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Biophysical Journal 87:2828-2837 (2004)
© 2004 The Biophysical Society

Biomechanics of Schlemm's Canal Endothelial Cells: Influence on F-Actin Architecture

C. Ross Ethier * {dagger}, A. Thomas Read * and Darren Chan *

Departments of * Mechanical and Industrial Engineering, and {dagger} Ophthalmology, University of Toronto, Toronto, Ontario, Canada

Correspondence: Address reprint requests to C. Ross Ethier, PhD, Dept. of Mechanical and Industrial Engineering, University of Toronto, 5 King's College Rd., Toronto, Ontario M5S 3G8, Canada. Tel.: 416-978-6728; Fax: 416-978-7753; E-mail: ethier{at}mie.utoronto.ca.

Aqueous humor drains from the eye through Schlemm's canal, a small endothelial-lined collecting duct. Schlemm's canal endothelial cells may be important in controlling the pressure within the eye (and hence are of interest in glaucoma), and are subject to an unusual combination of shear stress and a basal-to-apical pressure gradient. We sought to characterize this biomechanical environment and determine its effects on F-actin architecture in situ. A theoretical model of flow in Schlemm's canal was used to estimate shear stresses applied to endothelial cells by flowing aqueous humor. Alignment of Schlemm's canal endothelial cells in human eyes was quantified by scanning electron microscopy. F-actin architecture was visualized by fluorescent labeling and compared for closely adjacent cells exposed to different biomechanical environments. We found that, despite the relatively low flow rate of aqueous humor, shear stresses experienced by Schlemm's canal endothelial cells could reach those in the arterial system. Schlemm's canal endothelial cells showed a statistically significant preferential alignment, consistent with a shear-mediated effect. Schlemm's canal endothelial cells subjected to a basal-to-apical pressure gradient due to transendothelial flow showed a prominent marginal band of F-actin with relatively few cytoplasmic filaments. Adjacent cells not subject to this gradient showed little marginal F-actin, with a denser cytoplasmic random network. We conclude that Schlemm's canal endothelial cells experience physiologically significant levels of shear stress, promoting cell alignment. We speculate that this may help control the calibre of Schlemm's canal. F-actin distribution depends critically on the presence or absence of transendothelial flow and its associated pressure gradient. In the case of this pressure gradient, mechanical reinforcement around the cell periphery by F-actin seems to be critical.




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