Aqil Madeeha, Mallik Saurav, Bandyopadhyay Sanghamitra, Maulik Ujjwal, Jameel Shahid
Virology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi 110067, India ; Department of Oral Medicine and Diagnostic Sciences, College of Dentistry, University of Illinois at Chicago, Chicago, IL 60612, USA.
Machine Intelligence Unit, Indian Statistical Institute, Kolkata 700108, India.
Biomed Res Int. 2015;2015:492395. doi: 10.1155/2015/492395. Epub 2015 Apr 15.
The Nef protein of human immunodeficiency virus (HIV) promotes viral replication and progression to AIDS. Besides its well-studied effects on intracellular signaling, Nef also functions through its secretion in exosomes, which are nanovesicles containing proteins, microRNAs, and mRNAs and are important for intercellular communication. Nef expression enhances exosome secretion and these exosomes can enter uninfected CD4 T cells leading to apoptotic death. We have recently reported the first miRNome analysis of exosomes secreted from Nef-expressing U937monocytic cells. Here we show genome-wide transcriptome analysis of Nef-expressing U937 cells and their exosomes. We identified four key mRNAs preferentially retained in Nef-expressing cells; these code for MECP2, HMOX1, AARSD1, and ATF2 and are important for chromatin modification and gene expression. Interestingly, their target miRNAs are exported out in exosomes. We also identified three key mRNAs selectively secreted in exosomes from Nef-expressing U937 cells and their corresponding miRNAs being preferentially retained in cells. These are AATK, SLC27A1, and CDKAL and are important in apoptosis and fatty acid transport. Thus, our study identifies selectively expressed mRNAs in Nef-expressing U937 cells and their exosomes and supports a new mode on intercellular regulation by the HIV-1 Nef protein.
人类免疫缺陷病毒(HIV)的Nef蛋白可促进病毒复制及病情发展至艾滋病。除了其对细胞内信号传导的深入研究作用外,Nef还通过其在外泌体中的分泌发挥功能,外泌体是包含蛋白质、微小RNA和信使RNA的纳米囊泡,对细胞间通讯很重要。Nef表达增强外泌体分泌,这些外泌体可进入未感染的CD4 T细胞导致凋亡死亡。我们最近报道了对表达Nef的U937单核细胞分泌的外泌体进行的首次微小RNA组分析。在此我们展示了对表达Nef的U937细胞及其外泌体的全基因组转录组分析。我们鉴定出四个优先保留在表达Nef的细胞中的关键信使RNA;它们编码MECP2、HMOX1、AARSD1和ATF2,对染色质修饰和基因表达很重要。有趣的是,它们的靶微小RNA被输出到外泌体中。我们还鉴定出三个在表达Nef的U937细胞的外泌体中选择性分泌的关键信使RNA及其相应的微小RNA优先保留在细胞中。这些是AATK、SLC27A1和CDKAL,在细胞凋亡和脂肪酸转运中很重要。因此,我们的研究鉴定了表达Nef的U937细胞及其外泌体中选择性表达的信使RNA,并支持了HIV-1 Nef蛋白细胞间调节的新模式。