immune system
• immature B cells produce less surface IgM and IgD than wild-type
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• the number of IgM+B220lowIgD-/low immature B cells is reduced compared to wild-type
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• the number of IgM-B220lowCD43+ pro-B cells is increased compared to wild-type
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• small increase
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• the number of B220+IgM+ B cells in the spleen is decreased by 30% of wild-type
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• the number of circulating mature IgM+B220high B cells is slightly reduced (4% compared to 12% in wild-type mice)
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• the number of B1a B cells in the peritoneum is decreased 7-fold compared to wild-type
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• mice exhibit a 3- to 5-fold reduction in IgM and IgG response to T-dependent antigens such as NP-CGG and NP-Ficoll compared to wild-type mice
• despite normal levels of surface Cd40lg and Cd180, mice fail to response to Cd40lg, Cd180, CpG and LPS stimulation
• cell division in response to Cd40lg and Cd180 stimulation less and fewer cells are induced to divide in response to LPS and CpG stimulation compared to wild-type
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• the half-life of B cells in the spleen is increased (58.3 days compared to 23.4 days for wild-type)
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• B cells fail to proliferate in response to BCR cross-linking as wild-type mice do
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hematopoietic system
• immature B cells produce less surface IgM and IgD than wild-type
|
• the number of IgM+B220lowIgD-/low immature B cells is reduced compared to wild-type
|
• the number of IgM-B220lowCD43+ pro-B cells is increased compared to wild-type
|
• small increase
|
• the number of B220+IgM+ B cells in the spleen is decreased by 30% of wild-type
|
• the number of circulating mature IgM+B220high B cells is slightly reduced (4% compared to 12% in wild-type mice)
|
• the number of B1a B cells in the peritoneum is decreased 7-fold compared to wild-type
|
• the half-life of B cells in the spleen is increased (58.3 days compared to 23.4 days for wild-type)
|
• B cells fail to proliferate in response to BCR cross-linking as wild-type mice do
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cellular
• B cells fail to proliferate in response to BCR cross-linking as wild-type mice do
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