Fig. 4.
Fig. 4. sE-selectin induces a time-dependent increase in ERK1/2 phosphorylation. / HMVECs were stimulated with 50 nM sE-selectin for various time points as indicated (m indicates minutes; NS, nonstimulated). In the inhibition study, HMVECs were pretreated with PP2 (10 μM) for 2 hours prior to stimulating with sE-selectin, and PP2 was also present during the stimulation with sE-selectin. Cell extracts were prepared and the protein content in each sample was quantified. Samples (20 μg each) were resolved by 10% SDS-PAGE and probed with rabbit antihuman phospho-ERK1/2 (*p-ERK1/2) antibody. To verify equal loading, the blots were stripped and reprobed with rabbit antihuman ERK1/2 antibody. (A) Representative blot from 3 independent experiments. (B) The ratio of p-ERK1/2 to ERK1/2 band density ± SEM from 3 independent experiments. *Represents a significant difference (P < .05) between the respective groups. sE-selectin induced a marked increase in ERK1/2 phosphorylation at 10, 20, and 30 minutes after stimulation. Pretreatment of HMVECs with PP2 significantly inhibited ERK1/2 phosphorylation.

sE-selectin induces a time-dependent increase in ERK1/2 phosphorylation.

HMVECs were stimulated with 50 nM sE-selectin for various time points as indicated (m indicates minutes; NS, nonstimulated). In the inhibition study, HMVECs were pretreated with PP2 (10 μM) for 2 hours prior to stimulating with sE-selectin, and PP2 was also present during the stimulation with sE-selectin. Cell extracts were prepared and the protein content in each sample was quantified. Samples (20 μg each) were resolved by 10% SDS-PAGE and probed with rabbit antihuman phospho-ERK1/2 (*p-ERK1/2) antibody. To verify equal loading, the blots were stripped and reprobed with rabbit antihuman ERK1/2 antibody. (A) Representative blot from 3 independent experiments. (B) The ratio of p-ERK1/2 to ERK1/2 band density ± SEM from 3 independent experiments. *Represents a significant difference (P < .05) between the respective groups. sE-selectin induced a marked increase in ERK1/2 phosphorylation at 10, 20, and 30 minutes after stimulation. Pretreatment of HMVECs with PP2 significantly inhibited ERK1/2 phosphorylation.

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