Literature DB >> 11710808

Effects of desmin gene knockout on mice heart mitochondria.

M Lindén1, Z Li, D Paulin, T Gotow, J F Leterrier.   

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).

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Year:  2001        PMID: 11710808     DOI: 10.1023/a:1010611408007

Source DB:  PubMed          Journal:  J Bioenerg Biomembr        ISSN: 0145-479X            Impact factor:   2.945


  43 in total

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Journal:  Biochem Cell Biol       Date:  1992 Oct-Nov       Impact factor: 3.626

4.  Characterization of cytochrome oxidase purified from rat liver.

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Authors:  K T Tokuyasu; A H Dutton; S J Singer
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Authors:  V Prahlad; M Yoon; R D Moir; R D Vale; R D Goldman
Journal:  J Cell Biol       Date:  1998-10-05       Impact factor: 10.539

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7.  Autoimmunoreactive IgGs from patients with postural orthostatic tachycardia syndrome.

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9.  Bcl-2 overexpression corrects mitochondrial defects and ameliorates inherited desmin null cardiomyopathy.

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