hematopoietic system
• following induction with pIpC, CFU-GMs (colony forming units Granulocyte-Macrophage, myeloid) are increased and CFU-IL-7 (early B-lineage committed, lymphoid) are decreased compared to in control mice
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• following induction with pIpC, CFU-GEMMs (colony forming units Granulocyte, Erythroid, Macrophage, Megakaryocyte) are increased compared to in control mice
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• in repopulation assays, bone marrow cells from pIpC treated lead to reduced donor-derived lymphocyte numbers compared to when untreated cells are used
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• following pIpC treatment, myeloid progenitors are increased compared to in untreated mice
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• following pIpC treatment, common lymphoid progenitors and lymphoid-primed multipotential progenitor are decreased compared to in untreated mice
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• following induction with pIpC, BFU-Es (Burst-forming erythroid; early erythroid-committed, myeloid) are decreased compared to in controls
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• mild to moderate following pIpC treatment
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• mild to moderate following pIpC treatment
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• mild to moderate following pIpC treatment
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• B cells are gradually lost following pIpC treatment
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• following pIpC treatment, the long term repopulating hematopoietic stem cells are increased 10-fold compared to in untreated mice
• in repopulation assays, bone marrow cells from pIpC treated lead to a 10-fold increase in long term repopulation hematopoietic stem cells compared to when untreated cells are used
• following pIpC treatment, the total number of cycling hematopoietic stem cells compared to in untreated mice
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• the proportion of quiescent (G0) hematopoietic stem cells in the bone marrow of pIpC-treated mice is increased 17-fold compared with untreated controls
• following serum and cytokine withdrawal, the hematopoietic stem cells in the bone marrow of pIpC-treated mice exhibit increased apoptosis compared with untreated controls
• following induction with pIpC, hematopoietic stem cells used in serial transplantation experiments exhaust earlier than wild-type cells
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neoplasm
• following induction with pIpC and treatment with ENU, latency is shortened and a higher proportion of mice develop malignacy compared to control mice
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• following induction with pIpC and treatment with ENU, mice develop aggressive T cell leukemias with high blast counts and replacement of normal bone marrow with CD4+ CD8+ lymphoblasts unlike in control mice
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homeostasis/metabolism
• following induction with pIpC and treatment with ENU, latency is shortened and a higher proportion of mice develop malignacy compared to control mice
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immune system
N |
• T cell development is normal following pIpC induction
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• in repopulation assays, bone marrow cells from pIpC treated lead to reduced donor-derived lymphocyte numbers compared to when untreated cells are used
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• following pIpC treatment, myeloid progenitors are increased compared to in untreated mice
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• mild to moderate following pIpC treatment
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• mild to moderate following pIpC treatment
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• B cells are gradually lost following pIpC treatment
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