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Common and specific downstream signaling targets controlled by Tlr2 and Tlr5 innate immune signaling in zebrafish

BACKGROUND: Although the responses to many pathogen associated molecular patterns (PAMPs) in cell cultures and extracted organs are well characterized, there is little known of transcriptome responses to PAMPs in whole organisms. To characterize this in detail, we have performed RNAseq analysis of r...

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Autores principales: Yang, Shuxin, Marín-Juez, Rubén, Meijer, Annemarie H., Spaink, Herman P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514945/
https://www.ncbi.nlm.nih.gov/pubmed/26208853
http://dx.doi.org/10.1186/s12864-015-1740-9
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author Yang, Shuxin
Marín-Juez, Rubén
Meijer, Annemarie H.
Spaink, Herman P.
author_facet Yang, Shuxin
Marín-Juez, Rubén
Meijer, Annemarie H.
Spaink, Herman P.
author_sort Yang, Shuxin
collection PubMed
description BACKGROUND: Although the responses to many pathogen associated molecular patterns (PAMPs) in cell cultures and extracted organs are well characterized, there is little known of transcriptome responses to PAMPs in whole organisms. To characterize this in detail, we have performed RNAseq analysis of responses of zebrafish embryos to injection of PAMPs in the caudal vein at one hour after exposure. We have compared two ligands that in mammals have been shown to specifically activate the TLR2 and TLR5 receptors: Pam3CSK4 and flagellin, respectively. RESULTS: We identified a group of 80 common genes that respond with high stringency selection to stimulations with both PAMPs, which included several well-known immune marker genes such as il1b and tnfa. Surprisingly, we also identified sets of 48 and 42 genes that specifically respond to either Pam3CSK4 or flagellin, respectively, after a comparative filtering approach. Remarkably, in the Pam3CSK4 specific set, there was a set of transcription factors with more than 2 fold-change, as confirmed by qPCR analyses, including cebpb, fosb, nr4a1 and egr3. We also showed that the regulation of the Pam3CSK4 and flagellin specifically responding sets is inhibited by knockdown of tlr2 or tlr5, respectively. CONCLUSIONS: Our studies show that Pam3CSK4 and flagellin can stimulate the Tlr2 and Tlr5 signaling pathways leading to common and specific responses in the zebrafish embryo system. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1740-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-45149452015-07-26 Common and specific downstream signaling targets controlled by Tlr2 and Tlr5 innate immune signaling in zebrafish Yang, Shuxin Marín-Juez, Rubén Meijer, Annemarie H. Spaink, Herman P. BMC Genomics Research Article BACKGROUND: Although the responses to many pathogen associated molecular patterns (PAMPs) in cell cultures and extracted organs are well characterized, there is little known of transcriptome responses to PAMPs in whole organisms. To characterize this in detail, we have performed RNAseq analysis of responses of zebrafish embryos to injection of PAMPs in the caudal vein at one hour after exposure. We have compared two ligands that in mammals have been shown to specifically activate the TLR2 and TLR5 receptors: Pam3CSK4 and flagellin, respectively. RESULTS: We identified a group of 80 common genes that respond with high stringency selection to stimulations with both PAMPs, which included several well-known immune marker genes such as il1b and tnfa. Surprisingly, we also identified sets of 48 and 42 genes that specifically respond to either Pam3CSK4 or flagellin, respectively, after a comparative filtering approach. Remarkably, in the Pam3CSK4 specific set, there was a set of transcription factors with more than 2 fold-change, as confirmed by qPCR analyses, including cebpb, fosb, nr4a1 and egr3. We also showed that the regulation of the Pam3CSK4 and flagellin specifically responding sets is inhibited by knockdown of tlr2 or tlr5, respectively. CONCLUSIONS: Our studies show that Pam3CSK4 and flagellin can stimulate the Tlr2 and Tlr5 signaling pathways leading to common and specific responses in the zebrafish embryo system. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1740-9) contains supplementary material, which is available to authorized users. BioMed Central 2015-07-25 /pmc/articles/PMC4514945/ /pubmed/26208853 http://dx.doi.org/10.1186/s12864-015-1740-9 Text en © Yang et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Yang, Shuxin
Marín-Juez, Rubén
Meijer, Annemarie H.
Spaink, Herman P.
Common and specific downstream signaling targets controlled by Tlr2 and Tlr5 innate immune signaling in zebrafish
title Common and specific downstream signaling targets controlled by Tlr2 and Tlr5 innate immune signaling in zebrafish
title_full Common and specific downstream signaling targets controlled by Tlr2 and Tlr5 innate immune signaling in zebrafish
title_fullStr Common and specific downstream signaling targets controlled by Tlr2 and Tlr5 innate immune signaling in zebrafish
title_full_unstemmed Common and specific downstream signaling targets controlled by Tlr2 and Tlr5 innate immune signaling in zebrafish
title_short Common and specific downstream signaling targets controlled by Tlr2 and Tlr5 innate immune signaling in zebrafish
title_sort common and specific downstream signaling targets controlled by tlr2 and tlr5 innate immune signaling in zebrafish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514945/
https://www.ncbi.nlm.nih.gov/pubmed/26208853
http://dx.doi.org/10.1186/s12864-015-1740-9
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