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在稳态和感染期间对幼年反刍动物肠道单核吞噬细胞亚群的特征分析。

Characterization of intestinal mononuclear phagocyte subsets in young ruminants at homeostasis and during infection.

机构信息

Unité Mixte de Recherches (UMR)1282 Infectiologie et Santé Publique, INRAE Centre Val de Loire, Université François Rabelais de Tours, Nouzilly, France.

Phileo by Lesaffre, Marcq-en-Barœul, France.

出版信息

Front Immunol. 2024 May 2;15:1379798. doi: 10.3389/fimmu.2024.1379798. eCollection 2024.

DOI:10.3389/fimmu.2024.1379798
PMID:38756777
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11096452/
Abstract

INTRODUCTION

Cryptosporidiosis is a poorly controlled zoonosis caused by an intestinal parasite, , with a high prevalence in livestock (cattle, sheep, and goats). Young animals are particularly susceptible to this infection due to the immaturity of their intestinal immune system. In a neonatal mouse model, we previously demonstrated the importance of the innate immunity and particularly of type 1 conventional dendritic cells (cDC1) among mononuclear phagocytes (MPs) in controlling the acute phase of infection. These immune populations are well described in mice and humans, but their fine characterization in the intestine of young ruminants remained to be further explored.

METHODS

Immune cells of the small intestinal Peyer's patches and of the distal jejunum were isolated from naive lambs and calves at different ages. This was followed by their fine characterization by flow cytometry and transcriptomic analyses (q-RT-PCR and single cell RNAseq (lamb cells)). Newborn animals were infected with , clinical signs and parasite burden were quantified, and isolated MP cells were characterized by flow cytometry in comparison with age matched control animals.

RESULTS

Here, we identified one population of macrophages and three subsets of cDC (cDC1, cDC2, and a minor cDC subset with migratory properties) in the intestine of lamb and calf by phenotypic and targeted gene expression analyses. Unsupervised single-cell transcriptomic analysis confirmed the identification of these four intestinal MP subpopulations in lamb, while highlighting a deeper diversity of cell subsets among monocytic and dendritic cells. We demonstrated a weak proportion of cDC1 in the intestine of highly susceptible newborn lambs together with an increase of these cells within the first days of life and in response to the infection.

DISCUSSION

Considering cDC1 importance for efficient parasite control in the mouse model, one may speculate that the cDC1/cDC2 ratio plays also a key role for the efficient control of in young ruminants. In this study, we established the first fine characterization of intestinal MP subsets in young lambs and calves providing new insights for comparative immunology of the intestinal MP system across species and for future investigations on host-Cryptosporidium interactions in target species.

摘要

简介

隐孢子虫病是一种由肠道寄生虫引起的控制效果不佳的人畜共患病,在牲畜(牛、羊和山羊)中发病率很高。由于幼小动物的肠道免疫系统尚未成熟,它们特别容易感染这种寄生虫。在新生小鼠模型中,我们之前证明了单核吞噬细胞(MPs)中的固有免疫,特别是 1 型传统树突状细胞(cDC1),在控制 感染的急性期方面的重要性。这些免疫群体在小鼠和人类中得到了很好的描述,但它们在幼反刍动物肠道中的精细特征仍有待进一步探索。

方法

从小肠派尔集合淋巴结和回肠远端分离出不同年龄的新生羔羊和犊牛的小肠固有免疫细胞。然后通过流式细胞术和转录组分析(q-RT-PCR 和单细胞 RNAseq(羔羊细胞))对其进行精细表征。新生动物感染 后,量化临床症状和寄生虫负担,并通过流式细胞术对分离的 MP 细胞进行特征分析,与年龄匹配的对照动物进行比较。

结果

在这里,我们通过表型和靶向基因表达分析,在羔羊和犊牛的肠道中鉴定出一种巨噬细胞群体和三种 cDC 亚群(cDC1、cDC2 和具有迁移特性的次要 cDC 亚群)。未监督的单细胞转录组分析证实了在羔羊中鉴定出这四个肠道 MP 亚群,同时突出了单核细胞和树突状细胞中细胞亚群的更深层次多样性。我们证明了在高度易感的新生羔羊肠道中 cDC1 的比例较低,同时在生命的头几天以及感染后这些细胞的数量增加。

讨论

鉴于 cDC1 对小鼠模型中寄生虫有效控制的重要性,人们可能会推测,cDC1/cDC2 比值对于年轻反刍动物中 有效控制也起着关键作用。在这项研究中,我们首次对幼羔羊和犊牛的肠道 MP 亚群进行了精细特征描述,为跨物种肠道 MP 系统的比较免疫学提供了新的见解,并为宿主-隐孢子虫相互作用在目标物种中的未来研究提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb3f/11096452/80cadf103cac/fimmu-15-1379798-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb3f/11096452/0d4909e59553/fimmu-15-1379798-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb3f/11096452/d5a4e5fa22bb/fimmu-15-1379798-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb3f/11096452/80cadf103cac/fimmu-15-1379798-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb3f/11096452/ed9ea5812d40/fimmu-15-1379798-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb3f/11096452/0d4909e59553/fimmu-15-1379798-g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb3f/11096452/80cadf103cac/fimmu-15-1379798-g008.jpg

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