Immortalization of epithelial cells

被引:37
作者
Hopfer, U
Jacobberger, JW
Gruenert, DC
Eckert, RL
Jat, PS
Whitsett, JA
机构
[1] CASE WESTERN RESERVE UNIV, SCH MED, DEPT DERMATOL, CLEVELAND, OH 44106 USA
[2] CASE WESTERN RESERVE UNIV, SCH MED, DEPT GENET, CLEVELAND, OH 44106 USA
[3] CASE WESTERN RESERVE UNIV, SCH MED, DEPT BIOCHEM, CLEVELAND, OH 44106 USA
[4] CASE WESTERN RESERVE UNIV, SCH MED, CTR CANC, CLEVELAND, OH 44106 USA
[5] CHILDRENS HOSP, MED CTR, DIV PULM BIOL, CINCINNATI, OH 45229 USA
[6] UNIV CALIF SAN FRANCISCO, CARDIOVASC RES INST, DEPT LAB MED, GENE THERAPY CORE CTR, SAN FRANCISCO, CA 94143 USA
[7] UCL MED SCH BRANCH, LUDWIG INST CANC RES, LONDON W1P 8BT, ENGLAND
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1996年 / 270卷 / 01期
关键词
simian virus 40; papillomavirus; large T antigen; Papovaviridae; H-2K(b)tsA58 transgenic mouse; lung; intestine; kidney; cervix; human; rat; mouse; rabbit; cystic fibrosis;
D O I
10.1152/ajpcell.1996.270.1.C1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The methodologies for isolating cell lines have become very powerful, particularly in terms of retaining differentiated features of the parent cells. Cell lines can be developed from primary or early passage cells as well as from transgenic animals that carry an immortalizing gene. Cell lines from epithelia have been selected for their polar orientation, tight junction formation, and expression of differentiated markers or functions. These cell lines provide useful models for studying cell biology of specific tissues, tumorigenicity, genetic abnormalities, or to help screen for effective methods of gene therapy.
引用
收藏
页码:C1 / C11
页数:11
相关论文
共 93 条
[1]  
AGARWAL C, 1990, CANCER RES, V50, P5947
[2]  
AGARWAL C, 1994, CANCER RES, V54, P2108
[3]  
AGARWAL C, 1991, CANCER RES, V51, P3982
[4]   REGULATION OF INSULIN-LIKE GROWTH-FACTOR-1 BINDING-PROTEIN-3 LEVELS BY EPIDERMAL GROWTH-FACTOR AND RETINOIC ACID IN CERVICAL EPITHELIAL-CELLS [J].
ANDREATTAVANLEYEN, S ;
HEMBREE, JR ;
ECKERT, RL .
JOURNAL OF CELLULAR PHYSIOLOGY, 1994, 160 (02) :265-274
[5]   BINDING OF A NUCLEAR FACTOR TO A REGULATORY SEQUENCE IN THE PROMOTER OF THE MOUSE H-2KB CLASS-I MAJOR HISTOCOMPATIBILITY GENE [J].
BALDWIN, AS ;
SHARP, PA .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (01) :305-313
[6]   THE LUNG-SPECIFIC SURFACTANT PROTEIN-B GENE PROMOTER IS A TARGET FOR THYROID TRANSCRIPTION FACTOR-1 AND HEPATOCYTE NUCLEAR FACTOR-3, INDICATING COMMON FACTORS FOR ORGAN-SPECIFIC GENE-EXPRESSION ALONG THE FOREGUT AXIS [J].
BOHINSKI, RJ ;
DILAURO, R ;
WHITSETT, JA .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (09) :5671-5681
[7]  
BOND JA, 1994, ONCOGENE, V9, P1885
[8]   TRANSGENIC MICE HARBORING SV40 T-ANTIGEN GENES DEVELOP CHARACTERISTIC BRAIN-TUMORS [J].
BRINSTER, RL ;
CHEN, HY ;
MESSING, A ;
VANDYKE, T ;
LEVINE, AJ ;
PALMITER, RD .
CELL, 1984, 37 (02) :367-379
[9]  
BROWN AMC, 1987, DNA CLONING PRACTICA, P189
[10]   A RECOMBINANT MURINE RETROVIRUS FOR SIMIAN VIRUS-40 LARGE T-CDNA TRANSFORMS MOUSE FIBROBLASTS TO ANCHORAGE-INDEPENDENT GROWTH [J].
BROWN, M ;
MCCORMACK, M ;
ZINN, KG ;
FARRELL, MP ;
BIKEL, I ;
LIVINGSTON, DM .
JOURNAL OF VIROLOGY, 1986, 60 (01) :290-293