Effect of AAV-Mediated Rhodopsin Gene Augmentation on Retinal Degeneration Caused by the Dominant P23H Rhodopsin Mutation in a Knock-In Murine Model

2020 ◽  
Vol 31 (13-14) ◽  
pp. 730-742 ◽  
Author(s):  
Harry O. Orlans ◽  
Alun R. Barnard ◽  
Maria I. Patrício ◽  
Michelle E. McClements ◽  
Robert E. MacLaren

2016 ◽  
Vol 57 (6) ◽  
pp. 2770 ◽  
Author(s):  
Jing Wang ◽  
Xuezhi Cui ◽  
Penny Roon ◽  
Sylvia B. Smith




2014 ◽  
Vol 94 (6) ◽  
pp. 674-682 ◽  
Author(s):  
Yujuan Wang ◽  
Mones S Abu-Asab ◽  
Cheng-Rong Yu ◽  
Zhongshu Tang ◽  
Defen Shen ◽  
...  


2012 ◽  
Vol 9 (1) ◽  
Author(s):  
Jingsheng Tuo ◽  
Xiaoguang Cao ◽  
Defen Shen ◽  
Yujuan Wang ◽  
Jun Zhang ◽  
...  


2016 ◽  
Vol 57 (10) ◽  
pp. 4125 ◽  
Author(s):  
Elad Moisseiev ◽  
Zeljka Smit-McBride ◽  
Sharon Oltjen ◽  
Pengfei Zhang ◽  
Robert J. Zawadzki ◽  
...  


2017 ◽  
Vol 14 (1) ◽  
Author(s):  
Lei Zhao ◽  
Jun Li ◽  
Yingmei Fu ◽  
Mengxue Zhang ◽  
Bowen Wang ◽  
...  


2012 ◽  
Vol 53 (9) ◽  
pp. 5594 ◽  
Author(s):  
Wei Chieh Huang ◽  
Alan F. Wright ◽  
Alejandro J. Roman ◽  
Artur V. Cideciyan ◽  
Forbes D. Manson ◽  
...  


2021 ◽  
Vol 2021 ◽  
pp. 1-17
Author(s):  
Deokho Lee ◽  
Ayaka Nakai ◽  
Yukihiro Miwa ◽  
Yohei Tomita ◽  
Naho Serizawa ◽  
...  

Retinal degeneration is a progressive retinal damage in ocular vascular diseases. There are several reasons for this, such as occlusion of arteries or veins, diabetic retinopathy, or hereditary retinal diseases. To study pathological mechanisms of retinal degeneration, it is required to develop experimentally reproducible and clinically relevant models. In our previous studies, we developed a murine model of retinal hypoperfusion by unilateral common carotid artery occlusion (UCCAO) which mimics the pathophysiology of ocular ischemic syndrome (OIS) in humans, and described broad pathological mechanisms in the retina after UCCAO. However, there still remain missing pieces of the ocular pathologic process by UCCAO. In this study, we examined those unfound mechanisms. UCCAO was performed on adult mice. Ocular dysfunctions, histological deficits, and inflammation were examined after UCCAO, compared with sham-operated mice. Evaluation values were analyzed by electrophysiological, histological, and molecular biological methods. Eyelid drooping was permanently seen after UCCAO. Induction time point of acute reversible cataract under anesthesia was shortened. Retinal/visual dysfunctions were detected 2-4 weeks after UCCAO. Specifically, scotopic b-wave was more affected than a-wave, with the dysfunction of photopic b-wave. Impaired oscillatory potentials and visual evoked potential were constantly observed. Pathological Müller gliosis/inflammation was featured with NeuN-positive cell loss in the ganglion cell layer. Axial length, intraocular pressure, pupillary light reflex, and retinal pigment epithelium/choroidal thickness were not changed by UCCAO. A murine model of retinal ischemia by UCCAO can be useful for studying a series of degenerative process in the ischemic retina.



2015 ◽  
Vol 588 ◽  
pp. 108-113 ◽  
Author(s):  
Atsuko Kimura ◽  
Xiaoli Guo ◽  
Takahiko Noro ◽  
Chikako Harada ◽  
Kohichi Tanaka ◽  
...  


ASN NEURO ◽  
2013 ◽  
Vol 5 (5) ◽  
pp. AN20130028 ◽  
Author(s):  
Yujuan Wang ◽  
Preeti Subramanian ◽  
Defen Shen ◽  
Jingsheng Tuo ◽  
S. Patricia Becerra ◽  
...  


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