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

CARMEL, JASON B., GALANTE, ANTHONY, SOTEROPOULOS, PATRICIA, TOLIAS, PETER, RECCE, MICHAEL, YOUNG, WISE, HART, RONALD P.·2001·Physiological Genomics
DOI 10.1152/physiolgenomics.00074.2001
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Abstract

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.

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Metadata

Authors
CARMEL, J. B., GALANTE, A., SOTEROPOULOS, P., TOLIAS, P., RECCE, M., YOUNG, W., & HART, R. P.
Affiliations
  • W. M. Keck Center for Collaborative Neuroscience, Rutgers University, Piscataway 08854
  • Center for Applied Genomics, Public Health Research Institute and University of Medicine and Dentistry of New Jersey, New Jersey Medical School, Newark 07103
  • Center for Computational Biology and Bioengineering, New Jersey Institute of Technology, Newark, New Jersey 07103
Venue
Physiological Genomics
Publisher
American Physiological Society
Published
2001-12-21
Volume
7
Issue
2
Pages
201-213
ISSN
  • 1094-8341
  • 1531-2267
DOI
10.1152/physiolgenomics.00074.2001
Cited by
121
References
2
Language
en

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