immune system
• 4-fold increase in the number of CD43+IgM- Pro-B cells
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• relative number of CD21highCD23low marginal zone B cells is decreased
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• increase in the number of B cells at all stages of development in the bone marrow and spleen
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• a 3-5 fold increase in the numbers of transitional B cells
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• an increase in B-2 cell number, but not B-1 cells, from the peritoneal cavity
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• an increase in CD21intCD23high follicular B cells
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• a 4-fold increase in the number of IgM+ immature B cells
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• B cells are highly resistant to multiple cell death stimuli, including cytokine withdrawal, BCR crosslinking, steroid treatment, and DNA damage
• cell cycle progression of splenic B cells is impaired after stimulation with mitogens LPS and anti-IgM, but not CpG-DNA
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• all isotypes were 5-10 times higher than controls
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• increased IgG1, IgG2, IgG2b and IgG3
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hematopoietic system
• 4-fold increase in the number of CD43+IgM- Pro-B cells
|
• 2-fold increase in total cellularity of bone marrow cells, due to accumulation of developing B cells
|
• relative number of CD21highCD23low marginal zone B cells is decreased
|
• increase in the number of B cells at all stages of development in the bone marrow and spleen
|
• a 3-5 fold increase in the numbers of transitional B cells
|
• an increase in B-2 cell number, but not B-1 cells, from the peritoneal cavity
|
• an increase in CD21intCD23high follicular B cells
|
• a 4-fold increase in the number of IgM+ immature B cells
|
• B cells are highly resistant to multiple cell death stimuli, including cytokine withdrawal, BCR crosslinking, steroid treatment, and DNA damage
• cell cycle progression of splenic B cells is impaired after stimulation with mitogens LPS and anti-IgM, but not CpG-DNA
|
• all isotypes were 5-10 times higher than controls
|
• increased IgG1, IgG2, IgG2b and IgG3
|