The use of quantitative RT-PCR to measure mRNA expression in a rat model of focal ischemia - caspase-3 as a case study

被引:131
作者
Harrison, DC
Medhurst, AD
Bond, BC
Campbell, CA
Davis, RP
Philpott, KL
机构
[1] SmithKline Beecham Pharmaceut, Neurosci Res, Harlow CM19 5AW, Essex, England
[2] SmithKline Beecham Pharmaceut, Stat Sci, Harlow CM19 5AW, Essex, England
来源
MOLECULAR BRAIN RESEARCH | 2000年 / 75卷 / 01期
关键词
ischemia; caspase; mRNA; housekeeping genes;
D O I
10.1016/S0169-328X(99)00305-8
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Quantitative reverse transcription and polymerisation chain reaction (RT-PCR) using Taqman(TM) fluorogenic probes has been used to measure changes in gene expression in the cerebral cortex of rats in the permanent middle cerebral artery occlusion (pMCAO) model of focal ischemia. The mRNA levels of three housekeeping genes have been analysed in this model to determine which gene showed least change following experimental insult. In the lesioned cortex, beta-actin mRNA increased at 24 h, while the levels of cyclophilin and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) did not change. We have also used this methodology to examine modulations in the level of caspase-3 mRNA during focal ischemia in the rat. Caspase-3 mRNA showed a 41% increase at 6 h post-MCAO, which was specific to the lesioned cortex. This change became more pronounced with time, showing an increase of 220% at 24 h. This methodology enables changes in mRNA expression to be analysed more sensitively and quantitatively than other available techniques and highlights the need for careful choice of control or housekeeping genes used for RNA comparisons. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:143 / 149
页数:7
相关论文
共 32 条
[1]
Expression of interleukin-1 beta converting enzyme gene family and bcl-2 gene family in the rat brain following permanent occlusion of the middle cerebral artery [J].
Asahi, M ;
Hoshimaru, M ;
Uemura, Y ;
Tokime, T ;
Kojima, M ;
Ohtsuka, T ;
Matsuura, N ;
Aoki, T ;
Shibahara, K ;
Kikuchi, H .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1997, 17 (01) :11-18
[2]
ISCHEMIA-INDUCED CHANGES IN ALPHA-TUBULIN AND BETA-ACTIN MESSENGER-RNA IN THE GERBIL BRAIN AND EFFECTS OF BIFEMELANE HYDROCHLORIDE [J].
ASANUMA, M ;
OGAWA, N ;
HIRATA, H ;
CHOU, HH ;
KONDO, Y ;
MORI, A .
BRAIN RESEARCH, 1993, 600 (02) :243-248
[3]
Bhat RV, 1996, J NEUROSCI, V16, P4146
[4]
EARLY ENDONUCLEASE ACTIVATION FOLLOWING REVERSIBLE FOCAL ISCHEMIA IN THE RAT-BRAIN [J].
CHARRIAUTMARLANGUE, C ;
MARGAILL, I ;
PLOTKINE, M ;
BENARI, Y .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1995, 15 (03) :385-388
[5]
Chen J, 1998, J NEUROSCI, V18, P4914
[6]
Cochran W.G., 1957, EXPT DESIGNS, P82
[7]
Caspases: the executioners of apoptosis [J].
Cohen, GM .
BIOCHEMICAL JOURNAL, 1997, 326 :1-16
[8]
USES AND ABUSES OF ANALYSIS OF COVARIANCE IN CLINICAL-TRIALS [J].
EGGER, MJ ;
COLEMAN, ML ;
WARD, JR ;
READING, JC ;
WILLIAMS, HJ .
CONTROLLED CLINICAL TRIALS, 1985, 6 (01) :12-24
[9]
Eldadah BA, 1997, J NEUROSCI, V17, P6105
[10]
ALTERED GENE-EXPRESSION IN NEURONS DURING PROGRAMMED CELL-DEATH - IDENTIFICATION OF C-JUN AS NECESSARY FOR NEURONAL APOPTOSIS [J].
ESTUS, S ;
ZAKS, WJ ;
FREEMAN, RS ;
GRUDA, M ;
BRAVO, R ;
JOHNSON, EM .
JOURNAL OF CELL BIOLOGY, 1994, 127 (06) :1717-1727