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Efficient transfection of hepatocytes mediated by mRNA complexed to galactosylated cyclodextrins

Nathalie Symens UGent, Alejandro Méndez-Ardoy, Alejandro Diaz-Moscoso, Elena Sánchez-Fernéndez, Katrien Remaut UGent, Jo Demeester UGent, José M García Fernández, Stefaan De Smedt UGent and Joanna Rejman UGent (2012) BIOCONJUGATE CHEMISTRY. 23(6). p.1276-1289
abstract
In this study, we aimed at specific targeting of polycationic amphiphilic cyclodextrins (paCDs) to HepG2 cells via the asialoglycoprotein receptor (ASGPr). The transfection efficiencies of paCDs modified with galactose moieties were evaluated. In preliminary experiments, attempts to transfect HepG2 cells with pDNA complexed with different modified paCDs resulted in very low transfection levels. In additional series of experiments, we found out that nucleic acid/cyclodextrin complexes (CDplexes) were efficiently taken up by the cells and that photochemical internalization, which facilitates release from endosomes, did not improve transfection. Further experiments showed that pDNA can be readily released from the CDplexes when exposed to negatively charged vesicles. These observations imply that the lack of transfection cannot be attributed to a lack of internalization, release of CDplexes from the endosomal compartment, or release of free pDNA from the CDplexes. This in turn suggests that the nuclear entry of the pDNA represents the main limiting factor in the transfection process. To verify that HepG2 cells were transfected with targeted CDplexes containing mRNA, which does not require entry into the nucleus for being translated. With mRNA encoding the green fluorescent protein, fractions of GFP-positive cells of up to 31% were obtained. The results confirmed that the galactosylated complexes are specifically internalized via the ASGPr.
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
ASIALOGLYCOPROTEIN RECEPTOR, GENE DELIVERY-SYSTEMS, IN-VIVO, AMPHIPHILIC CYCLODEXTRINS, VIRAL VECTORS, GROWTH-FACTOR, PLASMID DNA, FACTOR-IX, ENDOCYTOSIS, LIGAND
journal title
BIOCONJUGATE CHEMISTRY
Bioconjugate Chem.
volume
23
issue
6
pages
1276 - 1289
Web of Science type
Article
Web of Science id
000305358700021
JCR category
CHEMISTRY, ORGANIC
JCR impact factor
4.58 (2012)
JCR rank
8/55 (2012)
JCR quartile
1 (2012)
ISSN
1043-1802
DOI
10.1021/bc3001003
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
2137184
handle
http://hdl.handle.net/1854/LU-2137184
date created
2012-06-08 11:30:08
date last changed
2012-09-12 11:26:12
@article{2137184,
  abstract     = {In this study, we aimed at specific targeting of polycationic amphiphilic cyclodextrins (paCDs) to HepG2 cells via the asialoglycoprotein receptor (ASGPr). The transfection efficiencies of paCDs modified with galactose moieties were evaluated. In preliminary experiments, attempts to transfect HepG2 cells with pDNA complexed with different modified paCDs resulted in very low transfection levels. In additional series of experiments, we found out that nucleic acid/cyclodextrin complexes (CDplexes) were efficiently taken up by the cells and that photochemical internalization, which facilitates release from endosomes, did not improve transfection. Further experiments showed that pDNA can be readily released from the CDplexes when exposed to negatively charged vesicles. These observations imply that the lack of transfection cannot be attributed to a lack of internalization, release of CDplexes from the endosomal compartment, or release of free pDNA from the CDplexes. This in turn suggests that the nuclear entry of the pDNA represents the main limiting factor in the transfection process. To verify that HepG2 cells were transfected with targeted CDplexes containing mRNA, which does not require entry into the nucleus for being translated. With mRNA encoding the green fluorescent protein, fractions of GFP-positive cells of up to 31\% were obtained. The results confirmed that the galactosylated complexes are specifically internalized via the ASGPr.},
  author       = {Symens, Nathalie and M{\'e}ndez-Ardoy, Alejandro and Diaz-Moscoso, Alejandro and S{\'a}nchez-Fern{\'e}ndez, Elena and Remaut, Katrien and Demeester, Jo and Garc{\'i}a Fern{\'a}ndez, Jos{\'e} M and De Smedt, Stefaan and Rejman, Joanna},
  issn         = {1043-1802},
  journal      = {BIOCONJUGATE CHEMISTRY},
  keyword      = {ASIALOGLYCOPROTEIN RECEPTOR,GENE DELIVERY-SYSTEMS,IN-VIVO,AMPHIPHILIC CYCLODEXTRINS,VIRAL VECTORS,GROWTH-FACTOR,PLASMID DNA,FACTOR-IX,ENDOCYTOSIS,LIGAND},
  language     = {eng},
  number       = {6},
  pages        = {1276--1289},
  title        = {Efficient transfection of hepatocytes mediated by mRNA complexed to galactosylated cyclodextrins},
  url          = {http://dx.doi.org/10.1021/bc3001003},
  volume       = {23},
  year         = {2012},
}

Chicago
Symens, Nathalie, Alejandro Méndez-Ardoy, Alejandro Diaz-Moscoso, Elena Sánchez-Fernéndez, Katrien Remaut, Jo Demeester, José M García Fernández, Stefaan De Smedt, and Joanna Rejman. 2012. “Efficient Transfection of Hepatocytes Mediated by mRNA Complexed to Galactosylated Cyclodextrins.” Bioconjugate Chemistry 23 (6): 1276–1289.
APA
Symens, N., Méndez-Ardoy, A., Diaz-Moscoso, A., Sánchez-Fernéndez, E., Remaut, K., Demeester, J., García Fernández, J. M., et al. (2012). Efficient transfection of hepatocytes mediated by mRNA complexed to galactosylated cyclodextrins. BIOCONJUGATE CHEMISTRY, 23(6), 1276–1289.
Vancouver
1.
Symens N, Méndez-Ardoy A, Diaz-Moscoso A, Sánchez-Fernéndez E, Remaut K, Demeester J, et al. Efficient transfection of hepatocytes mediated by mRNA complexed to galactosylated cyclodextrins. BIOCONJUGATE CHEMISTRY. 2012;23(6):1276–89.
MLA
Symens, Nathalie, Alejandro Méndez-Ardoy, Alejandro Diaz-Moscoso, et al. “Efficient Transfection of Hepatocytes Mediated by mRNA Complexed to Galactosylated Cyclodextrins.” BIOCONJUGATE CHEMISTRY 23.6 (2012): 1276–1289. Print.