Journal of Surgical Research
Volume 152, Issue 1 , Pages 3-17.e2, March 2009

Gene Expression Profiling of Long-Term Changes in Rat Liver Following Burn Injury1

  • Arul Jayaraman, Ph.D.

      Affiliations

    • Department of Surgery, Shriners Hospitals for Children and Massachusetts General Hospital, Boston, Massachusetts
    • Corresponding Author InformationTo whom correspondence and reprint requests should be addressed at Artie McFerrin Department of Chemical Engineering, Texas A&M University, College Station, Texas 77843-3122
  • ,
  • Tim Maguire, Ph.D.

      Affiliations

    • Department of Biomedical Engineering, Rutgers, the State University of New Jersey, Piscataway, New Jersey
  • ,
  • Murali Vemula, Ph.D.

      Affiliations

    • Department of Surgery, Shriners Hospitals for Children and Massachusetts General Hospital, Boston, Massachusetts
  • ,
  • Deukwoo W. Kwon, Ph.D.

      Affiliations

    • Department of Statistics, Texas A&M University, College Station, Texas
    • Current address: Radiation Epidemiology Branch, Division of Cancer, Epidemiology, and Genetics, National Cancer Institute, Bethesda, MD.
  • ,
  • Marina Vannucci, Ph.D.

      Affiliations

    • Department of Statistics, Texas A&M University, College Station, Texas
    • Current address: Department of Statistics, Rice University, Houston, TX.
  • ,
  • Francois Berthiaume, Ph.D.

      Affiliations

    • Department of Surgery, Shriners Hospitals for Children and Massachusetts General Hospital, Boston, Massachusetts
  • ,
  • Martin L. Yarmush, M.D., Ph.D.

      Affiliations

    • Department of Surgery, Shriners Hospitals for Children and Massachusetts General Hospital, Boston, Massachusetts

Received 3 February 2007 published online 30 August 2007.

The inflammatory response initiated upon burn injury is also associated with extensive metabolic adjustments. While there is a significant body of literature on the characterization of these changes at the metabolite level, little is known on the mechanisms of induction, especially with respect to the role of gene expression. We have comprehensively analyzed changes in gene expression in rat livers during the first 7 d after 20% total body surface area burn injury using Affymetrix microarrays. A total of 740 genes were significantly altered in expression at 1, 2, 4, and 7 d after burn injury compared to sham-burn controls. Functional classification based on gene ontology terms indicated that metabolism, transport, signaling, and defense/inflammation response accounted for more than 70% of the significantly altered genes. Fisher least-significant difference post-hoc testing of the 740 differentially expressed genes indicated that over 60% of the genes demonstrated significant changes in expression either on d 1 or on d 7 postburn. The gene expression trends were corroborated by biochemical measurements of triglycerides and fatty acids 24 h postburn but not at later time points. This suggests that fatty acids are used, at least in part, in the liver as energy substrates for the first 4 d after injury. Our data also suggest that long-term regulation of energy substrate utilization in the liver following burn injury is primarily at the posttranscriptional level. Last, relevance networks of significantly expressed genes indicate the involvement of key small molecules in the hepatic response to 20% total body surface area burn injury.

Key Words: liver gene expression, 20% burn injury, microarrays, energy expenditure

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

1 Arul Jayaraman and Tim Maguire contributed equally to this work.

PII: S0022-4804(07)00377-0

doi:10.1016/j.jss.2007.05.025

Journal of Surgical Research
Volume 152, Issue 1 , Pages 3-17.e2, March 2009