Retroviral transduction of alveolar bone cells with a temperature-sensitive SV40 large T antigen

被引:13
作者
Salih, V
Knowles, JC
O'Hare, MJ
Olsen, I
机构
[1] UCL, Eastman Dent Inst, Dept Periodontol, London WC1X 8LD, England
[2] UCL, Eastman Dent Inst, Dept Biomat, London WC1X 8LD, England
[3] UCL, Sch Med, Ludwig Inst Canc Res, Breast Canc Lab,Dept Surg, London W1P 7LD, England
关键词
osteoblasts; cell culture; flow cytometry; alveolar bone cells; human;
D O I
10.1007/s004410100391
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have transduced adult human alveolar bone (AB) cells with a gene construct encoding a temperature-sensitive mutation of the SV40 large T antigen (tsT). Such cells divided rapidly, for more than 50 passages thus far, at a permissive low temperature (34.5 degreesC), comparable to the non-transduced parental cells at 37 degreesC. However, the tsT-transduced AB cells failed to grow at a non-permissive high temperature (39 degreesC) at which the T antigen is inactivated. Nevertheless, the cells formed mineralised nodules in vitro at both the low and high temperatures. Flow cytometry analysis showed that the transduced cells cultured at 34.5 degreesC, like the parental cells at 37 degreesC, were smaller and less granular than the transduced cells incubated at 39 degreesC. Moreover, the transduced cells grown at 34.5 degreesC were also found to express bone sialoprotein. osteopontin and type I collagen at levels similar to those of the parental cells at 37 degreesC, although osteonectin and fibronectin were down-regulated. When the transduced cells were incubated at 39 degreesC, the expression of all antigens was up-regulated, particularly osteonectin. Thus, we have obtained long-term cultures of tsT-transduced AB cells whose growth is temperature-dependent and which express certain features characteristic of bone-derived cells.
引用
收藏
页码:371 / 376
页数:6
相关论文
共 31 条
[1]   1,25-DIHYDROXYVITAMIN-D3 AND HUMAN BONE-DERIVED CELLS-INVITRO - EFFECTS ON ALKALINE-PHOSPHATASE, TYPE-I COLLAGEN AND PROLIFERATION [J].
BERESFORD, JN ;
GALLAGHER, JA ;
RUSSELL, RGG .
ENDOCRINOLOGY, 1986, 119 (04) :1776-1785
[2]  
Bodine PVN, 1996, J BONE MINER RES, V11, P806
[3]   ARE MG-63 AND HOS TE85 HUMAN OSTEOSARCOMA CELL-LINES REPRESENTATIVE MODELS OF THE OSTEOBLASTIC PHENOTYPE [J].
CLOVER, J ;
GOWEN, M .
BONE, 1994, 15 (06) :585-591
[4]   Mineralization and the expression of matrix proteins during in vivo bone development [J].
Cowles, EA ;
DeRome, ME ;
Pastizzo, G ;
Brailey, LL ;
Gronowicz, GA .
CALCIFIED TISSUE INTERNATIONAL, 1998, 62 (01) :74-82
[5]   MODULATION OF CELL PHENOTYPE IN HUMAN OSTEOBLAST-LIKE CELLS BY THE SIMIAN-VIRUS-40 [J].
EVANS, CE ;
NG, K ;
ALLEN, J ;
GALLIMORE, P .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1995, 13 (03) :317-324
[6]   CHARACTERIZATION OF HUMAN UMBILICAL VEIN ENDOTHELIAL-CELL LINES PRODUCED BY TRANSFECTION WITH THE EARLY REGION OF SV40 [J].
FICKLING, SA ;
TOOZE, JA ;
WHITLEY, GS .
EXPERIMENTAL CELL RESEARCH, 1992, 201 (02) :517-521
[7]  
Globus RK, 1998, J CELL SCI, V111, P1385
[8]  
Gorczyca W, 1998, METH MOL B, V91, P217
[9]  
HARRIS SA, 1995, J BONE MINER RES, V10, P178
[10]   MODULATION OF CRYSTAL-FORMATION BY BONE PHOSPHOPROTEINS - STRUCTURAL SPECIFICITY OF THE OSTEOPONTIN-MEDIATED INHIBITION OF HYDROXYAPATITE FORMATION [J].
HUNTER, GK ;
KYLE, CL ;
GOLDBERG, HA .
BIOCHEMICAL JOURNAL, 1994, 300 :723-728