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The ultrastructural basis of corneal dysfunction and the development and optimization of novel therapeutic strategies

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AI plain-English summary

The cornea—the eye’s transparent front window—must be simultaneously clear, strong, and precisely curved, yet the microscopic arrangement of collagen that achieves this remains unknown. Without this structural blueprint, surgeons cannot predict how the cornea will respond to laser surgery, and researchers cannot fix what goes wrong in diseases that cloud or weaken the tissue. The team will use 3D imaging and X-ray techniques to map collagen fibrils and lamellae from the molecular level up, then build computer models that simulate how surgical cuts or treatments alter corneal shape. If successful, surgeons could plan incisions with far greater precision, reducing the risk of blurred vision after procedures. The work also targets specific corneal diseases: the researchers will test whether stem cell therapy or protein crosslinking can restore transparency and strength in damaged tissue. A deeper practical goal is to accelerate the development of an artificial cornea—a synthetic replacement needed because donor tissue remains in chronic global shortage. By revealing exactly how nature assembles the cornea’s structure to achieve its optical and mechanical properties, the project provides the engineering blueprint that other groups can use to build a functioning substitute.

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The cornea is the transparent window at the front of the eye and is its main focussing element. To fulfil its role it has to be very transparent, very strong and precisely shaped. Transparency, strength and shape are all controlled by the collagen fibrils that make up the cornea, and by the small molecules between them. This happens at different structural levels from the molecular level upwards: collagen molecules form fibrils, which in turn form larger structures called lamellae, which are then stacked up to form the tissue itself. From our previous work and work done by others, we know a lot about why the cornea is transparent and are beginning to understand the arrangement of collagen lamellae that gives rise to the cornea's shape and thus its focusing abilities. However, the precise details are still not known and, until they are, it will not be possible to understand why, in numerous diseases of the cornea, or after different types of surgery on the cornea - including laser surgery - transparency, strength and/or shape are abnormal and vision is lost or very blurred. We will use several new and exciting 3-D biological imaging and powerful X-ray measuring techniques, to explain how collagen fibrils and cells are arranged in the cornea to make it transparent, and how other proteins control this arrangement. We will also explain at a higher structural level how lamellae are arranged to provide form and strength. This will allow us to construct computer models from which to predict changes in corneal shape following given surgical incisions or other treatments to help inform surgeons. We will then explain what goes wrong in several important corneal diseases and investigate methods of preventing or correcting these changes, for example by using stem cell therapy or protein crosslinking. The methods will also allow us to explain why, when the cornea is wounded, tissue strength and transparency are compromised. Again, methods to improve this wound healing such as those mentioned above will be investigated, with the aim of strengthening the cornea whilst preserving transparency. Finally, several research groups in different countries are trying to develop a biological artificial cornea as there is, and is likely to continue to be, a worldwide shortage of donor corneal tissue for graft surgery. Synthetic biology depends on understanding how nature utilises the constituents of a tissue to achieve its vital properties. In the case of the cornea, the knowledge that we will obtain by elucidating the exact relationship between structure and function will be invaluable, and will allow us to collaborate with these groups to drive their constructs more quickly towards a fully functioning artificial cornea.

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Researchers

Andrew Quantock (Co-Investigator)Carlo Knupp (Co-Investigator)Craig Boote (Co-Investigator)Keith Meek (Principal Investigator)

Related Research

Grants with similar aims, by meaning.

A mechanistic understanding of corneal pathobiology and the development of therapeutic strategies for the treatment of connective tissue disorders
The Cellular Control of Corneal Development and Transparency and Generation of Biomimetic Corneal Tissue.
A Physical Characterisation of Assembly Mechanisms and Light Transmission in Cornea.
The collagen matrix in corneal pathology, and the effect of new therapies for loss of transparency and refractive status
Towards a functional understanding of proteoglycan-collagen associations in the cornea by 3-dimensional electron microscopy of gene-targeted mutants

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Research Grant

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