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. 2017 Mar 8;7:43838. doi: 10.1038/srep43838

Table 1. Summary of significant and dose-dependent cytokine responses mediated by NAP treatment.

Cell Type NAP [5 μM] Cytokine gene induction
Cytokine secretion
TNF IL6 IL10 INFA4 INFB1 INFG INFL2 TNF IL6 IL10 INFA4 INFB1 INFG INFL2
PHH REP 2006                   ≤4        
REP 2055                            
REP 2139                            
REP 2165                            
KC REP 2006 ≤4     ≤6     ≤6              
REP 2055 ≤2             ≤8            
REP 2139                            
REP 2165                           ≥8*
LSEC REP 2006               n.e. n.e. n.e. n.e. n.e. n.e. n.e.
REP 2055               n.e. n.e. n.e. n.e. n.e. n.e. n.e.
REP 2139               n.e. n.e. n.e. n.e. n.e. n.e. n.e.
REP 2165               n.e. n.e. n.e. n.e. n.e. n.e. n.e.
PMBC REP 2006 ≤4 ≤8           ≤4            
REP 2055 ≤2             ≤6#            
REP 2139 ≤8 ≤8           ≤4#   ≤4#        
REP 2165 ≤6 ≤8                        

Gene expression and protein secretion of cytokines was analyzed in primary human hepatocytes (PHH), Kupffer cells (KC), liver sinusoidal endothelial cells (LSEC) and peripheral blood mononuclear cells (PBMC) exposure to indicated NAPs [5 μM]. Numbers indicate statistically significant and dose-related fold induction in cytokine gene expression (left, 6 h exposure) or cytokine secretion (right, 24 h exposure) relative to untreated cells. #, significant increase was only determined for 50 μM high dose treatment; *, not considered biologically relevant (see discussion); n.e., not evaluated.