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结蛋白基因敲除对小鼠心脏线粒体的影响。

Effects of desmin gene knockout on mice heart mitochondria.

作者信息

Lindén M, Li Z, Paulin D, Gotow T, Leterrier J F

机构信息

Groupe de Biologie des Interactions Cellulaires, UMR CNRS 6558, Poitiers, France.

出版信息

J Bioenerg Biomembr. 2001 Aug;33(4):333-41. doi: 10.1023/a:1010611408007.

Abstract

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).

摘要

在缺乏中间丝(IF)结蛋白的小鼠心脏组织中,线粒体呈现出异常的形状和分布(托内尔等人,1997年)。在本研究中,我们从结蛋白基因敲除(D-/-)和对照(D+/+)小鼠中分离出心脏线粒体,并通过SDS-PAGE、免疫印迹和酶活性测定分析了它们的组成。我们发现,无论是在体外还是原位,传统驱动蛋白(一种与微管相关的向微管正端移动的分子马达)都经常与D+/+小鼠的心脏线粒体相关联,而不与D-/-小鼠的心脏线粒体相关联,这表明心脏中线粒体的定位是一个动态过程,涉及中间丝结蛋白、分子马达驱动蛋白,以及很可能还有微管(MT)网络。此外,我们发现能量产生能力有所增强,这表现为与D+/+小鼠相比,D-/-小鼠心脏线粒体中的肌酸激酶活性高出三倍。我们还观察到,D-/-小鼠心脏线粒体中的细胞色素c含量显著降低,并且Bcl-2发生了重新定位,这可能表明细胞处于凋亡状态,导致了先前报道的病理事件,如心肌细胞变性和心脏钙化(托内尔等人,1997年)。

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