Dendrons with spermine surface groups as potential building blocks for nonviral vectors in gene therapy

被引:73
作者
Hardy, JG
Kostiainen, MA
Smith, DK [1 ]
Gabrielson, NP
Pack, DW
机构
[1] Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
[2] Univ Illinois, Dept Chem & Biolmol Engn, Urbana, IL 61801 USA
关键词
D O I
10.1021/bc050212r
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This paper investigates a series of dendrons based on the Newkome dendritic scaffold that displays a naturally occurring polyamine (spermine) on their surface. These dendrons have previously been shown to interact with DNA in a generation dependent manner with the more highly branched dendrons exhibiting a strong multivalency effect for the spermine surface groups. In this paper, we investigate the ability of these dendrons to transfect DNA into cells (human breast carcinoma cells, MDA-MB-231, and murine myoblast cells, C2C12) as determined by the luciferase assay. Although the dendrons are unable to transfect DNA in their own right, they are capable of delivering DNA in vitro when administered with chloroquine, which assists with escape from endocytic vesicles. The cytotoxicity of the dendrons was determined using the XTT assay, and it was shown that the dendrons were nontoxic either alone or in the presence of DNA. However, when administered with DNA and chloroquine, the most highly branched dendron did exhibit some cytotoxicity. This paper elucidates the relationship between in vitro transfection efficiency and toxicity. While transfection efficiencies are modest, the low toxicity of the dendrons, both in their own right, and in the presence of DNA, provides encouragement that this type of building block, which has a relatively high affinity for DNA, will provide a useful starting point for the further synthetic development of more effective gene transfection agents.
引用
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页码:172 / 178
页数:7
相关论文
共 72 条
[1]   Hydrophobized dextran-spermine conjugate as potential vector for in vitro gene transfection [J].
Azzam, T ;
Eliyahu, H ;
Makovitzki, A ;
Linial, M ;
Domb, AJ .
JOURNAL OF CONTROLLED RELEASE, 2004, 96 (02) :309-323
[2]   SYNTHETIC GENE-TRANSFER VECTORS [J].
BEHR, JP .
ACCOUNTS OF CHEMICAL RESEARCH, 1993, 26 (05) :274-278
[3]   EFFICIENT GENE-TRANSFER INTO MAMMALIAN PRIMARY ENDOCRINE-CELLS WITH LIPOPOLYAMINE-COATED DNA [J].
BEHR, JP ;
DEMENEIX, B ;
LOEFFLER, JP ;
MUTUL, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (18) :6982-6986
[4]   DNA complexing with polyamidoamine dendrimers: Implications for transfection [J].
Bielinska, AU ;
Chen, CL ;
Johnson, J ;
Baker, JR .
BIOCONJUGATE CHEMISTRY, 1999, 10 (05) :843-850
[5]   Polyamines and novel polyamine conjugates interact with DNA in ways that can be exploited in non-viral gene therapy [J].
Blagbrough, IS ;
Geall, AJ ;
Neal, AP .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2003, 31 :397-406
[6]   Transfection with fluorinated lipoplexes based on new fluorinated cationic lipids and in the presence of a bile salt surfactant [J].
Boulanger, C ;
Di Giorgio, C ;
Gaucheron, J ;
Vierling, P .
BIOCONJUGATE CHEMISTRY, 2004, 15 (04) :901-908
[7]   Competition between condensation of monovalent and multivalent ions in DNA aggregation [J].
Burak, Y ;
Ariel, G ;
Andelman, D .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 2004, 9 (1-2) :53-58
[8]   Synthesis, activity, and structure-activity relationship studies of novel cationic lipids for DNA transfer [J].
Byk, G ;
Dubertret, C ;
Escriou, V ;
Frederic, M ;
Jaslin, G ;
Rangara, R ;
Pitard, B ;
Crouzet, J ;
Wils, P ;
Schwartz, B ;
Scherman, D .
JOURNAL OF MEDICINAL CHEMISTRY, 1998, 41 (02) :224-235
[9]   An improved synthesis of a trifurcated Newkome-type monomer and orthogonally protected two-generation dendrons [J].
Cardona, CM ;
Gawley, RE .
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (04) :1411-1413
[10]   Synthesis of a barbell-like triblock copolymer, poly(L-lysine) dendrimer-block-poly(ethylene glycol)-block-poly(L-lysine) dendrimer, and its self-assembly with plasmid DNA [J].
Choi, JS ;
Joo, DK ;
Kim, CH ;
Kim, K ;
Park, JS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (03) :474-480