Figure 3
Figure 3. Activation of ERK and cPLA2α and the ensuing LTC4 and PGD2 generation by BMMCs in response to Pam3CSK4 require TLR2 and MyD88. (A) BMMCs derived from Myd88-null (□) and wild-type C57BL/6 (■) mice were incubated for 60 minutes with the indicated concentrations of Pam3CSK4 for 60 minutes. The supernatants were assayed for LTC4 (left panel) and PGD2 (right panel) by EIA. (n = 3). Error bars indicate SEM. (B) BMMCs derived from Tlr2-null (n = 3), Myd88-null (n = 3), and wild-type C57BL/6 (n = 4) mice were incubated with 3 μg/mL Pam3CSK4 in a time-dependent manner. Pellets were analyzed for phosphorylated (left panels) or total (right panels) ERK and cPLA2α by Western blotting.

Activation of ERK and cPLA2α and the ensuing LTC4 and PGD2 generation by BMMCs in response to Pam3CSK4 require TLR2 and MyD88. (A) BMMCs derived from Myd88-null (□) and wild-type C57BL/6 (■) mice were incubated for 60 minutes with the indicated concentrations of Pam3CSK4 for 60 minutes. The supernatants were assayed for LTC4 (left panel) and PGD2 (right panel) by EIA. (n = 3). Error bars indicate SEM. (B) BMMCs derived from Tlr2-null (n = 3), Myd88-null (n = 3), and wild-type C57BL/6 (n = 4) mice were incubated with 3 μg/mL Pam3CSK4 in a time-dependent manner. Pellets were analyzed for phosphorylated (left panels) or total (right panels) ERK and cPLA2α by Western blotting.

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