Early stage of cytomegalovirus infection suppresses host microRNA expression regulation in human fibroblasts

被引:11
作者
Buzdin, Anton A. [1 ,2 ,3 ]
Artcibasova, Alina V. [1 ,4 ]
Fedorova, Natalya F. [5 ]
Suntsova, Maria V. [1 ,2 ]
Garazha, Andrew V. [1 ,6 ]
Sorokin, Maxim I. [7 ]
Allina, Daria [6 ,7 ]
Shalatonin, Mikhail [8 ]
Borisov, Nikolay M. [3 ,7 ]
Zhavoronkov, Alex A. [1 ,4 ]
Kovalchuk, Igor [9 ]
Kovalchuk, Olga [9 ]
Kushch, Alla A. [5 ]
机构
[1] D Rogachyov Fed Res Ctr Pediat Hematol Oncol & Im, Lab Bioinformat, Moscow, Russia
[2] Shemyakin Ovchinnikov Inst Bioorgan Chem, Grp Genom Regulat Cell Signaling Syst, Moscow, Russia
[3] Natl Res Ctr Kurchatov Inst, Ctr Convergence Nano Bio Informat & Cognit Sci &, Moscow, Russia
[4] Pathway Pharmaceut, Hong Kong, Hong Kong, Peoples R China
[5] Minist Hlth Russian Federat, NF Gamaleya Fed Res Ctr Epidemiol & Microbiol, Moscow, Russia
[6] Moscow Inst Phys & Technol, Dolgoprudnyi, Moscow Region, Russia
[7] First Oncol Res & Advisory Ctr, Moscow, Russia
[8] Morozov Childrens City Hosp, Moscow, Russia
[9] Univ Lethbridge, Dept Biol Sci, Lethbridge, AB, Canada
关键词
Cytomegalovirus infection; gene transcription; human fibroblasts; intracellular signaling pathway regulation; microRNA; total miRNAome; SIGNALING PATHWAY ACTIVATION; HUMAN BLADDER-CANCER; CELLS; RNAS; TRANSCRIPTION; DISEASE; MODELS; AGE;
D O I
10.1080/15384101.2016.1241928
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Responses to human cytomegalovirus (HCMV) infection are largely individual and cell type specific. We investigated molecular profiles in 2 primary cell cultures of human fibroblasts, which are highly or marginally sensitive to HCMV infection, respectively. We screened expression of genes and microRNAs (miRs) at the early (3 hours) stage of infection. To assess molecular pathway activation profiles, we applied bioinformatic algorithms OncoFinder and MiRImpact. In both cell types, pathway regulation properties at mRNA and miR levels were markedly different. Surprisingly, in the infected highly sensitive cells, we observed a "freeze" of miR expression profiles compared to uninfected controls. Our results evidence that in the sensitive cells, HCMV blocks intracellular regulation of microRNA expression already at the earliest stage of infection. These data suggest somewhat new functions for HCMV products and demonstrate dependence of miR expression arrest on the host-encoded factors.
引用
收藏
页码:3378 / 3389
页数:12
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