Cytokine Biology Group, Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong SAR, China.
Proc Natl Acad Sci U S A. 2011 Oct 25;108(43):17749-54. doi: 10.1073/pnas.1104892108. Epub 2011 Oct 12.
c-Myc (Myc) is a well known transcription factor that regulates many essential cellular processes; however, its role in modulating immunity is not known. Here, we showed different species of mycobacteria can induce Myc expression via ERK1/2 and JNK activation. Unexpectedly, the induced Myc is localized in the cytoplasm but not in the nucleus. This induced Myc expression is associated with the induction of TNF-α and IL-6 and with the suppression of intracellular mycobacterial growth. To delineate the underlying mechanisms, we demonstrated that Myc enhances IRAK1 degradation, leading to specific activations of ERK1/2 and p38 MAPK but not Akt, and reduces IκBα protein recovery upon degradation. Hence, our findings may provide insights into a potential role for Myc in regulating the antimicrobial responses.
c-Myc(Myc)是一种众所周知的转录因子,可调节许多基本的细胞过程;但是,其在调节免疫中的作用尚不清楚。在这里,我们表明不同种属的分枝杆菌可以通过 ERK1/2 和 JNK 的激活来诱导 Myc 的表达。出乎意料的是,诱导的 Myc 定位于细胞质中而不是细胞核中。这种诱导的 Myc 表达与 TNF-α和 IL-6 的诱导以及细胞内分枝杆菌生长的抑制有关。为了阐明潜在的机制,我们证明 Myc 增强了 IRAK1 的降解,从而特异性地激活了 ERK1/2 和 p38 MAPK,但不激活 Akt,并减少了降解后 IκBα 蛋白的恢复。因此,我们的发现可能为 Myc 在调节抗菌反应中的潜在作用提供了新的见解。