激活树突状细胞中的Notch靶点需要TLR和Dectin-1/Syk信号的参与

IF 2 Q3 INFECTIOUS DISEASES
Yuna Zhao, Chanyang Ju, K. Au, Jimmy Zhu, Baohong Zhao, Y. Shang, Xiaoyu Hu
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引用次数: 0

摘要

补充数字内容可在文本中获得摘要模式识别受体,如toll样受体(TLRs),检测广泛的微生物产物并启动先天免疫反应,从而产生炎症介质。此外,TLR信号传导还激活Notch靶基因的表达,这些基因在抑制TLR引发的炎症反应中起着至关重要的作用。然而,其他类型的模式识别受体参与的TLR信号通路是否诱导Notch靶基因的表达仍不清楚。在这里,我们证明酵母多糖,TLR2和dectin-1的刺激物,在人类和小鼠树突状细胞中强烈诱导多个Notch靶基因的表达。从机制上讲,酵母多糖对Notch靶点的诱导是TLR2-和Syk依赖性的,通过激活促分裂原活化的蛋白激酶和转录因子c-Fos。因此,我们的数据揭示了一种新的机制,即Notch靶基因的有效诱导需要TLR和dectin-1/Syk信号通路的参与。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Engagement of TLR and Dectin-1/Syk Signaling Is Required for Activation of Notch Targets in Dendritic Cells
Supplemental Digital Content is available in the text Abstract Pattern-recognition receptors, such as toll-like receptors (TLRs), detect a wide range of microbial products and initiate innate immune responses leading to the production of inflammatory mediators. In addition, TLR signaling also activates expression of Notch target genes that play crucial roles in suppression of TLR-triggered inflammatory responses. However, whether TLR signaling pathways engaged by other classes of pattern-recognition receptors induce expression of Notch target genes remains unclear. Here we demonstrate that zymosan, a stimulus for TLR2 and dectin-1, strongly induces expression of multiple Notch target genes in both human and murine dendritic cells. Mechanistically, induction of Notch targets by zymosan is both TLR2- and Syk-dependent through activation of mitogen-activated protein kinases and the transcription factor c-Fos. Hence, our data reveals a novel mechanism that efficient induction of Notch target genes requires engagement of TLR and dectin-1/Syk signaling pathways.
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