immune system
• deficient splenocytes injected into wild-type recipients which overexpress Th1 cytokines show lower efficiency in migrating to the spleen
• in a model of aseptic peritonitis, seven days after peritonitis induction, mutants have lower numbers of inflammatory cells in the peritoneal cavity compared to wild-type mice
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• in an aseptic peritonitis model, neutrophils display a defect in exiting the circulation into the peritoneal cavity; neutrophils are present in greater numbers in circulation of mutant animals compared to wild-type in aseptic peritonitis model
• after induction of peritonitis in Pscdbp-deficient mice, a limited reduction in circulating WBCs is observed compared to a 50% decrease in wild-type controls
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• reduced circulating WBCs in animals >6 months of age, with reduction of neutrophilic and monocytic fractions
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• reduced numbers of virus specific CTLs are observed infiltrating the tumors in null mice
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• lymphocyte numbers in tumor-draining lymph nodes are significantly reduced compared to controls mice, with fewer leukocytes infiltrating the tumors
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hematopoietic system
• deficient splenocytes injected into wild-type recipients which overexpress Th1 cytokines show lower efficiency in migrating to the spleen
• in a model of aseptic peritonitis, seven days after peritonitis induction, mutants have lower numbers of inflammatory cells in the peritoneal cavity compared to wild-type mice
|
• in an aseptic peritonitis model, neutrophils display a defect in exiting the circulation into the peritoneal cavity; neutrophils are present in greater numbers in circulation of mutant animals compared to wild-type in aseptic peritonitis model
• after induction of peritonitis in Pscdbp-deficient mice, a limited reduction in circulating WBCs is observed compared to a 50% decrease in wild-type controls
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• reduced circulating WBCs in animals >6 months of age, with reduction of neutrophilic and monocytic fractions
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• reduced numbers of virus specific CTLs are observed infiltrating the tumors in null mice
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neoplasm
• in null mice injected with Moloney murine sarcoma/Moloney murine leukemia virus, a higher (but nonsignificant) levelo of tumor incidence is observed (87% vs 70% in controls); mutant animals develop significantly larger sarcomas than wild-type mice
• regression of tumors occurs with slower kinetics than in wild-type controls
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cellular
• deficient splenocytes injected into wild-type recipients which overexpress Th1 cytokines show lower efficiency in migrating to the spleen
• in a model of aseptic peritonitis, seven days after peritonitis induction, mutants have lower numbers of inflammatory cells in the peritoneal cavity compared to wild-type mice
|
• in an aseptic peritonitis model, neutrophils display a defect in exiting the circulation into the peritoneal cavity; neutrophils are present in greater numbers in circulation of mutant animals compared to wild-type in aseptic peritonitis model
• after induction of peritonitis in Pscdbp-deficient mice, a limited reduction in circulating WBCs is observed compared to a 50% decrease in wild-type controls
|