Table 2.

The Quantification of ERK2 Activation on the Basis of Cell Equivalents by Densitometry Is Shown for Data Presented in Fig3 

Agonists Control [%]Panel
I Preincubation Sphingosine [%] II Sphingosine Alone [%] III DiC10 Alone [%]
(A) fMLP + EIgG  100  87 ± 12* <5* 132 ± 14 
(B) EIgG 49 ± 18* 59 ± 14* 0* 108 ± 19 
(C) Unstimulated  0* 13 ± 6 0  97 ± 16 
(D) fMLP 63 ± 17* 75 ± 10 <5* 114 ± 27 
Agonists Control [%]Panel
I Preincubation Sphingosine [%] II Sphingosine Alone [%] III DiC10 Alone [%]
(A) fMLP + EIgG  100  87 ± 12* <5* 132 ± 14 
(B) EIgG 49 ± 18* 59 ± 14* 0* 108 ± 19 
(C) Unstimulated  0* 13 ± 6 0  97 ± 16 
(D) fMLP 63 ± 17* 75 ± 10 <5* 114 ± 27 

For comparative purposes, the extent of fMLP-primed PMN (2 × 106/mL) undergoing phagocytosis with EIgG was determined to be 100%. Comparisons were made between sphingosine-treated PMN (panel II) versus sphingosine with DiC10-treated PMN (panel I), between control values versus sphingosine-treated PMN (panel II) and DiC10-treated PMN (panel III), and between different control values (A v B, C, and D).

*

P < .0001.

P < .05.

P < .001.

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