4.5 Article

In Situ Detection of Inflammatory Mediators in Post Mortem Human Brain Tissue after Traumatic Injury

期刊

JOURNAL OF NEUROTRAUMA
卷 27, 期 3, 页码 497-507

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/neu.2009.1120

关键词

cytokines; human brain; inflammation; post mortem tissue; traumatic brain injury

资金

  1. Victorian Neurotrauma Initiative
  2. National Trauma Research Institute
  3. University of Melbourne
  4. Mental Health Research Institute of Victoria
  5. Victorian Institute of Forensic Medicine
  6. Victorian Neurotrauma Initiative, Neurosciences Australia
  7. National Health and Medical Research Council of Australia

向作者/读者索取更多资源

Little is known about the molecular events following severe traumatic brain injury (TBI) in humans and to date there are no efficient therapies for the treatment of patients. In this study, the first of its kind in human tissue, a total of 21 post mortem trauma brain samples were analyzed. The inflammatory response within the brain tissue was explored by measuring the expression of various inflammatory cytokines at the mRNA and protein levels. These mediators were interleukin (IL)-1 beta, IL-2, IL-4, IL-6, IL-8, IL-10, tumor necrosis factor (TNF)-alpha, interferon (IFN)-gamma, and granulocyte-macrophage colony-stimulating factor (GM-CSF). This study shows for the first time in human brain tissue that 1) pro-inflammatory mediator protein levels are significantly increased in situ following acute brain injury while anti-inflammatory cytokines protein levels remain unchanged; 2) the cerebral inflammatory response begins within minutes of acute TBI, much earlier than previously thought; 3) IL-6, IL-8, TNF-alpha, and IL-1 beta mRNA levels are significantly increased following injury; 4) the rise in cytokine protein level coincides with increased levels of their mRNAs suggesting that traumatic injury elicits an immediate cerebral inflammatory response. Altogether these data confirm and extend previous observations on the release of cytokines in the cerebrospinal fluid of severe TBI patients. Finally, this study highlights the need to characterize the cell source of cytokines and elucidate their mode of action.

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