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Direct interaction of food derived colloidal micro/nano-particles with oral macrophages

Like any typical food system, bone soup (or broth), a traditional nourishing food in many cultures, contains a colloid dispersion of self-assembled micro/nano-particles. Food ingestion results in the direct contact of food colloidal MNPs with immune cells. Will they ever interact with each other? To...

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Autores principales: Ke, Lijing, Wang, Huiqin, Gao, Guanzhen, Rao, Pingfan, He, Lei, Zhou, Jianwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6548417/
https://www.ncbi.nlm.nih.gov/pubmed/31304245
http://dx.doi.org/10.1038/s41538-017-0003-3
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author Ke, Lijing
Wang, Huiqin
Gao, Guanzhen
Rao, Pingfan
He, Lei
Zhou, Jianwu
author_facet Ke, Lijing
Wang, Huiqin
Gao, Guanzhen
Rao, Pingfan
He, Lei
Zhou, Jianwu
author_sort Ke, Lijing
collection PubMed
description Like any typical food system, bone soup (or broth), a traditional nourishing food in many cultures, contains a colloid dispersion of self-assembled micro/nano-particles. Food ingestion results in the direct contact of food colloidal MNPs with immune cells. Will they ever interact with each other? To answer the question, MNPs and NPs were separated from porcine bone soup and labeled with Nile Red, and their uptake by murine oral macrophages and its consequent effects were investigated. Colloidal particle samples of UF-MNPs and SEC-NP were prepared from porcine bone soup by ultrafiltration (UF) and size-exclusion chromatography, respectively. Their mean hydrodynamic diameters were 248 ± 10 nm and 170 ± 1 nm with dominant composition of protein and lipid. Particles in both samples were found to be internalized by oral macrophages upon co-incubation at particle/cell ratios of 14,000/1. In normal oral macrophages, the particle uptake exerted influence neither on the cellular cytosolic membrane potential (V (mem)) nor mitochondrial superoxide level, as were indicated with fluorescent dyes of DiBAC(4)(3) and MitoSOX Red, respectively. However, when oral macrophages were challenged by peroxyl radical inducer AAPH, the engulfment of UF-MNPs and SEC-NPs mitigated the peroxyl radical induced membrane hyperpolarization effect by up to 70%, and the suppression on the oxygen respiration in mitochondria by up to 100%. Those results provide evidence of the direct interaction between food colloidal particles with immune cells, implying a possible new mode of food-body interaction.
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spelling pubmed-65484172019-07-12 Direct interaction of food derived colloidal micro/nano-particles with oral macrophages Ke, Lijing Wang, Huiqin Gao, Guanzhen Rao, Pingfan He, Lei Zhou, Jianwu NPJ Sci Food Article Like any typical food system, bone soup (or broth), a traditional nourishing food in many cultures, contains a colloid dispersion of self-assembled micro/nano-particles. Food ingestion results in the direct contact of food colloidal MNPs with immune cells. Will they ever interact with each other? To answer the question, MNPs and NPs were separated from porcine bone soup and labeled with Nile Red, and their uptake by murine oral macrophages and its consequent effects were investigated. Colloidal particle samples of UF-MNPs and SEC-NP were prepared from porcine bone soup by ultrafiltration (UF) and size-exclusion chromatography, respectively. Their mean hydrodynamic diameters were 248 ± 10 nm and 170 ± 1 nm with dominant composition of protein and lipid. Particles in both samples were found to be internalized by oral macrophages upon co-incubation at particle/cell ratios of 14,000/1. In normal oral macrophages, the particle uptake exerted influence neither on the cellular cytosolic membrane potential (V (mem)) nor mitochondrial superoxide level, as were indicated with fluorescent dyes of DiBAC(4)(3) and MitoSOX Red, respectively. However, when oral macrophages were challenged by peroxyl radical inducer AAPH, the engulfment of UF-MNPs and SEC-NPs mitigated the peroxyl radical induced membrane hyperpolarization effect by up to 70%, and the suppression on the oxygen respiration in mitochondria by up to 100%. Those results provide evidence of the direct interaction between food colloidal particles with immune cells, implying a possible new mode of food-body interaction. Nature Publishing Group UK 2017-10-30 /pmc/articles/PMC6548417/ /pubmed/31304245 http://dx.doi.org/10.1038/s41538-017-0003-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ke, Lijing
Wang, Huiqin
Gao, Guanzhen
Rao, Pingfan
He, Lei
Zhou, Jianwu
Direct interaction of food derived colloidal micro/nano-particles with oral macrophages
title Direct interaction of food derived colloidal micro/nano-particles with oral macrophages
title_full Direct interaction of food derived colloidal micro/nano-particles with oral macrophages
title_fullStr Direct interaction of food derived colloidal micro/nano-particles with oral macrophages
title_full_unstemmed Direct interaction of food derived colloidal micro/nano-particles with oral macrophages
title_short Direct interaction of food derived colloidal micro/nano-particles with oral macrophages
title_sort direct interaction of food derived colloidal micro/nano-particles with oral macrophages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6548417/
https://www.ncbi.nlm.nih.gov/pubmed/31304245
http://dx.doi.org/10.1038/s41538-017-0003-3
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