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Mutual modulation between norepinephrine and nitric oxide in haemocytes during the mollusc immune response
Nitric oxide (NO) is one of the most important immune molecules in innate immunity of invertebrates, and it can be regulated by norepinephrine in ascidian haemocytes. In the present study, the mutual modulation and underlying mechanism between norepinephrine and NO were explored in haemocytes of the...
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/PMC4223682/ https://www.ncbi.nlm.nih.gov/pubmed/25376551 http://dx.doi.org/10.1038/srep06963 |
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author | Jiang, Qiufen Zhou, Zhi Wang, Lingling Yang, Chuanyan Wang, Jingjing Wu, Tiantian Song, Linsheng |
author_facet | Jiang, Qiufen Zhou, Zhi Wang, Lingling Yang, Chuanyan Wang, Jingjing Wu, Tiantian Song, Linsheng |
author_sort | Jiang, Qiufen |
collection | PubMed |
description | Nitric oxide (NO) is one of the most important immune molecules in innate immunity of invertebrates, and it can be regulated by norepinephrine in ascidian haemocytes. In the present study, the mutual modulation and underlying mechanism between norepinephrine and NO were explored in haemocytes of the scallop Chlamys farreri. After lipopolysaccharide stimulation, NO production increased to a significant level at 24 h, and norepinephrine concentration rose to remarkable levels at 3 h and 12~48 h. A significant decrease of NO production was observed in the haemocytes concomitantly stimulated with lipopolysaccharide and α-adrenoceptor agonist, while a dramatic increase of NO production was observed in the haemocytes incubated with lipopolysaccharide and β-adrenoceptor agonist. Meanwhile, the concentration of cyclic adenosine monophosphate (cAMP) decreased significantly in the haemocytes treated by lipopolysaccharide and α/β-adrenoceptor agonist, while the content of Ca(2+) was elevated in those triggered by lipopolysaccharide and β-adrenoceptor agonist. When the haemocytes was incubated with NO donor, norepinephrine concentration was significantly enhanced during 1~24 h. Collectively, these results suggested that norepinephrine exerted varied effects on NO production at different immune stages via a novel α/β-adrenoceptor-cAMP/Ca(2+) regulatory pattern, and NO might have a feedback effect on the synthesis of norepinephrine in the scallop haemocytes. |
format | Online Article Text |
id | pubmed-4223682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42236822014-11-13 Mutual modulation between norepinephrine and nitric oxide in haemocytes during the mollusc immune response Jiang, Qiufen Zhou, Zhi Wang, Lingling Yang, Chuanyan Wang, Jingjing Wu, Tiantian Song, Linsheng Sci Rep Article Nitric oxide (NO) is one of the most important immune molecules in innate immunity of invertebrates, and it can be regulated by norepinephrine in ascidian haemocytes. In the present study, the mutual modulation and underlying mechanism between norepinephrine and NO were explored in haemocytes of the scallop Chlamys farreri. After lipopolysaccharide stimulation, NO production increased to a significant level at 24 h, and norepinephrine concentration rose to remarkable levels at 3 h and 12~48 h. A significant decrease of NO production was observed in the haemocytes concomitantly stimulated with lipopolysaccharide and α-adrenoceptor agonist, while a dramatic increase of NO production was observed in the haemocytes incubated with lipopolysaccharide and β-adrenoceptor agonist. Meanwhile, the concentration of cyclic adenosine monophosphate (cAMP) decreased significantly in the haemocytes treated by lipopolysaccharide and α/β-adrenoceptor agonist, while the content of Ca(2+) was elevated in those triggered by lipopolysaccharide and β-adrenoceptor agonist. When the haemocytes was incubated with NO donor, norepinephrine concentration was significantly enhanced during 1~24 h. Collectively, these results suggested that norepinephrine exerted varied effects on NO production at different immune stages via a novel α/β-adrenoceptor-cAMP/Ca(2+) regulatory pattern, and NO might have a feedback effect on the synthesis of norepinephrine in the scallop haemocytes. Nature Publishing Group 2014-11-07 /pmc/articles/PMC4223682/ /pubmed/25376551 http://dx.doi.org/10.1038/srep06963 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 Jiang, Qiufen Zhou, Zhi Wang, Lingling Yang, Chuanyan Wang, Jingjing Wu, Tiantian Song, Linsheng Mutual modulation between norepinephrine and nitric oxide in haemocytes during the mollusc immune response |
title | Mutual modulation between norepinephrine and nitric oxide in haemocytes during the mollusc immune response |
title_full | Mutual modulation between norepinephrine and nitric oxide in haemocytes during the mollusc immune response |
title_fullStr | Mutual modulation between norepinephrine and nitric oxide in haemocytes during the mollusc immune response |
title_full_unstemmed | Mutual modulation between norepinephrine and nitric oxide in haemocytes during the mollusc immune response |
title_short | Mutual modulation between norepinephrine and nitric oxide in haemocytes during the mollusc immune response |
title_sort | mutual modulation between norepinephrine and nitric oxide in haemocytes during the mollusc immune response |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4223682/ https://www.ncbi.nlm.nih.gov/pubmed/25376551 http://dx.doi.org/10.1038/srep06963 |
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