TY - JOUR
T1 - Differential modulation of astrocyte cytokine gene expression by TGF-β
AU - Benveniste, Etty N.
AU - Kwon, Jongbum
AU - Chung, Wook Joon
AU - Sampson, Jacinda
AU - Pandya, Kumar
AU - Tang, Li Ping
PY - 1994/12/1
Y1 - 1994/12/1
N2 - In this study, we demonstrate that TGF-β inhibits TNF-α expression, and induces/enhances IL-6 expression by primary rat astrocytes. Treatment of astrocytes with TGF-β alone had no effect on TNF-α mRNA or protein expression; however, TGF-β suppressed induction of TNF-α expression by three different stimuli (IFN-γ/LPS, IFN-γ/IL-1β, TNF-α) at both the protein and mRNA level. The extent of TGF-β-mediated inhibition was greatest when astrocytes were pretreated with TGF-β for 6 to 24 h, then exposed to the inducing stimuli. Inhibition of TNF-α mRNA steady-state levels by TGF- β was a result of inhibition of TNF-α gene transcription, rather than degradation of the TNF-α message. In contrast, TGF-β alone induced expression of IL-6 by astrocytes and synergized with two other cytokines, IL- 1β and TNF-α, for enhanced IL-6 expression. TGF-β-induced/enhanced IL-6 expression was mediated by transcriptional activation of the IL-6 gene. These results indicate that TGF-β is an important regulator of cytokine production by astrocytes under inflammatory conditions in the brain.
AB - In this study, we demonstrate that TGF-β inhibits TNF-α expression, and induces/enhances IL-6 expression by primary rat astrocytes. Treatment of astrocytes with TGF-β alone had no effect on TNF-α mRNA or protein expression; however, TGF-β suppressed induction of TNF-α expression by three different stimuli (IFN-γ/LPS, IFN-γ/IL-1β, TNF-α) at both the protein and mRNA level. The extent of TGF-β-mediated inhibition was greatest when astrocytes were pretreated with TGF-β for 6 to 24 h, then exposed to the inducing stimuli. Inhibition of TNF-α mRNA steady-state levels by TGF- β was a result of inhibition of TNF-α gene transcription, rather than degradation of the TNF-α message. In contrast, TGF-β alone induced expression of IL-6 by astrocytes and synergized with two other cytokines, IL- 1β and TNF-α, for enhanced IL-6 expression. TGF-β-induced/enhanced IL-6 expression was mediated by transcriptional activation of the IL-6 gene. These results indicate that TGF-β is an important regulator of cytokine production by astrocytes under inflammatory conditions in the brain.
UR - http://www.scopus.com/inward/record.url?scp=0028073808&partnerID=8YFLogxK
M3 - Article
C2 - 7963576
AN - SCOPUS:0028073808
SN - 0022-1767
VL - 153
SP - 5210
EP - 5221
JO - Journal of Immunology
JF - Journal of Immunology
IS - 11
ER -