Authors

Erwin P. Lobo1, Naomi C. Delic2,3, Alex Richardson4, Vanisri Raviraj2,3, Gary M. Halliday2, Nick Di Girolamo4,
Mary R. Myerscough1 & J Guy Lyons2,3,5

Affiliations

1 School of Mathematics and Statistics, Camperdown, New South Wales 2006, Australia. 2Discipline of Dermatology, Bosch Institute, Charles Perkins Centre,
University of Sydney, Camperdown, New South Wales 2006, Australia. 3 Immune Imaging Program, Centenary Institute for Cancer Medicine and Cell Biology,
Camperdown, New South Wales 2042, Australia. 4Department of Pathology, School of Medical Sciences, University of New South Wales, Randwick, New
South Wales 2052, Australia. 5 Sydney Head and Neck Cancer Institute, Cancer Services, Royal Prince Alfred Hospital, Camperdown, New South Wales
2050, Australia. Correspondence and requests for materials should be addressed to N.D.G. (email: n.digirolamo@unsw.edu.au) or to M.R.M.
(email: mary.myerscough@sydney.edu.au) or to J.G.L. (email: g.lyons@centenary.org.au).

Application Area

Neuroscience

Stimulation

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.

Extract

The mice were then anaesthetized with ketamine/
medetomidine and both corneas of each mouse were imaged using a Nikon AZ100
wide-field fluorescent microscope with CoolLED4000 light source, to obtain a
baseline measurement.

Product Associated Features

pE-4000: The universal LED illumination system for research fluorescence, with the broadest spectrum of illumination available from 16 selectable wavelengths, and extensive functionality that sets a new standard for industry.

Diascopic Technique

-

Live Cell Issues

-

Product Type

pE-4000

Journal

Nature Communications

Year of Publication

2016

Country of Publication

Australia