CD71 + erythroid cells promote intestinal symbiotic microbial communities in pregnancy and neonatal period.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY Microbiome Pub Date : 2024-07-30 DOI:10.1186/s40168-024-01859-0
Petya Koleva, Jia He, Garett Dunsmore, Najmeh Bozorgmehr, Julia Lu, Maia Huynh, Stephanie Tollenaar, Vivian Huang, Jens Walter, Sing Sing Way, Shokrollah Elahi
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Abstract

Background: The establishment of microbial communities in neonatal mammals plays a pivotal role in shaping their immune responses to infections and other immune-related conditions. This process is influenced by a combination of endogenous and exogenous factors. Previously, we reported that depletion of CD71 + erythroid cells (CECs) results in an inflammatory response to microbial communities in newborn mice.

Results: Here, we systemically tested this hypothesis and observed that the small intestinal lamina propria of neonatal mice had the highest frequency of CECs during the early days of life. This high abundance of CECs was attributed to erythropoiesis niches within the small intestinal tissues. Notably, the removal of CECs from the intestinal tissues by the anti-CD71 antibody disrupted immune homeostasis. This disruption was evident by alteration in the expression of antimicrobial peptides (AMPs), toll-like receptors (TLRs), inflammatory cytokines/chemokines, and resulting in microbial dysbiosis. Intriguingly, these alterations in microbial communities persisted when tested 5 weeks post-treatment, with a more notable effect observed in female mice. This illustrates a sex-dependent association between CECs and neonatal microbiome modulation. Moreover, we extended our studies on pregnant mice, observing that modulating CECs substantially alters the frequency and diversity of their microbial communities. Finally, we found a significantly lower proportion of CECs in the cord blood of pre-term human newborns, suggesting a potential role in dysregulated immune responses to microbial communities in the gut.

Conclusions: Our findings provide novel insights into pivotal role of CECs in immune homeostasis and swift adaptation of microbial communities in newborns. Despite the complexity of the cellular biology of the gut, our findings shed light on the previously unappreciated role of CECs in the dialogue between the microbiota and immune system. These findings have significant implications for human health. Video Abstract.

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CD71 + 红细胞可促进孕期和新生儿期肠道共生微生物群落的发展。
背景:新生哺乳动物体内微生物群落的建立在形成其对感染和其他免疫相关疾病的免疫反应方面起着关键作用。这一过程受到内源性和外源性因素的共同影响。以前,我们曾报道过消耗 CD71 + 红细胞(CECs)会导致新生小鼠对微生物群落产生炎症反应:结果:在这里,我们对这一假设进行了系统测试,并观察到新生小鼠的小肠固有层在其出生早期具有最高频率的 CECs。CECs的高丰度归因于小肠组织内的红细胞生成龛位。值得注意的是,抗 CD71 抗体从肠组织中清除 CECs 破坏了免疫平衡。这种破坏表现为抗菌肽(AMPs)、类收费受体(TLRs)、炎性细胞因子/趋化因子表达的改变,并导致微生物菌群失调。耐人寻味的是,这些微生物群落的改变在治疗后 5 周进行检测时仍然存在,而且在雌性小鼠身上观察到的影响更为显著。这说明了 CECs 与新生儿微生物群调节之间存在性别依赖关系。此外,我们还扩展了对怀孕小鼠的研究,观察到调节 CECs 会显著改变其微生物群落的频率和多样性。最后,我们发现早产新生儿脐带血中 CECs 的比例明显较低,这表明 CECs 在肠道微生物群落免疫反应失调中可能发挥作用:我们的研究结果为了解 CECs 在新生儿免疫平衡和迅速适应微生物群落中的关键作用提供了新的视角。尽管肠道细胞生物学非常复杂,但我们的研究结果揭示了 CECs 在微生物群和免疫系统之间的对话中所起的作用,而这一作用以前从未被人们所认识。这些发现对人类健康具有重要意义。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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