Original Article
Comparison of the uptake mechanisms of zwitterionic and negatively charged liposomes by HeLa cells

https://doi.org/10.1016/j.nano.2020.102300Get rights and content
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Abstract

Zwitterionic molecules are used as an alternative to PEGylation to reduce protein adsorption on nanocarriers. Nonetheless, little is known on the effect of zwitterionic modifications on the mechanisms cells use for nanocarrier uptake. In this study, the uptake mechanism of liposomes containing zwitterionic or negatively charged lipids was characterized using pharmacological inhibitors and RNA interference on HeLa cells to block endocytosis. As expected, introducing zwitterionic lipids reduced protein adsorption in serum, as well as uptake efficiency. Blocking clathrin-mediated endocytosis strongly decreased the uptake of the negatively charged liposomes, but not the zwitterionic ones. Additionally, inhibition of macropinocytosis reduced uptake of both liposomes, but blocking actin polymerization had effects only on the negatively charged ones. Overall, the results clearly indicated that the two liposomes were internalized by HeLa cells using different pathways. Thus, introducing zwitterionic lipids affects not only protein adsorption and uptake efficiency, but also the mechanisms of liposome uptake by cells.

Graphical Abstract

Zwitterionic lipids are used to reduce protein adsorption on liposomes. However, the effect of zwitterionic lipids on the mechanism of liposome uptake by cells is not well studied. In this context, the uptake mechanism of liposomes containing zwitterionic DOPC or negatively charged DOPG lipids was compared. Zwitterionic liposomes adsorbed much less proteins in serum, and their uptake efficacy was strongly reduced. Despite their similar size and charge after corona formation, zwitterionic and negatively charged liposomes were internalized by cells using different mechanisms, suggesting that the very different outcomes on cells may depend on the identity of the proteins adsorbed.

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Key words

Zwitterionic
Liposome
Uptake mechanism
Pharmacological inhibitor

Abbreviations

DOPC
1,2-dioleoyl-sn-glycero-3-phosphocholine
DOPG
1,2-dioleoyl-sn-glycero-3-phospho-(1′-rac-glycerol)
SRB
sulforhodamine B
CD47
cluster of differentiation 47
PBS
phosphate buffered saline
MWCO
molecular weight cut off
MEM
minimum essential medium
hsMEM
MEM medium supplemented with 4 mg/mL human serum
FBS
fetal bovine serum
cMEM
complete MEM medium supplemented with 10% FBS
sfMEM
serum-free MEM
SEC
size exclusion chromatography
SDS-PAGE
sodium dodecyl sulfate–polyacrylamide gel electrophoresis
EIPA
5-(N-ethyl-N-isopropyl)amiloride
MBCD
methyl-β-cyclodextrin
LDL
low-density lipoprotein
EDTA
ethylenediaminetetraacetic acid
TRITC
tetramethylrhodamine
DAPI
4′,6-diamidino-2-phenylindole
DLS
dynamic light scattering
CME
clathrin-mediated endocytosis
DNM
dynamin
GTPase
guanosine triphosphatase
Rac1
Ras-related C3 botulinum toxin substrate 1
Cdc42
cell division control protein 42 homolog

Cited by (0)

This work was funded by the European Research Council (ERC) under the European Union's Horizon 2020 Research and Innovation Programme under grant agreement no. 637614 (NanoPaths). K.Y. was supported by a PhD scholarship from the China Scholarship Council. A.S. would like to acknowledge additional funding from the University of Groningen (Rosalind Franklin Fellowship).

The authors declare no conflicts of interest.

1

These authors contributed equally to this publication.