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

Authors :
Naoyuki Tanimoto
Andreas Wenzel
Charlotte E. Remé
Mathias W. Seeliger
Rod Bremner
M. Dominik Fischer
Regine Muehlfriedel
Serge A. van de Pavert
Gesine Huber
Jan Wijnholds
Christian Grimm
Marek Pacal
Susanne C. Beck
E. Fahl
Molecular cell biology and Immunology
CCA - Immuno-pathogenesis
University of Zurich
Fischer, M D
Netherlands Institute for Neuroscience (NIN)
Source :
PLoS ONE, PLoS ONE, Vol 4, Iss 10, p e7507 (2009), PLoS ONE, 4(10), 1-7. Public Library of Science, Fischer, M D, Huber, G, Beck, S C, Tanimoto, N, Muehlfriedel, R, Fahl, E, Grimm, C, Wenzel, A, Reme, C E, van de Pavert, S A, Wijnholds, J, Pacal, M, Bremner, R & Seeliger, M W 2009, ' Noninvasive, In Vivo Assessment of Mouse Retinal Structure Using Optical Coherence Tomography ', PLoS ONE, vol. 4, no. 10, pp. 1-7 . https://doi.org/10.1371/journal.pone.0007507, PLoS One, 4. Public Library of Science
Publication Year :
2009

Abstract

BackgroundOptical 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 findingsWe 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/significanceWe 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.

Details

Language :
English
ISSN :
19326203
Volume :
4
Issue :
10
Database :
OpenAIRE
Journal :
PLoS ONE
Accession number :
edsair.doi.dedup.....75811cdb0ad1ad50c7f5be3c6e587d6e
Full Text :
https://doi.org/10.1371/journal.pone.0007507