hematopoietic system
N |
• normal frequencies of CD19+ B cells (including CD19+ AA4.1+ immature B cells), CD21int CD23+ follicular B and CD21hi CD23- MZ B cells, peritoneal B-1a and B-1b cells, and normal B220+ CD43+ pro-B-cell and B220int CD43- pre-B-cell compartments in the bone marrow
• equal proportion of wild-type and mutant splenic B cells in competitive bone marrow reconstitution experiments
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• increased percentage of bone marrow B220+ CD43- pro-B cells after intraperitoneal tunicamycin administration
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• significant reduction in bone marrow B220in CD43- pre-B cell compartment after intraperitoneal tunicamycin administration
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immune system
N |
• normal frequencies of CD19+ B cells (including CD19+ AA4.1+ immature B cells), CD21int CD23+ follicular B and CD21hi CD23- MZ B cells, peritoneal B-1a and B-1b cells, and normal B220+ CD43+ pro-B-cell and B220int CD43- pre-B-cell compartments in the bone marrow
• equal proportion of wild-type and mutant splenic B cells in competitive bone marrow reconstitution experiments
• normal IgM surface expression
• normal frequency of mature splenic B cells after intraperitoneal tunicamycin administration
• normal frequency of recirculating B220hi CD43- B cells after intraperitoneal tunicamycin administration
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• increased percentage of bone marrow B220+ CD43- pro-B cells after intraperitoneal tunicamycin administration
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• significant reduction in bone marrow B220in CD43- pre-B cell compartment after intraperitoneal tunicamycin administration
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• significantly reduced immune response after intravenous challenge with T-cell-independent type 2 (TI-2) antigen TNP-Ficoll or Streptococcus pneumoniae type 3 polysaccharide
• reduced amounts of anti-TNP-specific IgG3 isotype antibodies after intravenous challenge with TI-2 antigen TNP-Ficoll
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