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Updated: Sep 25, 2026

A Murine Model of a Burn Wound Reconstructed with an Allogeneic Skin Graft
Published on: August 8, 2020
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
Objective:
To investigate the expression sequence and distribution characteristics of the protooncogenes c-fos, c-myc and endogenous basic fibroblast growth factor (bFGF) genes in burned tissues, and to explore the possible effects of changes in these genes' functions on wound healing.
Methods:
Partial-thickness burns of 30% TBSA were established on backs of Wistar rats. In situ hybridization and histological methods were used to detect expression of c-fos, c-myc and bFGF genes in normal and burned tissue at 3 h, 6 h, 1 d, 3 d, 7 d and 14 d postburn.
Results:
Although expression of c-fos and c-myc genes and bFGF gene could be found in normal skin, the expression of all three were markedly induced by burn wounds and the expression models in sequence and distribution were quite different. Expression of c-fos gene increased and peaked at 6 h. Signals were mainly localized in both nuclei of dermal fibroblasts and monocytes. The expression of bFGF gene increased at 6 h and peaked at 1 d postburn, and was distributed in the cytoplasm of fibroblasts. C-myc gene peaked 3 d postburn and was also distributed in the cytoplasm of fibroblasts.
Conclusions:
These results indicated that thermal injury could induce the expression of c-fos, c-myc and bFGF at gene level, showing phasic control and regional distribution. The phasic expression of these genes suggests that there is an interaction between protooncogenes and bFGF, which may play an important role in wound healing. The different expressions of c-fos and c-myc play an inducing role in regulating bFGF, and in turn affect wound healing.
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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