Table 1.

Detection of vIL-6 in the culture supernatants of cell lines

Cell lineCulture without TPA (pg/mL)Culture with TPA (pg/mL)
BC-1*,   2880  26 300 
BCP-1* 19 200 118 100  
BCBL-1*   1680  29 100 
Daudi <30 <30 
v6O 88 600 ND 
VDS-O1,1-153 <30 ND 
Cell lineCulture without TPA (pg/mL)Culture with TPA (pg/mL)
BC-1*,   2880  26 300 
BCP-1* 19 200 118 100  
BCBL-1*   1680  29 100 
Daudi <30 <30 
v6O 88 600 ND 
VDS-O1,1-153 <30 ND 

To prepare conditioned media, suspension cells were seeded in 12-well plates at 1 × 106 cells/well in 2.5 mL RPMI 1640 medium supplemented with 10% fetal bovine serum and cultured with or without 20 ng/mL TPA (Sigma) for 48 hours. Adherent cells were seeded in 6-well plates at 1 × 106 cells/well in 2.5 mL culture media and cultured for 48 hours. The concentration of fetal bovine serum in each supernatant was adjusted to be 10%. Data represent the mean of duplicate assays.

*

KSHV-positive cell lines.4,20 22 

EBV-positive cell lines.12 

NIH3T3 cells stably transfected with vIL-6 expression vector.11 

F1-153

Lymphoblastoid cells stably transfected with hIL-6-expression vector.21 

ND, not determined.

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