Scaling and maintenance of corneal thickness during aging

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Scaling and maintenance of corneal thickness during aging

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Title: Scaling and maintenance of corneal thickness during aging
Author: Inomata, Takenori; Mashaghi, Alireza; Hong, Jiaxu; Nakao, Takeshi; Dana, Reza

Note: Order does not necessarily reflect citation order of authors.

Citation: Inomata, Takenori, Alireza Mashaghi, Jiaxu Hong, Takeshi Nakao, and Reza Dana. 2017. “Scaling and maintenance of corneal thickness during aging.” PLoS ONE 12 (10): e0185694. doi:10.1371/journal.pone.0185694. http://dx.doi.org/10.1371/journal.pone.0185694.
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Abstract: Corneal thickness is tightly regulated by its boundary endothelial and epithelial layers. The regulated set-point of corneal thickness likely shows inter-individual variations, changes by age, and response to stress. Using anterior segment-optical coherence tomography, we measure murine central corneal thickness and report on body size scaling of murine central corneal thickness during aging. For aged-matched mice, we find that corneal thickness depends on sex and strain. To shed mechanistic insights into these anatomical changes, we measure epithelial layer integrity and endothelial cell density during the life span of the mice using corneal fluorescein staining and in vivo confocal microscopy, respectively and compare their trends with that of the corneal thickness. Cornea thickness increases initially (1 month: 114.7 ± 3.0 μm, 6 months: 126.3 ± 1.6 μm), reaches a maximum (9 months: 129.3 ± 4.4 μm) and then reduces (12 months: 127 ± 2.9 μm, 13 months: 119.5 ± 7.6 μm, 14 months: 110.6 ± 10.6 μm), while the body size (weight) increases with age. We find that endothelial cell density reduces from 2 months old to 8 months old as the mice age and epithelial layer accumulates damages within this time frame. Finally, we compare murine corneal thickness with those of several other mammals including humans and show that corneal thickness has an allometric scaling with body size. Our results have relevance for organ size regulation, translational pharmacology, and veterinary medicine.
Published Version: doi:10.1371/journal.pone.0185694
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630165/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:34492177
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