Corneal collagen—its role in maintaining corneal shape and transparency

Meek, Keith Michael Andrew

doi:10.1007/s12551-009-0011-x

Cited by 143 publications

(130 citation statements)

References 98 publications

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“…The biomechanical properties of the cornea are influenced significantly by the organization of collagen fibrils that form the bulk of the corneal stroma [1]. Alterations in the alignment [2], [3], [4], diameter [5], [6], [7] and spatial order [5], [6] of stromal fibrils occurs after penetrating injury, and there is evidence that some of these changes persist long-term in and around the wound margin following some types of corneal surgery [3], [8], [9].…”

Section: Introductionmentioning

confidence: 99%

Quantification of Collagen Ultrastructure after Penetrating Keratoplasty – Implications for Corneal Biomechanics

et al. 2013

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PurposeTo quantify long-term changes in stromal collagen ultrastructure following penetrating keratoplasty (PK), and evaluate their possible implications for corneal biomechanics.MethodsA pair of 16 mm post-mortem corneo-scleral buttons was obtained from a patient receiving bilateral penetrating keratoplasty 12 (left)/28 (right) years previously. Small-angle x-ray scattering quantified collagen fibril spacing, diameter and spatial order at 0.5 mm or 0.25 mm intervals along linear scans across the graft margin. Corresponding control data was collected from two corneo-scleral buttons with no history of refractive surgery. Wide-angle x-ray scattering quantified collagen fibril orientation at 0.25 mm (horizontal)×0.25 mm (vertical) intervals across both PK specimens. Quantification of orientation changes in the graft margin were verified by equivalent analysis of data from a 13 year post-operative right PK specimen obtained from a second patient in a previous study, and comparison made with new and published data from normal corneas.ResultsMarked changes to normal fibril alignment, in favour of tangentially oriented collagen, were observed around the entire graft margin in all PK specimens. The total number of meridional fibrils in the wound margin was observed to decrease by up to 40%, with the number of tangentially oriented fibrils increasing by up to 46%. As a result, in some locations the number of fibrils aligned parallel to the wound outnumbered those spanning it by up to five times. Localised increases in fibril spacing and diameter, with an accompanying reduction in matrix order, were also evident.ConclusionsAbnormal collagen fibril size and spatial order within the PK graft margin are indicative of incomplete stromal wound remodelling and the long term persistence of fibrotic scar tissue. Lasting changes in collagen fibril orientation in and around PK wounds may alter corneal biomechanics and compromise the integrity of the graft-host interface in the long term.

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Section: Introductionmentioning

confidence: 99%

Quantification of Collagen Ultrastructure after Penetrating Keratoplasty – Implications for Corneal Biomechanics

et al. 2013

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“…P atm was set to zero, as IOP is defined as the pressure difference between IOP and extraocular pressure. In corneal tissue, ∼250 collagen lamellae (Meek, 2009) are stacked one over another, each running from limbus to limbus. Therefore, in approximation, the tissue can be considered being transversely isotropic, with distinct properties in the plane of collagen lamellae compared to their orthogonal direction.…”

Section: Estimation Of the Stress-strain Relationshipmentioning

confidence: 99%

Optical Coherence Elastography-Based Corneal Strain Imaging During Low-Amplitude Intraocular Pressure Modulation

Kling

Khodadadi

Göksel

2020

Front. Bioeng. Biotechnol.

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Purpose: Optical coherence elastography (OCE) is a promising technique for high-resolution strain imaging in ocular tissues. A major strain-inducing factor in the eye is intraocular pressure (IOP), with diurnal physiological fluctuations reaching up to 5 mmHg. We study herein low-amplitude IOP modulation to assess local corneal strain patterns.Methods: Ex vivo porcine eye globes were adjusted to an initial IOP of 15 mmHg and subsequently 25 mmHg. Corneal strain was induced by two subsequent pressure cycles, in which IOP was first increased and then decreased, each by a total of 5 mmHg. Two-dimensional optical coherence tomography (2D-OCT) B-scans were recorded after each loading step. Axial strain maps were obtained from magnitude and phase changes and supra-pixel displacements from cross-correlation. The strain detection sensitivity was evaluated in an isotropic material.Results: Deformations arising from a single 1-mmHg step could be resolved. The largest strain amplitudes (5.11·10 −3 ) were observed in the posterior stroma at a low initial IOP. Strain amplitude was 1.34 times higher at 15 mmHg than at 25 mmHg (p = 0.003). Upon IOP increase, the anterior cornea was compressed, whereas the posterior cornea showed axial expansion. Both morphological images and strain maps were sensitive to postmortem time. Strains that are larger than 2.44·10 −5 could be reliably measured.Conclusions: Low-amplitude IOP modulation, similar to diurnal physiological changes, induced measurable deformations in corneal tissue. Axial strain maps permit a localized comparison of the corneal biomechanical response. Small-strain OCE can likely be extended to other domains.

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“…In the stroma, collagen is composed of heterotypic fibrils containing mainly collagen type I and V and smaller amounts of type VI, XII, XIII, XIV and XXIV (Michelacci, 2003;Meek, 2009). Type XII collagen was detected in the stroma in the area near to Bowman's and Descemet's membranes, whereas type XIII was found in the posterior stroma (Meek, 2009). Type XVIII collagen is localized in the corneal epithelium and epithelial basement membrane (Michelacci, 2003).…”

Section: Collagen and Beta-actinmentioning

confidence: 99%

Role of biochemical factors in the pathogenesis of keratoconus.

et al. 2014

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Keratoconus (KC) is a corneal disease associated with structural abnormalities in the corneal epithelium, Bowman's layer and stroma and altered concentration of tear components. KC corneas show a different pattern of collagen lamellae than their normal counterparts. Also, a reduction of several collagen types in KC epithelium and stroma was observed. Altered expression and/or activity of lysyl oxidase, a critical enzyme of the biogenesis of connective tissue detected in KC corneas, may weaken covalent bonds between collagen and elastin fibrils, what may lead to biomechanical deterioration of the cornea. Increased activity of matrix metalloproteinases observed in KC may induce the degradation of the extracellular matrix causing damage to the cornea. Oxidative and nitrative stress play an important role in KC pathogenesis and KC corneas are characterized by the disturbed lipid peroxidation and nitric oxide pathways. Malfunctioning of these pathways may lead to accumulation of their toxic by-products inducing several detrimental effects, along with apoptosis of the corneal cells, which may result from the loss of β-actin or increased levels of cytokines, including interleukin-1 and -6. Change in the expression of genes associated with wound healing, including the nerve growth factor and the visual system homeobox 1, may contribute to increased susceptibility of KC corneas to injury. Consequently, biochemical changes may play an important role in KC pathophysiology and, therefore, can be considered in prevention, diagnosis, prognosis and in the therapy of this disease as well.

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Corneal collagen—its role in maintaining corneal shape and transparency

Cited by 143 publications

References 98 publications

Quantification of Collagen Ultrastructure after Penetrating Keratoplasty – Implications for Corneal Biomechanics

Quantification of Collagen Ultrastructure after Penetrating Keratoplasty – Implications for Corneal Biomechanics

Optical Coherence Elastography-Based Corneal Strain Imaging During Low-Amplitude Intraocular Pressure Modulation

Role of biochemical factors in the pathogenesis of keratoconus.

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