Journal of the American College of Surgeons · 2007 · 73 citations · 23 references
Life SciencesPathologySurgeryCell SignalingSignal TransductionWound HealingGrowth Factor SignalingWound ClosureWound ContractionWound Healing PhysiologyWound Healing ResponseWound InflammationRabbit ModelsTemporal ExpressionTemporal Gene ExpressionTransforming Growth Factor Beta ReceptorsTransforming Growth Factor Beta RegulationTransforming Growth Factor Beta Signaling ModulationTransforming Growth Factor-beta SignalingWound Healing Progression
BACKGROUND: Despite numerous studies that have investigated the cellular and molecular mechanisms underlying scar formation, this process still remains poorly understood. The importance of transforming growth factor-beta (TGF-beta) in these processes has been well recognized, and this study sought to define the temporal expression of the key members in this pathway in a well-established, clinically relevant, rabbit ear model of hypertrophic scarring. STUDY DESIGN: Seven-millimeter (hypertrophic) and 5-mm (nonhypertrophic) punch wounds were made on the ears of 12 rabbits. Wounds were harvested at days 0, 7, 15, 28, and 40. RESULTS: There were no appreciable histologic differences between the 5- and 7-mm wounds at days 7 and 15. At day 28, however, the 7-mm scars were considerably more hypertrophic compared with the 5-mm control scars (p<0.001). The mRNA levels of TGF-beta1 and collagen Ialpha2 were notably higher in the hypertrophic 7-mm scars at day 28 than in the nonhypertrophic 5-mm scars (p<0.03). Although not pronounced, levels of TGF-beta2 were higher in the hypertrophic scars. There were no other statistically significant differences between the 7- and 5-mm scars. CONCLUSIONS: Elevated levels of TGF-beta1, and possibly TGF-beta2, are associated with hypertrophic scar formation.
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Kee Yang Chung, A. Agarwal, Jouni Uitto et al. · Journal of Biological Chemistry · 1996 · 315 citations · Full text