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Identification of the novel 3′ UTR sequences of human IL-21 mRNA as potential targets of miRNAs
Hepatitis B virus (HBV) infection is a leading cause of hepatocellular carcinoma worldwide. However, the strategy of HBV to escape from the host immune system remains largely unknown. In this study, we examined extracellular vesicles (EVs) secreted from human hepatocytes infected with HBV. EVs inclu...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552845/ https://www.ncbi.nlm.nih.gov/pubmed/28798470 http://dx.doi.org/10.1038/s41598-017-07853-x |
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author | Enomoto, Yutaka Takagi, Rie Naito, Yutaka Kiniwa, Tsuyoshi Tanaka, Yasuhito Hamada-Tsutsumi, Susumu Kawano, Masaaki Matsushita, Sho Ochiya, Takahiro Miyajima, Atsushi |
author_facet | Enomoto, Yutaka Takagi, Rie Naito, Yutaka Kiniwa, Tsuyoshi Tanaka, Yasuhito Hamada-Tsutsumi, Susumu Kawano, Masaaki Matsushita, Sho Ochiya, Takahiro Miyajima, Atsushi |
author_sort | Enomoto, Yutaka |
collection | PubMed |
description | Hepatitis B virus (HBV) infection is a leading cause of hepatocellular carcinoma worldwide. However, the strategy of HBV to escape from the host immune system remains largely unknown. In this study, we examined extracellular vesicles (EVs) secreted from human hepatocytes infected with HBV. EVs includeing exosomes are nano-size vesicles with proteins, mRNAs, and microRNAs (miRNAs), which can be transmitted to different cells. We found that 104 EV associated miRNAs were increased in hepatocytes more than 2-fold by HBV infection. We then selected those that were potentially implicated in immune regulation. Among them, five HBV-induced miRNAs were found to potentially target multiple sequences in the 3′UTR of IL-21, a cytokine that induces anti-viral immunity. Moreover, expression of a reporter gene with the 3′ UTR of human IL-21 mRNA was suppressed by the five miRNAs individually. Finally, IL-21 expression in cloned human T cells was down-regulated by the five miRNAs. Collectively, this study identified the novel 3′ UTR sequences of human IL-21 mRNA and potential binding sites of HBV-induced EV-miRNAs. |
format | Online Article Text |
id | pubmed-5552845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55528452017-08-14 Identification of the novel 3′ UTR sequences of human IL-21 mRNA as potential targets of miRNAs Enomoto, Yutaka Takagi, Rie Naito, Yutaka Kiniwa, Tsuyoshi Tanaka, Yasuhito Hamada-Tsutsumi, Susumu Kawano, Masaaki Matsushita, Sho Ochiya, Takahiro Miyajima, Atsushi Sci Rep Article Hepatitis B virus (HBV) infection is a leading cause of hepatocellular carcinoma worldwide. However, the strategy of HBV to escape from the host immune system remains largely unknown. In this study, we examined extracellular vesicles (EVs) secreted from human hepatocytes infected with HBV. EVs includeing exosomes are nano-size vesicles with proteins, mRNAs, and microRNAs (miRNAs), which can be transmitted to different cells. We found that 104 EV associated miRNAs were increased in hepatocytes more than 2-fold by HBV infection. We then selected those that were potentially implicated in immune regulation. Among them, five HBV-induced miRNAs were found to potentially target multiple sequences in the 3′UTR of IL-21, a cytokine that induces anti-viral immunity. Moreover, expression of a reporter gene with the 3′ UTR of human IL-21 mRNA was suppressed by the five miRNAs individually. Finally, IL-21 expression in cloned human T cells was down-regulated by the five miRNAs. Collectively, this study identified the novel 3′ UTR sequences of human IL-21 mRNA and potential binding sites of HBV-induced EV-miRNAs. Nature Publishing Group UK 2017-08-10 /pmc/articles/PMC5552845/ /pubmed/28798470 http://dx.doi.org/10.1038/s41598-017-07853-x Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Enomoto, Yutaka Takagi, Rie Naito, Yutaka Kiniwa, Tsuyoshi Tanaka, Yasuhito Hamada-Tsutsumi, Susumu Kawano, Masaaki Matsushita, Sho Ochiya, Takahiro Miyajima, Atsushi Identification of the novel 3′ UTR sequences of human IL-21 mRNA as potential targets of miRNAs |
title | Identification of the novel 3′ UTR sequences of human IL-21 mRNA as potential targets of miRNAs |
title_full | Identification of the novel 3′ UTR sequences of human IL-21 mRNA as potential targets of miRNAs |
title_fullStr | Identification of the novel 3′ UTR sequences of human IL-21 mRNA as potential targets of miRNAs |
title_full_unstemmed | Identification of the novel 3′ UTR sequences of human IL-21 mRNA as potential targets of miRNAs |
title_short | Identification of the novel 3′ UTR sequences of human IL-21 mRNA as potential targets of miRNAs |
title_sort | identification of the novel 3′ utr sequences of human il-21 mrna as potential targets of mirnas |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552845/ https://www.ncbi.nlm.nih.gov/pubmed/28798470 http://dx.doi.org/10.1038/s41598-017-07853-x |
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