Table 1.

Quantitative analyses of mitochondria and CRUs in EDL muscles

ABCDEF
EDLNo. of mitochondria/100 μm2No. of altered mitochondria/100 μm2 (%)No. of CRUs/100 μm2% of oblique/longitudinal CRUs% of dyadsNo. of mitochondrion/CRU pairs/100 μm2
WT 22.8 ± 0.8 0.4 ± 0.1 (2%) 46.1 ± 0.9 4.3 ± 0.1 1.0 ± 0.9 18.6 ± 0.7 
Ho 16.8 ± 0.8*
(P = 2.25E-06) 
2.0 ± 0.3* (12%)
(P = 4.48E-06) 
36.5 ± 0.9*
(P = 2.42E-13) 
10.5 ± 0.1*
(P = 5.11E-06) 
3.9 ± 0.1*
(P = 0.0003) 
12.3 ± 0.7*
(P = 1.09E-09) 
ABCDEF
EDLNo. of mitochondria/100 μm2No. of altered mitochondria/100 μm2 (%)No. of CRUs/100 μm2% of oblique/longitudinal CRUs% of dyadsNo. of mitochondrion/CRU pairs/100 μm2
WT 22.8 ± 0.8 0.4 ± 0.1 (2%) 46.1 ± 0.9 4.3 ± 0.1 1.0 ± 0.9 18.6 ± 0.7 
Ho 16.8 ± 0.8*
(P = 2.25E-06) 
2.0 ± 0.3* (12%)
(P = 4.48E-06) 
36.5 ± 0.9*
(P = 2.42E-13) 
10.5 ± 0.1*
(P = 5.11E-06) 
3.9 ± 0.1*
(P = 0.0003) 
12.3 ± 0.7*
(P = 1.09E-09) 

In EDL fibers from Ho mice, the frequency of mitochondria, the number of CRUs, and the number of couples mitochondrion/CRU are significantly reduced compared with WT. On the other hand, the number of damaged mitochondria, dyads (i.e., incomplete CRUs), and misoriented CRUs (oblique/longitudinal) are significantly increased compared with WT littermates. Data are shown as mean ± SEM (* P < 0.001). Samples size: 32 fibers from three WT mice, 22 fibers from three Ho littermates, five micrographs/fiber.

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