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Lipoprotein Particles as Shuttles for Hydrophilic Cargo

Lipoprotein particles (LPs) are excellent transporters and have been intensively studied in cardiovascular diseases, especially regarding parameters such as their class distribution and accumulation, site-specific delivery, cellular internalization, and escape from endo/lysosomal compartments. The a...

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Autores principales: Weber, Florian, Axmann, Markus, Horner, Andreas, Schwarzinger, Bettina, Weghuber, Julian, Plochberger, Birgit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222575/
https://www.ncbi.nlm.nih.gov/pubmed/37233532
http://dx.doi.org/10.3390/membranes13050471
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author Weber, Florian
Axmann, Markus
Horner, Andreas
Schwarzinger, Bettina
Weghuber, Julian
Plochberger, Birgit
author_facet Weber, Florian
Axmann, Markus
Horner, Andreas
Schwarzinger, Bettina
Weghuber, Julian
Plochberger, Birgit
author_sort Weber, Florian
collection PubMed
description Lipoprotein particles (LPs) are excellent transporters and have been intensively studied in cardiovascular diseases, especially regarding parameters such as their class distribution and accumulation, site-specific delivery, cellular internalization, and escape from endo/lysosomal compartments. The aim of the present work is the hydrophilic cargo loading of LPs. As an exemplary proof-of-principle showcase, the glucose metabolism-regulating hormone, insulin, was successfully incorporated into high-density lipoprotein (HDL) particles. The incorporation was studied and verified to be successful using Atomic Force Microscopy (AFM) and Fluorescence Microscopy (FM). Single-molecule-sensitive FM together with confocal imaging visualized the membrane interaction of single, insulin-loaded HDL particles and the subsequent cellular translocation of glucose transporter type 4 (Glut4).
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spelling pubmed-102225752023-05-28 Lipoprotein Particles as Shuttles for Hydrophilic Cargo Weber, Florian Axmann, Markus Horner, Andreas Schwarzinger, Bettina Weghuber, Julian Plochberger, Birgit Membranes (Basel) Article Lipoprotein particles (LPs) are excellent transporters and have been intensively studied in cardiovascular diseases, especially regarding parameters such as their class distribution and accumulation, site-specific delivery, cellular internalization, and escape from endo/lysosomal compartments. The aim of the present work is the hydrophilic cargo loading of LPs. As an exemplary proof-of-principle showcase, the glucose metabolism-regulating hormone, insulin, was successfully incorporated into high-density lipoprotein (HDL) particles. The incorporation was studied and verified to be successful using Atomic Force Microscopy (AFM) and Fluorescence Microscopy (FM). Single-molecule-sensitive FM together with confocal imaging visualized the membrane interaction of single, insulin-loaded HDL particles and the subsequent cellular translocation of glucose transporter type 4 (Glut4). MDPI 2023-04-28 /pmc/articles/PMC10222575/ /pubmed/37233532 http://dx.doi.org/10.3390/membranes13050471 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Weber, Florian
Axmann, Markus
Horner, Andreas
Schwarzinger, Bettina
Weghuber, Julian
Plochberger, Birgit
Lipoprotein Particles as Shuttles for Hydrophilic Cargo
title Lipoprotein Particles as Shuttles for Hydrophilic Cargo
title_full Lipoprotein Particles as Shuttles for Hydrophilic Cargo
title_fullStr Lipoprotein Particles as Shuttles for Hydrophilic Cargo
title_full_unstemmed Lipoprotein Particles as Shuttles for Hydrophilic Cargo
title_short Lipoprotein Particles as Shuttles for Hydrophilic Cargo
title_sort lipoprotein particles as shuttles for hydrophilic cargo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222575/
https://www.ncbi.nlm.nih.gov/pubmed/37233532
http://dx.doi.org/10.3390/membranes13050471
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