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The immunomodulatory functions and molecular mechanism of a new bursal heptapeptide (BP7) in immune responses and immature B cells

The bursa of Fabricius (BF) is the acknowledged central humoural immune organ unique to birds and plays a vital role in B lymphocyte development. In addition, the unique molecular immune features of bursal-derived biological peptides involved in B cell development are rarely reported. In this paper,...

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Autores principales: Feng, Xiu Li, Zheng, Yang, Zong, Man Man, Hao, Shan Shan, Zhou, Guang Fang, Cao, Rui Bing, Chen, Pu Yan, Liu, Tao Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749628/
https://www.ncbi.nlm.nih.gov/pubmed/31533803
http://dx.doi.org/10.1186/s13567-019-0682-7
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author Feng, Xiu Li
Zheng, Yang
Zong, Man Man
Hao, Shan Shan
Zhou, Guang Fang
Cao, Rui Bing
Chen, Pu Yan
Liu, Tao Qing
author_facet Feng, Xiu Li
Zheng, Yang
Zong, Man Man
Hao, Shan Shan
Zhou, Guang Fang
Cao, Rui Bing
Chen, Pu Yan
Liu, Tao Qing
author_sort Feng, Xiu Li
collection PubMed
description The bursa of Fabricius (BF) is the acknowledged central humoural immune organ unique to birds and plays a vital role in B lymphocyte development. In addition, the unique molecular immune features of bursal-derived biological peptides involved in B cell development are rarely reported. In this paper, a novel bursal heptapeptide (BP7) with the sequence GGCDGAA was isolated from the BF and was shown to enhance the monoclonal antibody production of a hybridoma. A mouse immunization experiment showed that mice immunized with an AIV antigen and BP7 produced strong antibody responses and cell-mediated immune responses. Additionally, BP7 stimulated increased mRNA levels of sIgM in immature mouse WEHI-231 B cells. Gene microarray results confirmed that BP7 regulated 2465 differentially expressed genes in BP7-treated WEHI-231 cells and induced 13 signalling pathways and various immune-related functional processes. Furthermore, we found that BP7 stimulated WEHI-231 cell autophagy and AMPK-ULK1 phosphorylation and regulated Bcl-2 protein expression. Finally, chicken immunization showed that BP7 enhanced the potential antibody and cytokine responses to the AIV antigen. These results suggested that BP7 might be an active biological factor that functions as a potential immunopotentiator, which provided some novel insights into the molecular mechanisms of the effects of bursal peptides on immune functions and B cell differentiation.
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spelling pubmed-67496282019-09-23 The immunomodulatory functions and molecular mechanism of a new bursal heptapeptide (BP7) in immune responses and immature B cells Feng, Xiu Li Zheng, Yang Zong, Man Man Hao, Shan Shan Zhou, Guang Fang Cao, Rui Bing Chen, Pu Yan Liu, Tao Qing Vet Res Research Article The bursa of Fabricius (BF) is the acknowledged central humoural immune organ unique to birds and plays a vital role in B lymphocyte development. In addition, the unique molecular immune features of bursal-derived biological peptides involved in B cell development are rarely reported. In this paper, a novel bursal heptapeptide (BP7) with the sequence GGCDGAA was isolated from the BF and was shown to enhance the monoclonal antibody production of a hybridoma. A mouse immunization experiment showed that mice immunized with an AIV antigen and BP7 produced strong antibody responses and cell-mediated immune responses. Additionally, BP7 stimulated increased mRNA levels of sIgM in immature mouse WEHI-231 B cells. Gene microarray results confirmed that BP7 regulated 2465 differentially expressed genes in BP7-treated WEHI-231 cells and induced 13 signalling pathways and various immune-related functional processes. Furthermore, we found that BP7 stimulated WEHI-231 cell autophagy and AMPK-ULK1 phosphorylation and regulated Bcl-2 protein expression. Finally, chicken immunization showed that BP7 enhanced the potential antibody and cytokine responses to the AIV antigen. These results suggested that BP7 might be an active biological factor that functions as a potential immunopotentiator, which provided some novel insights into the molecular mechanisms of the effects of bursal peptides on immune functions and B cell differentiation. BioMed Central 2019-09-18 2019 /pmc/articles/PMC6749628/ /pubmed/31533803 http://dx.doi.org/10.1186/s13567-019-0682-7 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Feng, Xiu Li
Zheng, Yang
Zong, Man Man
Hao, Shan Shan
Zhou, Guang Fang
Cao, Rui Bing
Chen, Pu Yan
Liu, Tao Qing
The immunomodulatory functions and molecular mechanism of a new bursal heptapeptide (BP7) in immune responses and immature B cells
title The immunomodulatory functions and molecular mechanism of a new bursal heptapeptide (BP7) in immune responses and immature B cells
title_full The immunomodulatory functions and molecular mechanism of a new bursal heptapeptide (BP7) in immune responses and immature B cells
title_fullStr The immunomodulatory functions and molecular mechanism of a new bursal heptapeptide (BP7) in immune responses and immature B cells
title_full_unstemmed The immunomodulatory functions and molecular mechanism of a new bursal heptapeptide (BP7) in immune responses and immature B cells
title_short The immunomodulatory functions and molecular mechanism of a new bursal heptapeptide (BP7) in immune responses and immature B cells
title_sort immunomodulatory functions and molecular mechanism of a new bursal heptapeptide (bp7) in immune responses and immature b cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749628/
https://www.ncbi.nlm.nih.gov/pubmed/31533803
http://dx.doi.org/10.1186/s13567-019-0682-7
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