State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, Department of Infectious Diseases, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang 310003, China.
FEBS Lett. 2012 Jul 30;586(16):2459-67. doi: 10.1016/j.febslet.2012.06.004. Epub 2012 Jun 16.
miR-21 has been shown to regulate multiple mRNAs and cause tumor progression and metastasis. However, whether miR-21-mediated posttranscriptional regulation is involved in antigen presentation and anti-mycobacterial responses remains unclear. Here, we report that miR-21 can be induced after Bacillus Calmette-Guerin (BCG) vaccination by NF-kB activation. miR-21 suppressed IL-12 production by targeting IL-12p35, which impaired anti-mycobacterial T cell responses both in vitro and in vivo. Additionally, miR-21 also promoted dendritic cell (DC) apoptosis by targeting Bcl-2. Therefore, miR-21 may potentially be involved in fine-tuning of the anti-mycobacterial Th1 response and in regulating the efficacy of BCG vaccination.
miR-21 已被证明可以调节多个 mRNA,并导致肿瘤的进展和转移。然而,miR-21 介导的转录后调控是否参与抗原呈递和抗分枝杆菌反应尚不清楚。在这里,我们报告说,NF-kB 的激活可以诱导卡介苗(BCG)接种后的 miR-21。miR-21 通过靶向 IL-12p35 抑制 IL-12 的产生,从而损害了体外和体内的抗分枝杆菌 T 细胞反应。此外,miR-21 还通过靶向 Bcl-2 促进树突状细胞(DC)凋亡。因此,miR-21 可能参与微调抗分枝杆菌 Th1 反应,并调节 BCG 接种的效果。