A cautionary note on the use of stable transformed cells

被引:2
作者
Blum, D
Torch, S
Nissou, MF
Verna, JM
机构
[1] Dept Neurosci, Neurophysiol Lab, Brain Res Unit, B-1070 Brussels, Belgium
[2] CHU Michallon, NDP, LAPSEN, F-38043 Grenoble 9, France
关键词
apoptosis; Bcl-2; Bfl-1; 6-hydroxydopamine; PC12; cells; stable transformants;
D O I
10.1023/A:1009668210150
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Gene transfection and ectopic expression is a widely used method in experimental biology. In the present report, we would like to point out that this approach may, in certain circumstances, lead to a modification of the transfected cell phenotype. Indeed, we observed that after transfection of bcl-2 gene in the neuronal PC12 cell line some of the selected clones have lost their neuronal and catecholaminergic characteristics, i.e. TH expression and ability to grow neurites in response to NGF. Thus, the resistance of some PC12-Bcl-2 clones against neurotoxic insults may not necessarily reflect the potential benefit afforded by Bcl-2 expression. We therefore encouraged authors to verify cell phenotype after stable transfection to avoid misinterpretation of their results.
引用
收藏
页码:115 / 116
页数:2
相关论文
共 6 条
[1]
BATISTANOU A, 1996, J NEUROSCI, V13, P4422
[2]
ESTABLISHMENT OF A NORADRENERGIC CLONAL LINE OF RAT ADRENAL PHEOCHROMOCYTOMA CELLS WHICH RESPOND TO NERVE GROWTH-FACTOR [J].
GREENE, LA ;
TISCHLER, AS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (07) :2424-2428
[3]
ISAACSON S, 1997, MOVEMENT DISORD, V12, P6
[4]
THE PROTOONCOGENE BCL-2 INHIBITS APOPTOSIS IN PC12 CELLS [J].
MAH, SP ;
ZHONG, LT ;
LIU, Y ;
ROGHANI, A ;
EDWARDS, RH ;
BREDESEN, DE .
JOURNAL OF NEUROCHEMISTRY, 1993, 60 (03) :1183-1186
[5]
Transgenic mice expressing human Bcl-2 in their neurons are resistant to 6-hydroxydopamine and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine neurotoxicity [J].
Offen, D ;
Beart, PM ;
Cheung, NS ;
Pascoe, CJ ;
Hochman, A ;
Gorodin, S ;
Melamed, E ;
Bernard, R ;
Bernard, O .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (10) :5789-5794
[6]
OH YJ, 1994, NEUROBIOL DIS, V220, P157