May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Corneal Basement Membrane Changes in Postnatal Life
Author Affiliations & Notes
  • A.V. Ljubimov
    Ophthalmology Research Laboratories, Cedars–Sinai Medical Center, Los Angeles, CA
    UCLA School of Medicine, Los Angeles, CA
  • A. Kabosova
    Ophthalmology Research Laboratories, Cedars–Sinai Medical Center, Los Angeles, CA
  • M.C. Kenney
    Ophthalmology, UCI College of Medicine, Orange, CA
  • Footnotes
    Commercial Relationships  A.V. Ljubimov, None; A. Kabosova, None; M.C. Kenney, None.
  • Footnotes
    Support  Skirball Program in Molecular Ophthalmology and seed grant from the Department of Surgery, Cedars–Sinai Medical Center
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 2709. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      A.V. Ljubimov, A. Kabosova, M.C. Kenney; Corneal Basement Membrane Changes in Postnatal Life . Invest. Ophthalmol. Vis. Sci. 2006;47(13):2709.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

Purpose: : We have previously shown that corneal basement membranes (BMs) are composed of different structural components. The adult epithelial BM displays "horizontal" heterogeneity in laminin and type IV collagen isoforms between central area (with Bowman's layer present) and peripheral corneoscleral limbus. Descemet's membrane (DM) shows "vertical" heterogeneity, with different composition of its stromal and endothelial faces. Our purpose was to identify corneal basement membrane changes during postnatal development.

Methods: : Thirty adult healthy corneas and 10 corneas from six 12–day to 3 year–old children (within 30 h postmortem, obtained from NDRI) were studied by immunofluorescence with antibodies to BM components.

Results: : Children's corneas had type IV collagen α1/α2 chains in central epithelial BM that changed after 3 years of life to α3/α4 chains, with α1/α2 chains retained only in the limbal BM. Compared to children's corneas, laminin α2 and ß2 chains appeared in the adult limbal BM. In 3 year–old corneas, laminin ß2 chain already had an adult distribution. In children's DM, laminin–10, type IV collagen α1–α6 chains, perlecan, nidogen–1, nidogen–2 and ß–netrin were found on both faces but they all remained only on the endothelial face in adult DM. Stromal face of the children's but not the adult DM stained for tenascin–C (containing A–1 repeat), fibrillin–1, BM–40/SPARC, and laminin–5. DM type VIII collagen shifted from the endothelial face in the children's to the stromal face in the adult, and matrilin–4 completely disappeared after 3 years. Corneas of a 13–year old individual already had adult patterns of all markers studied. We provide the first description of corneal distribution of nidogen–2, ß–netrin, matrilin–2, matrilin–4, and type XXIII collagen.

Conclusions: : The observed differences may relate to changes in corneal cell adhesion, differentiation and mechanical strength of corneal BMs in the process of postnatal corneal maturation.

Keywords: cornea: epithelium • extracellular matrix • development 
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×