mortality/aging
• mice have a median survival of 14 days after birth
• 65% of mice die between 11 and 18 days of age
• some mice die as early as 1 day after birth and one mouse of 17 survived into adulthood
• lethality can be rescued by transfusion
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hematopoietic system
• spleen as a percentage of bodyweight is 14-fold greater than controls
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• extramedullary hematopoiesis occurs in the spleen and liver
• large clusters of erythroblasts disrupt the architecture of the spleen and liver
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• mice die of a lethal anemia
• anemia resembles beta thalassemia in humans
• anemia can be rescued by transfusion
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• blood smears showed numerous damaged RBCs
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• proerythroblast and early erythroblast numbers are increased in the bone marrow and spleen
• there is a higher ratio of early erythroblasts to late erythroblasts in both tissues
• increased levels of apoptosis occur to early and late erythroblasts in the bone marrow
• increased levels of apoptosis occur to late erythroblasts in the spleen
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• red blood cell count is about 75% lower than controls
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• hemoglobin content is decreased by more than 4-fold
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• packed cell volume is decreased by almost two thirds
• red cell distribution width is greatly expanded
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• visible in blood smears
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• nucleated cells with polychromatophilia are visible in blood smears
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• visible in blood smears
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• percentage of reticulocytes in the blood is almost 72% compared to 3% in controls
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• spleen architecture is disrupted by the presence of large numbers of erythroblasts
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homeostasis/metabolism
• bilirubin levels are increased 150-fold in the blood
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immune system
• spleen as a percentage of bodyweight is 14-fold greater than controls
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• spleen architecture is disrupted by the presence of large numbers of erythroblasts
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growth/size/body
• spleen as a percentage of bodyweight is 14-fold greater than controls
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Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
beta thalassemia | DOID:12241 |
OMIM:613985 |
J:148521 |