Dietary protein modulates intestinal dendritic cells to establish mucosal homeostasis

Dietary proteins are taken up by intestinal dendritic cells (DCs), cleaved into peptides, loaded to major histocompatibility complexes, and presented to T cells to generate an immune response. Amino acid (AA)-diets do not have the same effects because AAs cannot bind to major histocompatibility comp...

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Veröffentlicht in:Mucosal immunology 2024-10, Vol.17 (5), p.911-922
Hauptverfasser: Moreira, Thais G., Cox, Laura M., Da Silva, Patrick, Mangani, Davide, De Oliveira, Marilia G., Escobar, Giulia, Lanser, Toby B., Murphy, Liam, Lobo, Eduardo.L.C., Milstein, Omer, Gauthier, Christian D., Clara Guimarāes, Ana, Schwerdtfeger, Luke, Ekwudo, Mellicient N., Wasén, Caroline, Liu, Shirong, Menezes, Gustavo B., Ferreira, Enio, Gabriely, Galina, Anderson, Ana C., Faria, Ana Maria C., Rezende, Rafael M., Weiner, Howard L.
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container_end_page 922
container_issue 5
container_start_page 911
container_title Mucosal immunology
container_volume 17
creator Moreira, Thais G.
Cox, Laura M.
Da Silva, Patrick
Mangani, Davide
De Oliveira, Marilia G.
Escobar, Giulia
Lanser, Toby B.
Murphy, Liam
Lobo, Eduardo.L.C.
Milstein, Omer
Gauthier, Christian D.
Clara Guimarāes, Ana
Schwerdtfeger, Luke
Ekwudo, Mellicient N.
Wasén, Caroline
Liu, Shirong
Menezes, Gustavo B.
Ferreira, Enio
Gabriely, Galina
Anderson, Ana C.
Faria, Ana Maria C.
Rezende, Rafael M.
Weiner, Howard L.
description Dietary proteins are taken up by intestinal dendritic cells (DCs), cleaved into peptides, loaded to major histocompatibility complexes, and presented to T cells to generate an immune response. Amino acid (AA)-diets do not have the same effects because AAs cannot bind to major histocompatibility complex to activate T cells. Here, we show that impairment in regulatory T cell generation and loss of tolerance in mice fed a diet lacking whole protein is associated with major transcriptional changes in intestinal DCs including downregulation of genes related to DC maturation, activation and decreased gene expression of immune checkpoint molecules. Moreover, the AA-diet had a profound effect on microbiome composition, including an increase in Akkermansia muciniphilia and Oscillibacter and a decrease in Lactococcus lactis and Bifidobacterium. Although microbiome transfer experiments showed that AA-driven microbiome modulates intestinal DC gene expression, most of the unique transcriptional change in DC was linked to the absence of whole protein in the diet. Our findings highlight the importance of dietary proteins for intestinal DC function and mucosal tolerance.
doi_str_mv 10.1016/j.mucimm.2024.06.006
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