Tumor necrosis factor alpha (TNFalpha) is a pro-inflammatory cytokine involved in innate immune response, as well as in the pathogenesis of many inflammatory diseases. Although several response elements in the TNFalpha promoter region are involved in the activation of gene transcription, few studies have examined the regulatory mechanism that controls TNFalpha autoregulation. In this study, we investigated the role of the Early Growth Response-1 (EGR-1) transcription factor in TNFalpha autoregulation in HaCaT human keratinocytes. The requirement for EGR-1 in TNFalpha autoregulation was confirmed using a construct harboring a point mutation in the EGR-1 binding site within the TNFalpha promoter and the introduction of EGR-1 siRNA. Inhibition of the ERK or JNK pathway suppressed TNFalpha-induced EGR-1 expression, resulting in the inhibition of TNFalpha-induced TNFalpha promoter activation. These results reveal that the ERK and JNK MAPK pathways contribute to the autoregulation of TNFalpha synthesis via EGR-1 induction in HaCaT keratinocytes.