人乳细胞外囊泡-肠屏障相互作用的机理研究。

Journal of extracellular biology Pub Date : 2025-01-09 eCollection Date: 2025-01-01 DOI:10.1002/jex2.70032
Xiang Luo, Yunyue Zhang, Ning Ding, Jana Javorovic, Bahijja Tolulope Raimi-Abraham, Steven Lynham, Xiaoping Yang, Natalie Shenker, Driton Vllasaliu
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引用次数: 0

摘要

母乳细胞外囊泡(EVs)是母婴传递生物信号的重要信使。据报道,这些ev在消化过程中存活下来,并通过肠道运输。乳汁ev与肠黏膜相互作用的机制,包括上皮摄取,目前尚不清楚。在这里,我们研究了母乳ev与肠道屏障成分的相互作用,包括肠道生物体液、酶、粘液和上皮。此外,我们还探讨了介导EV肠摄取的内吞机制。最后,通过蛋白质组学分析,我们确定了肠上皮运输的EV部分中富集的蛋白质的存在和鉴定。我们发现,人乳ev在生化肠道屏障中基本稳定,并表现出高粘液扩散性。ev表现出高水平的上皮细胞摄取(约70%)和高效的Caco-2单层运输。虽然ev的细胞摄取是通过多种途径介导的,但没有一种途径特异性抑制剂能抑制它们的上皮易位。通过Caco-2单层运输的EV蛋白组学分析,鉴定出14种可能促进肠道运输的富集EV蛋白。这些发现大大扩展了我们对人乳ev与肠道屏障之间相互作用的理解,包括它们的肠道吸收。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanistic insight into human milk extracellular vesicle-intestinal barrier interactions.

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.

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