Microarray expression analysis of the early N-methy-N-nitrosourea-induced retinal degeneration in rat

被引:9
作者
Yang, Liu
Li, Dai
Chen, Jinmao
Yang, Jinnan
Xue, Liping
Hu, Shixing
Wu, Kaili
机构
[1] Sun Yat Sen Univ, Zhongshan Ophthalm Ctr, State Key Lab Opthalmol, Guangzhou 510060, Peoples R China
[2] Xianning Med Coll, Hubei 437100, Xianning, Peoples R China
[3] Guangxi Med Univ, Affiliated Hosp 1, Dept Ophthalmol, Nanning 530021, Peoples R China
[4] Hosp Eye, China Acad Tradit Chinese Med, Beijing 100040, Peoples R China
基金
中国国家自然科学基金;
关键词
retinal degeneration; N-methy-N-nitrosourea; animal model; microarray analysis; real time RT-PCR;
D O I
10.1016/j.neulet.2007.02.084
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The study was undertaken to investigate the gene expressions in N-methy-N-nitrosourea (MNU)-induced rat retinal degeneration (RD) by performing microarray analysis of retinal RNA at 12 h. All rats were randomly divided into a normal group, a 12 h model group and a 24 It model group. Rats in the two model groups received a single intraperitoneal injection of 40 mg/kg body weight of MNU, while those in the normal group were injected with equivalent volume of physiological saline. After 12 h and 24 h of the injection, rats in each respective group were sacrificed, respectively. One eye of each animal was used for hematoxylin and erosin (H&E) staining, and fresh retinas of the other eye of each animal in the both normal group and 12 h model group were used to extract total RNA, which was analyzed by microarray and real time RT-PCR. Retinal histological alteration was found in the 24 h model group. There were 75 genes differently expressed (ratio >= 2.0), including 64 genes up-regulated and I I genes down-regulated. Seven genes were assayed by real time RT-PCR and demonstrated the same alteration tendency as in microarray analysis. These genes that expressed differently mainly involved signal transduction, development, immune and defense, and apoptosis, etc. The major pathways were MAP-kinase signaling pathways, Toll-like receptor signaling pathway and apoptosis pathway involved. The results suggest that there are significant changes of gene expression in the early stage of MNU-induced RD. These microarray results provide clues to understand the molecular pathways underlying photoreceptor degeneration and indicate directions for future studies. (c) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:38 / 43
页数:6
相关论文
共 42 条
[1]  
Abler AS, 1996, RES COMMUN MOL PATH, V92, P177
[2]   Absence of p53 delays apoptotic photoreceptor cell death in the rds mouse [J].
Ali, RR ;
Reichel, MB ;
Kanuga, N ;
Munro, PM ;
Alexander, RA ;
Clarke, AR ;
Luthert, PJ ;
Bhattacharya, SS ;
Hunt, DM .
CURRENT EYE RESEARCH, 1998, 17 (09) :917-923
[3]   ANIMAL SPECIES IN WHICH N-NITROSO COMPOUNDS INDUCE CANCER [J].
BOGOVSKI, P ;
BOGOVSKI, S .
INTERNATIONAL JOURNAL OF CANCER, 1981, 27 (04) :471-474
[4]   METHYL NITROSOUREA INDUCED UNSCHEDULED DNA-SYNTHESIS INVIVO IN MICE - EFFECTS OF BACKGROUND GENOTYPE ON EXCISION REPAIR DURING AGING [J].
BOND, SL ;
SINGH, SM .
MECHANISMS OF AGEING AND DEVELOPMENT, 1987, 41 (03) :177-187
[5]   Apoptosis in the developing visual system [J].
Cellerino, A ;
Bähr, M ;
Isenmann, S .
CELL AND TISSUE RESEARCH, 2000, 301 (01) :53-69
[6]   Light damage induced changes in mouse retinal gene expression [J].
Chen, L ;
Wu, W ;
Dentchev, T ;
Zeng, Y ;
Wang, JH ;
Tsui, I ;
Tobias, JW ;
Bennett, J ;
Baldwin, D ;
Dunaief, JL .
EXPERIMENTAL EYE RESEARCH, 2004, 79 (02) :239-247
[7]   MEMORIES OF FOS [J].
CURRAN, T ;
MORGAN, JI .
BIOESSAYS, 1987, 7 (06) :255-258
[8]   Apoptosis: A potential therapeutic target for retinal degenerations [J].
Doonan, F ;
Cotter, TG .
CURRENT NEUROVASCULAR RESEARCH, 2004, 1 (01) :41-53
[9]  
Grimm C, 2000, MOL VIS, V6, P252
[10]   The absence of c-fos prevents light-induced apoptotic cell death of photoreceptors in retinal degeneration in vivo [J].
Hafezi, F ;
Steinbach, JP ;
Marti, A ;
Munz, K ;
Wang, ZQ ;
Wagner, EF ;
Aguzzi, A ;
Reme, CE .
NATURE MEDICINE, 1997, 3 (03) :346-349