Table 2.

Impact of PPAR-γ activation on TLR ligand-induced DC functions



No TLR ligand

+ TLR2L

+ TLR3L

+ TLR4L

+ TLR7L

DMSO
TGZ
DMSO
TGZ
DMSO
TGZ
DMSO
TGZ
DMSO
TGZ
DC maturation marker   –   –   ++   –   +++   –   +++   –   +++   –  
RANTES, MIP-1α, IL-10, IL-12   –   –   – (+)   –   +++   +   +++   +   – (+)   –  
MCP-1   +   ++   +   ++   ++   +++   ++   +++   +   ++  
Dextran uptake   +   ++   –   ++   –   ++   –   ++   +   ++  
Migration   –   –   ++   –   +++   –   +++   –   ++   –  
Nuclear c-Rel   –   –   +   –   +   –   +++   –   +   –  
ERK phosphorylation   –   –   +   –   +   –   +   –   +   –  
p38 phosphorylation
 

 

 
(+)
 
(+)
 
+
 
+
 
++
 

 

 

 


No TLR ligand

+ TLR2L

+ TLR3L

+ TLR4L

+ TLR7L

DMSO
TGZ
DMSO
TGZ
DMSO
TGZ
DMSO
TGZ
DMSO
TGZ
DC maturation marker   –   –   ++   –   +++   –   +++   –   +++   –  
RANTES, MIP-1α, IL-10, IL-12   –   –   – (+)   –   +++   +   +++   +   – (+)   –  
MCP-1   +   ++   +   ++   ++   +++   ++   +++   +   ++  
Dextran uptake   +   ++   –   ++   –   ++   –   ++   +   ++  
Migration   –   –   ++   –   +++   –   +++   –   ++   –  
Nuclear c-Rel   –   –   +   –   +   –   +++   –   +   –  
ERK phosphorylation   –   –   +   –   +   –   +   –   +   –  
p38 phosphorylation
 

 

 
(+)
 
(+)
 
+
 
+
 
++
 

 

 

 

Peripheral blood adhering monocytes were incubated for 6 days in the presence of GM-CSF and IL-4 with or without 5 μM TGZ starting from the first day of culture. The cells were incubated with different TLR ligands as a maturation stimulus 24 hours before harvesting. - indicates negative; +, positive; ++, up-regulated, highly positive; +++, highly up-regulated, very highly positive; and (+), scarcely positive.

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