mortality/aging
|
• 80% of mice die after E. coli infection unlike wild-type mice within 18 hours
• 60% of mice die after E. coli infection unlike wild-type mice after 30 hours
|
|
• following cecal ligation and puncture surgery
|
immune system
| N |
• mice exhibit normal LPS- and LTA-induced TNFalpha and IL6 production in peritoneal macrophages
|
|
• in E. coli-infected mice or following intraperitoneal CpG injection
• however, levels are normal after thioglycollate treatment and LPS challenge
|
|
• in E. coli-infected mice or following intraperitoneal CpG injection
• however, levels are normal after thioglycollate treatment and LPS challenge
|
|
• from CpG-induced peritoneal macrophage
|
|
• from CpG-induced peritoneal macrophage
|
|
• E. coli-infected mice exhibit increased serum TNFalpha and IL6 concentration and increased mortality compared with wild-type mice
|
|
• 80% of mice die after E. coli infection unlike wild-type mice within 18 hours
• 60% of mice die after E. coli infection unlike wild-type mice after 30 hours
|
homeostasis/metabolism
|
• in E. coli-infected mice or following intraperitoneal CpG injection
• however, levels are normal after thioglycollate treatment and LPS challenge
|
|
• in E. coli-infected mice or following intraperitoneal CpG injection
• however, levels are normal after thioglycollate treatment and LPS challenge
|
|
• following cecal ligation and puncture surgery, mice exhibit worse disease scores with earlier and increased mortality compared with wild-type mice
|


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