ICAM-1 induction in the mouse CNS following irradiation

John A. Olschowka, Stephanos Kyrkanides, Brandon K. Harvey, M. Kerry O'Banion, Jacqueline P. Williams, Philip Rubin, John T. Hansen

Research output: Contribution to journalArticlepeer-review

63 Scopus citations


Injury to the central nervous system (CNS) results in inflammation, increased trafficking of leukocytes into the CNS, induction of cytokines, and exacerbation of the primary injury. The increased trafficking of neutrophils into the CNS has been described following a number of injury models including stab, stroke, and excitotoxin-induced injury. This enhanced trafficking has largely been ascribed to the adhesion molecule intercellular adhesion molecule-1 (ICAM-1, CD54). In the current study, we wished to determine if the inflammation caused by irradiation of the CNS resulted in a similar induction of ICAM -1 C3H/HeJ mice were irradiated using gamma irradiation aimed over the right cerebral hemisphere The relative induction of ICAM-1 mRNA levels was determined using quantitative RT-PCR 6 hours following irradiation with either 0, 5, 15 25 or 35 Gy. ICAM-1 message was seen to exhibit a normal dose response curve with increasing mRNA levels seen at 15 Gy and higher. To determine the cellular distribution of the ICAM-1 protein following irradiation, mice were sacrificed at 4 hrs, 24 hrs, 48 hrs and 7 days following 25 Gy irradiation and the tissue was processed for ICAM-1 immunocytochemistry. ICAM-1 staining was seen to increase in both endothelial cells and astrocytes beginning as early as 4 hrs. The staining intensity continued to increase throughout the 7 day period observed. Together, these results suggest that irradiation of the CNS causes a rapid induction of both ICAM-1 mRNA and protein. This suggests that increased leukocyte trafficking into the CNS may exacerbate the inflammation induced by radiation injury.

Original languageEnglish
Pages (from-to)273-285
Number of pages13
JournalBrain, Behavior, and Immunity
Issue number4
StatePublished - Dec 1997

Bibliographical note

Funding Information:
This work was supported by PHS Grant CA 11051 and by the Lucille P. Markey Charitable Trust.

ASJC Scopus subject areas

  • Immunology
  • Endocrine and Autonomic Systems
  • Behavioral Neuroscience


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