Noninvasive, In Vivo Assessment of Mouse Retinal Structure Using Optical Coherence Tomography

被引:176
作者
Fischer, M. Dominik
Huber, Gesine
Beck, Susanne C.
Tanimoto, Naoyuki
Muehlfriedel, Regine
Fahl, Edda
Grimm, Christian
Wenzel, Andreas
Reme, Charlotte E.
van de Pavert, Serge A.
Wijnholds, Jan
Pacal, Marek
Bremner, Rod
Seeliger, Mathias W.
机构
[1] Division of Ocular Neurodegeneration, Centre for Ophthalmology, University of Tuebingen, Tuebingen
[2] Institute of Animal Welfare Ethology and Animal Hygiene, Faculty of Veterinary Medicine, Ludwig-Maximilians-University, Munich
[3] Laboratory of Retinal Cell Biology, University of Zurich, Zurich
[4] Neuromedical Genetics, Netherlands Institute for Neuroscience, Amsterdam
[5] Toronto Western Research Institute, University Health Network, University of Toronto, Toronto, ON
[6] Novartis Pharma Schweiz AG, Berne
[7] VU University Medical Center, Department of Molecular Cell Biology and Immunology, Amsterdam
来源
PLOS ONE | 2009年 / 4卷 / 10期
关键词
MICE; NRL; DEFICIENT; ORIGIN; RPE65; GENE;
D O I
10.1371/journal.pone.0007507
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Optical coherence tomography (OCT) is a novel method of retinal in vivo imaging. In this study, we assessed the potential of OCT to yield histology-analogue sections in mouse models of retinal degeneration. Methodology/Principal Findings: We achieved to adapt a commercial 3(rd) generation OCT system to obtain and quantify high-resolution morphological sections of the mouse retina which so far required in vitro histology. OCT and histology were compared in models with developmental defects, light damage, and inherited retinal degenerations. In conditional knockout mice deficient in retinal retinoblastoma protein Rb, the gradient of Cre expression from center to periphery, leading to a gradual reduction of retinal thickness, was clearly visible and well topographically quantifiable. In Nrl knockout mice, the layer involvement in the formation of rosette-like structures was similarly clear as in histology. OCT examination of focal light damage, well demarcated by the autofluorescence pattern, revealed a practically complete loss of photoreceptors with preservation of inner retinal layers, but also more subtle changes like edema formation. In Crb1 knockout mice (a model for Leber's congenital amaurosis), retinal vessels slipping through the outer nuclear layer towards the retinal pigment epithelium (RPE) due to the lack of adhesion in the subapical region of the photoreceptor inner segments could be well identified. Conclusions/Significance: We found that with the OCT we were able to detect and analyze a wide range of mouse retinal pathology, and the results compared well to histological sections. In addition, the technique allows to follow individual animals over time, thereby reducing the numbers of study animals needed, and to assess dynamic processes like edema formation. The results clearly indicate that OCT has the potential to revolutionize the future design of respective short- and long-term studies, as well as the preclinical assessment of therapeutic strategies.
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页数:7
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