Thermal injuries induce gene expression of endogenous c-fos, c-myc and bFGF in burned tissues

Xiaobing Fu1, Xiaoman Gu, Tongzhu Sun

  • 1Key Research Laboratory of Wound Repair of PLA, Burn Institute, 304th Hospital, Trauma Center of Postgraduate Medical College, Beijing 100037, China. fuxb@cgw.net.cn

Abstract

Insights

Burn wounds significantly alter the expression of c-fos, c-myc, and basic fibroblast growth factor (bFGF) genes. These changes in gene expression, occurring in distinct phases and locations, are crucial for effective wound healing.

Area of Science:

  • Molecular biology
  • Wound healing research
  • Burn injury mechanisms

Background:

  • Protooncogenes c-fos and c-myc, and basic fibroblast growth factor (bFGF) are implicated in cellular processes.
  • Understanding their role in burn wound healing is critical for therapeutic development.

Purpose of the Study:

  • To investigate the expression patterns of c-fos, c-myc, and bFGF genes in burn tissues.
  • To explore the functional impact of these genes on wound healing processes.

Main Methods:

  • Induction of partial-thickness burns (30% TBSA) in Wistar rats.
  • Utilized in situ hybridization and histological methods to analyze gene expression at multiple time points post-burn (3h to 14d).

Main Results:

  • Burn wounds markedly induced c-fos, c-myc, and bFGF gene expression compared to normal skin.
  • c-fos peaked at 6h (fibroblasts, monocytes nuclei); bFGF peaked at 1d (fibroblast cytoplasm); c-myc peaked at 3d (fibroblast cytoplasm).
  • Distinct temporal and spatial expression patterns were observed for each gene.

Conclusions:

  • Thermal injury triggers a coordinated, time-dependent, and spatially regulated gene expression response involving c-fos, c-myc, and bFGF.
  • The interplay between protooncogenes and bFGF, as indicated by their phasic expression, is vital for effective wound healing.
  • c-fos and c-myc appear to induce bFGF expression, thereby influencing the overall wound healing cascade.

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