, Institute of Genetics and Cancer, The University of Edinburgh, Crewe Road South, Edinburgh EH4 2XU, UK.
Princess Alexandra Eye Pavilion, NHS Lothian, Chalmers Street, Edinburgh EH3 9HA, UK.
Genes (Basel). 2025 Sep 16;16(9):1088. doi: 10.3390/genes16091088.
Inherited retinal dystrophies (IRDs) represent a diverse group of disorders caused by mutations in genes essential for retinal function and maintenance. Traditional bulk RNA sequencing techniques provide valuable information for deciphering disease pathogenesis but lack the resolution to capture variation among specific cell clusters during disease progression. In contrast, single-cell transcriptomics, including single-cell RNA sequencing (scRNA-seq), enables detailed examination of distinct retinal clusters in both healthy and diseased states, uncovering unique gene expression signatures and early molecular changes preceding photoreceptor cell death in IRDs. These insights not only deepen our understanding of the complex pathogenesis of IRDs but also highlight potential targets for novel therapeutic interventions. In this review, we examine the recent literature on the application of single-cell transcriptomics in IRDs to explore how these techniques enhance our understanding of disease mechanisms and contribute to the identification of new therapeutic targets.
遗传性视网膜营养不良(IRDs)是由视网膜功能和维持所必需的基因突变引起的一组多样的疾病。传统的批量RNA测序技术为解读疾病发病机制提供了有价值的信息,但缺乏在疾病进展过程中捕捉特定细胞簇间差异的分辨率。相比之下,单细胞转录组学,包括单细胞RNA测序(scRNA-seq),能够详细检查健康和患病状态下不同的视网膜细胞簇,揭示IRD中独特的基因表达特征以及光感受器细胞死亡之前的早期分子变化。这些见解不仅加深了我们对IRDs复杂发病机制的理解,还突出了新型治疗干预的潜在靶点。在本综述中,我们研究了关于单细胞转录组学在IRDs中应用的最新文献,以探讨这些技术如何增强我们对疾病机制的理解并有助于确定新的治疗靶点。