April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
Effect of Pneumatic Dissection of Descemet's Membrane on Endothelial Cell Viability and Morphology
Author Affiliations & Notes
  • A. Chew
    Singapore National Eye Centre, Singapore, Singapore
  • R. Poh
    Singapore Eye Research Institute, Singapore, Singapore
  • H. Cajucom-Uy
    Singapore National Eye Centre, Singapore, Singapore
  • R. W. Beuerman
    Singapore Eye Research Institute, Singapore, Singapore
  • D. T. H. Tan
    Singapore National Eye Centre, Singapore, Singapore
    Singapore Eye Research Institute, Singapore, Singapore
  • J. S. Mehta
    Singapore National Eye Centre, Singapore, Singapore
    Singapore Eye Research Institute, Singapore, Singapore
  • Footnotes
    Commercial Relationships  A. Chew, None; R. Poh, None; H. Cajucom-Uy, None; R.W. Beuerman, None; D.T.H. Tan, None; J.S. Mehta, None.
  • Footnotes
    Support  NMRC R472
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 1823. doi:
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      A. Chew, R. Poh, H. Cajucom-Uy, R. W. Beuerman, D. T. H. Tan, J. S. Mehta; Effect of Pneumatic Dissection of Descemet's Membrane on Endothelial Cell Viability and Morphology. Invest. Ophthalmol. Vis. Sci. 2009;50(13):1823.

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

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Abstract

Purpose: : To describe the effect of pneumatic dissection of Descement's membrane (DM) on endothelial cell viability and morphology.

Methods: : 18 human corneoscleral rims underwent pneumatic air dissection of DM. Following cleavage the tissue was examined by either vital dye exclusion (n=9) or live/dead cell assay (n=9). Ultrastructural examination of the endothelial cell morphology was performed by electron microscopy (EM). Corneal tissue was also sectioned for histology and TUNEL assay.

Results: : Air dissection alone was successful in 66% of cases, but with the addition of OVD 100% cleavage was achieved. Histology demonstrated complete clean separation of the DM from overlying stroma. There was no significant loss of endothelial cells by apoptosis on TUNEL assay. Vital dye staining of the endothelial cells showed staining of the nuclei of the cells located at the apex of the bubble. Those located at the base showed no staining. Live dead cell assay show mean percentage cell loss of 10% (SD 5%). EM showed distension of the cellular borders at the apex of the bubble.

Conclusions: : Pneumatic dissection of DM causes minimal cellular damage and achieves clean dissection of DM. However there is disruption of the intercellular borders at the apex of the bubble which did not affect cell viability.

Keywords: cornea: endothelium 
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