Transient induction of metallothionein isoform 3 (MT-3), c- fos, c- jun and c- myc in human proximal tubule cells exposed to cadmium

Cadmium (Cd +2) has been shown to transiently increase the expression of mRNA for the third isoform of the metallothionein (MT-3) gene family in cultured human proximal tubule (HPT) cells. The goal of the present study was to further define the expression of MT-3 in mortal (HPT) and immortal (HK-2)...

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Veröffentlicht in:Toxicology letters 2002-01, Vol.126 (1), p.69-80
Hauptverfasser: Garrett, Scott H, Phillips, Veronica, Somji, Seema, Sens, Mary Ann, Dutta, Rana, Park, Seongmi, Kim, Doyeob, Sens, Donald A
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Sprache:eng
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Zusammenfassung:Cadmium (Cd +2) has been shown to transiently increase the expression of mRNA for the third isoform of the metallothionein (MT-3) gene family in cultured human proximal tubule (HPT) cells. The goal of the present study was to further define the expression of MT-3 in mortal (HPT) and immortal (HK-2) cultures of HPT cells when exposed to lethal and sub-lethal concentrations of Cd +2 under both acute and chronic time periods of exposure. Expression of MT-3 mRNA and protein was determined in cultured HPT cells and HK-2 cells using reverse-transcription-polymerase chain reaction (RT-PCR) and immuno-blotting, and expression of c- fos, c- jun and c- myc mRNA by RT-PCR. The results confirmed that exposure of the HPT cells to Cd +2 induced a transient increase in MT-3 mRNA and extended the induction to include a subsequent transient increase in the level of the MT-3 protein. The induction of MT-3 was rapid and returned to control values within 48 h of exposure despite the continued presence of lethal and sublethal concentrations of Cd +2. It was also demonstrated that the pattern of expression of MT-3 mRNA was similar to that of the early response genes, c- fos, c- jun and c- myc. It was shown that the HK-2 cells did not express MT-3 when exposed to Cd +2, but had similar expression of the c- fos, c- jun and c- myc genes. The results demonstrate that MT-3 expression is metal responsive in HPT cells.
ISSN:0378-4274
1879-3169
DOI:10.1016/S0378-4274(01)00448-9