Journal article
Genetic dependence of central corneal thickness among inbred strains of mice
Investigative ophthalmology & visual science, Vol.51(1), pp.160-171
01/2010
DOI: 10.1167/iovs.09-3429
PMCID: PMC2869057
PMID: 19710407
Abstract
Central corneal thickness (CCT) exhibits broad variability. For unknown reasons, CCT also associates with diseases not typically considered corneal, particularly glaucoma. The purpose of this study was to test the strain dependence of CCT variability among inbred mice and identify cellular and molecular factors associated with differing CCT. Methodology for measuring murine CCT with ultrasound pachymetry was developed and used to measure CCT among 17 strains of mice. Corneas from three strains with nonoverlapping differences in CCT (C57BLKS/J, C57BL/6J, and SJL/J) were compared by histology, transmission electron microscopy, and expression profiling with gene microarrays. CCT in mice was highly strain dependent. CCT exhibited continuous variation from 89.2 microm in C57BLKS/J to 123.8 microm in SJL/J. Stromal thickness was the major determinant of the varying murine CCT, with epithelial thickness also contributing. Corneal expression levels of many genes differed between strains with differing CCT, but most of these changes did not correlate with the changes observed in previously studied corneal diseases nor did they correlate with genes encoding major structural proteins of the cornea. Murine CCT has been measured with a variety of different techniques, but only among a limited number of different strains. Here, pachymetry was established as an additional tool and used to conduct a broad survey of different strains of inbred mice. These results demonstrated that murine CCT was highly influenced by genetic background and established a baseline for future genetic approaches to further elucidate mechanisms regulating CCT and its disease associations.
Details
- Title: Subtitle
- Genetic dependence of central corneal thickness among inbred strains of mice
- Creators
- Geoffrey D Lively - Department of Molecular Physiology and Biophysics, The University of Iowa, Iowa City, Iowa, USABing JiangAdam Hedberg-BuenzBo ChangGreg E PetersenKai WangMarkus H KuehnMichael G Anderson
- Resource Type
- Journal article
- Publication Details
- Investigative ophthalmology & visual science, Vol.51(1), pp.160-171
- DOI
- 10.1167/iovs.09-3429
- PMID
- 19710407
- PMCID
- PMC2869057
- NLM abbreviation
- Invest Ophthalmol Vis Sci
- ISSN
- 0146-0404
- eISSN
- 1552-5783
- Publisher
- United States
- Grant note
- R01 EY019485 / NEI NIH HHS R01 EY018825 / NEI NIH HHS EY018825 / NEI NIH HHS
- Language
- English
- Date published
- 01/2010
- Academic Unit
- Molecular Physiology and Biophysics; Biostatistics; Ophthalmology and Visual Sciences
- Record Identifier
- 9983980012602771
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