In vitro uptake of polystyrene microspheres: effect of particle size, cell line and cell density

被引:329
作者
Zauner, W [1 ]
Farrow, NA [1 ]
Haines, AMR [1 ]
机构
[1] Cobra Therapeut Ltd, Keele ST5 5SP, Staffs, England
关键词
polystyrene microspheres; particle size; uptake; polyplex; DNA;
D O I
10.1016/S0168-3659(00)00358-8
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Uptake of polycation-DNA particles is the first step in achieving gene delivery with non-viral vehicles. One of the important characteristics determining uptake of DNA particles is their size. Here we have characterized the ability of several cell lines to internalise labelled polystyrene microspheres of different sizes. All the cell lines tested ingested 20-nm microspheres avidly. With larger microspheres (93, 220, 560 and 1010 nm) cell type as well as growth related differences were observed. Whereas some cell lines (HUVEC, ECV 304 and HNX 14C) took up microspheres up to 1010 nm even when the cells were confluent, others did not take up many microspheres larger than 93 nm (Hepa 1-6 and HepG2). In one cell line (KLN 205), uptake of 93-, 220- and 560-nm microspheres was avid in growing cells, but not detectable when they were confluent. In KLN 205 cells, a good correlation was found between the uptake of 560-nm microspheres and the uptake of a peptide-DNA polyplex formulation, when it was prepared under conditions leading to small particle sizes. Little correlation was found when the polyplex formulation was allowed to aggregate. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:39 / 51
页数:13
相关论文
共 41 条
[1]   ESTABLISHED CELL LINE OF URINARY-BLADDER CARCINOMA (T-24) CONTAINING TUMOR-SPECIFIC ANTIGEN [J].
BUBENIK, J ;
BARESOVA, M ;
VIKLICKY, V ;
JAKOUBKOVA, J ;
SAINEROVA, H ;
DONNER, J .
INTERNATIONAL JOURNAL OF CANCER, 1973, 11 (03) :765-773
[2]  
DARLINGTON GJ, 1980, J NATL CANCER I, V64, P809
[3]   Gene transfer mediated by polyarginine requires a formation of big carrier-complex of DNA aggregate [J].
Emi, N ;
Kidoaki, S ;
Yoshikawa, K ;
Saito, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 231 (02) :421-424
[4]   A low rate of cell proliferation and reduced DNA uptake limit cationic lipid-mediated gene transfer to primary cultures of ciliated human airway epithelia [J].
Fasbender, A ;
Zabner, J ;
Zeiher, BG ;
Welsh, MJ .
GENE THERAPY, 1997, 4 (11) :1173-1180
[5]   Nomenclature for synthetic gene delivery systems [J].
Felgner, PL ;
Barenholz, Y ;
Behr, JP ;
Cheng, SH ;
Cullis, P ;
Huang, L ;
Jessee, JA ;
Seymour, L ;
Szoka, F ;
Thierry, AR ;
Wagner, E ;
Wu, G .
HUMAN GENE THERAPY, 1997, 8 (05) :511-512
[6]  
FUJITA H, 1987, CELL TISSUE RES, V250, P251
[7]   LECTIN-MEDIATED ATTACHMENT AND INGESTION OF YEAST-CELLS AND ERYTHROCYTES BY HAMSTER FIBROBLASTS [J].
GOLDMAN, R .
EXPERIMENTAL CELL RESEARCH, 1977, 104 (02) :325-334
[8]   Polyethylenimine-based intravenous delivery of transgenes to mouse lung [J].
Goula, D ;
Benoist, C ;
Mantero, S ;
Merlo, G ;
Levi, G ;
Demeneix, BA .
GENE THERAPY, 1998, 5 (09) :1291-1295
[9]   Size, diffusibility and transfection performance of linear PEI/DNA complexes in the mouse central nervous system [J].
Goula, D ;
Remy, JS ;
Erbacher, P ;
Wasowicz, M ;
Levi, G ;
Abdallah, B ;
Demeneix, BA .
GENE THERAPY, 1998, 5 (05) :712-717
[10]   Smaller sized particles are preferentially taken up by alveolar type II pneumocytes [J].
Griese, M ;
Reinhardt, D .
JOURNAL OF DRUG TARGETING, 1998, 5 (06) :471-+