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首页> 外文期刊>FEBS letters. >Divergent intracellular pathways regulate interleukin-1beta-induced miR-146a and miR-146b expression and chemokine release in human alveolar epithelial cells.
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Divergent intracellular pathways regulate interleukin-1beta-induced miR-146a and miR-146b expression and chemokine release in human alveolar epithelial cells.

机译:不同的细胞内途径调节人肺泡上皮细胞中白介素-1β诱导的miR-146a和miR-146b表达以及趋化因子释放。

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摘要

We have previously reported that IL-beta-induced miR-146a and miR-146b expression negatively regulates IL-8 and RANTES release in human alveolar A549 epithelial cells. To determine the intracellular pathways that regulate this response, we demonstrate IL-1beta-induced activation of the nuclear factor (NF)-kappaB, extracellular regulated kinase (ERK)-1/2, c-jun N-terminal kinase (JNK)-1/2 and p38 mitogen activated kinase (MAP) kinase pathways. Subsequent pharmacological studies show that IL-1beta-induced miR-146a, IL-8 and RANTES production was regulated via NF-kappaB and JNK-1/2 whilst miR-146b expression was mediated via MEK-1/2 and JNK-1/2. These divergent intracellular pathways likely explain the differential expression and biological action of the miR-146 isoforms.
机译:我们以前曾报道过,IL-β诱导的miR-146a和miR-146b表达负面调节人肺泡A549上皮细胞中的IL-8和RANTES释放。为了确定调节这种应答的细胞内途径,我们证明了IL-1beta诱导的核因子(NF)-kappaB,细胞外调节激酶(ERK)-1 / 2,c-jun N末端激酶(JNK)-的激活1/2和p38丝裂原活化激酶(MAP)激酶途径。随后的药理研究表明,IL-1beta诱导的miR-146a,IL-8和RANTES的产生是通过NF-kappaB和JNK-1 / 2来调节的,而miR-146b的表达是通过MEK-1 / 2和JNK-1 / 2。这些不同的细胞内途径可能解释了miR-146同工型的差异表达和生物学作用。

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