Gene profiling in muscle of severely burned children: age- and sex-dependent changes

Mohan R K Dasu1, Robert E Barrow, David N Herndon

  • 1Department of Surgery, The University of Texas Medical Branch, Shriners Hospitals for Children, Galveston, Texas, USA.

Insights

Severe burns significantly alter gene expression in children's skeletal muscle, affecting metabolism and immune responses. This study highlights key molecular changes following thermal injury in pediatric patients.

Area of Science:

  • Pediatric critical care
  • Molecular biology
  • Burn research

Background:

  • Severe thermal injury triggers a significant catabolic response in skeletal muscle.
  • Understanding the molecular mechanisms of this response is crucial for effective treatment.

Purpose of the Study:

  • To identify gene expression alterations in the skeletal muscle of children with severe burns.
  • To compare gene expression profiles between burned children and a control group.

Main Methods:

  • Utilized high-density oligonucleotide microarrays (Affymetrix HG-U95 Av.2) to analyze gene expression.
  • Compared messenger RNA (mRNA) expression patterns between six burn patients and six control subjects.
  • RNA was isolated, transcribed in vitro, and hybridized to arrays for analysis using Affymetrix GeneChip Analysis Suite 5.2 and dChip.

Main Results:

  • Significant differential expression was observed in 77 genes (increased) and 21 genes (decreased) in burn children compared to controls (P < 0.05).
  • Specific genes with altered expression were identified in both male and female burn patients.
  • Affected genes were categorized into key functional groups including metabolism, immune response, stress response, and signal transduction.

Conclusions:

  • Burn injury leads to differential gene expression in pediatric skeletal muscle, impacting various cellular functions.
  • Identified genes, including transcription factors and signaling pathway proteins, warrant further investigation.
  • Further research is needed to establish functional relevance and molecular pathology of burn injury in muscle tissue.
Abstract