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The properties of chondrocyte membrane reservoirs and their role in impact-induced cell death.

Authors :
Moo EK
Amrein M
Epstein M
Duvall M
Abu Osman NA
Pingguan-Murphy B
Herzog W
Source :
Biophysical journal [Biophys J] 2013 Oct 01; Vol. 105 (7), pp. 1590-600.
Publication Year :
2013

Abstract

Impact loading of articular cartilage causes extensive chondrocyte death. Cell membranes have a limited elastic range of 3-4% strain but are protected from direct stretch during physiological loading by their membrane reservoir, an intricate pattern of membrane folds. Using a finite-element model, we suggested previously that access to the membrane reservoir is strain-rate-dependent and that during impact loading, the accessible membrane reservoir is drastically decreased, so that strains applied to chondrocytes are directly transferred to cell membranes, which fail when strains exceed 3-4%. However, experimental support for this proposal is lacking. The purpose of this study was to measure the accessible membrane reservoir size for different membrane strain rates using membrane tethering techniques with atomic force microscopy. We conducted atomic force spectroscopy on isolated chondrocytes (n = 87). A micron-sized cantilever was used to extract membrane tethers from cell surfaces at constant pulling rates. Membrane tethers could be identified as force plateaus in the resulting force-displacement curves. Six pulling rates were tested (1, 5, 10, 20, 40, and 80 μm/s). The size of the membrane reservoir, represented by the membrane tether surface areas, decreased exponentially with increasing pulling rates. The current results support our theoretical findings that chondrocytes exposed to impact loading die because of membrane ruptures caused by high tensile membrane strain rates.<br /> (Copyright © 2013 Biophysical Society. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1542-0086
Volume :
105
Issue :
7
Database :
MEDLINE
Journal :
Biophysical journal
Publication Type :
Academic Journal
Accession number :
24094400
Full Text :
https://doi.org/10.1016/j.bpj.2013.08.035