Kuo Cheng-Chin, Lin Wen-Ting, Liang Chi-Ming, Liang Shu-Mei
Institute of BioAgricultural Sciences, Academia Sinica, 128 Academia Road Section 2, Taipei, Taiwan.
J Immunol. 2006 May 15;176(10):5943-9. doi: 10.4049/jimmunol.176.10.5943.
PI3K involvement has been implicated in the TLR signal pathway. However, the precise roles of the different classes of PI3K in the pathway remain elusive. In this study, we have explored the functions of class I and class III PI3K in the TLR signal pathway using specific kinase mutants and PI3K lipid products. Our results reveal that class III PI3K specifically regulates CpG oligodeoxynucleotide (ODN)-induced cytokine and NO production as well as NF-kappaB activation, whereas class I PI3K regulates both CpG ODN- and LPS-induced IL-12 production and NF-kappaB activation. Additional studies of CpG ODN uptake with flow cytometric analysis show that class III PI3K, but not class I, regulates cellular CpG ODN uptake. Furthermore, experiments with MyD88-overexpressing fibroblast cells transfected with dominant-negative mutants of PI3K demonstrate that class III PI3K regulates CpG ODN-mediated signaling upstream of MyD88, while class I PI3K regulation is downstream of MyD88. These results suggest that class I and class III PI3K play distinct roles in not only the uptake of CpG ODN, but also responses elicited by CpG ODN and LPS.
PI3K参与了TLR信号通路。然而,不同类别的PI3K在该通路中的具体作用仍不清楚。在本研究中,我们使用特异性激酶突变体和PI3K脂质产物探索了I类和III类PI3K在TLR信号通路中的功能。我们的结果表明,III类PI3K特异性调节CpG寡脱氧核苷酸(ODN)诱导的细胞因子和NO产生以及NF-κB激活,而I类PI3K调节CpG ODN和LPS诱导的IL-12产生和NF-κB激活。通过流式细胞术分析对CpG ODN摄取的进一步研究表明,III类PI3K而非I类PI3K调节细胞对CpG ODN的摄取。此外,用PI3K显性负性突变体转染的过表达MyD88的成纤维细胞进行的实验表明,III类PI3K在MyD88上游调节CpG ODN介导的信号传导,而I类PI3K的调节在MyD88下游。这些结果表明,I类和III类PI3K不仅在CpG ODN的摄取中,而且在CpG ODN和LPS引发的反应中都发挥着不同的作用。