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人乳细胞外囊泡与肠道屏障相互作用的机制洞察

Mechanistic insight into human milk extracellular vesicle-intestinal barrier interactions.

作者信息

Luo Xiang, Zhang Yunyue, Ding Ning, Javorovic Jana, Raimi-Abraham Bahijja Tolulope, Lynham Steven, Yang Xiaoping, Shenker Natalie, Vllasaliu Driton

机构信息

Institute of Pharmaceutical Science School of Cancer and Pharmaceutical Science King's College London London UK.

Centre of Excellence for Mass Spectrometry, The James Black Centre King's College London London UK.

出版信息

J Extracell Biol. 2025 Jan 9;4(1):e70032. doi: 10.1002/jex2.70032. eCollection 2025 Jan.

Abstract

Human milk extracellular vesicles (EVs) are crucial mother-to-baby messengers that transfer biological signals. These EVs are reported to survive digestion and transport across the intestine. The mechanisms of interaction between human milk EVs and the intestinal mucosa, including epithelial uptake remain unclear. Here, we studied the interaction of human milk EVs with the gut barrier components, including intestinal biofluids, enzymes, mucus and epithelium. Additionally, we probed the endocytic mechanisms mediating the EV intestinal uptake. Finally, using proteomic analysis, we determined the existence and identification of proteins enriched in the EV fraction transported across the intestinal epithelium. We show that human milk EVs are largely stable in the biochemical gut barriers and demonstrate high mucus diffusivity. EVs show a high level of epithelial cell uptake (∼70%) and efficient transport across Caco-2 monolayers. Whilst cell uptake of EVs was mediated by multiple routes, none of the pathway-specific inhibitors inhibited their epithelial translocation. Proteomic analysis of EVs transported across Caco-2 monolayers identified 14 enriched EV proteins that may facilitate intestinal transport. These findings significantly expand our understanding of the interactions between human milk EVs and the gut barriers, including their intestinal uptake.

摘要

人乳细胞外囊泡(EVs)是传递生物信号的关键母婴信使。据报道,这些EVs能在消化过程中存活并穿过肠道运输。人乳EVs与肠黏膜之间的相互作用机制,包括上皮细胞摄取,仍不清楚。在此,我们研究了人乳EVs与肠道屏障成分之间的相互作用,包括肠生物流体、酶、黏液和上皮细胞。此外,我们探究了介导EVs肠道摄取的内吞机制。最后,通过蛋白质组学分析,我们确定了跨肠上皮运输的EVs组分中富集蛋白质的存在和鉴定。我们发现人乳EVs在生化肠道屏障中基本稳定,并表现出高黏液扩散性。EVs显示出高水平的上皮细胞摄取(约70%),并能有效穿过Caco-2单层细胞。虽然EVs的细胞摄取是由多种途径介导的,但没有一种途径特异性抑制剂能抑制它们的上皮转运。对跨Caco-2单层细胞运输的EVs进行蛋白质组学分析,鉴定出14种富集的EV蛋白,这些蛋白可能有助于肠道运输。这些发现显著扩展了我们对人乳EVs与肠道屏障之间相互作用的理解,包括它们的肠道摄取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9aa3/11714171/885127503735/JEX2-4-e70032-g006.jpg

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