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DARC技术介绍。

An introduction to DARC technology.

作者信息

Ahmad Syed Shoeb

机构信息

Department of Ophthalmology, Queen Elizabeth Hospital, Kota Kinabalu, Malaysia.

出版信息

Saudi J Ophthalmol. 2017 Jan-Mar;31(1):38-41. doi: 10.1016/j.sjopt.2016.08.001. Epub 2016 Aug 22.

DOI:10.1016/j.sjopt.2016.08.001
PMID:28337061
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5352956/
Abstract

Glaucoma is a multi-factorial neurodegenerative disorder. The common denominator in all types of glaucomas is retinal ganglion cell death through apoptosis. However, this cellular demise in glaucoma is detected late by structural or functional analyses. There can be a 10-year delay prior to the appearance of visual field defects and pre-perimetric glaucoma is an issue still being addressed. However, a new cutting-edge technology called detection of apoptosing retinal cells (DARC) is being developed. This technique is capable of non-invasive, real-time visualization of apoptotic changes at the cellular level. It can detect glaucomatous cell damage at a very early stage, at the moment apoptosis starts, and thus management can be initiated even prior to development of visual field changes. In future, this technique will also be able to provide conclusive evidence of the effectiveness of treatment protocol and the need for any modifications which may be required. This article aims to provide a concise review of DARC technology.

摘要

青光眼是一种多因素神经退行性疾病。所有类型青光眼的共同特征是视网膜神经节细胞通过凋亡而死亡。然而,通过结构或功能分析在青光眼患者中检测到这种细胞死亡的时间较晚。在视野缺损出现之前可能会有10年的延迟,而视野缺损前青光眼仍是一个有待解决的问题。然而,一种名为凋亡视网膜细胞检测(DARC)的前沿新技术正在研发中。这项技术能够在细胞水平上对凋亡变化进行非侵入性实时可视化。它可以在细胞凋亡刚开始的非常早期阶段检测到青光眼性细胞损伤,从而甚至在视野变化出现之前就可以开始治疗。未来,这项技术还将能够为治疗方案的有效性以及是否需要进行任何修改提供确凿证据。本文旨在对DARC技术进行简要综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a8b/5352956/741a7773cde9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a8b/5352956/646d6dfb0044/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a8b/5352956/741a7773cde9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a8b/5352956/646d6dfb0044/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a8b/5352956/741a7773cde9/gr2.jpg

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本文引用的文献

1
Current Concepts in the Biochemical Mechanisms of Glaucomatous Neurodegeneration.青光眼性神经变性生化机制的当前概念
J Curr Glaucoma Pract. 2013 May-Aug;7(2):49-53. doi: 10.5005/jp-journals-10008-1137. Epub 2013 May 9.
2
A semi-automated technique for labeling and counting of apoptosing retinal cells.一种用于标记和计数凋亡视网膜细胞的半自动技术。
BMC Bioinformatics. 2014 Jun 5;15:169. doi: 10.1186/1471-2105-15-169.
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The potential of annexin-labelling for the diagnosis and follow-up of glaucoma. Annexin 标记在青光眼诊断和随访中的潜力。
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Advances in Retinal Optical Imaging.视网膜光学成像的进展
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Glaucoma suspects: A practical approach.青光眼疑似病例:一种实用方法。
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Regenerative medicine in the retina: from stem cells to cell replacement therapy.视网膜再生医学:从干细胞到细胞替代疗法。
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Eye (Lond). 2011 May;25(5):545-53. doi: 10.1038/eye.2011.64. Epub 2011 Mar 25.
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Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo.成像神经退行性变的多个阶段:评估体内细胞死亡的新方法。
Cell Death Dis. 2010;1(1):e3. doi: 10.1038/cddis.2009.3.
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Mechanisms of retinal ganglion cell injury and defense in glaucoma.青光眼中原发性神经节细胞损伤和防御的机制。
Exp Eye Res. 2010 Jul;91(1):48-53. doi: 10.1016/j.exer.2010.04.002. Epub 2010 Apr 13.
8
Real-time in vivo imaging of retinal cell apoptosis after laser exposure.激光照射后视网膜细胞凋亡的实时体内成像。
Invest Ophthalmol Vis Sci. 2008 Jun;49(6):2773-80. doi: 10.1167/iovs.07-1335. Epub 2008 Feb 15.
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Assessment of rat and mouse RGC apoptosis imaging in vivo with different scanning laser ophthalmoscopes.使用不同的扫描激光检眼镜对大鼠和小鼠视网膜神经节细胞凋亡进行体内成像评估。
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