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The early life immune dynamics and cellular drivers at single-cell resolution in lamb forestomachs and abomasum
BACKGROUND: Four-chambered stomach including the forestomachs (rumen, reticulum, and omasum) and abomasum allows ruminants convert plant fiber into high-quality animal products. The early development of this four-chambered stomach is crucial for the health and well-being of young ruminants, especial...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568933/ https://www.ncbi.nlm.nih.gov/pubmed/37821933 http://dx.doi.org/10.1186/s40104-023-00933-1 |
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author | Huang, Kailang Yang, Bin Xu, Zebang Chen, Hongwei Wang, Jiakun |
author_facet | Huang, Kailang Yang, Bin Xu, Zebang Chen, Hongwei Wang, Jiakun |
author_sort | Huang, Kailang |
collection | PubMed |
description | BACKGROUND: Four-chambered stomach including the forestomachs (rumen, reticulum, and omasum) and abomasum allows ruminants convert plant fiber into high-quality animal products. The early development of this four-chambered stomach is crucial for the health and well-being of young ruminants, especially the immune development. However, the dynamics of immune development are poorly understood. RESULTS: We investigated the early gene expression patterns across the four-chambered stomach in Hu sheep, at 5, 10, 15, and 25 days of age. We found that forestomachs share similar gene expression patterns, all four stomachs underwent widespread activation of both innate and adaptive immune responses from d 5 to 25, whereas the metabolic function were significantly downregulated with age. We constructed a cell landscape of the four-chambered stomach using single-cell sequencing. Integrating transcriptomic and single-cell transcriptomic analyses revealed that the immune-associated module hub genes were highly expressed in T cells, monocytes and macrophages, as well as the defense-associated module hub genes were highly expressed in endothelial cells in the four-stomach tissues. Moreover, the non-immune cells such as epithelial cells play key roles in immune maturation. Cell communication analysis predicted that in addition to immune cells, non-immune cells recruit immune cells through macrophage migration inhibitory factor signaling in the forestomachs. CONCLUSIONS: Our results demonstrate that the immune and defense responses of four stomachs are quickly developing with age in lamb's early life. We also identified the gene expression patterns and functional cells associated with immune development. Additionally, we identified some key receptors and signaling involved in immune regulation. These results help to understand the early life immune development at single-cell resolution, which has implications to develop nutritional manipulation and health management strategies based on specific targets including key receptors and signaling pathways. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40104-023-00933-1. |
format | Online Article Text |
id | pubmed-10568933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105689332023-10-13 The early life immune dynamics and cellular drivers at single-cell resolution in lamb forestomachs and abomasum Huang, Kailang Yang, Bin Xu, Zebang Chen, Hongwei Wang, Jiakun J Anim Sci Biotechnol Research BACKGROUND: Four-chambered stomach including the forestomachs (rumen, reticulum, and omasum) and abomasum allows ruminants convert plant fiber into high-quality animal products. The early development of this four-chambered stomach is crucial for the health and well-being of young ruminants, especially the immune development. However, the dynamics of immune development are poorly understood. RESULTS: We investigated the early gene expression patterns across the four-chambered stomach in Hu sheep, at 5, 10, 15, and 25 days of age. We found that forestomachs share similar gene expression patterns, all four stomachs underwent widespread activation of both innate and adaptive immune responses from d 5 to 25, whereas the metabolic function were significantly downregulated with age. We constructed a cell landscape of the four-chambered stomach using single-cell sequencing. Integrating transcriptomic and single-cell transcriptomic analyses revealed that the immune-associated module hub genes were highly expressed in T cells, monocytes and macrophages, as well as the defense-associated module hub genes were highly expressed in endothelial cells in the four-stomach tissues. Moreover, the non-immune cells such as epithelial cells play key roles in immune maturation. Cell communication analysis predicted that in addition to immune cells, non-immune cells recruit immune cells through macrophage migration inhibitory factor signaling in the forestomachs. CONCLUSIONS: Our results demonstrate that the immune and defense responses of four stomachs are quickly developing with age in lamb's early life. We also identified the gene expression patterns and functional cells associated with immune development. Additionally, we identified some key receptors and signaling involved in immune regulation. These results help to understand the early life immune development at single-cell resolution, which has implications to develop nutritional manipulation and health management strategies based on specific targets including key receptors and signaling pathways. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40104-023-00933-1. BioMed Central 2023-10-12 /pmc/articles/PMC10568933/ /pubmed/37821933 http://dx.doi.org/10.1186/s40104-023-00933-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Huang, Kailang Yang, Bin Xu, Zebang Chen, Hongwei Wang, Jiakun The early life immune dynamics and cellular drivers at single-cell resolution in lamb forestomachs and abomasum |
title | The early life immune dynamics and cellular drivers at single-cell resolution in lamb forestomachs and abomasum |
title_full | The early life immune dynamics and cellular drivers at single-cell resolution in lamb forestomachs and abomasum |
title_fullStr | The early life immune dynamics and cellular drivers at single-cell resolution in lamb forestomachs and abomasum |
title_full_unstemmed | The early life immune dynamics and cellular drivers at single-cell resolution in lamb forestomachs and abomasum |
title_short | The early life immune dynamics and cellular drivers at single-cell resolution in lamb forestomachs and abomasum |
title_sort | early life immune dynamics and cellular drivers at single-cell resolution in lamb forestomachs and abomasum |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568933/ https://www.ncbi.nlm.nih.gov/pubmed/37821933 http://dx.doi.org/10.1186/s40104-023-00933-1 |
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