Glaucoma, More than Meets the Eye: Patterns of Demyelination Revealed in Human Postmortem Glaucomatous Optic Nerve.

IF 7 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Gabriella E Parrilla, Akanksha Salkar, Roshana Vander Wall, Vivek Gupta, Stuart L Graham, Yuyi You
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Abstract

Glaucoma is a neurodegenerative disease affecting millions worldwide, characterised by retinal ganglion cell (RGC) degeneration which leads to blindness in more advanced cases. Although the pathogenesis and underlying mechanisms of glaucoma are not fully understood, there are theories that hint at demyelination playing a role in the disease process. Demyelination, or the degeneration of the myelin sheath surrounding axons, has been found in previous studies using animal models of glaucoma and clinical assessments of glaucoma patients. However, this has not been fully realised or quantified in glaucoma patients. Utilising postmortem optic nerve samples from glaucoma and healthy subjects, various immunohistochemical and morphological assessments were performed to determine the extent, if any, of demyelination in glaucomatous optic nerves. Our findings revealed that alongside nerve shrinkage and degeneration of nerve tissue fascicles, there were significantly less myelin proteins, specifically myelin basic protein (MBP), in glaucoma optic nerves. Additionally, the loss of MBP was correlated with decreased oligodendrocyte (OLG) precursors and increasing glial activity. This further supports previous evidence that demyelination may be a secondary degenerative process associated with glaucoma disease progression. Not only do these results provide evidence for potential disease mechanisms, but this is also the first study to quantify optic nerve demyelination in glaucoma postmortem tissue.

青光眼,远不止眼睛看到的那么简单:人类青光眼死后视神经脱髓鞘的模式。
青光眼是一种影响全球数百万人的神经退行性疾病,其特点是视网膜神经节细胞(RGC)变性,晚期病例会导致失明。虽然青光眼的发病机理和内在机制尚未完全明了,但有理论认为脱髓鞘在疾病过程中发挥了作用。在以往使用青光眼动物模型进行的研究和对青光眼患者进行的临床评估中发现,脱髓鞘或围绕轴突的髓鞘发生了变性。然而,这种现象在青光眼患者身上尚未得到充分认识或量化。利用青光眼和健康受试者的死后视神经样本,我们进行了各种免疫组化和形态学评估,以确定青光眼视神经脱髓鞘的程度(如果有的话)。我们的研究结果表明,在神经萎缩和神经组织束变性的同时,青光眼视神经中的髓鞘蛋白,特别是髓鞘碱性蛋白(MBP)明显减少。此外,髓鞘蛋白的减少还与少突胶质细胞(OLG)前体的减少和胶质细胞活动的增加有关。这进一步支持了之前的证据,即脱髓鞘可能是与青光眼疾病进展相关的继发性变性过程。这些结果不仅为潜在的疾病机制提供了证据,也是第一项量化青光眼死后组织中视神经脱髓鞘的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Aging and Disease
Aging and Disease GERIATRICS & GERONTOLOGY-
CiteScore
14.60
自引率
2.70%
发文量
138
审稿时长
10 weeks
期刊介绍: Aging & Disease (A&D) is an open-access online journal dedicated to publishing groundbreaking research on the biology of aging, the pathophysiology of age-related diseases, and innovative therapies for conditions affecting the elderly. The scope encompasses various diseases such as Stroke, Alzheimer's disease, Parkinson’s disease, Epilepsy, Dementia, Depression, Cardiovascular Disease, Cancer, Arthritis, Cataract, Osteoporosis, Diabetes, and Hypertension. The journal welcomes studies involving animal models as well as human tissues or cells.
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