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Synthetic mimetics of the endogenous gastrointestinal nanomineral: Silent constructs that trap macromolecules for intracellular delivery

Amorphous magnesium-substituted calcium phosphate (AMCP) nanoparticles (75-150 nm) form constitutively in large numbers in the mammalian gut. Collective evidence indicates that they trap and deliver luminal macromolecules to mucosal antigen presenting cells (APCs) and facilitate gut immune homeostas...

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Autores principales: Pele, Laetitia C., Haas, Carolin T., Hewitt, Rachel E., Robertson, Jack, Skepper, Jeremy, Brown, Andy, Hernandez-Garrido, Juan Carlos, Midgley, Paul A., Faria, Nuno, Chappell, Helen, Powell, Jonathan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339085/
https://www.ncbi.nlm.nih.gov/pubmed/27478107
http://dx.doi.org/10.1016/j.nano.2016.07.008
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author Pele, Laetitia C.
Haas, Carolin T.
Hewitt, Rachel E.
Robertson, Jack
Skepper, Jeremy
Brown, Andy
Hernandez-Garrido, Juan Carlos
Midgley, Paul A.
Faria, Nuno
Chappell, Helen
Powell, Jonathan J.
author_facet Pele, Laetitia C.
Haas, Carolin T.
Hewitt, Rachel E.
Robertson, Jack
Skepper, Jeremy
Brown, Andy
Hernandez-Garrido, Juan Carlos
Midgley, Paul A.
Faria, Nuno
Chappell, Helen
Powell, Jonathan J.
author_sort Pele, Laetitia C.
collection PubMed
description Amorphous magnesium-substituted calcium phosphate (AMCP) nanoparticles (75-150 nm) form constitutively in large numbers in the mammalian gut. Collective evidence indicates that they trap and deliver luminal macromolecules to mucosal antigen presenting cells (APCs) and facilitate gut immune homeostasis. Here, we report on a synthetic mimetic of the endogenous AMCP and show that it has marked capacity to trap macromolecules during formation. Macromolecular capture into AMCP involved incorporation as shown by STEM tomography of the synthetic AMCP particle with 5 nm ultra-fine iron (III) oxohydroxide. In vitro, organic cargo-loaded synthetic AMCP was taken up by APCs and tracked to lysosomal compartments. The AMCP itself did not regulate any gene, or modify any gene regulation by its cargo, based upon whole genome transcriptomic analyses. We conclude that synthetic AMCP can efficiently trap macromolecules and deliver them to APCs in a silent fashion, and may thus represent a new platform for antigen delivery.
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spelling pubmed-53390852017-03-13 Synthetic mimetics of the endogenous gastrointestinal nanomineral: Silent constructs that trap macromolecules for intracellular delivery Pele, Laetitia C. Haas, Carolin T. Hewitt, Rachel E. Robertson, Jack Skepper, Jeremy Brown, Andy Hernandez-Garrido, Juan Carlos Midgley, Paul A. Faria, Nuno Chappell, Helen Powell, Jonathan J. Nanomedicine Original Article Amorphous magnesium-substituted calcium phosphate (AMCP) nanoparticles (75-150 nm) form constitutively in large numbers in the mammalian gut. Collective evidence indicates that they trap and deliver luminal macromolecules to mucosal antigen presenting cells (APCs) and facilitate gut immune homeostasis. Here, we report on a synthetic mimetic of the endogenous AMCP and show that it has marked capacity to trap macromolecules during formation. Macromolecular capture into AMCP involved incorporation as shown by STEM tomography of the synthetic AMCP particle with 5 nm ultra-fine iron (III) oxohydroxide. In vitro, organic cargo-loaded synthetic AMCP was taken up by APCs and tracked to lysosomal compartments. The AMCP itself did not regulate any gene, or modify any gene regulation by its cargo, based upon whole genome transcriptomic analyses. We conclude that synthetic AMCP can efficiently trap macromolecules and deliver them to APCs in a silent fashion, and may thus represent a new platform for antigen delivery. Elsevier 2017-02 /pmc/articles/PMC5339085/ /pubmed/27478107 http://dx.doi.org/10.1016/j.nano.2016.07.008 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Pele, Laetitia C.
Haas, Carolin T.
Hewitt, Rachel E.
Robertson, Jack
Skepper, Jeremy
Brown, Andy
Hernandez-Garrido, Juan Carlos
Midgley, Paul A.
Faria, Nuno
Chappell, Helen
Powell, Jonathan J.
Synthetic mimetics of the endogenous gastrointestinal nanomineral: Silent constructs that trap macromolecules for intracellular delivery
title Synthetic mimetics of the endogenous gastrointestinal nanomineral: Silent constructs that trap macromolecules for intracellular delivery
title_full Synthetic mimetics of the endogenous gastrointestinal nanomineral: Silent constructs that trap macromolecules for intracellular delivery
title_fullStr Synthetic mimetics of the endogenous gastrointestinal nanomineral: Silent constructs that trap macromolecules for intracellular delivery
title_full_unstemmed Synthetic mimetics of the endogenous gastrointestinal nanomineral: Silent constructs that trap macromolecules for intracellular delivery
title_short Synthetic mimetics of the endogenous gastrointestinal nanomineral: Silent constructs that trap macromolecules for intracellular delivery
title_sort synthetic mimetics of the endogenous gastrointestinal nanomineral: silent constructs that trap macromolecules for intracellular delivery
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339085/
https://www.ncbi.nlm.nih.gov/pubmed/27478107
http://dx.doi.org/10.1016/j.nano.2016.07.008
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