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Comparative functional analysis of macrophage phagocytosis in Dagu chickens and Wenchang chickens

Phagocytosis of macrophages constitutes a powerful barrier to innate immunity. Differences in the phagocytic function of macrophages among chicken breeds have rarely been reported, and the molecular mechanisms underlying phagocytosis remain poorly understood. This study compared functional differenc...

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Autores principales: Zhang, Jin, Wang, Qiao, Li, Qinghe, Wang, Zixuan, Zheng, Maiqing, Wen, Jie, Zhao, Guiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941738/
https://www.ncbi.nlm.nih.gov/pubmed/36825012
http://dx.doi.org/10.3389/fimmu.2023.1064461
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author Zhang, Jin
Wang, Qiao
Li, Qinghe
Wang, Zixuan
Zheng, Maiqing
Wen, Jie
Zhao, Guiping
author_facet Zhang, Jin
Wang, Qiao
Li, Qinghe
Wang, Zixuan
Zheng, Maiqing
Wen, Jie
Zhao, Guiping
author_sort Zhang, Jin
collection PubMed
description Phagocytosis of macrophages constitutes a powerful barrier to innate immunity. Differences in the phagocytic function of macrophages among chicken breeds have rarely been reported, and the molecular mechanisms underlying phagocytosis remain poorly understood. This study compared functional difference of macrophages in Dagu chickens, originated in Zhuanghe, Liaoning Province, China, and Wenchang chickens, originated from Hainan Island in the South China Sea, and explored the potential molecular mechanisms by integrated analysis of mRNA expression profiles of macrophages and whole genome sequencing. Immunological parameters in peripheral blood indicated that Dagu chickens were more resistant to Salmonella challenge at 28 days old. Phagocytosis index and phagocytosis rate of macrophages displayed Dagu chickens performed a significantly higher phagocytic ability of macrophages at 14 and 28 days old. Furthermore, comparative analysis of mRNA expression profiles of macrophages of two breeds at 28 days old revealed that 1136 differentially expressed genes (DEGs), and 22 DEGs (e.g., H2AFZ, SNRPA1, CUEDC2, S100A12) were found to be hub genes regulating phagocytosis by participating in different immunological biological signaling pathways. In addition, many DEGs and hub genes were under strong differentiation in genome between two breeds, the H2AFZ gene was an intersection of DEGs and hub genes. These results provided a comprehensive functional comparison and transcriptomic profiles of macrophages in Chinese native chicken breeds, and deepened our understanding of the genetic mechanism of innate immunity.
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spelling pubmed-99417382023-02-22 Comparative functional analysis of macrophage phagocytosis in Dagu chickens and Wenchang chickens Zhang, Jin Wang, Qiao Li, Qinghe Wang, Zixuan Zheng, Maiqing Wen, Jie Zhao, Guiping Front Immunol Immunology Phagocytosis of macrophages constitutes a powerful barrier to innate immunity. Differences in the phagocytic function of macrophages among chicken breeds have rarely been reported, and the molecular mechanisms underlying phagocytosis remain poorly understood. This study compared functional difference of macrophages in Dagu chickens, originated in Zhuanghe, Liaoning Province, China, and Wenchang chickens, originated from Hainan Island in the South China Sea, and explored the potential molecular mechanisms by integrated analysis of mRNA expression profiles of macrophages and whole genome sequencing. Immunological parameters in peripheral blood indicated that Dagu chickens were more resistant to Salmonella challenge at 28 days old. Phagocytosis index and phagocytosis rate of macrophages displayed Dagu chickens performed a significantly higher phagocytic ability of macrophages at 14 and 28 days old. Furthermore, comparative analysis of mRNA expression profiles of macrophages of two breeds at 28 days old revealed that 1136 differentially expressed genes (DEGs), and 22 DEGs (e.g., H2AFZ, SNRPA1, CUEDC2, S100A12) were found to be hub genes regulating phagocytosis by participating in different immunological biological signaling pathways. In addition, many DEGs and hub genes were under strong differentiation in genome between two breeds, the H2AFZ gene was an intersection of DEGs and hub genes. These results provided a comprehensive functional comparison and transcriptomic profiles of macrophages in Chinese native chicken breeds, and deepened our understanding of the genetic mechanism of innate immunity. Frontiers Media S.A. 2023-02-06 /pmc/articles/PMC9941738/ /pubmed/36825012 http://dx.doi.org/10.3389/fimmu.2023.1064461 Text en Copyright © 2023 Zhang, Wang, Li, Wang, Zheng, Wen and Zhao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Zhang, Jin
Wang, Qiao
Li, Qinghe
Wang, Zixuan
Zheng, Maiqing
Wen, Jie
Zhao, Guiping
Comparative functional analysis of macrophage phagocytosis in Dagu chickens and Wenchang chickens
title Comparative functional analysis of macrophage phagocytosis in Dagu chickens and Wenchang chickens
title_full Comparative functional analysis of macrophage phagocytosis in Dagu chickens and Wenchang chickens
title_fullStr Comparative functional analysis of macrophage phagocytosis in Dagu chickens and Wenchang chickens
title_full_unstemmed Comparative functional analysis of macrophage phagocytosis in Dagu chickens and Wenchang chickens
title_short Comparative functional analysis of macrophage phagocytosis in Dagu chickens and Wenchang chickens
title_sort comparative functional analysis of macrophage phagocytosis in dagu chickens and wenchang chickens
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941738/
https://www.ncbi.nlm.nih.gov/pubmed/36825012
http://dx.doi.org/10.3389/fimmu.2023.1064461
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