Human milk extracellular vesicles target nodes in interconnected signalling pathways that enhance oral epithelial barrier function and dampen immune responses

Publication date

2020-05-01

Authors

Zonneveld, M.I.ISNI 0000000395610444
van Herwijnen, Martijn J CORCID 0000-0002-3158-1026ISNI 0000000419432284
Fernandez-Gutierrez, Marcela
Giovanazzi, AlbertaISNI 0000000506582109
de Groot, A.M.ISNI 0000000505985424
Kleinjan, MarijeISNI 0000000419445579
van Capel, T.M.
Sijts, AliceORCID 0000-0003-3815-4788ISNI 0000000394812562
Taams, L.S.
Garssen, JohanORCID 0000-0002-8678-9182ISNI 0000000034097251

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Document Type

/dk/atira/pure/researchoutput/researchoutputtypes/workingpaper/preprint
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cc_by

Abstract

Maternal milk is nature’s first functional food. It plays a crucial role in the development of the infant’s gastrointestinal (GI) tract and the immune system. Extracellular vesicles (EVs) are a heterogeneous population of lipid bilayer enclosed vesicles released by cells for intercellular communication and are a component of milk. Recently, we discovered that human milk EVs contain a unique proteome compared to other milk components. Here, we show that physiological concentrations of milk EVs support epithelial barrier function by increasing cell migration via the p38 MAPK pathway. Additionally, milk EVs inhibit agonist-induced activation of endosomal Toll like receptors TLR3 and TLR9. Furthermore, milk EVs directly inhibit activation of CD4+ T cells by temporarily suppressing T cell activation without inducing tolerance. We show that milk EV proteins target key hotspots of signalling networks that can modulate cellular processes in various cell types of the GI tract.

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Citation

Zonneveld, M I, van Herwijnen, M J C, Fernandez-Gutierrez, M, Giovanazzi, A, de Groot, A M, Kleinjan, M, van Capel, T M, Sijts, E J A M, Taams, L S, Garssen, J, de Jong, E, Kleerebezem, M, t Hoen, E N M, Redegeld, F A M & Wauben, M H M 2020 'Human milk extracellular vesicles target nodes in interconnected signalling pathways that enhance oral epithelial barrier function and dampen immune responses' bioRxiv. https://doi.org/10.1101/2020.04.29.068841