Publication: Sodium transport systems in human chondrocytes II. Expression of ENaC, Na+ K+ 2CI- cotransporter and Na+ H+ exchangers in healthy
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Date
1999
Authors
Trujillo, E. ; Alvarez de la Rosa, D. ; Mobasheri, A. ; Gonzalez, T. ; Canessa, C.M. ; Martín Vasallo, P.
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Publisher
Murcia : F. Hernández
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DOI
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info:eu-repo/semantics/article
Description
Abstract
In this article, the second of two, we continue
our studies of sodium-dependent transport systems in
human cartilage from healthy individuals and with
osteoarthritis (OA) and rheumatoid arthritis (RA). We
demonstrate the presence of the epithelia1 sodium
channel (ENaC), previously undescribed in chondrocytes.
This system is composed of three subunits, a, 13
and y. We have shown that the human chondrocytes
express at least the a and the l3 subunit of ENaC. The
expression of these subunits is altered in arthritic
chondrocytes. In RA samples the quantity of a and B is
significantly higher than in control samples. On the other
hand, ENaC a and B subunits are absent in the
chondrocytes of OA cartilage. Human chondrocytes also
possess three isoforms of the Na+/H+ exchanger (NHE),
NHE1, NHE2 and NHE3. The NHE system is composed
of a single protein and is believed to participate in
intracellular pH regulation. Furthermore, our studies
indicate that at least one isoform of the electroneutral
Naf/K+/2C1- cotransporter (NKCC) is present in human
chondrocytes. There are no obvious variations in the
relative expression of NHE isoforms or NKCC between
healthy and arthritic cartilage. Our data suggests that
chondrocytes from arthritic cartilage may adapt to
changes in their environmental sodium concentration
through variations in ENaC protein levels. ENaC is also
likely to serve as a major sodium entry mechanism, a
process that, along with cytoskeletal proteins, may be
part of mechanotransduction in cartilage.
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