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Departments of 1 Urology and 2 Pathology, Erasmus University and Academic Hospital Dijkzigt, 3000 DR Rotterdam, The Netherlands
The retention of
crystals in the kidney is considered to be a crucial step in the
development of a renal stone. This study demonstrates the
time-dependent alterations in the extent of calcium oxalate (CaOx)
monohydrate (COM) crystal binding to Madin-Darby canine kidney (MDCK)
cells during their growth to confluence and during the healing of
wounds made in confluent monolayers. As determined by radiolabeled COM
crystal binding studies and confirmed by confocal-scanning laser
microscopy, relatively large amounts of crystals (10.4 ± 0.4 µg/cm2) bound to subconfluent
cultures that still exhibited a low transepithelial electrical
resistance (TER < 400
· cm2).
The development of junctional integrity, indicated by a high resistance
(TER > 1,500
· cm2),
was followed by a decrease of the crystal binding capacity to almost
undetectable low levels (0.13 ± 0.03 µg/cm2). Epithelial injury
resulted in increased crystal adherence. The highest level of crystal
binding was observed 2 days postinjury when the wounds were already
morphologically closed but TER was still low. Confocal images showed
that during the repair process, crystals selectively adhered to
migrating cells at the wound border and to stacked cells at sites were
the wounds were closed. After the barrier integrity was restored,
crystal binding decreased again to the same low levels as in undamaged
controls. These results indicate that, whereas functional MDCK
monolayers are largely protected against COM crystal adherence,
epithelial injury and the subsequent process of wound healing lead to
increased crystal binding.
nephrolithiasis; Madin-Darby canine kidney cells; injury; epithelial barrier integrity
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