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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...

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Autores principales: Chen, Hao, Zhou, Zhi, Wang, Lingling, Wang, Hao, Liu, Rui, Zhang, Huan, Song, Linsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2016
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.
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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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