Department of Ophthalmology and Visual Sciences, the University of Iowa Carver College of Medicine, Iowa City, IA 52242, USA.
Institute for Vision Research, the University of Iowa, Iowa City, IA 52242, USA.
Cells. 2020 Feb 13;9(2):438. doi: 10.3390/cells9020438.
Degenerative diseases affecting retinal photoreceptor cells have numerous etiologies and clinical presentations. We clinically and molecularly studied the retina of a 70-year-old patient with retinal degeneration attributed to autoimmune retinopathy. The patient was followed for 19 years for progressive peripheral visual field loss and pigmentary changes. Single-cell RNA sequencing was performed on foveal and peripheral retina from this patient and four control patients, and cell-specific gene expression differences were identified between healthy and degenerating retina. Distinct populations of glial cells, including astrocytes and Müller cells, were identified in the tissue from the retinal degeneration patient. The glial cell populations demonstrated an expression profile consistent with reactive gliosis. This report provides evidence that glial cells have a distinct transcriptome in the setting of human retinal degeneration and represents a complementary clinical and molecular investigation of a case of progressive retinal disease.
影响视网膜光感受器细胞的退行性疾病有多种病因和临床表现。我们对一名 70 岁患者的视网膜进行了临床和分子研究,该患者的视网膜退化归因于自身免疫性视网膜炎。该患者因进行性周边视野丧失和色素变化而接受了 19 年的随访。对来自该患者和 4 名对照患者的中心凹和周边视网膜进行了单细胞 RNA 测序,并确定了健康和变性视网膜之间的细胞特异性基因表达差异。在来自视网膜变性患者的组织中鉴定出了包括星形胶质细胞和 Müller 细胞在内的不同胶质细胞群体。这些神经胶质细胞群体表现出与反应性胶质增生一致的表达谱。本报告提供了证据表明,在人类视网膜变性的情况下,神经胶质细胞具有独特的转录组,这代表了对进行性视网膜疾病的案例的临床和分子补充研究。