Skip to main navigation Skip to search Skip to main content

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
  • , Jose Antonio Martinez-Lopez
  • , Rafael Fernandez-Chacon
  • , Wolfgang J. Parak
  • , Hans Peter Elsasser
  • , Pilar Rivera Gil

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

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.

Original languageEnglish
Title of host publicationBio-Nano Interfaces
Subtitle of host publicationPerspectives, Properties, and Applications
PublisherJenny Stanford Publishing
Pages1103-1138
Number of pages36
ISBN (Electronic)9781000618907
ISBN (Print)9789814877831
DOIs
StatePublished - 1 Jan 2024
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2024 by Jenny Stanford Publishing Pte. Ltd.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Fingerprint

Dive into the research topics of 'Multiple Internalization Pathways of Polyelectrolyte Multilayer Capsules into Mammalian Cells'. Together they form a unique fingerprint.

Cite this