Screening Genes Related to Development and Injury of the Mouse Optic Nerve by cDNA Microarrays

被引:3
作者
Liu, Yunlai [1 ]
Huang, Minghui [2 ]
Zhang, Yanqi [3 ]
Li, Hongli [1 ]
Xiao, Lan [1 ]
Liu, Jianjun [1 ]
Yuan, Bibo [1 ]
Qin, Maolin [1 ]
Li, Chengren [1 ]
Yang, Micheal [2 ]
Cai, Wenqin [1 ]
机构
[1] Third Mil Med Univ, Dept Histol & Embryol, Chongqing 400038, Peoples R China
[2] City Univ Hong Kong, Dept Biochem, Kowloon, Hong Kong, Peoples R China
[3] Third Mil Med Univ, Dept Stat, Chongqing 400038, Peoples R China
关键词
cDNA microarray; Optic nerve; Development; Injury; REGENERATION; EXPRESSION; SYSTEM;
D O I
10.1007/s10571-010-9515-y
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The aim of this study was to screen genes related to the development and injury of the mouse optic nerve so as to provide possible target genes for gene-engineering therapy of central nervous system (CNS) injury. Gene expression was profiled by cDNA microarrays in the mouse superior colliculus at 8-time points during the development or following injury of the optic nerve; consequently, 1,095 highly expressed genes (ratio a parts per thousand yen2) were identified. Then, these genes were categorized functionally; there were 561 genes (51.19%) with unidentified functions and 534 genes (48.81%) with identified or partially identified functions. After discounting the overlapping genes, 486 genes with identified or partially identified functions were categorized into 17 functional groups. The 17 functional groups were as follows: I transcription regulation, II signal transduction, III protein synthesis, IV materials transporting, V RNA processing, VI metabolism-related genes, VII cell cycle or apoptosis-related genes, VIII extracellular matrix, IX protein folding and degradation, X cytoskeleton, XI histone metabolism, XII nervous system specific functional genes, XIII tumor related genes, XIV DNA replication and repair, XV axon growth and guidance, XVI immune response, and XVII cell adhesion. These genes may play key roles in the development, injury, and repairment of the optic nerve.
引用
收藏
页码:869 / 876
页数:8
相关论文
共 17 条
[1]   Dynamic regulation of middle neurofilament RNA pools during optic nerve regeneration [J].
Ananthakrishnan, L. ;
Gervasi, C. ;
Szaro, B. G. .
NEUROSCIENCE, 2008, 153 (01) :144-153
[2]   Pleiotrophin cellular localization in nerve regeneration after peripheral nerve injury [J].
Blondet, B ;
Carpentier, G ;
Lafdil, F ;
Courty, J .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2005, 53 (08) :971-977
[3]  
Brüstle O, 1999, BRAIN PATHOL, V9, P527
[4]   Roles of neuropilins in neuronal development, angiogenesis, and cancers [J].
Chen, CY ;
Li, M ;
Chai, H ;
Yang, H ;
Fisher, WE ;
Yao, QH .
WORLD JOURNAL OF SURGERY, 2005, 29 (03) :271-275
[5]   Brain derived neurotrophic factor and trk B mRNA expression in the brain of a brain stem-spinal cord regenerating model, the European eel, after spinal cord injury [J].
Dalton, Victoria S. ;
Roberts, Barry L. ;
Borich, Suzanne M. .
NEUROSCIENCE LETTERS, 2009, 461 (03) :275-279
[6]   Regenerating optic axons restore topography after incomplete optic nerve injury [J].
Dunlop, Sarah A. ;
Tee, Lisa B. G. ;
Goossens, Michel A. L. ;
Stirling, R. Victoria ;
Hool, Livia ;
Rodger, Jenny ;
Beazley, L. D. .
JOURNAL OF COMPARATIVE NEUROLOGY, 2007, 505 (01) :46-57
[7]   Drebrin A regulates dendritic spine plasticity and synaptic function in mature cultured hippocampal neurons [J].
Ivanov, Anton ;
Esclapez, Monique ;
Pellegrino, Christophe ;
Shirao, Tomoaki ;
Ferhat, Lotfi .
JOURNAL OF CELL SCIENCE, 2009, 122 (04) :524-534
[8]   Cell Therapy for CNS Trauma [J].
Jain, K. K. .
MOLECULAR BIOTECHNOLOGY, 2009, 42 (03) :367-376
[9]   Soluble Nogo-A, an inhibitor of axonal regeneration, as a biomarker for multiple sclerosis [J].
Jurewicz, Anna ;
Matysiak, Mariola ;
Raine, Cedric S. ;
Selmaj, Krzysztof .
NEUROLOGY, 2007, 68 (04) :283-287
[10]  
Katoh Y, 2006, ONCOL REP, V15, P1391