Premium
Ochratoxin A impairs Nrf2‐dependent gene expression in porcine kidney tubulus cells
Author(s) -
BoeschSaadatmandi C.,
Wagner A. E.,
Graeser A. C.,
Hundhausen C.,
Wolffram S.,
Rimbach G.
Publication year - 2009
Publication title -
journal of animal physiology and animal nutrition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.651
H-Index - 56
eISSN - 1439-0396
pISSN - 0931-2439
DOI - 10.1111/j.1439-0396.2008.00838.x
Subject(s) - transactivation , nephrotoxicity , ochratoxin a , activator (genetics) , transcription factor , glutathione , biology , glutathione s transferase , biochemistry , chemistry , kidney , microbiology and biotechnology , enzyme , gene , mycotoxin , endocrinology , botany
Summary The mycotoxin, ochratoxin A (OTA), which is produced by Aspergillus and Penicillium subspecies, is frequently present in feedstuffs. Ochratoxin A exhibits a wide range of toxic activities including nephrotoxicity. However, the underlying molecular mechanisms of OTA‐induced cellular nephrotoxicity have yet not been fully elucidated. Nrf2 is a basic leucine zipper transcriptional activator essential for the coordinated transcriptional induction of antioxidant and xenobiotic metabolizing enzymes in the kidney. Therefore, in the present study, the effects of OTA on the nuclear translocation and transactivation of the transcription factor Nrf2 as well as mRNA levels of Nrf2 target genes including glutathione‐ S ‐transferase and γ‐glutamylcysteinyl synthetase have been studied in cultured porcine kidney tubulus cells (LLC‐PK1). Nrf2 was induced by sulforaphane, a well‐known activator of this transcription factor. Ochratoxin A significantly decreased γ‐glutamylcysteinyl synthetase and glutathione‐ S ‐transferase mRNA levels in LLC‐PK1 cells. Decreased mRNA levels of γ‐glutamylcysteinyl synthetase and glutathione‐ S ‐transferase were accompanied by a lowered nuclear translocation and transactivation of Nrf2. Furthermore, OTA also lowered Nrf2 mRNA levels. Current data indicate that OTA nephrotoxicity may be, at least partly, mediated by an Nrf2‐dependent signal transduction pathway.