immune system
• Dapp1-deficient B cell proliferation is reduced by 50% compared to wild-type B cells in response to BCR crosslinking; this decrease is limited to signaling by the BCR since stimulation with other B cell mitogens such as anti-CD40 or LPS results in normal or enhanced mutant B cell proliferation
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• null mice display defective responses to T cell independent type II antigens like TNP-Ficoll; production of IgG3 is markedly reduced
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• vaccination of Dapp1-deficient mice with capsular polysaccharide from S. pneumoniae results in production of type 3 polysaccharide-specific IgM antibodies but failure to produce of type 3 polysaccharide-specific IgG3 antibodies
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• wild-type mice vaccinated with live S. pneumoniae via IP injection show100% survival but all vaccinated Dapp1-deficient die
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hematopoietic system
• Dapp1-deficient B cell proliferation is reduced by 50% compared to wild-type B cells in response to BCR crosslinking; this decrease is limited to signaling by the BCR since stimulation with other B cell mitogens such as anti-CD40 or LPS results in normal or enhanced mutant B cell proliferation
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• vaccination of Dapp1-deficient mice with capsular polysaccharide from S. pneumoniae results in production of type 3 polysaccharide-specific IgM antibodies but failure to produce of type 3 polysaccharide-specific IgG3 antibodies
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cellular
• Dapp1-deficient B cell proliferation is reduced by 50% compared to wild-type B cells in response to BCR crosslinking; this decrease is limited to signaling by the BCR since stimulation with other B cell mitogens such as anti-CD40 or LPS results in normal or enhanced mutant B cell proliferation
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