Table 2.

H7 and cycloheximide inhibit IL-6– and IFN-γ–induced fusion of macrophages with T-tropic envelope-expressing cells

Cytokine*InhibitorNo. of syncytia
None None 7 ± 4 
IL-6 None 72 ± 9  
IL-6 Cx 6 ± 2 
IL-6 H7 9 ± 1  
None Cx 8 ± 4 
None H7 3 ± 0  
None None 14 ± 1 
IFN-γ None 61 ± 13  
IFN-γ Cx 13 ± 1 
IFN-γ H7 12 ± 2  
None Cx 11 ± 1 
None H7 9 ± 1 
Cytokine*InhibitorNo. of syncytia
None None 7 ± 4 
IL-6 None 72 ± 9  
IL-6 Cx 6 ± 2 
IL-6 H7 9 ± 1  
None Cx 8 ± 4 
None H7 3 ± 0  
None None 14 ± 1 
IFN-γ None 61 ± 13  
IFN-γ Cx 13 ± 1 
IFN-γ H7 12 ± 2  
None Cx 11 ± 1 
None H7 9 ± 1 

IL-6 indicates interleukin 6; IFN-γ, interferon γ.

*

Cytokines were added for the last 24 hours of the monocyte-derived macrophage culture.

Cycloheximide (Cx) at 5 ng/mL and 1-(5-isoquinolinesulfonyl)-2-methyl-piperazine (H7) at 100 μmol were added to MDMs 1 hour prior to cytokines.

Syncytia were scored after 18 hours of co-culture of the macrophages (untreated or pretreated with cytokines) and TF228 cells expressing IIIB envelope.

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