Author
Listed:
- John W. Wills
(University of Cambridge)
- Alicja Dabrowska
(University of Cambridge)
- Jack Robertson
(University of Cambridge)
- Michelle Miniter
(University of Cambridge)
- Sebastian Riedle
(Massey University
Food & Bio-based Products Group, AgResearch, Grasslands Research Centre, Tennent Drive)
- Huw D. Summers
(Swansea University)
- Rachel E. Hewitt
(University of Cambridge)
- Adeeba Fathima
(University of Cambridge)
- Alessandra Barreto Silva
(University of Cambridge)
- Carlos A. P. Bastos
(University of Cambridge)
- Stuart Micklethwaite
(University of Leeds)
- Åsa V. Keita
(Linköping University)
- Johan D. Söderholm
(Linköping University)
- Nicole C. Roy
(Massey University
University of Otago
High-Value Nutrition Ko Ngā Kai Whai Painga National Science Challenge)
- Don Otter
(Auckland University of Technology)
- Ravin Jugdaohsingh
(University of Cambridge)
- Pietro Mastroeni
(University of Cambridge)
- Andy P. Brown
(University of Leeds)
- Paul Rees
(Swansea University
Broad Institute of MIT and Harvard)
- Jonathan J. Powell
(University of Cambridge)
Abstract
Food-grade titanium dioxide (fgTiO2) is a bio-persistent particle under intense regulatory scrutiny. Yet paradoxically, the only known cell reservoirs for fgTiO2 are graveyard intestinal pigment cells which are metabolically and immunologically quiescent. Here we identify immunocompetent cell targets of fgTiO2 in humans, most notably in the subepithelial dome region of intestinal Peyer’s patches. Using multimodal microscopies with single-particle detection and per-cell / vesicle image analysis we achieve correlative dosimetry, quantitatively recapitulating human cellular exposures in the ileum of mice fed a fgTiO2-containing diet. Epithelial microfold cells selectively funnel fgTiO2 into LysoMac and LysoDC cells with ensuing accumulation. Notwithstanding, proximity extension analyses for 92 protein targets reveal no measureable perturbation of cell signalling pathways. When chased with oral ΔaroA-Salmonella, pro-inflammatory signalling is confirmed, but no augmentation by fgTiO2 is revealed despite marked same-cell loading. Interestingly, Salmonella causes the fgTiO2-recipient cells to migrate within the patch and, sporadically, to be identified in the lamina propria, thereby fully recreating the intestinal tissue distribution of fgTiO2 in humans. Immunocompetent cells that accumulate fgTiO2 in vivo are now identified and we demonstrate a mouse model that finally enables human-relevant risk assessments of ingested, bio-persistent (nano)particles.
Suggested Citation
John W. Wills & Alicja Dabrowska & Jack Robertson & Michelle Miniter & Sebastian Riedle & Huw D. Summers & Rachel E. Hewitt & Adeeba Fathima & Alessandra Barreto Silva & Carlos A. P. Bastos & Stuart M, 2025.
"Immunocompetent cell targeting by food-additive titanium dioxide,"
Nature Communications, Nature, vol. 16(1), pages 1-19, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-60248-9
DOI: 10.1038/s41467-025-60248-9
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