February 1997
Volume 38, Issue 2
Free
Articles  |   February 1997
Human lens epithelial cell proliferation in a protein-free medium.
Author Affiliations
  • I M Wormstone
    School of Biological Sciences, University of East Auglia, Norwich, UK.
  • C S Liu
    School of Biological Sciences, University of East Auglia, Norwich, UK.
  • J M Rakic
    School of Biological Sciences, University of East Auglia, Norwich, UK.
  • J M Marcantonio
    School of Biological Sciences, University of East Auglia, Norwich, UK.
  • G F Vrensen
    School of Biological Sciences, University of East Auglia, Norwich, UK.
  • G Duncan
    School of Biological Sciences, University of East Auglia, Norwich, UK.
Investigative Ophthalmology & Visual Science February 1997, Vol.38, 396-404. doi:
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      I M Wormstone, C S Liu, J M Rakic, J M Marcantonio, G F Vrensen, G Duncan; Human lens epithelial cell proliferation in a protein-free medium.. Invest. Ophthalmol. Vis. Sci. 1997;38(2):396-404.

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

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Abstract

PURPOSE: The ocular humors are relatively low in protein, yet cell growth in the human capsular bag still occurs after extracapsular cataract extraction (ECCE) surgery. This resilient growth gives rise to posterior capsule opacification (PCO) in a significant proportion (30%) of patients. This study compared the ability of human lens cells to proliferate in serum-supplemented and protein-free medium. METHODS: Sham cataract operations were performed on human donor eyes. The capsular bag was dissected free, pinned flat on a petri dish, and incubated in Eagle's minimal essential medium (EMEM) alone or in EMEM supplemented with 10% fetal calf serum. Observations were made by phase-contrast microscopy. At the endpoint, capsules were studied by fluorescence or electron microscopy. Mitotic activity was identified using Bromo-2-deoxyuridine labeling and detection techniques. When required, an intraocular lens was implanted when surgery was performed. RESULTS: It was found that human lens cells from a wide age spectrum of donors proliferate and migrate on the lens capsule in the absence of added protein. The rate of growth was age-dependent, such that the posterior capsule was completely confluent after 8.0 +/- 0 days (n = 3) and 24.4 +/- 5.3 days (n = 3) for donor lenses aged < 40 years and > 60 years, respectively. The outgrowth of epithelial cells gave rise to capsular contraction, wrinkling, and increased light scatter. Growth on the anterior surface of the intraocular lens was less prolific than on the posterior capsule. CONCLUSION: The protein-free model replicates many features of clinically-observed PCO. The resilient cell growth on the natural collagen capsule explains the high prevalence of PCO, especially in younger patients, and suggests that inflammation and external growth factors are not necessary for PCO. Furthermore, the protein-free capsular bag system can be used to explore fundamental questions concerning the autocrine control of lens epithelial cell survival and growth.

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