IL-32-PAR2 axis is an innate immunity sensor providing alternative signaling for LPS-TRIF axis.

IL-32-PAR2 axis is an innate immunity sensor providing alternative signaling for LPS-TRIF axis.
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IL-32-PAR2轴是一种先天免疫传感器,为LPS-TRIF轴提供了替代信号。

DOI:
10.1038/srep02960
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发表时间:
2013-10-16
期刊:
影响因子:
4.6
通讯作者:
Miyamoto, Takeshi
Miyamoto, Takeshi
中科院分区:
综合性期刊3区
文献类型:
--
作者:
Nakayama, Masanori;Niki, Yasuo;Kawasaki, Toshiki;Takeda, Yuki;Ikegami, Hiroyasu;Toyama, Yoshiaki;Miyamoto, Takeshi

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白细胞介素(IL)-32对先天性免疫应答具有明显的促进作用,但其受体和下游信号通路尚不清楚。我们发现IL-32γ上调蛋白酶-3(PR 3)的丝氨酸蛋白酶活性,进而触发蛋白酶激活受体2(PAR 2)信号传导。有趣的是,使用siRNA沉默PR 3或PAR 2显著降低IL-32γ诱导的TNFα和IFN-β mRNA表达。IL-32γ-PAR 2轴利用TRIF和Ras-Raf-1途径。在脂多糖(LPS)刺激下,蛋白激酶C亚型的差异活化调节LPS-TLR 4-TRIF和IL-32-PAR 2-TRIF轴之间的平衡,因为LPS是IL-32γ的强诱导剂。IL-32-PAR 2-TRIF轴不仅是细菌和自体蛋白酶的细胞外传感器,而且在感染过程中也是先天性和适应性免疫的调节剂。
Interleukin (IL)-32 is known to exert adujvant effects on innate immune response, however, receptors and downstream signaling pathways remain to be clarified. Here we found that IL-32γ upregulated serine protease activity of proteinase-3 (PR3), in turn triggering protease-activated receptor 2 (PAR2) signaling. Interestingly, silencing of PR3 or PAR2 using siRNA markedly diminished IL-32γ-induced TNFα and IFN-β mRNA expression. IL-32γ-PAR2 axis utilized TRIF and Ras-Raf-1 pathways. On stimulation with lipopolysaccharide (LPS), differential activation of protein kinase C isoforms modulated the balance between LPS-TLR4-TRIF and IL-32-PAR2-TRIF axes, because LPS was a strong inducer of IL-32γ. IL-32-PAR2-TRIF axis might serve not only as an extracellular sensor of bacterial and autologous proteases, but also as a modulator of innate and adaptive immunity during infection.
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