کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1937609 1050721 2007 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Enhanced IL-1β-induced IL-8 production in cystic fibrosis lung epithelial cells is dependent of both mitogen-activated protein kinases and NF-κB signaling
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Enhanced IL-1β-induced IL-8 production in cystic fibrosis lung epithelial cells is dependent of both mitogen-activated protein kinases and NF-κB signaling
چکیده انگلیسی

Transcription nuclear factor-κB (NF-κB) is hyperactivated in cystic fibrosis (CF) lung epithelial cells, and participates in exaggerated IL-8 production in the CF lung. We recently found that rapid activation of NF-κB occurred in a CF lung epithelial IB3-1 cell line (CF cells) upon IL-1β stimulation, which was not observed in its CFTR-corrected lung epithelial S9 cell line (corrected cells). To test whether other signaling pathways such as that of mitogen-activated protein kinases (MAPKs) could be involved in IL-1β-induced IL-8 production of CF cells, we investigated ERK1/2, JNK, and p38MAP signaling compared to NF-κB. Within 30 min, exposure to IL-1β caused high activation of NF-κB, ERK1/2, p38MAP but not JNK in CF cells compared to corrected cells. Treatment of IL-1β-stimulated CF cells with a series of chemical inhibitors of NF-κB, ERK1/2, and p38MAP, when used separately, reduced slightly IL-8 production. However, when used together, these inhibitors caused a blockade in IL-1β-induced IL-8 production in CF cells. Understanding of the cross-talk between NF-κB and MAPKs signaling in CF lung epithelial cells may help in developing new therapeutics to reduce lung inflammation in patients with CF.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochemical and Biophysical Research Communications - Volume 357, Issue 2, 1 June 2007, Pages 402–407
نویسندگان
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