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The role of TGF-β signaling and apoptosis in innate and adaptive immunity in zebrafish: a systems biology approach
BACKGROUND: The immune system is a key biological system present in vertebrates. Exposure to pathogens elicits various defensive immune mechanisms that protect the host from potential threats and harmful substances derived from pathogens such as parasites, bacteria, and viruses. The complex immune s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4224695/ https://www.ncbi.nlm.nih.gov/pubmed/25341656 http://dx.doi.org/10.1186/s12918-014-0116-0 |
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author | Lin, Che Lin, Chin-Nan Wang, Yu-Chao Liu, Fang-Yu Chuang, Yung-Jen Lan, Chung-Yu Hsieh, Wen-Ping Chen, Bor-Sen |
author_facet | Lin, Che Lin, Chin-Nan Wang, Yu-Chao Liu, Fang-Yu Chuang, Yung-Jen Lan, Chung-Yu Hsieh, Wen-Ping Chen, Bor-Sen |
author_sort | Lin, Che |
collection | PubMed |
description | BACKGROUND: The immune system is a key biological system present in vertebrates. Exposure to pathogens elicits various defensive immune mechanisms that protect the host from potential threats and harmful substances derived from pathogens such as parasites, bacteria, and viruses. The complex immune system of humans and many other vertebrates can be divided into two major categories: the innate and the adaptive immune systems. At present, analysis of the complex interactions between the two subsystems that regulate host defense and inflammatory responses remains challenging. RESULTS: Based on time-course microarray data following primary and secondary infection of zebrafish by Candida albicans, we constructed two intracellular protein–protein interaction (PPI) networks for primary and secondary responses of the host. 57 proteins and 341 PPIs were identified for primary infection while 90 proteins and 385 PPIs were identified for secondary infection. There were 20 proteins in common while 37 and 70 proteins specific to primary and secondary infection. By inspecting the hub proteins of each network and comparing significant changes in the number of linkages between the two PPI networks, we identified TGF-β signaling and apoptosis as two of the main functional modules involved in primary and secondary infection. Smad7, a member of the inhibitor SMADs, was identified to be a key protein in TGF-β signaling involved in secondary infection only. Indeed, the Smad7-dependent feedback system is related to the TGF-β signaling pathway and the immune response, suggesting that Smad7 may be an important regulator of innate and adaptive immune responses in zebrafish. Furthermore, we found that apoptosis was differentially involved in the two infection phases; more specifically, whereas apoptosis was promoted in response to primary infection, it was inhibited during secondary infection. CONCLUSIONS: Our initial in silico analyses pave the way for further investigation into the interesting roles played by the TGF-β signaling pathway and apoptosis in innate and adaptive immunity in zebrafish. Such insights could lead to therapeutic advances and improved drug design in the continual battle against infectious diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12918-014-0116-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4224695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42246952014-11-14 The role of TGF-β signaling and apoptosis in innate and adaptive immunity in zebrafish: a systems biology approach Lin, Che Lin, Chin-Nan Wang, Yu-Chao Liu, Fang-Yu Chuang, Yung-Jen Lan, Chung-Yu Hsieh, Wen-Ping Chen, Bor-Sen BMC Syst Biol Research Article BACKGROUND: The immune system is a key biological system present in vertebrates. Exposure to pathogens elicits various defensive immune mechanisms that protect the host from potential threats and harmful substances derived from pathogens such as parasites, bacteria, and viruses. The complex immune system of humans and many other vertebrates can be divided into two major categories: the innate and the adaptive immune systems. At present, analysis of the complex interactions between the two subsystems that regulate host defense and inflammatory responses remains challenging. RESULTS: Based on time-course microarray data following primary and secondary infection of zebrafish by Candida albicans, we constructed two intracellular protein–protein interaction (PPI) networks for primary and secondary responses of the host. 57 proteins and 341 PPIs were identified for primary infection while 90 proteins and 385 PPIs were identified for secondary infection. There were 20 proteins in common while 37 and 70 proteins specific to primary and secondary infection. By inspecting the hub proteins of each network and comparing significant changes in the number of linkages between the two PPI networks, we identified TGF-β signaling and apoptosis as two of the main functional modules involved in primary and secondary infection. Smad7, a member of the inhibitor SMADs, was identified to be a key protein in TGF-β signaling involved in secondary infection only. Indeed, the Smad7-dependent feedback system is related to the TGF-β signaling pathway and the immune response, suggesting that Smad7 may be an important regulator of innate and adaptive immune responses in zebrafish. Furthermore, we found that apoptosis was differentially involved in the two infection phases; more specifically, whereas apoptosis was promoted in response to primary infection, it was inhibited during secondary infection. CONCLUSIONS: Our initial in silico analyses pave the way for further investigation into the interesting roles played by the TGF-β signaling pathway and apoptosis in innate and adaptive immunity in zebrafish. Such insights could lead to therapeutic advances and improved drug design in the continual battle against infectious diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12918-014-0116-0) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-24 /pmc/articles/PMC4224695/ /pubmed/25341656 http://dx.doi.org/10.1186/s12918-014-0116-0 Text en © Lin et al.; licensee BioMed Central Ltd. 2014 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 Lin, Che Lin, Chin-Nan Wang, Yu-Chao Liu, Fang-Yu Chuang, Yung-Jen Lan, Chung-Yu Hsieh, Wen-Ping Chen, Bor-Sen The role of TGF-β signaling and apoptosis in innate and adaptive immunity in zebrafish: a systems biology approach |
title | The role of TGF-β signaling and apoptosis in innate and adaptive immunity in zebrafish: a systems biology approach |
title_full | The role of TGF-β signaling and apoptosis in innate and adaptive immunity in zebrafish: a systems biology approach |
title_fullStr | The role of TGF-β signaling and apoptosis in innate and adaptive immunity in zebrafish: a systems biology approach |
title_full_unstemmed | The role of TGF-β signaling and apoptosis in innate and adaptive immunity in zebrafish: a systems biology approach |
title_short | The role of TGF-β signaling and apoptosis in innate and adaptive immunity in zebrafish: a systems biology approach |
title_sort | role of tgf-β signaling and apoptosis in innate and adaptive immunity in zebrafish: a systems biology approach |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4224695/ https://www.ncbi.nlm.nih.gov/pubmed/25341656 http://dx.doi.org/10.1186/s12918-014-0116-0 |
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