Selective chemokine mRNA accumulation in the rat spinal cord after contusion injury
Autor: | Dana M. McTigue, Bradford T. Stokes, Gregory S. Kelner, Kimberly Krivacic, Dominique Maciejewski, Richard A. Maki, Ann Chernosky, Richard M. Ransohoff, Marie Tani |
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Rok vydání: | 1998 |
Předmět: |
medicine.medical_specialty
Chemokine biology business.industry Monocyte medicine.medical_treatment Inflammation Chemotaxis Spinal cord medicine.disease Lesion Cellular and Molecular Neuroscience medicine.anatomical_structure Cytokine Endocrinology Internal medicine Immunology medicine biology.protein medicine.symptom business Spinal cord injury |
Zdroj: | Journal of Neuroscience Research. 53:368-376 |
ISSN: | 1097-4547 0360-4012 |
DOI: | 10.1002/(sici)1097-4547(19980801)53:3<368::aid-jnr11>3.0.co;2-1 |
Popis: | Following traumatic injury to the spinal cord, hematogenous inflammatory cells including neutrophils, monocytes, and lymphocytes infiltrate the lesion in a distinct temporal sequence. To examine potential mechanisms for their recruitment, we measured chemokine mRNAs in the contused rat spinal cord, using specific and sensitive reverse transcriptase polymerase chain reaction (RT-PCR) dot-blot hybridization assays. The neutrophil chemoattractant GRO-alpha was 30-fold higher than control values at 6 hr postinjury and decayed rapidly thereafter. LIX, a highly related alpha-chemokine, also was elevated early postinjury. Monocyte chemoattractant peptide (MCP)-1 and MCP-5 mRNAs, potent chemoattractants for monocytes, were significantly elevated at the lesion epicenter at 12 and 24 hr postinjury and declined thereafter. Interferon-gamma-inducible protein, 10 kDa (IP-10), chemoattractant towards activated T-lymphocytes, was significantly elevated at 6 and 12 hr postinjury. The dendritic cell chemoattractant MIP-3alpha also was increased, perhaps contributing to the development of T-cell autoreactivity to neural components after spinal cord injury (SCI) in rats. Other beta-chemokines, including MIP-1alpha and RANTES (regulated on expression normal T-cell expressed and secreted), were minimally affected by SCI. Expression of chemokines, therefore, directly precedes the influx of target neutrophils, monocytes, and T-cells into the spinal cord postinjury, as noted previously. Thus, selective chemokine expression may be integral to inflammatory processes within the injured spinal cord as a mechanism of recruitment for circulating leukocytes. |
Databáze: | OpenAIRE |
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