mortality/aging
• mice die postnatally due to severe submucosal lymphedema of the small intestine
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• in 30% of mice die before E10.5
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immune system
N |
• B cell development is normal with normal numbers of mature B cells
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• the number of IL7 colony progenitors that form from E14.5 fetal liver cells is increased compared to when wild-type fetal liver cells are similarly treated
• serial replating of E14.5 fetal liver cells with IL7, SCF (stem cell factor), and Flt3L (Flt3 ligand) leads to an increase in colony numbers compared to when wild-type fetal liver cells are similarly treated
• however, fetal liver cell generated colonies are factor-dependent and not transformed
• bone marrow transplanted into irradiated Rag null mice fail to reconstitute the lymphocyte, pro-B cell, pre-B cells and IgM+ B cell compartments unlike when wild-type cells are transplanted
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digestive/alimentary system
• mice die postnatally due to severe submucosal lymphedema of the small intestine
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growth/size/body
• mice fail to thrive
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homeostasis/metabolism
• mice die postnatally due to severe submucosal lymphedema of the small intestine
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neoplasm
embryo
N |
• unlike in other mice lacking Etv6 expression, yolk vascular development is normal in mice that survive beyond E10.5
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hematopoietic system
• the number of IL7 colony progenitors that form from E14.5 fetal liver cells is increased compared to when wild-type fetal liver cells are similarly treated
• serial replating of E14.5 fetal liver cells with IL7, SCF (stem cell factor), and Flt3L (Flt3 ligand) leads to an increase in colony numbers compared to when wild-type fetal liver cells are similarly treated
• however, fetal liver cell generated colonies are factor-dependent and not transformed
• bone marrow transplanted into irradiated Rag null mice fail to reconstitute the lymphocyte, pro-B cell, pre-B cells and IgM+ B cell compartments unlike when wild-type cells are transplanted
|