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Noninvasive, In Vivo Assessment of Mouse Retinal Structure Using Optical Coherence Tomography
- 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.
- Subjects :
- Retinal degeneration
Male
Pathology
Light
genetic structures
Retinoblastoma Protein
chemistry.chemical_compound
Mice
0302 clinical medicine
Conditional gene knockout
Mice, Knockout
0303 health sciences
Multidisciplinary
medicine.diagnostic_test
Retinal Degeneration
Ophthalmology/Inherited Eye Disorders
medicine.anatomical_structure
Basic-Leucine Zipper Transcription Factors
Medicine
Female
Neuroscience/Neurobiology of Disease and Regeneration
Preclinical imaging
Tomography, Optical Coherence
Research Article
10018 Ophthalmology Clinic
medicine.medical_specialty
Science
610 Medicine & health
Nerve Tissue Proteins
1100 General Agricultural and Biological Sciences
Biology
Retina
03 medical and health sciences
Optical coherence tomography
1300 General Biochemistry, Genetics and Molecular Biology
medicine
Animals
Outer nuclear layer
Eye Proteins
030304 developmental biology
1000 Multidisciplinary
Retinal pigment epithelium
Neuroscience/Sensory Systems
Lasers
Retinal
medicine.disease
eye diseases
Mice, Inbred C57BL
Ophthalmoscopy
chemistry
Genetics and Genomics/Disease Models
Cell Biology/Neuronal and Glial Cell Biology
030221 ophthalmology & optometry
sense organs
Subjects
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