mortality/aging
• by 1 year of age, 21 of 62 mice are moribund compared with no wild-type mice
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hematopoietic system
• increased numbers of granulocyte and macrophage precursors (CFU-GM) in the bone marrow and spleen
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• 12 of 21 mice develop myelodysplastic syndrome with erythroid predominance
• 4 of 21 mice develop myeloproliferative-like myeloid leukemia
• 4 of 21 mice develop chronic myelomonocytic leukemia
• 1 of 21 mice develop myeloid leukemia with maturation
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• at 1 year of age, one-third of moribund mice exhibit pale footpads suggesting anemia unlike wild-type mice
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• in most mice at 2 and 4 months
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• in most mice at 2 and 4 months
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• in most mice at 2 and 4 months
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• in most mice at 2 and 4 months
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• in most mice at 2 and 4 months
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• in most mice at 2 and 4 months
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• increased proliferation and altered differentiation potential in vitro
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neoplasm
• 12 of 21 mice develop myelodysplastic syndrome with erythroid predominance
• 4 of 21 mice develop myeloproliferative-like myeloid leukemia
• 4 of 21 mice develop chronic myelomonocytic leukemia
• 1 of 21 mice develop myeloid leukemia with maturation
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• 4 of 21 mice develop chronic myelomonocytic leukemia
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immune system
• 12 of 21 mice develop myelodysplastic syndrome with erythroid predominance
• 4 of 21 mice develop myeloproliferative-like myeloid leukemia
• 4 of 21 mice develop chronic myelomonocytic leukemia
• 1 of 21 mice develop myeloid leukemia with maturation
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• in most mice at 2 and 4 months
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• in most mice at 2 and 4 months
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• in most mice at 2 and 4 months
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liver/biliary system
• at 2 and 4 months
• 2 to 5 times in moribund mice at 1 year of age
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growth/size/body
• at 2 and 4 months
• 2 to 5 times in moribund mice at 1 year of age
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