A model of giant vacuole dynamics in human Schlemm's canal endothelial cells

Ryan M Pedrigi, David Simon, Ashley Reed, W. Daniel Stamer, Darryl R. Overby

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

Aqueous humour transport across the inner wall endothelium of Schlemm's canal likely involves flow through giant vacuoles and pores, but the mechanics of how these structures form and how they influence the regulation of intraocular pressure (IOP) are not well understood. In this study, we developed an in vitro model of giant vacuole formation in human Schlemm's canal endothelial cells (HSCECs) perfused in the basal-to-apical direction (i.e., the direction that flow crosses the inner wall in vivo) under controlled pressure drops (2 or 6 mmHg). The system was mounted on a confocal microscope for time-lapse en face imaging, and cells were stained with calcein, a fluorescent vital dye. At the onset of perfusion, elliptical void regions appeared within an otherwise uniformly stained cytoplasm, and 3-dimensional reconstructions revealed that these voids were dome-like outpouchings of the cell to form giant vacuole-like structures or GVLs that reproduced the classic " signet ring" appearance of true giant vacuoles. Increasing pressure drop from 2 to 6 mmHg increased GVL height (14 ± 4 vs. 21 ± 7 μm, p < 0.0001) and endothelial hydraulic conductivity (1.15 ± 0.04 vs. 2.11 ± 0.49 μl min-1 mmHg-1 cm-2; p < 0.001), but there was significant variability in the GVL response to pressure between cell lines isolated from different donors. During perfusion, GVLs were observed " migrating" and agglomerating about the cell layer and often collapsed despite maintaining the same pressure drop. GVL formation was also observed in human umbilical vein and porcine aortic endothelial cells, suggesting that giant vacuole formation is not a unique property of Schlemm's canal cells. However, in these other cell types, GVLs were rarely observed " migrating" or contracting during perfusion, suggesting that Schlemm's canal endothelial cells may be better adapted to withstand basal-to-apical directed pressure gradients. In conclusion, we have established an in vitro model system to study giant vacuole dynamics, and we have demonstrated that this system reproduces key aspects of giant vacuole morphology and behaviour. This model offers promising opportunities to investigate the role of endothelial cell biomechanics in the regulation of intraocular pressure in normal and glaucomatous eyes.

Original languageEnglish (US)
Pages (from-to)57-66
Number of pages10
JournalExperimental Eye Research
Volume92
Issue number1
DOIs
StatePublished - Jan 1 2011

Fingerprint

Vacuoles
Endothelial Cells
Pressure
Perfusion
Intraocular Pressure
Umbilical Veins
Aqueous Humor
Mechanics
Fluorescent Dyes
Biomechanical Phenomena
Endothelium
Cytoplasm
Swine
Cell Line

Keywords

  • Aqueous humour outflow resistance
  • Cellular biomechanics
  • Endothelial transport
  • Giant vacuole
  • Intraocular pressure
  • Schlemm's canal

ASJC Scopus subject areas

  • Ophthalmology
  • Sensory Systems
  • Cellular and Molecular Neuroscience

Cite this

A model of giant vacuole dynamics in human Schlemm's canal endothelial cells. / Pedrigi, Ryan M; Simon, David; Reed, Ashley; Stamer, W. Daniel; Overby, Darryl R.

In: Experimental Eye Research, Vol. 92, No. 1, 01.01.2011, p. 57-66.

Research output: Contribution to journalArticle

Pedrigi, Ryan M ; Simon, David ; Reed, Ashley ; Stamer, W. Daniel ; Overby, Darryl R. / A model of giant vacuole dynamics in human Schlemm's canal endothelial cells. In: Experimental Eye Research. 2011 ; Vol. 92, No. 1. pp. 57-66.
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