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Vol. 293, Issue 3, 837-844, June 2000
Physiologisches Institut, Würzburg, Germany (M.G., G.S.,
R.F., S.M.); and Department of Physiology, University of Innsbruck,
Innsbruck, Austria (D.W., V.P., M.D., H.S.)
Ochratoxin A (OTA) is a ubiquitous fungal metabolite with
nephritogenic, carcinogenic, and teratogenic action. Epidemiological studies indicate that OTA may be involved in the pathogenesis of
different forms of human nephropathies. Previously we have shown that
OTA activates extracellular signal-regulated kinases 1 and 2, members of the mitogen-activated protein kinases (MAPK) family,
in the C7-clone but not in the C11-clone of renal epithelial Madin-Darby canine kidney (MDCK) cells. Here we show that
nanomolar concentrations of OTA lead to activation of a second member
of the MAPK family, namely, c-jun amino-terminal-kinase (JNK) in MDCK-C7 cells but virtually not in MDCK-C11 cells, as determined by
kinase assay and Western blot. Furthermore, OTA potentiated the effect
of tumor necrosis factor-
on JNK activation. In parallel to its
effects on JNK, nanomolar OTA induced apoptosis in MDCK-C7 cells but
not in MDCK-C11 cells, as determined by DNA fragmentation, DNA ladder
formation, and caspase activation. In addition, OTA potentiated the
proapoptotic action of tumor necrosis factor-
. Our data provide
additional evidence that OTA interacts in a cell type-specific way with
distinct members of the MAPK family at concentrations where no acute
toxic effect can be observed. Induction of apoptosis via the JNK
pathway can explain some of the OTA-induced changes in renal function
as well as part of its teratogenic action.
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