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Self-organized centripetal movement of corneal epithelium in the absence of external cues

Author

Listed:
  • Erwin P. Lobo

    (School of Mathematics and Statistics)

  • Naomi C. Delic

    (Discipline of Dermatology, Bosch Institute, Charles Perkins Centre, University of Sydney
    Immune Imaging Program, Centenary Institute for Cancer Medicine and Cell Biology)

  • Alex Richardson

    (School of Medical Sciences, University of New South Wales)

  • Vanisri Raviraj

    (Discipline of Dermatology, Bosch Institute, Charles Perkins Centre, University of Sydney
    Immune Imaging Program, Centenary Institute for Cancer Medicine and Cell Biology)

  • Gary M. Halliday

    (Discipline of Dermatology, Bosch Institute, Charles Perkins Centre, University of Sydney)

  • Nick Di Girolamo

    (School of Medical Sciences, University of New South Wales)

  • Mary R. Myerscough

    (School of Mathematics and Statistics)

  • J. Guy Lyons

    (Discipline of Dermatology, Bosch Institute, Charles Perkins Centre, University of Sydney
    Immune Imaging Program, Centenary Institute for Cancer Medicine and Cell Biology
    Sydney Head and Neck Cancer Institute, Cancer Services, Royal Prince Alfred Hospital)

Abstract

Maintaining the structure of the cornea is essential for high-quality vision. In adult mammals, corneal epithelial cells emanate from stem cells in the limbus, driven by an unknown mechanism towards the centre of the cornea as cohesive clonal groups. Here we use complementary mathematical and biological models to show that corneal epithelial cells can self-organize into a cohesive, centripetal growth pattern in the absence of external physiological cues. Three conditions are required: a circumferential location of stem cells, a limited number of cell divisions and mobility in response to population pressure. We have used these complementary models to provide explanations for the increased rate of centripetal migration caused by wounding and the potential for stem cell leakage to account for stable transplants derived from central corneal tissue, despite the predominantly limbal location of stem cells.

Suggested Citation

  • Erwin P. Lobo & Naomi C. Delic & Alex Richardson & Vanisri Raviraj & Gary M. Halliday & Nick Di Girolamo & Mary R. Myerscough & J. Guy Lyons, 2016. "Self-organized centripetal movement of corneal epithelium in the absence of external cues," Nature Communications, Nature, vol. 7(1), pages 1-8, November.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms12388
    DOI: 10.1038/ncomms12388
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