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Evaluation of topical cysteamine therapy in the CTNS(−/−) knockout mouse using in vivo confocal microscopy
PURPOSE: The purpose of this study was to assess the ability of quantitative in vivo confocal microscopy (CM) to detect changes in cystine crystal volume in the cystinosisn (Ctns(−/−))mouse cornea following topical cysteamine therapy. METHODS: Fifteen Ctns(−/−) mice were sequentially followed using...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3209421/ https://www.ncbi.nlm.nih.gov/pubmed/22065917 |
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author | Simpson, Jennifer L. Nien, Chyong Jy Flynn, Kevin J. Jester, James V. |
author_facet | Simpson, Jennifer L. Nien, Chyong Jy Flynn, Kevin J. Jester, James V. |
author_sort | Simpson, Jennifer L. |
collection | PubMed |
description | PURPOSE: The purpose of this study was to assess the ability of quantitative in vivo confocal microscopy (CM) to detect changes in cystine crystal volume in the cystinosisn (Ctns(−/−))mouse cornea following topical cysteamine therapy. METHODS: Fifteen Ctns(−/−) mice were sequentially followed using in vivo CM from 3 to 10 months of age. In a second experiment, five mice receiving topical cysteamine eyedrops (0.55%) for 4 weeks were compared to five untreated mice. The volume of corneal cystine crystals was determined by thresholding and counting high intensity pixels in the in vivo CM scans and dividing by the stromal volume to calculate a crystal volume index (CVI). RESULTS: Corneal crystals progressively increased in density with age, reaching a peak density at 6–8 months and showing a 70 fold increase in CVI. Eyes treated with cysteamine drops showed significantly less crystal accumulation compared to control eyes (p<0.001) with only a 15% increase in treated eyes (p=ns) compared to 173% increase (p<0.04) for untreated eyes. CONCLUSIONS: Measurement of CVI shows that there is a progressive increase in cystine crystal volume up to 8 months of age and that cysteamine eyedrops significantly inhibits progression in the Ctns(−/−) mouse. These findings are similar to those seen clinically in patients with cystinosis, and suggest that measurement of CVI in the Ctns(−/−) mouse may be used as a model to develop novel therapeutic strategies for treating corneal cystinosis. |
format | Online Article Text |
id | pubmed-3209421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Molecular Vision |
record_format | MEDLINE/PubMed |
spelling | pubmed-32094212011-11-07 Evaluation of topical cysteamine therapy in the CTNS(−/−) knockout mouse using in vivo confocal microscopy Simpson, Jennifer L. Nien, Chyong Jy Flynn, Kevin J. Jester, James V. Mol Vis Research Article PURPOSE: The purpose of this study was to assess the ability of quantitative in vivo confocal microscopy (CM) to detect changes in cystine crystal volume in the cystinosisn (Ctns(−/−))mouse cornea following topical cysteamine therapy. METHODS: Fifteen Ctns(−/−) mice were sequentially followed using in vivo CM from 3 to 10 months of age. In a second experiment, five mice receiving topical cysteamine eyedrops (0.55%) for 4 weeks were compared to five untreated mice. The volume of corneal cystine crystals was determined by thresholding and counting high intensity pixels in the in vivo CM scans and dividing by the stromal volume to calculate a crystal volume index (CVI). RESULTS: Corneal crystals progressively increased in density with age, reaching a peak density at 6–8 months and showing a 70 fold increase in CVI. Eyes treated with cysteamine drops showed significantly less crystal accumulation compared to control eyes (p<0.001) with only a 15% increase in treated eyes (p=ns) compared to 173% increase (p<0.04) for untreated eyes. CONCLUSIONS: Measurement of CVI shows that there is a progressive increase in cystine crystal volume up to 8 months of age and that cysteamine eyedrops significantly inhibits progression in the Ctns(−/−) mouse. These findings are similar to those seen clinically in patients with cystinosis, and suggest that measurement of CVI in the Ctns(−/−) mouse may be used as a model to develop novel therapeutic strategies for treating corneal cystinosis. Molecular Vision 2011-10-08 /pmc/articles/PMC3209421/ /pubmed/22065917 Text en Copyright © 2011 Molecular Vision. http://creativecommons.org/licenses/by/3.0/ 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 work is properly cited. |
spellingShingle | Research Article Simpson, Jennifer L. Nien, Chyong Jy Flynn, Kevin J. Jester, James V. Evaluation of topical cysteamine therapy in the CTNS(−/−) knockout mouse using in vivo confocal microscopy |
title | Evaluation of topical cysteamine therapy in the CTNS(−/−) knockout mouse using in vivo confocal microscopy |
title_full | Evaluation of topical cysteamine therapy in the CTNS(−/−) knockout mouse using in vivo confocal microscopy |
title_fullStr | Evaluation of topical cysteamine therapy in the CTNS(−/−) knockout mouse using in vivo confocal microscopy |
title_full_unstemmed | Evaluation of topical cysteamine therapy in the CTNS(−/−) knockout mouse using in vivo confocal microscopy |
title_short | Evaluation of topical cysteamine therapy in the CTNS(−/−) knockout mouse using in vivo confocal microscopy |
title_sort | evaluation of topical cysteamine therapy in the ctns(−/−) knockout mouse using in vivo confocal microscopy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3209421/ https://www.ncbi.nlm.nih.gov/pubmed/22065917 |
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