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Regulation of T cell proliferation by JMJD6 and PDGF-BB during chronic hepatitis B infection
T cell functional exhaustion during chronic hepatitis B virus (HBV) infection may contribute to the failed viral clearance; however, the underlying molecular mechanisms remain largely unknown. Here we demonstrate that jumonji domain-containing protein 6 (JMJD6) is a potential regulator of T cell pro...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163673/ https://www.ncbi.nlm.nih.gov/pubmed/25219359 http://dx.doi.org/10.1038/srep06359 |
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author | Chen, Cai-Feng Feng, Xia Liao, Hui-Yu Jin, Wen-Jing Zhang, Jian Wang, Yu Gong, Lu-Lu Liu, Jing-Jun Yuan, Xiao-Hui Zhao, Bin-Bin Zhang, Ding Chen, Guo-Feng Wan, Ying Guo, Jian Yan, Hui-Ping He, You-Wen |
author_facet | Chen, Cai-Feng Feng, Xia Liao, Hui-Yu Jin, Wen-Jing Zhang, Jian Wang, Yu Gong, Lu-Lu Liu, Jing-Jun Yuan, Xiao-Hui Zhao, Bin-Bin Zhang, Ding Chen, Guo-Feng Wan, Ying Guo, Jian Yan, Hui-Ping He, You-Wen |
author_sort | Chen, Cai-Feng |
collection | PubMed |
description | T cell functional exhaustion during chronic hepatitis B virus (HBV) infection may contribute to the failed viral clearance; however, the underlying molecular mechanisms remain largely unknown. Here we demonstrate that jumonji domain-containing protein 6 (JMJD6) is a potential regulator of T cell proliferation during chronic HBV infection. The expression of JMJD6 was reduced in T lymphocytes in chronic hepatitis B (CHB) patients, and this reduction in JMJD6 expression was associated with impaired T cell proliferation. Moreover, silencing JMJD6 expression in primary human T cells impaired T cell proliferation. We found that JMJD6 promotes T cell proliferation by suppressing the mRNA expression of CDKN3. Furthermore, we have identified platelet derived growth factor-BB (PDGF-BB) as a regulator of JMJD6 expression. PDGF-BB downregulates JMJD6 expression and inhibits the proliferation of human primary T cells. Importantly, the expression levels of JMJD6 and PDGF-BB in lymphocytes from CHB patients were correlated with the degree of liver damage and the outcome of chronic HBV infection treatment. Our results demonstrate that PDGF-BB and JMJD6 regulate T cell function during chronic HBV infection and may provide insights for the treatment strategies for CHB patients. |
format | Online Article Text |
id | pubmed-4163673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-41636732014-09-22 Regulation of T cell proliferation by JMJD6 and PDGF-BB during chronic hepatitis B infection Chen, Cai-Feng Feng, Xia Liao, Hui-Yu Jin, Wen-Jing Zhang, Jian Wang, Yu Gong, Lu-Lu Liu, Jing-Jun Yuan, Xiao-Hui Zhao, Bin-Bin Zhang, Ding Chen, Guo-Feng Wan, Ying Guo, Jian Yan, Hui-Ping He, You-Wen Sci Rep Article T cell functional exhaustion during chronic hepatitis B virus (HBV) infection may contribute to the failed viral clearance; however, the underlying molecular mechanisms remain largely unknown. Here we demonstrate that jumonji domain-containing protein 6 (JMJD6) is a potential regulator of T cell proliferation during chronic HBV infection. The expression of JMJD6 was reduced in T lymphocytes in chronic hepatitis B (CHB) patients, and this reduction in JMJD6 expression was associated with impaired T cell proliferation. Moreover, silencing JMJD6 expression in primary human T cells impaired T cell proliferation. We found that JMJD6 promotes T cell proliferation by suppressing the mRNA expression of CDKN3. Furthermore, we have identified platelet derived growth factor-BB (PDGF-BB) as a regulator of JMJD6 expression. PDGF-BB downregulates JMJD6 expression and inhibits the proliferation of human primary T cells. Importantly, the expression levels of JMJD6 and PDGF-BB in lymphocytes from CHB patients were correlated with the degree of liver damage and the outcome of chronic HBV infection treatment. Our results demonstrate that PDGF-BB and JMJD6 regulate T cell function during chronic HBV infection and may provide insights for the treatment strategies for CHB patients. Nature Publishing Group 2014-09-15 /pmc/articles/PMC4163673/ /pubmed/25219359 http://dx.doi.org/10.1038/srep06359 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Article Chen, Cai-Feng Feng, Xia Liao, Hui-Yu Jin, Wen-Jing Zhang, Jian Wang, Yu Gong, Lu-Lu Liu, Jing-Jun Yuan, Xiao-Hui Zhao, Bin-Bin Zhang, Ding Chen, Guo-Feng Wan, Ying Guo, Jian Yan, Hui-Ping He, You-Wen Regulation of T cell proliferation by JMJD6 and PDGF-BB during chronic hepatitis B infection |
title | Regulation of T cell proliferation by JMJD6 and PDGF-BB during chronic hepatitis B infection |
title_full | Regulation of T cell proliferation by JMJD6 and PDGF-BB during chronic hepatitis B infection |
title_fullStr | Regulation of T cell proliferation by JMJD6 and PDGF-BB during chronic hepatitis B infection |
title_full_unstemmed | Regulation of T cell proliferation by JMJD6 and PDGF-BB during chronic hepatitis B infection |
title_short | Regulation of T cell proliferation by JMJD6 and PDGF-BB during chronic hepatitis B infection |
title_sort | regulation of t cell proliferation by jmjd6 and pdgf-bb during chronic hepatitis b infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163673/ https://www.ncbi.nlm.nih.gov/pubmed/25219359 http://dx.doi.org/10.1038/srep06359 |
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