論文

査読有り 国際誌
2011年

High Glucose Increases Metallothionein Expression in Renal Proximal Tubular Epithelial Cells

Experimental Diabetes Research
  • Daisuke Ogawa
  • Masato Asanuma
  • Ikuko Miyazaki
  • Hiromi Tachibana
  • Jun Wada
  • Norio Sogawa
  • Takeshi Sugaya
  • Shinji Kitamura
  • Yohei Maeshima
  • Kenichi Shikata
  • Hirofumi Makino
  • 全て表示

2011
開始ページ
1
終了ページ
8
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1155/2011/534872
出版者・発行元
Hindawi Limited

Metallothionein (MT) is an intracellular metal-binding, cysteine-rich protein, and is a potent antioxidant that protects cells and tissues from oxidative stress. Although the major isoforms MT-1 and -2 (MT-1/-2) are highly inducible in many tissues, the distribution and role of MT-1/-2 in diabetic nephropathy are poorly understood. In this study, diabetes was induced in adult male rats by streptozotocin, and renal tissues were stained with antibodies for MT-1/-2. MT-1/-2 expression was also evaluated in mProx24 cells, a mouse renal proximal tubular epithelial cell line, stimulated with high glucose medium and pretreated with the antioxidant vitamin E. MT-1/-2 expression was gradually and dramatically increased, mainly in the proximal tubular epithelial cells and to a lesser extent in the podocytes in diabetic rats, but was hardly observed in control rats. MT-1/-2 expression was also increased by high glucose stimulation in mProx24 cells. Because the induction of MT was suppressed by pretreatment with vitamin E, the expression of MT-1/-2 is induced, at least in part, by high glucose-induced oxidative stress. These observations suggest that MT-1/-2 is induced in renal proximal tubular epithelial cells as an antioxidant to protect the kidney from oxidative stress, and may offer a novel therapeutic target against diabetic nephropathy.

リンク情報
DOI
https://doi.org/10.1155/2011/534872
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/21960990
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3179884
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000296809500001&DestApp=WOS_CPL
URL
http://downloads.hindawi.com/journals/jdr/2011/534872.pdf
URL
http://downloads.hindawi.com/journals/jdr/2011/534872.xml
ID情報
  • DOI : 10.1155/2011/534872
  • ISSN : 1687-5214
  • eISSN : 1687-5303
  • PubMed ID : 21960990
  • PubMed Central 記事ID : PMC3179884
  • Web of Science ID : WOS:000296809500001

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