Table 2.

Induction of Skin Vasculitis by Injection of FcR+ Mast Cells Into FcRγ −/− Mice

Inoculation FcRγ 6-19 No. Cell Transfer Ear Lesions
IV  −/−  +  4  Macrophage* 0/4 
   5  LPS-macrophage 0/5  
   BMMC 5/9  
 −/−  −  3  Macrophage 0/3  
   3  BMMC  0/3  
SC  −/−  6  Macrophage  0/6  
   6  LPS-macrophage 0/6  
   8  BMMC  6/8  
 −/−  − 3  Macrophage  0/3  
   3  LPS-macrophage 0/3  
   3  BMMC  0/3 
Inoculation FcRγ 6-19 No. Cell Transfer Ear Lesions
IV  −/−  +  4  Macrophage* 0/4 
   5  LPS-macrophage 0/5  
   BMMC 5/9  
 −/−  −  3  Macrophage 0/3  
   3  BMMC  0/3  
SC  −/−  6  Macrophage  0/6  
   6  LPS-macrophage 0/6  
   8  BMMC  6/8  
 −/−  − 3  Macrophage  0/3  
   3  LPS-macrophage 0/3  
   3  BMMC  0/3 

FcRγ −/− mice were inoculated with 6-19 hybridoma cells as described in Table 1. Seven days later, various FcR+ cells were IV or SC transferred into 6-19–treated FcRγ −/− mice.

*

Adherent populations from the thioglycolate-induced peritoneal exudate cells were used as macrophages.

Peritoneal macrophages as in the asterisk note were activated with LPS.

Bone marrow cells were cultured in the presence of IL-3 and used after 4 weeks of culture as BMMC.

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