Mechanistic insight into human milk extracellular vesicle-intestinal barrier interactions

Xiang Luo, Yunyue Zhang, Ning Ding, Jana Javorovic, Bahijja Tolulope Raimi-Abraham, Steven Lynham, Xiaoping Yang, Natalie Shenker, Driton Vllasaliu
{"title":"Mechanistic insight into human milk extracellular vesicle-intestinal barrier interactions","authors":"Xiang Luo,&nbsp;Yunyue Zhang,&nbsp;Ning Ding,&nbsp;Jana Javorovic,&nbsp;Bahijja Tolulope Raimi-Abraham,&nbsp;Steven Lynham,&nbsp;Xiaoping Yang,&nbsp;Natalie Shenker,&nbsp;Driton Vllasaliu","doi":"10.1002/jex2.70032","DOIUrl":null,"url":null,"abstract":"<p>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.</p>","PeriodicalId":73747,"journal":{"name":"Journal of extracellular biology","volume":"4 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11714171/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of extracellular biology","FirstCategoryId":"1085","ListUrlMain":"https://isevjournals.onlinelibrary.wiley.com/doi/10.1002/jex2.70032","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

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.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
人乳细胞外囊泡-肠屏障相互作用的机理研究。
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。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
A One-Step Workflow for Size-Based Separation of Extracellular Vesicles With Integrated Surface Marker Detection. Proteomic Epithelial-To-Mesenchymal Transition Signature in Fetoplacental Small Extracellular Vesicles of Early-Onset Preeclampsia. Small Extracellular Vesicles in Gestational Diabetes Mellitus: Current Landscape and Emerging Diagnostic Horizons. Molecular Characterization of Extracellular Vesicles From Human B Cell Lymphomas: Methodological Comparison to Vesicles From Patient Serum Extracellular Vesicle Properties and Functions Are Defined by the Originating Cell's Fitness Status
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1