mortality/aging
• lower median survival rate
|
muscle
• about 20% of mice develop fibrosis in the cardiac muscle after 30 weeks of age and some cardiomyocytes show amyloid deposition and rimmed vacuoles
|
• 5 of 12 mice that died displayed rimmed vacuoles in the skeletal muscles
• muscle cross sections are positive for Congo red stained protein deposits and about 62% of rimmed vesicles contain amyloid proteins
• accumulation of these proteins starts at 32 to 34 weeks of age
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• after 40 weeks of age, rimmed vacuoless and occasional inclusion bodies are seen in scattered fibers
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• some fibers appear atrophic by 40 weeks of age
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• increase in variation of fiber size with age that preferentially affects the gastrocnemius and quadriceps muscles
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• 3 of 12 mice had fibrosis and a few rimmed vacuoles in the diaphragm
|
• some muscles, particularly the gastrocnemius, are atrophic
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• vacuolated muscle fibers shows signs of the unfolded protein response and activation of autophagy
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• reduced muscle strength noted after 30 weeks of age
|
growth/size/body
• after 30 weeks of age, mice weigh significantly less than control littermates
• lower body weight is more pronounced and develops earlier in females compred to males
|
homeostasis/metabolism
• elevated serum creatine kinase activity compared to littermate controls starting at 30 weeks of age
|
cardiovascular system
• about 20% of mice develop fibrosis in the cardiac muscle after 30 weeks of age and some cardiomyocytes show amyloid deposition and rimmed vacuoles
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
inclusion body myositis | DOID:3429 |
OMIM:147421 |
J:117854 |