hematopoietic system
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• mice develop microcytic and hypochromic anemia following polyinosinicpolycytidylic acid (pIpC) treatment
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• decreased number of mature (R4) erythroblasts in the spleen in proportion to number of R2 erythroblasts
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• increased numbers of immature (R2) erythroblasts in the spleen in proportion to number of R4 erythroblasts
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• variation in red blood cell size and shape
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• impaired transition of stage III (poly-chromatophilic) to stage IV (ortho-chromatophilic) erythroblasts
• increase in erythroblast apoptosis
• decrease in number of fully-formed clathrin coated pits in erythroblast
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• reduced numbers of red blood cells in peripheral blood following pIpC treatment
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• reduced hematocrit levels in peripheral blood following pIpC treatment
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• reduced hemoglobin levels in peripheral blood following pIpC treatment
• reticulocytes have a low hemoglobin content
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• decreased mean corpuscular volume following pIpC treatment
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• decreased mean corpuscular hemoglobin following pIpC treatment
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• increased red cell distribution width in peripheral blood following pIpC treatment
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• decreased numbers of CD4+ T cells beginning 3 months after pIpC treatment
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• decreased numbers of CD8+ T cells beginning 5 months after pIpC treatment
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• elevated reticulocyte counts
• increase in percentage of immature reticulocyte fraction
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homeostasis/metabolism
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• high serum erythropoietin levels beginning 2 months after pIpC treatment
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• increased amounts of surface-bound transferrin in relation to internalized transferrin on erythroblasts as compaired to wild-type
• transferrin receptor endocytosis is 25% as efficient as wild-type
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• elevated serum iron levels
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immune system
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• decreased numbers of CD4+ T cells beginning 3 months after pIpC treatment
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• decreased numbers of CD8+ T cells beginning 5 months after pIpC treatment
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growth/size/body


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