Allergy and Clinical Immunology Branch, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Centers for Disease Control and Prevention, Morgantown, WV 26505-2888, USA.
Virology. 2013 Dec;447(1-2):84-94. doi: 10.1016/j.virol.2013.08.031. Epub 2013 Sep 20.
Understanding the host response to influenza A virus infection is essential for developing intervention approaches. We show that infection of human alveolar epithelial cells and human bronchial epithelial cells with influenza A for 3h resulted in down-regulation of host hsa-miRNA-548an (miRNA-548an) which triggered the overexpression of influenza non-structural-1A binding protein (IVNS1ABP, herein referred to as NS1ABP). Reduced NS1ABP mRNA and NS1ABP protein expression after transfection of miRNA-548an mimic or increased NS1ABP mRNA and NS1ABP protein expression after transfection of miRNA-548an inhibitor provided evidence that miRNA-548an is involved in the regulation of NS1ABP. Transfection of cells with inhibitor led to reduced apoptosis of infected cells while transfection of mimic led to increased apoptosis and reduced influenza copy number suggesting that NS1ABP has a role in viral maintenance. Thus, miRNA-548an may be an important target in controlling the early stage infection of influenza A.
了解宿主对甲型流感病毒感染的反应对于开发干预措施至关重要。我们表明,甲型流感病毒感染人肺泡上皮细胞和人支气管上皮细胞 3 小时后,宿主 hsa-miRNA-548an(miRNA-548an)下调,导致流感非结构蛋白 1A 结合蛋白(IVNS1ABP,以下简称 NS1ABP)过表达。miRNA-548an 模拟物转染后 NS1ABP mRNA 和 NS1ABP 蛋白表达减少,miRNA-548an 抑制剂转染后 NS1ABP mRNA 和 NS1ABP 蛋白表达增加,这表明 miRNA-548an 参与了 NS1ABP 的调节。抑制剂转染细胞导致感染细胞凋亡减少,而模拟物转染导致凋亡增加和流感拷贝数减少,表明 NS1ABP 在病毒维持中起作用。因此,miRNA-548an 可能是控制甲型流感早期感染的重要靶标。