Qu Shuo-Yao, Lin Jia-Ji, Zhang Jian, Song Li-Qiang, Yang Xue-Min, Wu Chang-Gui
Department of Pulmonary and Critical Care Medicine, Xijing Hospital, Fourth Military Medical University, China.
Department of Neurology, Tangdu Hospital, Fourth Military Medical University, China.
Cell Immunol. 2017 Aug;318:29-34. doi: 10.1016/j.cellimm.2017.05.005. Epub 2017 May 27.
Basophils (BAs) are the least common granulocytes of all leukocytes, but they play an important role in orchestrating of chronic allergic inflammation. The Notch signaling pathway is a highly conserved pathway that influences cell lineage decisions and differentiation during various stages of development. However, the relationship between Notch signaling and BA remains to be elucidate. Here, we report that several Notch signaling molecules were found to be expressed in BAs. γ-secretase inhibitor (GSI) treatment increase BAs apoptosis, and suppress BAs proliferation. Furthermore, GSI reduced BAs in the S phase, with a concomitant accumulation in G1 and G2 phases. In addition, GSI also significantly down-regulated mRNA levels of cytokines IL-4, IL-6 and IL-13 induced by A23187, and this effect was dependent on MAPK pathway. Finally, IL-6 inhibition was specifically associated with ERK and IL-13 with JNK. Therefore, Notch signaling regulates BA biological function, at least partially via the modulation of MAPK.
嗜碱性粒细胞(BAs)是所有白细胞中最不常见的粒细胞,但它们在协调慢性过敏性炎症中发挥着重要作用。Notch信号通路是一条高度保守的通路,在发育的各个阶段影响细胞谱系决定和分化。然而,Notch信号与嗜碱性粒细胞之间的关系仍有待阐明。在此,我们报告发现几种Notch信号分子在嗜碱性粒细胞中表达。γ-分泌酶抑制剂(GSI)处理可增加嗜碱性粒细胞凋亡,并抑制嗜碱性粒细胞增殖。此外,GSI使处于S期的嗜碱性粒细胞减少,同时G1期和G2期细胞蓄积。另外,GSI还显著下调了由A23187诱导的细胞因子IL-4、IL-6和IL-13的mRNA水平,且这种作用依赖于丝裂原活化蛋白激酶(MAPK)通路。最后,IL-6的抑制与细胞外信号调节激酶(ERK)特异性相关,而IL-13的抑制与应激活化蛋白激酶(JNK)相关。因此,Notch信号至少部分通过调节MAPK来调控嗜碱性粒细胞的生物学功能。