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  3. Different endocytotic uptake mechanisms for nanoparticles in epithelial cells and macrophages.

Different endocytotic uptake mechanisms for nanoparticles in epithelial cells and macrophages.

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DOI
10.7892/boris.64402
Publisher DOI
10.3762/bjnano.5.174
PubMed ID
25383275
Abstract
Precise knowledge regarding cellular uptake of nanoparticles is of great importance for future biomedical applications. Four different endocytotic uptake mechanisms, that is, phagocytosis, macropinocytosis, clathrin- and caveolin-mediated endocytosis, were investigated using a mouse macrophage (J774A.1) and a human alveolar epithelial type II cell line (A549). In order to deduce the involved pathway in nanoparticle uptake, selected inhibitors specific for one of the endocytotic pathways were optimized regarding concentration and incubation time in combination with fluorescently tagged marker proteins. Qualitative immunolocalization showed that J774A.1 cells highly expressed the lipid raft-related protein flotillin-1 and clathrin heavy chain, however, no caveolin-1. A549 cells expressed clathrin heavy chain and caveolin-1, but no flotillin-1 uptake-related proteins. Our data revealed an impeded uptake of 40 nm polystyrene nanoparticles by J774A.1 macrophages when actin polymerization and clathrin-coated pit formation was blocked. From this result, it is suggested that macropinocytosis and phagocytosis, as well as clathrin-mediated endocytosis, play a crucial role. The uptake of 40 nm nanoparticles in alveolar epithelial A549 cells was inhibited after depletion of cholesterol in the plasma membrane (preventing caveolin-mediated endocytosis) and inhibition of clathrin-coated vesicles (preventing clathrin-mediated endocytosis). Our data showed that a combination of several distinguishable endocytotic uptake mechanisms are involved in the uptake of 40 nm polystyrene nanoparticles in both the macrophage and epithelial cell line.
Date Issued
2014
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Subjects
cell lines
•
endocytosis
•
inhibition
•
nanoparticles
•
uptake proteins
Language(s)
en
Author(s)
Kuhn, Dagmar A
Vanhecke, Dimitri
Michen, Benjamin
Blank, Fabian  
Departement Klinische Forschung, Forschungsgruppe Pneumologie (Erwachsene)  
UniversitƤtsklinik für Pneumologie  
Gehr, Peter  
Emeriti, Medizinische FakultƤt  
Petri-Fink, Alke
Rothen-Rutishauser, Barbara  
Departement Klinische Forschung, Forschungsgruppe Pneumologie (Erwachsene)  
UniversitƤtsklinik für Pneumologie  
Additional Credits
UniversitƤtsklinik für Pneumologie  
Departement Klinische Forschung, Forschungsgruppe Pneumologie (Erwachsene)  
Emeriti, Medizinische FakultƤt  
Journal
Beilstein journal of nanotechnology
Publisher
Beilstein-Institut zur Förderung der Chemischen Wissenschaften
ISSN
2190-4286
Access(Rights)
open.access
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