María Llorián-Salvador, Alerie G. de Fuente, Christopher E. McMurran, Amy Dashwood, James Dooley, Adrian Liston, Rosana Penalva, Yvonne Dombrowski, Alan W. Stitt, Denise C. Fitzgerald
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引用次数: 0
Abstract
Ageing is the principal risk factor for retinal degenerative diseases, which are the commonest cause of blindness in the developed countries. These conditions include age-related macular degeneration or diabetic retinopathy. Regulatory T cells play a vital role in immunoregulation of the nervous system by limiting inflammation and tissue damage in health and disease. Because the retina was long-considered an immunoprivileged site, the precise contribution of regulatory T cells in retinal homeostasis and in age-related retinal diseases remains unknown. Regulatory T cells were selectively depleted in both young (2–4 months) and aged (18–23 months) FoxP3-DTR mice. We evaluated neuroretinal degeneration, gliosis, subretinal space phagocyte infiltration, and retinal pigmented epithelium morphology through immunofluorescence analysis. Subsequently, aged Treg depleted animals underwent adoptive transfer of both young and aged regulatory T cells from wild-type mice, and the resulting impact on neurodegeneration was assessed. Statistical analyses employed included the U-Mann Whitney test, and for comparisons involving more than two groups, 1-way ANOVA analysis followed by Bonferroni’s post hoc test. Our study shows that regulatory T cell elimination leads to retinal pigment epithelium cell dysmorphology and accumulation of phagocytes in the subretinal space of young and aged mice. However, only aged mice experience retinal neurodegeneration and gliosis. Surprisingly, adoptive transfer of young but not aged regulatory T cells reverse these changes. Our findings demonstrate an essential role for regulatory T cells in maintaining age retinal homeostasis and preventing age-related neurodegeneration. This previously undescribed role of regulatory T cells in limiting retinal inflammation, RPE/choroid epithelium damage and subsequently photoreceptor loss with age, opens novel avenues to explore regulatory T cell neuroprotective and anti-inflammatory properties as potential therapeutic approaches for age-related retinal diseases.
老龄化是视网膜变性疾病的主要风险因素,也是发达国家最常见的致盲原因。这些疾病包括老年黄斑变性或糖尿病视网膜病变。调节性 T 细胞通过限制健康和疾病中的炎症和组织损伤,在神经系统的免疫调节中发挥着重要作用。由于视网膜长期以来被认为是免疫特权部位,调节性 T 细胞在视网膜稳态和与年龄相关的视网膜疾病中的确切贡献仍然未知。我们选择性地消耗了幼年(2-4 个月)和老年(18-23 个月)FoxP3-DTR 小鼠的调节性 T 细胞。我们通过免疫荧光分析评估了神经视网膜变性、胶质增生、视网膜下间隙吞噬细胞浸润和视网膜色素上皮形态。随后,老年Treg耗竭动物接受了来自野生型小鼠的年轻和老年调节性T细胞的收养性转移,并评估了其对神经退行性变的影响。采用的统计分析方法包括U-Mann Whitney检验,对于涉及两组以上的比较,则采用单因素方差分析,然后进行Bonferroni事后检验。我们的研究表明,调节性 T 细胞的清除会导致视网膜色素上皮细胞畸形和吞噬细胞在年轻小鼠和老年小鼠视网膜下间隙的聚集。然而,只有老年小鼠出现视网膜神经变性和胶质细胞病变。令人惊讶的是,年轻而非衰老的调节性 T 细胞的收养性转移能逆转这些变化。我们的研究结果表明,调节性 T 细胞在维持年龄视网膜稳态和防止与年龄相关的神经变性方面起着至关重要的作用。调节性 T 细胞在限制视网膜炎症、RPE/蛛网膜上皮细胞损伤以及随之而来的感光细胞随年龄增长而丧失方面的作用以前从未被描述过,这为探索调节性 T 细胞的神经保护和抗炎特性作为老年相关视网膜疾病的潜在治疗方法开辟了新的途径。
期刊介绍:
Molecular Neurodegeneration, an open-access, peer-reviewed journal, comprehensively covers neurodegeneration research at the molecular and cellular levels.
Neurodegenerative diseases, such as Alzheimer's, Parkinson's, Huntington's, and prion diseases, fall under its purview. These disorders, often linked to advanced aging and characterized by varying degrees of dementia, pose a significant public health concern with the growing aging population. Recent strides in understanding the molecular and cellular mechanisms of these neurodegenerative disorders offer valuable insights into their pathogenesis.