Transcriptome analysis of human cornea tissue

  • Research type

    Research Study

  • Full title

    Single-cell gene expression analysis of human cornea epithelial and endothelial cells for the development of novel cell conversions and advanced medicinal therapy products (ATMPs) that restore vision loss after corneal blindness.

  • IRAS ID

    276001

  • Contact name

    Geraint Parfitt

  • Contact email

    geraint.parfitt@mogrify.co.uk

  • Sponsor organisation

    Mogrify

  • Duration of Study in the UK

    1 years, 0 months, 1 days

  • Research summary

    Corneal transplants (keratoplasty) are used to surgically treat corneal disease, however, they are not effective in the treatment of epithelial defects, such as limbal stem cell deficiency, as they do not replace the stem cells located at the peripheral cornea. Furthermore, there is a shortage of donor cornea tissue in the UK for keratoplasty, particularly in cases of corneal endothelial dystrophy, a condition that leads to cell death in the corneal endothelial cell layer and loss of sight.

    We propose to overcome these issues by developing novel cell therapies to corneal diseases, including limbal stem cell deficiency and Fuch's endothelial corneal dystrophy. Our project is based on the conversion of readily available source cells, such as skin fibroblasts, to cornea epithelia and endothelia cells for transplantation. To achieve this, Mogrify has developed an algorithm that predicts the optimal set of transcription factors to convert any cell type from RNA-sequencing data of source and target cell types. Therefore, we seek to perform RNA-sequencing of human primary corneal limbus and endothelium to establish the factors required for their conversion from source cells.

  • REC name

    East of England - Cambridge Central Research Ethics Committee

  • REC reference

    20/EE/0067

  • Date of REC Opinion

    8 Apr 2020

  • REC opinion

    Further Information Favourable Opinion