Fig. 3.
Fig. 3. Restoration of ERK2 phosphorylation by DiC10 in PMN treated with sphingosine. PMN (2 × 106/mL) were pretreated for 30 minutes with 10 μmol/L sphingosine followed by incubation for 30 minutes with 200 μmol/L DiC10 (panel I) or treated with 10 μmol/L sphingosine alone (panel II) or 200 μmol/L DiC10 alone (panel III). The PMN were then primed with 10−7mol/L fMLP and then challenged with EIgG (column A), challenged with EIgG alone (column B), were not treated (column C), or were stimulated with 10−7 mol/L fMLP (column D). ERK2 phosphorylation was determined by Western blotting. See Fig 2B for an example of control values.

Restoration of ERK2 phosphorylation by DiC10 in PMN treated with sphingosine. PMN (2 × 106/mL) were pretreated for 30 minutes with 10 μmol/L sphingosine followed by incubation for 30 minutes with 200 μmol/L DiC10 (panel I) or treated with 10 μmol/L sphingosine alone (panel II) or 200 μmol/L DiC10 alone (panel III). The PMN were then primed with 10−7mol/L fMLP and then challenged with EIgG (column A), challenged with EIgG alone (column B), were not treated (column C), or were stimulated with 10−7 mol/L fMLP (column D). ERK2 phosphorylation was determined by Western blotting. See Fig 2B for an example of control values.

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