Analysis of gene expression following sciatic nerve crush and spinal cord hemisection in the mouse by microarray expression profiling

被引:36
作者
Fan, M
Mi, RF
Yew, DT
Chan, WY [1 ]
机构
[1] Chinese Univ Hong Kong, Fac Med, Dept Anat, Shatin, Hong Kong, Peoples R China
[2] Chinese Acad Med Sci, Inst Basic Med Sci, Beijing 100730, Peoples R China
关键词
nerve injury; sciatic nerve; spinal cord; crush; hemisection; microarray; gene expression; gene profiling; periphery nervous system; central nervous system;
D O I
10.1023/A:1013867306555
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
1. The responses of periphery (PNS) and central nervous systems (CNS) towards nerve injury are different: while injured mammalian periphery nerons can successfully undergo regeneration, axons in the central nervous system are usually not able to regenerate. 2. In the present study, the genes which were differentially expressed in the PNS and CNS following nerve injury were identified and compared by microarray profiling techniques. 3. Sciatic nerve crush and hemisection of the spinal cord of adult mice were used as the models for nerve injury in PNS and CNS respectively. 4. It was found that of all the genes examined, 14% (80/588) showed changes in expression following either PNS or CNS injury, and only 3% (18/588) showed changes in both types of injuries. 5. Among all the differentially expressed genes, only 8% (6/80) exhibited similar changes in gene expression (either up- or down-regulation) following injury in both PNS and CNS nerve injuries. 6. Our results indicated that microarray expression profiling is an efficient and useful method to identify genes that are involved in the regeneration process following nerve injuries, and several genes which are differentially expressed in the PNS and/or CNS following nerve injuries were identified in the present study.
引用
收藏
页码:497 / 508
页数:12
相关论文
共 32 条
[1]   Constitutive expression of GAP-43 correlates with rapid, but not slow regrowth of injured dorsal root axons in the adult rat [J].
Andersen, LB ;
Schreyer, DJ .
EXPERIMENTAL NEUROLOGY, 1999, 155 (02) :157-164
[2]  
BRAY GM, 1991, ANN NY ACAD SCI, V633, P214
[3]   Exploring the new world of the genome with DNA microarrays [J].
Brown, PO ;
Botstein, D .
NATURE GENETICS, 1999, 21 (Suppl 1) :33-37
[4]   Induction of c-Erb A-AP-1 interactions and c-Erb A transcriptional activity in myoblasts by RXR - Consequences for muscle differentiation [J].
CassarMalek, I ;
Marchal, S ;
Rochard, P ;
Casas, F ;
Wrutniak, C ;
Samarut, J ;
Cabello, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (19) :11392-11399
[5]   GROWTH-FACTOR SIGNALING - WHERE IS THE SPECIFICITY [J].
CHAO, MV .
CELL, 1992, 68 (06) :995-997
[6]   AXONAL ELONGATION INTO PERIPHERAL NERVOUS-SYSTEM BRIDGES AFTER CENTRAL NERVOUS-SYSTEM INJURY IN ADULT-RATS [J].
DAVID, S ;
AGUAYO, AJ .
SCIENCE, 1981, 214 (4523) :931-933
[7]  
DELEON M, 1991, J NEUROSCI RES, V29, P437
[8]   EVIDENCE FOR 2 ORGANIZATIONAL PLANS WITHIN THE SOMATIC SENSORY-MOTOR CORTEX OF THE RAT [J].
DONOGHUE, JP ;
KERMAN, KL ;
EBNER, FF .
JOURNAL OF COMPARATIVE NEUROLOGY, 1979, 183 (03) :647-663
[9]   Microarray technology - enhanced versatility, persistent challenge [J].
Epstein, CB ;
Butow, RA .
CURRENT OPINION IN BIOTECHNOLOGY, 2000, 11 (01) :36-41
[10]   Involvement of thyroid hormone and its α receptor in avian neurulation [J].
Flamant, F ;
Samarut, J .
DEVELOPMENTAL BIOLOGY, 1998, 197 (01) :1-11