Toxicological Research

  • 제32권1호
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  • Pages.73-80
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  • 2016
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  • 1976-8257(pISSN)
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  • 2234-2753(eISSN)
한국독성학회 (Korean Society of Toxicology & Korea Environmental Mutagen Society)
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Different Regulation of p53 Expression by Cadmium Exposure in Kidney, Liver, Intestine, Vasculature, and Brain Astrocytes

  • Lee, Jin-Yong (Laboratory of Pharmaceutical Health Sciences, School of Pharmacy, Aichi Gakuin University) ;
  • Tokumoto, Maki (Laboratory of Pharmaceutical Health Sciences, School of Pharmacy, Aichi Gakuin University) ;
  • Hattori, Yuta (Laboratory of Pharmaceutical Health Sciences, School of Pharmacy, Aichi Gakuin University) ;
  • Fujiwara, Yasuyuki (Laboratory of Pharmaceutical Health Sciences, School of Pharmacy, Aichi Gakuin University) ;
  • Shimada, Akinori (Laboratory of Pathology, Department of Medical Technology, School of Life and Environmental Science, Azabu University) ;
  • Satoh, Masahiko (Laboratory of Pharmaceutical Health Sciences, School of Pharmacy, Aichi Gakuin University)
  • 투고 : 2015.11.14
  • 심사 : 2016.01.04
  • 발행 : 2016.01.15
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초록

Chronic exposure to cadmium (Cd) is known to adversely affect renal function. Our previous studies indicated that Cd induces p53-dependent apoptosis by inhibiting gene expression of the ubiquitin-conjugating enzyme (Ube) 2d family in both human and rat proximal tubular cells. In this study, the effects of Cd on protein expression of p53 and apoptotic signals in the kidney and liver of mice exposed to Cd for 12 months were examined, as well as the effects of Cd on p53 protein levels and gene expression of the Ube2d family in various cell lines. Results showed that in the kidney of mice exposed to 300 ppm Cd for 12 months, there was overaccumulation of p53 proteins in addition to the induction of apoptosis, which was triggered specifically in the proximal tubules. Interestingly, the site of apoptosis was the same as that of p53 accumulation in the proximal tubules. In the liver of mice chronically exposed to Cd, gene expression of the Ube2d family tended to be slightly decreased, together with slight apoptosis without the accumulation of p53 protein. In rat small intestine epithelial (IEC-6) cells, Cd decreased not only the p53 protein level but also gene expression of Ube2d1, Ube2d2 and Ube2d4. In human brain microvascular endothelial cells (HBMECs), Cd did not suppress gene expression of the Ube2d family, but increased the p53 protein level. In human brain astrocytes (HBASTs), Cd only increased gene expression of UBE2D3. These results suggest that Cd-induced apoptosis through p53 protein is associated with renal toxicity but not hepatic toxicity, and the modification of p53 protein by Cd may vary depending on cell type.

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참고문헌

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