Effects of desmin gene knockout on mice heart mitochondria

被引:52
作者
Lindén, M
Li, ZL
Paulin, D
Gotow, T
Leterrier, JF
机构
[1] CNRS, UMR 6558, Grp Biol Interact Cellulaires, F-86022 Poitiers, France
[2] Univ Stockholm, Dept Biochem, S-10691 Stockholm, Sweden
[3] Univ Paris 07, UFR Biochim, F-75005 Paris, France
[4] Koshien Univ, Coll Nutr, Cell Biol Lab, Takarazuka, Hyogo 6650006, Japan
关键词
desmin; intermediate filament; mitochondria; creatine kinase; cytochrome c; Bcl-2; apoptosis; kinesin; porin;
D O I
10.1023/A:1010611408007
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In heart tissue from mice lacking the intermediate filament (IF) desmin, mitochondria show an abnormal shape and distribution (Thornell et al., 1997). In the present study we have isolated heart mitochondria from desmin null (D-/-) and control (D+/+) mice. and analyzed their composition by SDS-PAGE, immunoblotting, and enzyme measurements. We found both in vitro and in situ that the conventional kinesin, the microtubule-associated plus-end directed motor, was frequently associated with D+/+ heart mitochondria, but not with D-/- heart mitochondria, suggesting that the positioning of mitochondria in heart is a dynamic event involving the IF desmin, the molecular motor kinesin, and, most likely, the microtubules (MT) network. Furthermore, an increased capacity in energy production was found, as indicated by a threefold higher creatine kinase activity in heart mitochondria from D-/- compared to D+/+ mice. We also observed a significantly lower amount of cytochrome c in heart mitochondria from D-/- mice, and a relocalization of Bcl-2, which may indicate an apoptotic condition in the cell leading to the earlier reported pathological events, such as cardiomyocytes degeneration and calcinosis of the heart (Thornell et al., 1997).
引用
收藏
页码:333 / 341
页数:9
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