羔羊前胃和胃单细胞分辨率的早期免疫动力学和细胞驱动因素。

IF 6.3 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE Journal of Animal Science and Biotechnology Pub Date : 2023-10-12 DOI:10.1186/s40104-023-00933-1
Kailang Huang, Bin Yang, Zebang Xu, Hongwei Chen, Jiakun Wang
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引用次数: 1

摘要

背景:包括前胃(瘤胃、网胃和胃)和胃的四腔胃使反刍动物能够将植物纤维转化为高质量的动物产品。这种四腔胃的早期发育对幼年反刍动物的健康和福祉至关重要,尤其是免疫发育。然而,人们对免疫发育的动力学知之甚少。结果:我们研究了湖羊在5、10、15和25日龄时四腔胃的早期基因表达模式。我们发现,前胃具有相似的基因表达模式,从第5天到第25天,所有四个胃都经历了先天和适应性免疫反应的广泛激活,而代谢功能随着年龄的增长而显著下调。我们使用单细胞测序构建了四腔胃的细胞景观。综合转录组学和单细胞转录组学分析显示,免疫相关模块hub基因在T细胞、单核细胞和巨噬细胞中高表达,防御相关模块hub基因在四种胃组织的内皮细胞中高表达。此外,上皮细胞等非免疫细胞在免疫成熟中起着关键作用。细胞通讯分析预测,除了免疫细胞外,非免疫细胞还通过前胃中巨噬细胞迁移抑制因子的信号传导来招募免疫细胞。结论:我们的研究结果表明,在羔羊的早期,四个胃的免疫和防御反应随着年龄的增长而迅速发展。我们还鉴定了与免疫发育相关的基因表达模式和功能细胞。此外,我们还鉴定了一些参与免疫调节的关键受体和信号传导。这些结果有助于了解单细胞分辨率下的早期免疫发育,这对开发基于特定靶点(包括关键受体和信号通路)的营养操作和健康管理策略具有启示意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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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, 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.

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822
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