Cargando…
Cross-tissue single-cell transcriptomic landscape reveals the key cell subtypes and their potential roles in the nutrient absorption and metabolism in dairy cattle
INTRODUCTION: Dairy cattle are a vitally important ruminant in meeting the demands for high-quality animal protein production worldwide. The complicated biological process of converting human indigestible biomass into highly digestible and nutritious milk is orchestrated by various tissues. However,...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039752/ https://www.ncbi.nlm.nih.gov/pubmed/35499046 http://dx.doi.org/10.1016/j.jare.2021.11.009 |
_version_ | 1784694197891104768 |
---|---|
author | Wu, Jia-Jin Zhu, Senlin Gu, Fengfei Valencak, Teresa G. Liu, Jian-Xin Sun, Hui-Zeng |
author_facet | Wu, Jia-Jin Zhu, Senlin Gu, Fengfei Valencak, Teresa G. Liu, Jian-Xin Sun, Hui-Zeng |
author_sort | Wu, Jia-Jin |
collection | PubMed |
description | INTRODUCTION: Dairy cattle are a vitally important ruminant in meeting the demands for high-quality animal protein production worldwide. The complicated biological process of converting human indigestible biomass into highly digestible and nutritious milk is orchestrated by various tissues. However, poorly understanding of the cellular composition and function of the key metabolic tissues hinders the improvement of health and performance of domestic ruminants. OBJECTIVES: The cellular heterogeneity, metabolic features, interactions across ten tissue types of lactating dairy cattle were studied at single-cell resolution in the current study. METHODS: Unbiased single-cell RNA-sequencing and analysis were performed on the rumen, reticulum, omasum, abomasum, ileum, rectum, liver, salivary gland, mammary gland, and peripheral blood of lactating dairy cattle. Immunofluorescences and fluorescence in situ hybridization were performed to verify cell identity. RESULTS: In this study, we constructed a single-cell landscape covering 88,013 high-quality (500 < genes < 4,000, UMI < 50, 000, and mitochondrial gene ratio < 40% or 15%) single cells and identified 55 major cell types in lactating dairy cattle. Our systematic survey of the gene expression profiles and metabolic features of epithelial cells related to nutrient transport revealed cell subtypes that have preferential absorption of different nutrients. Importantly, we found that T helper type 17 (Th17) cells (highly expressing CD4 and IL17A) were specifically enriched in the forestomach tissues and predominantly interacted with the epithelial cell subtypes with high potential uptake capacities of short-chain fatty acids through IL-17 signaling. Furthermore, the comparison between IL17RA(high)IL17RC(high) cells (epithelial cells with IL17RA and IL17RC expression levels both greater than 0.25) and other cells explained the importance of Th17 cells in regulating the epithelial cellular transcriptional response to nutrient transport in the forestomach. CONCLUSION: The findings enhance our understanding of the cellular biology of ruminants and open new avenues for improved animal production of dairy cattle. |
format | Online Article Text |
id | pubmed-9039752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-90397522022-04-27 Cross-tissue single-cell transcriptomic landscape reveals the key cell subtypes and their potential roles in the nutrient absorption and metabolism in dairy cattle Wu, Jia-Jin Zhu, Senlin Gu, Fengfei Valencak, Teresa G. Liu, Jian-Xin Sun, Hui-Zeng J Adv Res Agriculture INTRODUCTION: Dairy cattle are a vitally important ruminant in meeting the demands for high-quality animal protein production worldwide. The complicated biological process of converting human indigestible biomass into highly digestible and nutritious milk is orchestrated by various tissues. However, poorly understanding of the cellular composition and function of the key metabolic tissues hinders the improvement of health and performance of domestic ruminants. OBJECTIVES: The cellular heterogeneity, metabolic features, interactions across ten tissue types of lactating dairy cattle were studied at single-cell resolution in the current study. METHODS: Unbiased single-cell RNA-sequencing and analysis were performed on the rumen, reticulum, omasum, abomasum, ileum, rectum, liver, salivary gland, mammary gland, and peripheral blood of lactating dairy cattle. Immunofluorescences and fluorescence in situ hybridization were performed to verify cell identity. RESULTS: In this study, we constructed a single-cell landscape covering 88,013 high-quality (500 < genes < 4,000, UMI < 50, 000, and mitochondrial gene ratio < 40% or 15%) single cells and identified 55 major cell types in lactating dairy cattle. Our systematic survey of the gene expression profiles and metabolic features of epithelial cells related to nutrient transport revealed cell subtypes that have preferential absorption of different nutrients. Importantly, we found that T helper type 17 (Th17) cells (highly expressing CD4 and IL17A) were specifically enriched in the forestomach tissues and predominantly interacted with the epithelial cell subtypes with high potential uptake capacities of short-chain fatty acids through IL-17 signaling. Furthermore, the comparison between IL17RA(high)IL17RC(high) cells (epithelial cells with IL17RA and IL17RC expression levels both greater than 0.25) and other cells explained the importance of Th17 cells in regulating the epithelial cellular transcriptional response to nutrient transport in the forestomach. CONCLUSION: The findings enhance our understanding of the cellular biology of ruminants and open new avenues for improved animal production of dairy cattle. Elsevier 2021-11-24 /pmc/articles/PMC9039752/ /pubmed/35499046 http://dx.doi.org/10.1016/j.jare.2021.11.009 Text en © 2022 The Authors. Published by Elsevier B.V. on behalf of Cairo University. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Agriculture Wu, Jia-Jin Zhu, Senlin Gu, Fengfei Valencak, Teresa G. Liu, Jian-Xin Sun, Hui-Zeng Cross-tissue single-cell transcriptomic landscape reveals the key cell subtypes and their potential roles in the nutrient absorption and metabolism in dairy cattle |
title | Cross-tissue single-cell transcriptomic landscape reveals the key cell subtypes and their potential roles in the nutrient absorption and metabolism in dairy cattle |
title_full | Cross-tissue single-cell transcriptomic landscape reveals the key cell subtypes and their potential roles in the nutrient absorption and metabolism in dairy cattle |
title_fullStr | Cross-tissue single-cell transcriptomic landscape reveals the key cell subtypes and their potential roles in the nutrient absorption and metabolism in dairy cattle |
title_full_unstemmed | Cross-tissue single-cell transcriptomic landscape reveals the key cell subtypes and their potential roles in the nutrient absorption and metabolism in dairy cattle |
title_short | Cross-tissue single-cell transcriptomic landscape reveals the key cell subtypes and their potential roles in the nutrient absorption and metabolism in dairy cattle |
title_sort | cross-tissue single-cell transcriptomic landscape reveals the key cell subtypes and their potential roles in the nutrient absorption and metabolism in dairy cattle |
topic | Agriculture |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039752/ https://www.ncbi.nlm.nih.gov/pubmed/35499046 http://dx.doi.org/10.1016/j.jare.2021.11.009 |
work_keys_str_mv | AT wujiajin crosstissuesinglecelltranscriptomiclandscaperevealsthekeycellsubtypesandtheirpotentialrolesinthenutrientabsorptionandmetabolismindairycattle AT zhusenlin crosstissuesinglecelltranscriptomiclandscaperevealsthekeycellsubtypesandtheirpotentialrolesinthenutrientabsorptionandmetabolismindairycattle AT gufengfei crosstissuesinglecelltranscriptomiclandscaperevealsthekeycellsubtypesandtheirpotentialrolesinthenutrientabsorptionandmetabolismindairycattle AT valencakteresag crosstissuesinglecelltranscriptomiclandscaperevealsthekeycellsubtypesandtheirpotentialrolesinthenutrientabsorptionandmetabolismindairycattle AT liujianxin crosstissuesinglecelltranscriptomiclandscaperevealsthekeycellsubtypesandtheirpotentialrolesinthenutrientabsorptionandmetabolismindairycattle AT sunhuizeng crosstissuesinglecelltranscriptomiclandscaperevealsthekeycellsubtypesandtheirpotentialrolesinthenutrientabsorptionandmetabolismindairycattle |