Michaux Hélène, Halouani Aymen, Trussart Charlotte, Renard Chantal, Jaïdane Hela, Martens Henri, Geenen Vincent, Hober Didier
GIGA-I3 Center of Immunoendocrinology, GIGA Research Institute, University of Liège, 4000 Liège, Belgium.
Laboratoire des Maladies Transmissibles et Substances Biologiquement Actives LR99ES27, Université de Monastir, 5000 Monastir, Tunisia.
Microorganisms. 2021 Feb 15;9(2):402. doi: 10.3390/microorganisms9020402.
Coxsackievirus B4 (CV-B4) can infect human and murine thymic epithelial cells (TECs). In a murine TEC cell line, CV-B4 can downregulate the transcription of the insulin-like growth factor 2 () gene coding for the self-peptide of the insulin family. In this study, we show that CV-B4 infections of a murine TEC cell line decreased P3 promoter activity by targeting a region near the transcription start site; however, the stability of transcripts remained unchanged, indicating a regulation of transcription. Furthermore, CV-B4 infections decreased STAT3 phosphorylation in vitro. We also showed that mice infected with CV-B4 had an altered expression of isoforms as detected in TECs, followed by a decrease in the pro-IGF2 precursor in the thymus. Our study sheds new light on the intrathymic regulation of transcription during CV-B4 infections and supports the hypothesis that a viral infection can disrupt central self-tolerance to insulin by decreasing transcription in the thymic epithelium.
柯萨奇病毒B4(CV - B4)可感染人和小鼠的胸腺上皮细胞(TECs)。在小鼠TEC细胞系中,CV - B4可下调编码胰岛素家族自身肽的胰岛素样生长因子2(IGF2)基因的转录。在本研究中,我们发现CV - B4感染小鼠TEC细胞系通过靶向转录起始位点附近的区域降低了IGF2 P3启动子活性;然而,IGF2转录本的稳定性保持不变,表明存在对IGF2转录的调控。此外,CV - B4感染在体外降低了STAT3磷酸化。我们还表明,感染CV - B4的小鼠在TECs中检测到的IGF2亚型表达发生改变,随后胸腺中前IGF2前体减少。我们的研究为CV - B4感染期间胸腺内IGF2转录调控提供了新的见解,并支持病毒感染可通过降低胸腺上皮细胞中IGF2转录来破坏对胰岛素的中枢自身耐受这一假说。