DOI QR코드

DOI QR Code

Increased expression of the F1Fo ATP synthase in response to iron in heart mitochondria

  • Kim, Mi-Sun (Division of Life Science, College of Natural Sciences, Sookmyung Women's University) ;
  • Kim, Jin-Sun (Division of Life Science, College of Natural Sciences, Sookmyung Women's University) ;
  • Cheon, Choong-Ill (Division of Life Science, College of Natural Sciences, Sookmyung Women's University) ;
  • Cho, Dae-Ho (Division of Life Science, College of Natural Sciences, Sookmyung Women's University) ;
  • Park, Jong-Hoon (Division of Life Science, College of Natural Sciences, Sookmyung Women's University) ;
  • Kim, Keun-Il (Division of Life Science, College of Natural Sciences, Sookmyung Women's University) ;
  • Lee, Kyo-Young (Department of Pathology, Saint Mary's Hospital) ;
  • Song, Eun-Sook (Division of Life Science, College of Natural Sciences, Sookmyung Women's University)
  • 투고 : 2007.09.07
  • 심사 : 2007.12.17
  • 발행 : 2008.02.29

초록

The objective of the present study was to identify mitochondrial components associated with the damage caused by iron to the rat heart. Decreased cell viability was assessed by increased presence of lactate dehydrogenase (LDH) in serum. To assess the functional integrity of mitochondria, Reactive Oxygen Species (ROS), the Respiratory Control Ratio (RCR), ATP and chelatable iron content were measured in the heart. Chelatable iron increased 15-fold in the mitochondria and ROS increased by 59%. Deterioration of mitochondrial function in the presence of iron was demonstrated by low RCR (46% decrease) and low ATP content (96% decrease). Using two dimensional gel electrophoresis (2DE), we identified alterations in 21 mitochondrial proteins triggered by iron overload. Significantly, expression of the $\alpha$, $\beta$, and d subunits of $F_1F_o$ ATP synthase increased along with the loss of ATP. This suggests that the $F_1F_o$ ATP synthase participates in iron metabolism.

키워드

참고문헌

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