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c-Myc 在调控抗分枝杆菌反应中的作用。

A role for c-Myc in regulating anti-mycobacterial responses.

机构信息

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.

出版信息

Proc Natl Acad Sci U S A. 2011 Oct 25;108(43):17749-54. doi: 10.1073/pnas.1104892108. Epub 2011 Oct 12.

Abstract

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.

摘要

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。

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