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Regulatory T cells protected against abdominal aortic aneurysm by suppression of the COX‐2 expression
CD4(+)CD25(+) regulatory T cells (Tregs) have been shown to protect against the development of abdominal aortic aneurysm (AAA). Cyclooxygenase‐2 (COX‐2), a pro‐inflammatory protein, can convert arachidonic acid into prostaglandins (PGs). The present study was aimed to investigate the effect of Tregs...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787467/ https://www.ncbi.nlm.nih.gov/pubmed/31328426 http://dx.doi.org/10.1111/jcmm.14554 |
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author | Liu, Bin Kong, Jing An, Guipeng Zhang, Kai Qin, Weidong Meng, Xiao |
author_facet | Liu, Bin Kong, Jing An, Guipeng Zhang, Kai Qin, Weidong Meng, Xiao |
author_sort | Liu, Bin |
collection | PubMed |
description | CD4(+)CD25(+) regulatory T cells (Tregs) have been shown to protect against the development of abdominal aortic aneurysm (AAA). Cyclooxygenase‐2 (COX‐2), a pro‐inflammatory protein, can convert arachidonic acid into prostaglandins (PGs). The present study was aimed to investigate the effect of Tregs on COX‐2 expression in angiotension II (Ang II)‐induced AAA in ApoE(−/−) mice. Tregs were injected via tail vein in every 2 weeks. Ang II was continuously infused by a micropump for 28 days to induce AAA. In vivo, compared with the control group, adoptive transfer of Tregs significantly reduced the incidence of AAA, maximal diameter, and the mRNA and protein expression of COX‐2 in mice. Immunofluorescence showed that Tregs treatment reduced COX‐2 expression both in smooth muscle cells (SMCs) and macrophages in AAA. In vitro, the Western blot analysis showed that Tregs reduced Ang II‐induced COX‐2 expression in macrophages and SMCs. Meanwhile, ELISA showed that Tregs reduced Ang II‐induced prostaglandin E(2) (PGE(2)) secretion. Moreover, Tregs increased SMC viability and induced transition of macrophages phenotype from M1 to M2. In conclusion, Tregs treatment dramatically decreased the expression of COX‐2 in vivo and in vitro, suggesting that Tregs could protect against AAA through inhibition of COX‐2. The study may shed light on the immune treatment of AAA. |
format | Online Article Text |
id | pubmed-6787467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67874672019-10-17 Regulatory T cells protected against abdominal aortic aneurysm by suppression of the COX‐2 expression Liu, Bin Kong, Jing An, Guipeng Zhang, Kai Qin, Weidong Meng, Xiao J Cell Mol Med Original Articles CD4(+)CD25(+) regulatory T cells (Tregs) have been shown to protect against the development of abdominal aortic aneurysm (AAA). Cyclooxygenase‐2 (COX‐2), a pro‐inflammatory protein, can convert arachidonic acid into prostaglandins (PGs). The present study was aimed to investigate the effect of Tregs on COX‐2 expression in angiotension II (Ang II)‐induced AAA in ApoE(−/−) mice. Tregs were injected via tail vein in every 2 weeks. Ang II was continuously infused by a micropump for 28 days to induce AAA. In vivo, compared with the control group, adoptive transfer of Tregs significantly reduced the incidence of AAA, maximal diameter, and the mRNA and protein expression of COX‐2 in mice. Immunofluorescence showed that Tregs treatment reduced COX‐2 expression both in smooth muscle cells (SMCs) and macrophages in AAA. In vitro, the Western blot analysis showed that Tregs reduced Ang II‐induced COX‐2 expression in macrophages and SMCs. Meanwhile, ELISA showed that Tregs reduced Ang II‐induced prostaglandin E(2) (PGE(2)) secretion. Moreover, Tregs increased SMC viability and induced transition of macrophages phenotype from M1 to M2. In conclusion, Tregs treatment dramatically decreased the expression of COX‐2 in vivo and in vitro, suggesting that Tregs could protect against AAA through inhibition of COX‐2. The study may shed light on the immune treatment of AAA. John Wiley and Sons Inc. 2019-07-21 2019-10 /pmc/articles/PMC6787467/ /pubmed/31328426 http://dx.doi.org/10.1111/jcmm.14554 Text en © 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Liu, Bin Kong, Jing An, Guipeng Zhang, Kai Qin, Weidong Meng, Xiao Regulatory T cells protected against abdominal aortic aneurysm by suppression of the COX‐2 expression |
title | Regulatory T cells protected against abdominal aortic aneurysm by suppression of the COX‐2 expression |
title_full | Regulatory T cells protected against abdominal aortic aneurysm by suppression of the COX‐2 expression |
title_fullStr | Regulatory T cells protected against abdominal aortic aneurysm by suppression of the COX‐2 expression |
title_full_unstemmed | Regulatory T cells protected against abdominal aortic aneurysm by suppression of the COX‐2 expression |
title_short | Regulatory T cells protected against abdominal aortic aneurysm by suppression of the COX‐2 expression |
title_sort | regulatory t cells protected against abdominal aortic aneurysm by suppression of the cox‐2 expression |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787467/ https://www.ncbi.nlm.nih.gov/pubmed/31328426 http://dx.doi.org/10.1111/jcmm.14554 |
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