Table 2.

Quantitative analyses of mitochondria and CRUs in soleus muscles

ABCDEF
No. of mitochondria
/100 μm2
No. of altered mitochondria
/100 μm2 (%)
No. of CRUs
/100 μm2
% of oblique/longitudinal CRUs% of dyadsNo. of mitochondrion/CRU pairs/100 μm2
WT 42.5 ± 1.1 2.1 ± 0.3 (1%) 34.8 ± 1.1 4.2 ± 0.1 6.5 ± 0.1 21.6 ± 1.2 
Ho 30.9 ± 1.1*
(P = 8.46E-13) 
3.0 ± 0.4* (10%)
(P = 2.70E-07) 
28.0 ± 1.0*
(P = 1.19E-05) 
14.9 ± 0.1*
(P = 8.12E-13) 
14.1 ± 0.1*
(P = 3.0E-05) 
12.9 ± 0.7*
(P = 2.08E-09) 
ABCDEF
No. of mitochondria
/100 μm2
No. of altered mitochondria
/100 μm2 (%)
No. of CRUs
/100 μm2
% of oblique/longitudinal CRUs% of dyadsNo. of mitochondrion/CRU pairs/100 μm2
WT 42.5 ± 1.1 2.1 ± 0.3 (1%) 34.8 ± 1.1 4.2 ± 0.1 6.5 ± 0.1 21.6 ± 1.2 
Ho 30.9 ± 1.1*
(P = 8.46E-13) 
3.0 ± 0.4* (10%)
(P = 2.70E-07) 
28.0 ± 1.0*
(P = 1.19E-05) 
14.9 ± 0.1*
(P = 8.12E-13) 
14.1 ± 0.1*
(P = 3.0E-05) 
12.9 ± 0.7*
(P = 2.08E-09) 

In soleus 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: 28 fibers from three WT mice, 28 fibers from three Ho littermates, five micrographs/fiber.

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