journal article·2013-08-27

Multiple Internalization Pathways of Polyelectrolyte Multilayer Capsules into Mammalian Cells

Lena Kastl, Daniel Sasse, Verena Wulf, Raimo Hartmann, Josif Mircheski, Christiane Ranke, Susana Carregal-Romero, José Antonio Martínez-López, Rafael Fernández-Chacón, Wolfgang J. Parak, Hans-Peter Elsasser, Pilar Rivera_Gil

ACS Nano· Volume 7· Issue 8
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Abstract

Polyelectrolyte multilayer (PEM) capsules are carrier vehicles with great potential for biomedical applications. With the future aim of designing biocompatible, effective therapeutic delivery systems (e.g., for cancer), the pathway of internalization (uptake and fate) of PEM capsules was investigated. In particular the following experiments were performed: (i) the study of capsule co-localization with established endocytic markers, (ii) switching-off endocytotic pathways with pharmaceutical/chemical inhibitors, and (iii) characterization and quantification of capsule uptake with confocal and electron microscopy. As result, capsules co-localized with lipid rafts and with phagolysosomes, but not with other endocytic vesicles. Chemical interference of endocytosis with chemical blockers indicated that PEM capsules enter the investigated cell lines through a mechanism slightly sensitive to electrostatic interactions, independent of clathrin and caveolae, and strongly dependent on cholesterol-rich domains and organelle acidification. Microscopic characterization of cells during capsule uptake showed the formation of phagocytic cups (vesicles) to engulf the capsules, an increased number of mitochondria, and a final localization in the perinuclear cytoplasma. Combining all these indicators we conclude that PEM capsule internalization in general occurs as a combination of different sequential mechanisms. Initially, an adsorptive mechanism due to strong electrostatic interactions governs the stabilization of the capsules at the cell surface. Membrane ruffling and filopodia extensions are responsible for capsule engulfing through the formation of a phagocytic cup. Co-localization with lipid raft domains activates the cell to initiate a lipid-raft-mediated macropinocytosis. Internalization vesicles are very acidic and co-localize only with phagolysosome markers, excluding caveolin-mediated pathways and indicating that upon phagocytosis the capsules are sorted to heterophagolysosomes.
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Research context

OpenAlex topics: Polymer Surface Interaction Studies · Blood properties and coagulation · Dendrimers and Hyperbranched Polymers

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Fachbereich Physik, Philipps-Universität Marburg, Renthof 7, 35037 Marburg, Germany

Instituto de Biomedicina de Sevilla (IBiS) Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Departamento de Fisiologia Medica y Biofísica, and CIBERNED, Avenida Manuel Siurot s/n, 41013, Sevilla, Spain

Andalusian Center for Nanomedicine and Biotechnology (BIONAND), Andalusian Technological Park, C/Severo Ochoa, 35, 29590 Campanillas, Málaga, Spain

Institute of Cytology and Cytopathology, Philipps-Universität Marburg, Robert-Koch Straße 6, 35033 Marburg, Germany

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