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An invertebrate-specific miRNA targeted the ancient cholinergic neuroendocrine system of oyster
Acetylcholine (ACh) is the main neurotransmitter in the cholinergic neuroendocrine system and plays an indispensable role in modulating diverse immune responses. As important transporters in choline uptake, choline transporter-like proteins (CTLs) can control ACh synthesis and release indirectly in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008008/ https://www.ncbi.nlm.nih.gov/pubmed/27488375 http://dx.doi.org/10.1098/rsob.160059 |
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author | Chen, Hao Zhou, Zhi Wang, Lingling Wang, Hao Liu, Rui Zhang, Huan Song, Linsheng |
author_facet | Chen, Hao Zhou, Zhi Wang, Lingling Wang, Hao Liu, Rui Zhang, Huan Song, Linsheng |
author_sort | Chen, Hao |
collection | PubMed |
description | Acetylcholine (ACh) is the main neurotransmitter in the cholinergic neuroendocrine system and plays an indispensable role in modulating diverse immune responses. As important transporters in choline uptake, choline transporter-like proteins (CTLs) can control ACh synthesis and release indirectly in multiple organisms. In this study, cgi-miR-2d, an invertebrate-specific miRNA in oyster Crassostrea gigas, is proved to repress the synthesis/release of ACh by targeting CgCTL1 and choline uptake in haemocytes during the early stage of pathogen infection. In short, an opposite expression pattern between CgCTL1 and cgi-miR-2d is observed during Vibrio splendidus infection, accompanied by changes in haemolymph ACh. In addition, the expression level of CgCTL1 is found to be significantly repressed after cgi-miR-2d overexpression in vivo, while both haemocyte choline and haemolymph ACh are also decreased simultaneously, similar to the finding in CgCTL1 knock-down assay. As a result, the expression of two tumour necrosis factor-like proteins and the bacteriostatic activity of oyster haemocytes are found to be altered significantly by either gain-of-function cgi-miR-2d or knock-down of CgCTL1. To our knowledge, this is the first miRNA identified in invertebrates that can target the ancient cholinergic system and augment immune response during infection. |
format | Online Article Text |
id | pubmed-5008008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-50080082016-09-09 An invertebrate-specific miRNA targeted the ancient cholinergic neuroendocrine system of oyster Chen, Hao Zhou, Zhi Wang, Lingling Wang, Hao Liu, Rui Zhang, Huan Song, Linsheng Open Biol Research Acetylcholine (ACh) is the main neurotransmitter in the cholinergic neuroendocrine system and plays an indispensable role in modulating diverse immune responses. As important transporters in choline uptake, choline transporter-like proteins (CTLs) can control ACh synthesis and release indirectly in multiple organisms. In this study, cgi-miR-2d, an invertebrate-specific miRNA in oyster Crassostrea gigas, is proved to repress the synthesis/release of ACh by targeting CgCTL1 and choline uptake in haemocytes during the early stage of pathogen infection. In short, an opposite expression pattern between CgCTL1 and cgi-miR-2d is observed during Vibrio splendidus infection, accompanied by changes in haemolymph ACh. In addition, the expression level of CgCTL1 is found to be significantly repressed after cgi-miR-2d overexpression in vivo, while both haemocyte choline and haemolymph ACh are also decreased simultaneously, similar to the finding in CgCTL1 knock-down assay. As a result, the expression of two tumour necrosis factor-like proteins and the bacteriostatic activity of oyster haemocytes are found to be altered significantly by either gain-of-function cgi-miR-2d or knock-down of CgCTL1. To our knowledge, this is the first miRNA identified in invertebrates that can target the ancient cholinergic system and augment immune response during infection. The Royal Society 2016-08-03 /pmc/articles/PMC5008008/ /pubmed/27488375 http://dx.doi.org/10.1098/rsob.160059 Text en © 2016 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Chen, Hao Zhou, Zhi Wang, Lingling Wang, Hao Liu, Rui Zhang, Huan Song, Linsheng An invertebrate-specific miRNA targeted the ancient cholinergic neuroendocrine system of oyster |
title | An invertebrate-specific miRNA targeted the ancient cholinergic neuroendocrine system of oyster |
title_full | An invertebrate-specific miRNA targeted the ancient cholinergic neuroendocrine system of oyster |
title_fullStr | An invertebrate-specific miRNA targeted the ancient cholinergic neuroendocrine system of oyster |
title_full_unstemmed | An invertebrate-specific miRNA targeted the ancient cholinergic neuroendocrine system of oyster |
title_short | An invertebrate-specific miRNA targeted the ancient cholinergic neuroendocrine system of oyster |
title_sort | invertebrate-specific mirna targeted the ancient cholinergic neuroendocrine system of oyster |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008008/ https://www.ncbi.nlm.nih.gov/pubmed/27488375 http://dx.doi.org/10.1098/rsob.160059 |
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