CINC-1 is an acute-phase protein induced by focal brain injury causing leukocyte mobilization and liver injury.

Sandra J. Campbell*, Paula M. Hughes, John P. Iredale, David C. Wilcockson, Sara Waters, Fabian Docagne, V. Hugh Perry, Daniel C. Anthony

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

113 Citations (SciVal)

Abstract

Following injury or infection, the liver releases acute-phase proteins (APP). After a severe focal injury, this systemic response can be excessive and may lead to multiorgan dysfunction (MODS). CINC-1 is a neutrophil chemoattractant, and we have now established that it also functions as an early APP after injury to the brain or to peripheral tissues. After induction of a focal inflammatory lesion in the brain, there is rapid hepatic and serum CINC-1 induction, which is associated with increases in neutrophil numbers within the liver and within the circulation. CINC-1-mediated recruitment of neutrophils to organs distant from the primary injury site may contribute to MODS. Indeed, we found that enzyme markers of liver tissue injury are increased in the serum following generation of a focal inflammatory lesion in the brain. Neutralization of CINC-1 in the periphery reversed brain-injury-induced neutrophil mobilization and inhibited recruitment of neutrophils to the brain and to the liver. Thus, a significant component of the hepatic acute-phase response is the release of chemokines by the liver, which act to amplify the inflammatory response and modulate the subsequent leukocytosis and secondary tissue damage. Hepatic CINC-1 synthesis following injury presents a novel focus for treatment of inflammation.

Original languageEnglish
Pages (from-to)1168-1170
Number of pages20
JournalFASEB Journal
Volume17
Issue number9
Early online date22 Apr 2003
DOIs
Publication statusPublished - 01 Jun 2003
Externally publishedYes

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