Interleukin-4 regulates connective tissue growth factor expression in human lung fibroblasts

被引:27
作者
Rishikof, DC
Ricupero, DA
Kuang, PP
Liu, HQ
Goldstein, RH
机构
[1] Boston Univ, Sch Med, Ctr Pulm, Boston, MA 02118 USA
[2] Boston VA Med Ctr, Boston, MA 02130 USA
关键词
transforming growth factor-beta; Smad; Stat; fibrosis;
D O I
10.1002/jcb.10144
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transforming growth factor-beta (TGF-beta) and interleukin-4 (IL-4) have fibrogenic properties and induce extracellular matrix production in a variety of lung diseases. Connective tissue growth factor (CTCF) is a matrix signaling molecule stimulated by TGF-beta that in part mediates alpha1 (1) collagen mRNA expression, In these studies, the regulation of CTGF expression by IL-4 in human lung fibroblasts was examined. Following 6 h of stimulation with IL-4 basal CTGF mRNA levels were unchanged as assessed by Northern blot analysis. However, IL-4 attenuated the TGF-beta-stimulated induction of CTGF mRNA expression by 50%. This effect was selective because IL-4 did not affect, fibronectin or alpha1(1) collagen mRNA expression induced by TGF-beta. Experiments employing the transcriptional inhibitor actinomycin D suggest that IL-4 did not affect the stability of the CTGF mRNA. Transient transfection assays with 3TP-Lux, a luciferase gene controlled by a TGF-beta inducible promoter, and with a CTGF promoter construct indicate that IL-4 interfered with the TGF-beta-induced transcriptional activation of the CTCF gene.
引用
收藏
页码:496 / 504
页数:9
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