Gene expression profiling of acute spinal cord injury reveals spreading inflammatory signals and neuron loss

被引:125
|
作者
Carmel, JB
Galante, A
Soteropoulos, P
Tolias, P
Recce, M
Young, W
Hart, RP
机构
[1] Rutgers State Univ, WM Keck Ctr Collaborat Neurosci, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Dept Biol Sci, Newark, NJ 07102 USA
[3] Ctr Appl Genom, Inst Publ Hlth, Newark, NJ 07103 USA
[4] Univ Med & Dent New Jersey, New Jersey Med Sch, Newark, NJ 07103 USA
[5] New Jersey Inst Technol, Ctr Computat Biol & Bioengn, Newark, NJ 07103 USA
关键词
spinal cord injury; microarray; gene expression; regeneration-associated genes; inflammation; cell death;
D O I
10.1152/physiolgenomics.00074.2001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have completed the first large- scale gene expression study of acute spinal cord injury (SCI) in rat. Oligonucleotide microarrays containing 1,200 gene- specific probes were used to quantify mRNA levels, relative to uninjured controls, in spinal cords injured using a standard contusion model. Our results revealed a marked loss of neuron- specific mRNAs at the injury site. The surviving cells showed a characteristic inflammatory response that started at the injury site and spread to the distal cord. Changes in several mRNA levels were associated with putative regenerative responses in the spinal cord. Notably, phosphodiesterase 4, nestin, glia- derived neurite promoting factor, and GAP- 43 mRNAs increased significantly. Other mRNAs clustered temporally and spatially with these regeneration- associated genes. Thus we have described global patterns of gene expression following acute SCI, and we have identified targets for future study and possible therapeutic intervention.
引用
收藏
页码:201 / 213
页数:13
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