Table 3.

Bioactive lipids and human macrophage survival


Treatment (prior to apoptosis induction)

Caspase-3 activity, fold of control*

SD

P, n ≥ 3
None   30.6   ± 4   ND  
ACM   5.3   ± 3.6   .02  
LPA    
   1 μM   30.1   ± 12.8   .35  
   10 μM   33.8   ± 19.7   .49  
   100 μM   39.5   ± 20.8   .35  
SIP    
   1 μM   13.2   ± 9.2   .05  
   10 μM   10   ± 6.3   .02  
   100 μM   6.1   ± 4   .006  
PAF    
   1 μM   40.5   ± 5.1   .4  
   10 μM   61.1   ± 41.3   .15  
   100 μM   97.2   ± 59.6   .09  
LPC    
   1 μM   54.2   ± 27.8   .25  
   10 μM   32.1   ± 18.4   .44  
   100 μM
 
20
 
± 5.2
 
.2
 

Treatment (prior to apoptosis induction)

Caspase-3 activity, fold of control*

SD

P, n ≥ 3
None   30.6   ± 4   ND  
ACM   5.3   ± 3.6   .02  
LPA    
   1 μM   30.1   ± 12.8   .35  
   10 μM   33.8   ± 19.7   .49  
   100 μM   39.5   ± 20.8   .35  
SIP    
   1 μM   13.2   ± 9.2   .05  
   10 μM   10   ± 6.3   .02  
   100 μM   6.1   ± 4   .006  
PAF    
   1 μM   40.5   ± 5.1   .4  
   10 μM   61.1   ± 41.3   .15  
   100 μM   97.2   ± 59.6   .09  
LPC    
   1 μM   54.2   ± 27.8   .25  
   10 μM   32.1   ± 18.4   .44  
   100 μM
 
20
 
± 5.2
 
.2
 

ND indicates not determined

*

Human primary macrophages were exposed to ACM, LPA, S1P, PAF, or LPC at the indicated concentrations for 16 hours. Apoptosis was induced with 10 ng/mL TNF-α and 10 μg/mL CHX for 8 hours. Caspase-3 activity in whole-cell lysates was quantified as described in “Material and methods”

Statistical analysis was performed using the paired Student t test

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