Cited by 15Cellular Mechanics and InteractionsNanoparticle-Based Drug DeliveryRNA Interference and Gene Delivery

Influence of HepG2 cell shape on nanoparticle uptake

Prats‐Mateu, Batirtze, Ertl, Peter, Toca‐Herrera, José Luis·2014·Microscopy Research and Technique

Abstract

Cell mechanics provides insights in cell responses to external stress, which is an important parameter known to influence a variety of cell functions. Understanding the interdependence between mechanical stimulus, cell shape and function is essential in controlling cell culture microenvironment. In this paper, we report on the effect of cationic and anionic interfaces on cell shape and nanoparticle uptake activity of hepatocellular carcinoma cells HepG2. The shape of HepG2 cells changed from a round‐like shape to a spread‐like form exhibiting lamellar protrusions by incubating them on coated polystyrene well plates with polystyrene sulfonate and poly‐ethylene imine (PEI), respectively. This change in shape of HepG2 cells did not influence the uptake of 49‐nm particles (which entered the cells by diffusion). However, the internalization of 240‐nm diameter particles was larger on cells seeded on cationic PEI. Particle uptake was measured at 4°C and 37°C; the optimal incubation time was 6 h. Cell shape and particle uptake were monitored by fluorescence and confocal microscopy. Quantification of particle internalization was carried out with flow cytometry. Microsc. Res. Tech. 77:560–565, 2014. © 2014 Wiley Periodicals, Inc.

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Crossref · 10.1002/jemt.22374

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  • HepG2 seeded on polystyrene well plates with and without coating exhibited significant differences in morphology, distribution, and functions such as particle uptake or P450-dependent detoxification.

    “The hepatoma cell line cell line HepG2, which is widely used not only for liver-associated research, seeded on polystyrene well plates with and without coating exhibited significant differences in their morphology, distribution, and functions such as particle uptake or P450-dependent detoxification (Saravia and Toca-Herrera, 2009; Prats-Mateu et al., 2014).”

    From In Vitro research Reproducibility: Keeping up High Standards (2019) · cites this paper as Prats-Mateu et al., 2014

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Authors
Prats‐Mateu, B., Ertl, P., & Toca‐Herrera, J. L.
Affiliations
  • AIT Austrian Institute of Technology GmbH (AT)
  • Department of Nanobiotechnology Institute for Biophysics, University of Natural Resources and Life Sciences 1190 Vienna Austria
Venue
Microscopy Research and Technique
Publisher
Wiley
Published
2014-05-08
Volume
77
Issue
8
Pages
560-565
ISSN
  • 1059-910X (ISSN-L)
  • 1097-0029
OpenAlex
W1836982097
Cited by
15
References
0
Citations by year
2026: 4 · 2025: 1 · 2024: 2 · 2023: 1 · 2020: 2 · 2019: 1 · 2018: 1 · 2017: 1 · 2016: 1 · 2015: 1
FWCI
0.50
Type
journal article
Language
en
Open access
closed
Locations
  • Microscopy Research and Technique (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
  • Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
Keywords
HepG2 cells, cell shape, nanoparticle uptake, cell mechanics, hepatocellular carcinoma, cationic surfaces, anionic surfaces, polyethyleneimine, polystyrene sulfonate, particle internalization, cell spreading
MeSH terms
Biological Transport, Diffusion, Humans, Microscopy, Fluorescence, Polyethyleneimine, Polystyrenes, Cell Culture Techniques, Cell Shape, Nanoparticles, Hep G2 Cells, Cellular Microenvironment

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