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The effect of fibre cell remodelling on the power and optical quality of the lens
Vertebrate eye lenses are uniquely adapted to form a refractive index gradient (GRIN) for improved acuity, and to grow slowly in size despite constant cell proliferation. The mechanisms behind these adaptations remain poorly understood. We hypothesize that cell compaction contributes to both. To tes...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509584/ https://www.ncbi.nlm.nih.gov/pubmed/37727073 http://dx.doi.org/10.1098/rsif.2023.0316 |
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author | Rodriguez, J. Tan, Q. Šikić, H. Taber, L. A. Bassnett, S. |
author_facet | Rodriguez, J. Tan, Q. Šikić, H. Taber, L. A. Bassnett, S. |
author_sort | Rodriguez, J. |
collection | PubMed |
description | Vertebrate eye lenses are uniquely adapted to form a refractive index gradient (GRIN) for improved acuity, and to grow slowly in size despite constant cell proliferation. The mechanisms behind these adaptations remain poorly understood. We hypothesize that cell compaction contributes to both. To test this notion, we examined the relationship between lens size and shape, refractive characteristics and the cross-sectional areas of constituent fibre cells in mice of different ages. We developed a block-face imaging method to visualize cellular cross sections and found that the cross-sectional areas of fibre cells rose and then decreased over time, with the most significant reduction occurring in denucleating cells in the adult lens cortex, followed by cells in the embryonic nucleus. These findings help reconcile differences between the predictions of lens growth models and empirical data. Biomechanical simulations suggested that compressive forces generated from continuous deposition of fibre cells could contribute to cellular compaction. However, optical measurements revealed that the GRIN did not mirror the pattern of cellular compaction, implying that compaction alone cannot account for GRIN formation and that additional mechanisms are likely to be involved. |
format | Online Article Text |
id | pubmed-10509584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-105095842023-09-21 The effect of fibre cell remodelling on the power and optical quality of the lens Rodriguez, J. Tan, Q. Šikić, H. Taber, L. A. Bassnett, S. J R Soc Interface Life Sciences–Physics interface Vertebrate eye lenses are uniquely adapted to form a refractive index gradient (GRIN) for improved acuity, and to grow slowly in size despite constant cell proliferation. The mechanisms behind these adaptations remain poorly understood. We hypothesize that cell compaction contributes to both. To test this notion, we examined the relationship between lens size and shape, refractive characteristics and the cross-sectional areas of constituent fibre cells in mice of different ages. We developed a block-face imaging method to visualize cellular cross sections and found that the cross-sectional areas of fibre cells rose and then decreased over time, with the most significant reduction occurring in denucleating cells in the adult lens cortex, followed by cells in the embryonic nucleus. These findings help reconcile differences between the predictions of lens growth models and empirical data. Biomechanical simulations suggested that compressive forces generated from continuous deposition of fibre cells could contribute to cellular compaction. However, optical measurements revealed that the GRIN did not mirror the pattern of cellular compaction, implying that compaction alone cannot account for GRIN formation and that additional mechanisms are likely to be involved. The Royal Society 2023-09-20 /pmc/articles/PMC10509584/ /pubmed/37727073 http://dx.doi.org/10.1098/rsif.2023.0316 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Life Sciences–Physics interface Rodriguez, J. Tan, Q. Šikić, H. Taber, L. A. Bassnett, S. The effect of fibre cell remodelling on the power and optical quality of the lens |
title | The effect of fibre cell remodelling on the power and optical quality of the lens |
title_full | The effect of fibre cell remodelling on the power and optical quality of the lens |
title_fullStr | The effect of fibre cell remodelling on the power and optical quality of the lens |
title_full_unstemmed | The effect of fibre cell remodelling on the power and optical quality of the lens |
title_short | The effect of fibre cell remodelling on the power and optical quality of the lens |
title_sort | effect of fibre cell remodelling on the power and optical quality of the lens |
topic | Life Sciences–Physics interface |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509584/ https://www.ncbi.nlm.nih.gov/pubmed/37727073 http://dx.doi.org/10.1098/rsif.2023.0316 |
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