## Abstract In recent studies, treatment with IL‐1β of cultured Caco‐2 cells, a human intestinal epithelial cell line, resulted in transcriptional upregulation of IL‐6 production. The role of C/EBP‐β and ‐δ in enterocyte IL‐6 production is not known. Stimulation with IL‐1β of Caco‐2 cells transient
Pro-inflammatory cytokines induce the transcription factors C/EBPβ and C/EBPδ in astrocytes
✍ Scribed by Jean-René Cardinaux; Igor Allaman; Pierre J. Magistretti
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 178 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0894-1491
No coin nor oath required. For personal study only.
✦ Synopsis
The transcription factors CCAAT/enhancer binding protein (C/EBP)- and -␦ are key regulators for the expression of the acute phase genes in the liver, such as complement component C3 and antichymotrypsin. In the brain, these acute phase proteins are produced in response to pro-inflammatory cytokines by the reactive astrocytes, in particular those surrounding the amyloid plaques of Alzheimer's disease brains. Here we show that lipopolysaccharides (LPS), IL-1, and TNF␣ induce the expression of the c/ebp and -␦ genes in mouse primary astrocytes. This induction precedes the expression of the acute phase genes coding for the complement component C3 and the mouse homologue of antichymotrypsin. The induction of these two acute phase genes by LPS is blocked by cycloheximide, whereas this protein synthesis inhibitor does not affect the expression of the c/ebp genes. Altogether, our data support a role as immediate-early genes for c/ebp and -␦, whose expression is induced by proinflammatory cytokines in mouse cortical astrocytes. In the liver, these transcription factors are known to play an important role in inflammation and energy metabolism regulation. Therefore, C/EBP and -␦ could be pivotal transcription factors involved in brain inflammation, in addition to their previously demonstrated role in brain glycogen metabolism regulation (Cardinaux and Magistretti.
📜 SIMILAR VOLUMES
## Abstract Transcription of the HIV‐1 genome is a complex event that requires functional and physical communication of cellular proteins that recognize the LTR sequence with viral proteins, most notably, Tat. Moreover, studies have revealed the ability of Tat to induce transcription of a variety o
Previous analyses of the mechanism of the transcriptional induction of the rat haptoglobin (Hp) gene during acute-phase (AP)-reaction have revealed the involvement of several trans-acting nucleoproteins (NPs) in controlling this process. In this study, by using antibodies against C/EBPbeta factor in
## Abstract Signal transducer and activator of transcription 3 (STAT3) was reported to be involved in adipogenesis. However, the regulating mechanism of STAT3 remains unclear. The present results showed that STAT3 was activated within 2‐h adipogenic induction, in which the phosphorylated STAT3 tran
## Abstract The G~0~ growth arrest (quiescent) state is highly conserved in evolution to promote survival under adverse environmental conditions. To maintain viability, G~0~ growth arrested cells limit gene expression to essential growth control and pro‐survival genes. CCAAT enhancer binding protei