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

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) generatio...

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Autores principales: Fischer, M. Dominik, Huber, Gesine, Beck, Susanne C., Tanimoto, Naoyuki, Muehlfriedel, Regine, Fahl, Edda, Grimm, Christian, Wenzel, Andreas, Remé, Charlotte E., van de Pavert, Serge A., Wijnholds, Jan, Pacal, Marek, Bremner, Rod, Seeliger, Mathias W.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2759518/
https://www.ncbi.nlm.nih.gov/pubmed/19838301
http://dx.doi.org/10.1371/journal.pone.0007507
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author Fischer, M. Dominik
Huber, Gesine
Beck, Susanne C.
Tanimoto, Naoyuki
Muehlfriedel, Regine
Fahl, Edda
Grimm, Christian
Wenzel, Andreas
Remé, Charlotte E.
van de Pavert, Serge A.
Wijnholds, Jan
Pacal, Marek
Bremner, Rod
Seeliger, Mathias W.
author_facet Fischer, M. Dominik
Huber, Gesine
Beck, Susanne C.
Tanimoto, Naoyuki
Muehlfriedel, Regine
Fahl, Edda
Grimm, Christian
Wenzel, Andreas
Remé, Charlotte E.
van de Pavert, Serge A.
Wijnholds, Jan
Pacal, Marek
Bremner, Rod
Seeliger, Mathias W.
author_sort Fischer, M. Dominik
collection PubMed
description 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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spelling pubmed-27595182009-10-19 Noninvasive, In Vivo Assessment of Mouse Retinal Structure Using Optical Coherence Tomography Fischer, M. Dominik Huber, Gesine Beck, Susanne C. Tanimoto, Naoyuki Muehlfriedel, Regine Fahl, Edda Grimm, Christian Wenzel, Andreas Remé, Charlotte E. van de Pavert, Serge A. Wijnholds, Jan Pacal, Marek Bremner, Rod Seeliger, Mathias W. PLoS One Research Article 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. Public Library of Science 2009-10-19 /pmc/articles/PMC2759518/ /pubmed/19838301 http://dx.doi.org/10.1371/journal.pone.0007507 Text en Fischer et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fischer, M. Dominik
Huber, Gesine
Beck, Susanne C.
Tanimoto, Naoyuki
Muehlfriedel, Regine
Fahl, Edda
Grimm, Christian
Wenzel, Andreas
Remé, Charlotte E.
van de Pavert, Serge A.
Wijnholds, Jan
Pacal, Marek
Bremner, Rod
Seeliger, Mathias W.
Noninvasive, In Vivo Assessment of Mouse Retinal Structure Using Optical Coherence Tomography
title Noninvasive, In Vivo Assessment of Mouse Retinal Structure Using Optical Coherence Tomography
title_full Noninvasive, In Vivo Assessment of Mouse Retinal Structure Using Optical Coherence Tomography
title_fullStr Noninvasive, In Vivo Assessment of Mouse Retinal Structure Using Optical Coherence Tomography
title_full_unstemmed Noninvasive, In Vivo Assessment of Mouse Retinal Structure Using Optical Coherence Tomography
title_short Noninvasive, In Vivo Assessment of Mouse Retinal Structure Using Optical Coherence Tomography
title_sort noninvasive, in vivo assessment of mouse retinal structure using optical coherence tomography
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2759518/
https://www.ncbi.nlm.nih.gov/pubmed/19838301
http://dx.doi.org/10.1371/journal.pone.0007507
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