Carmel J B, Galante A, Soteropoulos P, Tolias P, Recce M, Young W, Hart R P
W. M. Keck Center for Collaborative Neuroscience, Rutgers University, Piscataway 08854, USA.
Physiol Genomics. 2001 Dec 21;7(2):201-13. doi: 10.1152/physiolgenomics.00074.2001.
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.
我们已经完成了大鼠急性脊髓损伤(SCI)的首次大规模基因表达研究。使用包含1200个基因特异性探针的寡核苷酸微阵列来定量脊髓中相对于未受伤对照的mRNA水平,脊髓损伤采用标准挫伤模型。我们的结果显示损伤部位神经元特异性mRNA明显减少。存活的细胞表现出特征性的炎症反应,始于损伤部位并扩散至脊髓远端。几种mRNA水平的变化与脊髓中假定的再生反应相关。值得注意的是,磷酸二酯酶4、巢蛋白、胶质细胞衍生的神经突促进因子和GAP - 43 mRNA显著增加。其他mRNA在时间和空间上与这些再生相关基因聚集在一起。因此,我们描述了急性脊髓损伤后基因表达的整体模式,并且我们已经确定了未来研究和可能的治疗干预目标。