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Comparative transcriptome analyses of immune responses to LPS in peripheral blood mononuclear cells from the giant panda, human, mouse, and monkey

Gram-negative bacteria are major pathogens that can cause illnesses in giant pandas. Lipopolysaccharides (LPS), components of Gram-negative bacteria, can activate immune responses in mammals (i.e., humans and mice) through recognition by toll-like receptors (TLRs). However, the giant pandas’ immune...

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Autores principales: Li, Shun, Li, Caiwu, Chen, Lixiang, Yang, Hua, Ren, Xiaonan, Xu, Chunhua, Wu, Bin, Wang, Chao, Ling, Yun, Shen, Yinzhong, Lu, Hongzhou, Liu, Weiping, Zhou, Xiaohui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9852843/
https://www.ncbi.nlm.nih.gov/pubmed/36685921
http://dx.doi.org/10.3389/fgene.2022.1053655
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author Li, Shun
Li, Caiwu
Chen, Lixiang
Yang, Hua
Ren, Xiaonan
Xu, Chunhua
Wu, Bin
Wang, Chao
Ling, Yun
Shen, Yinzhong
Lu, Hongzhou
Liu, Weiping
Zhou, Xiaohui
author_facet Li, Shun
Li, Caiwu
Chen, Lixiang
Yang, Hua
Ren, Xiaonan
Xu, Chunhua
Wu, Bin
Wang, Chao
Ling, Yun
Shen, Yinzhong
Lu, Hongzhou
Liu, Weiping
Zhou, Xiaohui
author_sort Li, Shun
collection PubMed
description Gram-negative bacteria are major pathogens that can cause illnesses in giant pandas. Lipopolysaccharides (LPS), components of Gram-negative bacteria, can activate immune responses in mammals (i.e., humans and mice) through recognition by toll-like receptors (TLRs). However, the giant pandas’ immune response to LPS stimulation and the differences between the giant panda and other mammals are not fully known. In this study, we administrated peripheral blood mononuclear cells (PBMCs) from giant pandas, humans, C57BL/6 mice, and rhesus monkeys by LPS treatment at 6 h followed by RNA sequencing (RNA-seq), respectively, with control of non-stimulation. KEGG analyses of differentially expressed genes (DEGs) pathways indicated that LPS could activate the classic signaling pathway of NF-κB in PBMCs from those four tested species. Thus, similar to the other three species, NF-κB is an LPS-responsive regulator of innate immune responses in giant pandas. Furthermore, the expression patterns of adapter genes, inflammatory cytokine genes, chemokines, interferon genes, cytokine genes related to cell growth and development, costimulatory molecules, Th1/Th2 cytokine genes, Th17 cytokine genes, Th9, and Th22 cytokine genes were compared among giant pandas and three other species. Our data indicated that in addition to the similar expression patterns of certain genes among giant pandas and other species, the unique expression pattern response to LPS in giant pandas was also discovered. Furthermore, Th9, Th17, and Th22 cells might be involved in the response to LPS in giant pandas at this tested time point. This study reveals that LPS-induced immune responses have different sensitivities and response timelines in giant pandas compared with other mammals. This study facilitates further understanding of the role of the TLR signaling pathway and the immune system in giant pandas, which might be helpful for disease prevention and protection.
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spelling pubmed-98528432023-01-21 Comparative transcriptome analyses of immune responses to LPS in peripheral blood mononuclear cells from the giant panda, human, mouse, and monkey Li, Shun Li, Caiwu Chen, Lixiang Yang, Hua Ren, Xiaonan Xu, Chunhua Wu, Bin Wang, Chao Ling, Yun Shen, Yinzhong Lu, Hongzhou Liu, Weiping Zhou, Xiaohui Front Genet Genetics Gram-negative bacteria are major pathogens that can cause illnesses in giant pandas. Lipopolysaccharides (LPS), components of Gram-negative bacteria, can activate immune responses in mammals (i.e., humans and mice) through recognition by toll-like receptors (TLRs). However, the giant pandas’ immune response to LPS stimulation and the differences between the giant panda and other mammals are not fully known. In this study, we administrated peripheral blood mononuclear cells (PBMCs) from giant pandas, humans, C57BL/6 mice, and rhesus monkeys by LPS treatment at 6 h followed by RNA sequencing (RNA-seq), respectively, with control of non-stimulation. KEGG analyses of differentially expressed genes (DEGs) pathways indicated that LPS could activate the classic signaling pathway of NF-κB in PBMCs from those four tested species. Thus, similar to the other three species, NF-κB is an LPS-responsive regulator of innate immune responses in giant pandas. Furthermore, the expression patterns of adapter genes, inflammatory cytokine genes, chemokines, interferon genes, cytokine genes related to cell growth and development, costimulatory molecules, Th1/Th2 cytokine genes, Th17 cytokine genes, Th9, and Th22 cytokine genes were compared among giant pandas and three other species. Our data indicated that in addition to the similar expression patterns of certain genes among giant pandas and other species, the unique expression pattern response to LPS in giant pandas was also discovered. Furthermore, Th9, Th17, and Th22 cells might be involved in the response to LPS in giant pandas at this tested time point. This study reveals that LPS-induced immune responses have different sensitivities and response timelines in giant pandas compared with other mammals. This study facilitates further understanding of the role of the TLR signaling pathway and the immune system in giant pandas, which might be helpful for disease prevention and protection. Frontiers Media S.A. 2023-01-06 /pmc/articles/PMC9852843/ /pubmed/36685921 http://dx.doi.org/10.3389/fgene.2022.1053655 Text en Copyright © 2023 Li, Li, Chen, Yang, Ren, Xu, Wu, Wang, Ling, Shen, Lu, Liu and Zhou. 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 Genetics
Li, Shun
Li, Caiwu
Chen, Lixiang
Yang, Hua
Ren, Xiaonan
Xu, Chunhua
Wu, Bin
Wang, Chao
Ling, Yun
Shen, Yinzhong
Lu, Hongzhou
Liu, Weiping
Zhou, Xiaohui
Comparative transcriptome analyses of immune responses to LPS in peripheral blood mononuclear cells from the giant panda, human, mouse, and monkey
title Comparative transcriptome analyses of immune responses to LPS in peripheral blood mononuclear cells from the giant panda, human, mouse, and monkey
title_full Comparative transcriptome analyses of immune responses to LPS in peripheral blood mononuclear cells from the giant panda, human, mouse, and monkey
title_fullStr Comparative transcriptome analyses of immune responses to LPS in peripheral blood mononuclear cells from the giant panda, human, mouse, and monkey
title_full_unstemmed Comparative transcriptome analyses of immune responses to LPS in peripheral blood mononuclear cells from the giant panda, human, mouse, and monkey
title_short Comparative transcriptome analyses of immune responses to LPS in peripheral blood mononuclear cells from the giant panda, human, mouse, and monkey
title_sort comparative transcriptome analyses of immune responses to lps in peripheral blood mononuclear cells from the giant panda, human, mouse, and monkey
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9852843/
https://www.ncbi.nlm.nih.gov/pubmed/36685921
http://dx.doi.org/10.3389/fgene.2022.1053655
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