Integrated mRNA-microRNA profiling of human NK cell differentiation identifies MiR-583 as a negative regulator of IL2Rγ expression.

Natural killer (NK) cells are innate immune effector cells that protect against cancer and some viral infections. Until recently, most studies have investigated the molecular signatures of human or mouse NK cells to identify genes that are specifically expressed during NK cell development. However,...

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Autores principales: Sohyun Yun, Su Ui Lee, Jung Min Kim, Hyun-Jun Lee, Hae Young Song, Young Kyeung Kim, Haiyoung Jung, Young-Jun Park, Suk Ran Yoon, Sei-Ryang Oh, Tae-Don Kim, Inpyo Choi
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Publicado: Public Library of Science (PLoS) 2014
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Acceso en línea:https://doaj.org/article/cd05017aad19401ba29fd2e703d0e7ec
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spelling oai:doaj.org-article:cd05017aad19401ba29fd2e703d0e7ec2021-11-25T05:56:47ZIntegrated mRNA-microRNA profiling of human NK cell differentiation identifies MiR-583 as a negative regulator of IL2Rγ expression.1932-620310.1371/journal.pone.0108913https://doaj.org/article/cd05017aad19401ba29fd2e703d0e7ec2014-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0108913https://doaj.org/toc/1932-6203Natural killer (NK) cells are innate immune effector cells that protect against cancer and some viral infections. Until recently, most studies have investigated the molecular signatures of human or mouse NK cells to identify genes that are specifically expressed during NK cell development. However, the mechanism regulating NK cell development remains unclear. Here, we report a regulatory network of potential interactions during in vitro differentiation of human NK cells, identified using genome-wide mRNA and miRNA databases through hierarchical clustering analysis, gene ontology analysis and a miRNA target prediction program. The microRNA (miR)-583, which demonstrated the largest ratio change in mature NK cells, was highly correlated with IL2 receptor gamma (IL2Rγ) expression. The overexpression of miR-583 had an inhibitory effect on NK cell differentiation. In a reporter assay, the suppressive effect of miR-583 was ablated by mutating the putative miR-583 binding site of the IL2Rγ 3' UTR. Therefore, we show that miR-583 acts as a negative regulator of NK cell differentiation by silencing IL2Rγ. Additionally, we provide a comprehensive database of genome-wide mRNA and miRNA expression during human NK cell differentiation, offering a better understanding of basic human NK cell biology for the application of human NK cells in immunotherapy.Sohyun YunSu Ui LeeJung Min KimHyun-Jun LeeHae Young SongYoung Kyeung KimHaiyoung JungYoung-Jun ParkSuk Ran YoonSei-Ryang OhTae-Don KimInpyo ChoiPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 10, p e108913 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Sohyun Yun
Su Ui Lee
Jung Min Kim
Hyun-Jun Lee
Hae Young Song
Young Kyeung Kim
Haiyoung Jung
Young-Jun Park
Suk Ran Yoon
Sei-Ryang Oh
Tae-Don Kim
Inpyo Choi
Integrated mRNA-microRNA profiling of human NK cell differentiation identifies MiR-583 as a negative regulator of IL2Rγ expression.
description Natural killer (NK) cells are innate immune effector cells that protect against cancer and some viral infections. Until recently, most studies have investigated the molecular signatures of human or mouse NK cells to identify genes that are specifically expressed during NK cell development. However, the mechanism regulating NK cell development remains unclear. Here, we report a regulatory network of potential interactions during in vitro differentiation of human NK cells, identified using genome-wide mRNA and miRNA databases through hierarchical clustering analysis, gene ontology analysis and a miRNA target prediction program. The microRNA (miR)-583, which demonstrated the largest ratio change in mature NK cells, was highly correlated with IL2 receptor gamma (IL2Rγ) expression. The overexpression of miR-583 had an inhibitory effect on NK cell differentiation. In a reporter assay, the suppressive effect of miR-583 was ablated by mutating the putative miR-583 binding site of the IL2Rγ 3' UTR. Therefore, we show that miR-583 acts as a negative regulator of NK cell differentiation by silencing IL2Rγ. Additionally, we provide a comprehensive database of genome-wide mRNA and miRNA expression during human NK cell differentiation, offering a better understanding of basic human NK cell biology for the application of human NK cells in immunotherapy.
format article
author Sohyun Yun
Su Ui Lee
Jung Min Kim
Hyun-Jun Lee
Hae Young Song
Young Kyeung Kim
Haiyoung Jung
Young-Jun Park
Suk Ran Yoon
Sei-Ryang Oh
Tae-Don Kim
Inpyo Choi
author_facet Sohyun Yun
Su Ui Lee
Jung Min Kim
Hyun-Jun Lee
Hae Young Song
Young Kyeung Kim
Haiyoung Jung
Young-Jun Park
Suk Ran Yoon
Sei-Ryang Oh
Tae-Don Kim
Inpyo Choi
author_sort Sohyun Yun
title Integrated mRNA-microRNA profiling of human NK cell differentiation identifies MiR-583 as a negative regulator of IL2Rγ expression.
title_short Integrated mRNA-microRNA profiling of human NK cell differentiation identifies MiR-583 as a negative regulator of IL2Rγ expression.
title_full Integrated mRNA-microRNA profiling of human NK cell differentiation identifies MiR-583 as a negative regulator of IL2Rγ expression.
title_fullStr Integrated mRNA-microRNA profiling of human NK cell differentiation identifies MiR-583 as a negative regulator of IL2Rγ expression.
title_full_unstemmed Integrated mRNA-microRNA profiling of human NK cell differentiation identifies MiR-583 as a negative regulator of IL2Rγ expression.
title_sort integrated mrna-microrna profiling of human nk cell differentiation identifies mir-583 as a negative regulator of il2rγ expression.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/cd05017aad19401ba29fd2e703d0e7ec
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