Figure 5
Figure 5. A proposed scheme for regulation of TNFα induction in the LPS-stimulated human PMN. (Left) In the resting cell, RhoA suppresses NF-κB activation and TNFα expression. This may occur through its inhibition of Cdc42 and possibly also through a Cdc42-independent mechanism. RhoA activity in the resting PMN is p38- and Cdc42-independent. (Right) In the LPS-stimulated PMN, we have previously reported that p38 is activated8 and promotes the activation of NF-κB8 and Cdc42.30 LPS-activated Cdc42 regulates RhoA activation. Downstream of RhoA, ROCKα is activated and promotes TNFα protein expression. LPS-activated p38 and Cdc42 may regulate TNFα protein through ROCKα, but ROCKα-independent pathways are also possible (not shown).

A proposed scheme for regulation of TNFα induction in the LPS-stimulated human PMN. (Left) In the resting cell, RhoA suppresses NF-κB activation and TNFα expression. This may occur through its inhibition of Cdc42 and possibly also through a Cdc42-independent mechanism. RhoA activity in the resting PMN is p38- and Cdc42-independent. (Right) In the LPS-stimulated PMN, we have previously reported that p38 is activated8 and promotes the activation of NF-κB8 and Cdc42.30  LPS-activated Cdc42 regulates RhoA activation. Downstream of RhoA, ROCKα is activated and promotes TNFα protein expression. LPS-activated p38 and Cdc42 may regulate TNFα protein through ROCKα, but ROCKα-independent pathways are also possible (not shown).

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