immune system
|
• at 2 months but not 4 months
|
|
• reduced lobularity with some bilobed and ovoid nuclei
|
|
• profound and progressive lymphopenia
|
|
• pyknotic with signs of blebbing and nuclear clumping
|
|
• mice exhibit a decrease T to B cell ratio compared with wild-type mice
|
|
• profound and progressive lymphopenia
• repopulation assays confirm that lymphopenia is cell intrinsic
|
|
• in the spleen and lymph node at 2 months
|
|
• to a greater extent than B cells
|
|
• in the spleen and lymph node at 2 months
|
|
• in the spleen and lymph node at 2 months
|
|
• at 2 and 4 months
|
|
• B cells exhibit an increase in surface IgM
|
|
• non-dividing lymphocyte lifespan is reduced
|
|
• homeotstatic
|
|
• at 2 and 4 months
|
skeleton
| N |
• mice exhibit nor obvious skeletal abnormalities
|
hematopoietic system
|
• at 2 months but not 4 months
|
|
• bone marrow cells used to re-constitute irradiated wild-type mice are deficient in restoring neutrophils, eosinophils, and red blood cells
|
|
• reduced lobularity with some bilobed and ovoid nuclei
|
|
• profound and progressive lymphopenia
|
|
• pyknotic with signs of blebbing and nuclear clumping
|
|
• mice exhibit a decrease T to B cell ratio compared with wild-type mice
|
|
• profound and progressive lymphopenia
• repopulation assays confirm that lymphopenia is cell intrinsic
|
|
• in the spleen and lymph node at 2 months
|
|
• to a greater extent than B cells
|
|
• in the spleen and lymph node at 2 months
|
|
• in the spleen and lymph node at 2 months
|
|
• at 2 and 4 months
|
|
• B cells exhibit an increase in surface IgM
|
|
• non-dividing lymphocyte lifespan is reduced
|
|
• homeotstatic
|
endocrine/exocrine glands
|
• at 2 months but not 4 months
|
cellular
|
• homeotstatic
|


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