immune system
| N |
• in a model of passive systemic anaphylaxis, mice sensitized i.p. with anti-DNP IgE and challenged i.p. with DNP-HAS exhibit a normal hypothermic response at 50 min post-challenge
|
|
• plasma membrane capacitance (Cm) recordings of single peritoneal mast cells (MCs) after stimulation by intracellular dialysis of GTPgammaS and Ca2+ show that MCs achieve the same total increase in plasma membrane area (deltaCm) at a significantly lower rate than wild-type MCs; however, time between cell access and beginning of the exocytic burst is normal
• after stimulation with PMA/ionomycin, peritoneal MCs show a significant reduction in intracellular multigranular compartments, indicating a partial defect in compound exocytosis
|
hematopoietic system
|
• plasma membrane capacitance (Cm) recordings of single peritoneal mast cells (MCs) after stimulation by intracellular dialysis of GTPgammaS and Ca2+ show that MCs achieve the same total increase in plasma membrane area (deltaCm) at a significantly lower rate than wild-type MCs; however, time between cell access and beginning of the exocytic burst is normal
• after stimulation with PMA/ionomycin, peritoneal MCs show a significant reduction in intracellular multigranular compartments, indicating a partial defect in compound exocytosis
|
mortality/aging
| N |
• mice are viable, grossly normal, and exhibit a normal life span when raised in a specific pathogen-free facility
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cellular
|
• plasma membrane capacitance (Cm) recordings of single peritoneal mast cells (MCs) after stimulation by intracellular dialysis of GTPgammaS and Ca2+ show that MCs achieve the same total increase in plasma membrane area (deltaCm) at a significantly lower rate than wild-type MCs; however, time between cell access and beginning of the exocytic burst is normal
• after stimulation with PMA/ionomycin, peritoneal MCs show a significant reduction in intracellular multigranular compartments, indicating a partial defect in compound exocytosis
|


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