Ejarque-Ortiz et al. [9] have also shown that the restoration of C/EBP-α levels may be a strategy for attenuating neurotoxic effects. Moreover, LPS can induce C/EBP-β expression by astrocytes and microglia in primary mouse
glial cultures. It has been demonstrated by Straccia et al. [8] that C/EBP-β-null glial culture in activated microglia abrogates neurotoxicity, implying that C/EBP-β is a possible therapeutic Stem Cells inhibitor target for ameliorating neuronal damage due to neuroinflammation. However, the relationships between the response of microglial cells to environmental damage or inflammatory processes and the profound changes of gene expression associated with ER stress-related signaling have not been clearly established [10, 11]. This study hypothesizes that enhancement of calpain-II-regulated C/EBP-β downregulation by IL-13 through the induction of ER stress-related signaling in activated microglia may exacerbate microglial cell death and lead to the inhibition of proinflammatory cytokines release from deteriorated microglia. Neuronal cells will no longer be exposed to toxic damage. Thus, this change may reduce neuronal damage due to neuroinflammation. The present study also shows that IL-13-enhanced ER stress-related calpain activation plays an important role in the downregulation of C/EBP-β-regulated PPAR-γ/HO-1 expression in activated
microglia. In activated microglia, IL-13 may potentially many confer functional and therapeutic benefits in neurologic disorders by abrogating neurodegeneration. Previously, PGE2 production was reportedly involved in activated microglial death [6]. Here, find more the role of C/EBP-α and C/EBP-β was analyzed using specific small interfering RNA (siRNA) to elucidate whether IL-13-enhanced activated microglia PGE2 expression using ELISA. IL-13 increased PGE2 expressions in LPS-induced primary and BV-2 microglial cells (Fig. 1A). C/EBP is thought to play a crucial role in the activation of microglia following brain injury. Moreover, transfection of siRNA targeting C/EBP-α significantly decreased PGE2 production, whereas
silencing C/EBP-β alone resulted in minor effects. To more directly assess IL-13 enhancement on NO induction in activated microglia, NO production was examined by Griess reagents. NO production was detected in LPS-treated cells (Fig. 1B). The combination of IL-13 in LPS showed no effects. These suggested that C/EBP-α could be a factor mediating IL-13-induced PGE2 production and death of activated microglia. IL-13-enhanced apoptotic cell death in activated microglia has been shown to be involved in neurodegenerative disorders [5-7, 12, 13]. Related genes in activated microglia were analyzed to determine whether they were regulated by C/EBP-α and C/EBP-β. LPS significantly increased C/EBP-α and C/EBP-β in primary microglia cells and BV-2 microglia (Fig. 2).