Cited by 76Corneal surgery and disordersCorneal Surgery and TreatmentsConnective tissue disorders research

Elastic microfibril distribution in the cornea: Differences between normal and keratoconic stroma

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White, Tomas L., Lewis, Philip N., Young, Robert D., Kitazawa, Koji, Inatomi, Tsutomu, Kinoshita, Shigeru, Meek, Keith M.·2017·Experimental Eye Research

Abstract

The optical and biomechanical properties of the cornea are largely governed by the collagen-rich stroma, a layer that represents approximately 90% of the total thickness. Within the stroma, the specific arrangement of superimposed lamellae provides the tissue with tensile strength, whilst the spatial arrangement of individual collagen fibrils within the lamellae confers transparency. In keratoconus, this precise stromal arrangement is lost, resulting in ectasia and visual impairment. In the normal cornea, we previously characterised the three-dimensional arrangement of an elastic fiber network spanning the posterior stroma from limbus-to-limbus. In the peripheral cornea/limbus there are elastin-containing sheets or broad fibers, most of which become microfibril bundles (MBs) with little or no elastin component when reaching the central cornea. The purpose of the current study was to compare this network with the elastic fiber distribution in post-surgical keratoconic corneal buttons, using serial block face scanning electron microscopy and transmission electron microscopy. We have demonstrated that the MB distribution is very different in keratoconus. MBs are absent from a region of stroma anterior to Descemet's membrane, an area that is densely populated in normal cornea, whilst being concentrated below the epithelium, an area in which they are absent in normal cornea. We contend that these latter microfibrils are produced as a biomechanical response to provide additional strength to the anterior stroma in order to prevent tissue rupture at the apex of the cone. A lack of MBs anterior to Descemet's membrane in keratoconus would alter the biomechanical properties of the tissue, potentially contributing to the pathogenesis of the disease.

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Authors
White, T. L., Lewis, P. N., Young, R. D., Kitazawa, K., Inatomi, T., Kinoshita, S., & Meek, K. M.
Affiliations
  • Cardiff University (GB)
  • Kyoto Prefectural University (JP)
Corresponding author
Meek, Keith M.
Venue
Experimental Eye Research
Publisher
Elsevier BV
Published
2017-06
Volume
159
Pages
40-48
ISSN
0014-4835 (ISSN-L)
OpenAlex
W2603759820
Cited by
76
References
1
Citations by year
2026: 7 · 2025: 8 · 2024: 9 · 2023: 4 · 2022: 6 · 2021: 8 · 2020: 13 · 2019: 9 · 2018: 11 · 2017: 1
FWCI
6.92
Type
journal article
Language
en
Open access
Locations
  • Experimental Eye Research (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • ORCA Online Research @Cardiff (Cardiff University) (acceptedVersion)
Funders
  • Medical Research Council (MR/K000837/1)
  • Biotechnology and Biological Sciences Research Council (BB/M025349/1)
Topics
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Corneal surgery and disorders
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Corneal Surgery and Treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Connective tissue disorders research
Keywords
keratoconus, corneal stroma, elastic fiber network, collagen fibrils, Descemet's membrane, corneal biomechanics, corneal transparency, corneal ectasia, corneal buttons
MeSH terms
Adult, Aged, Corneal Stroma, Elasticity, Extracellular Matrix, Female, Humans, Keratoconus, Male, Microscopy, Electron, Scanning, Middle Aged, Microscopy, Confocal, Microfibrils

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