期刊
MOLECULAR AND CELLULAR ENDOCRINOLOGY
卷 176, 期 1-2, 页码 1-12出版社
ELSEVIER IRELAND LTD
DOI: 10.1016/S0303-7207(01)00484-1
关键词
IGF-1 receptor; interferon-alpha; interferon-gamma; transcription; tumer necrosis factor-alpha
The insulin-like growth factor-I receptor (IGF-1-R) plays a critical role in normal and pathological growth processes. The expression of the IGF-1-R gene is regulated by various stimuli, including hormones and growth factors. We have investigated the molecular mechanisms by which two inhibitory cytokines, tumor necrosis factor-alpha (TNF-alpha) and interferon-gamma (IFN-gamma), regulate IGF-1-R gene expression. TNF-alpha and IFN-gamma reduced the proliferation rates of the osteogenic sarcoma cell line, Saos-2, and the human salivary gland cell line, HSG, in a dose- and time-dependent fashion. This effect was associated with significant reductions in the levels of IGF-I-R mRNA and protein, and with inhibition of IGF-I-R promoter activity, suggesting that TNF-alpha and IFN-gamma affect IGF-I-R gene expression at the transcriptional level. In addition, TNF-alpha significantly decreased IGF-I-R mRNA stability. Combined cytokine treatment inhibited cellular proliferation and promoter activity in an additive manner. Taken together, these results suggest that a novel potential mechanism by which TNF-alpha and IFN-gamma affect cellular proliferation involves suppression of IGF-I-R promoter activity, as well as destabilization of IGF-1-R transcripts. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
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