Stony Brook University School of Medicine, Stony Brook, New York, USA.
Wound Repair Regen. 2011 Sep-Oct;19(5):622-32. doi: 10.1111/j.1524-475X.2011.00725.x.
Burns are dynamic injuries, characterized by progressive death of surrounding tissue over time. Although central to an understanding of burn injury progression, the spatiotemporal degrees and rates of cellular necrosis and apoptosis in the zone of ischemia surrounding burns are not well characterized. Using a validated porcine hot comb model, we probed periburn tissue at 1, 4, and 24 hours after injury for high-mobility group box 1 as a marker of necrosis and activated cleaved caspase-3 as a marker of apoptosis, followed by spatiotemporal morphometric analysis. We found that necrosis was the most prominent mechanism of cell death in burn injury progression, with significant progression between 1 and 4 hours postburn. Apoptosis appeared not to play a role in early burn injury progression but was observed in cells at the interface of necrotic and viable tissue at 24 hours postburn. Our findings imply that intervention within the first 4 hours following injury is likely necessary to limit burn injury progression. Additionally, based on high-mobility group box 1 staining patterns, we define distinct early, intermediate, and late pathological signs of cell necrosis that may facilitate delineation of causal mechanistic relationships of burn injury progression in vivo.
烧伤是一种动态损伤,其特征是周围组织随着时间的推移逐渐死亡。尽管这是理解烧伤进展的核心,但烧伤周围缺血区域细胞坏死和凋亡的时空程度和速率尚未得到很好的描述。我们使用经过验证的猪热梳模型,在损伤后 1、4 和 24 小时探查烧伤周围组织中的高迁移率族蛋白 1(作为坏死的标志物)和活化的切割半胱氨酸天冬氨酸蛋白酶-3(作为凋亡的标志物),然后进行时空形态计量学分析。我们发现,坏死是烧伤进展中细胞死亡的最主要机制,伤后 1 至 4 小时内有显著进展。凋亡似乎在早期烧伤进展中不起作用,但在伤后 24 小时观察到坏死和存活组织交界处的细胞中出现凋亡。我们的研究结果表明,在损伤后 4 小时内进行干预可能是限制烧伤进展所必需的。此外,根据高迁移率族蛋白 1 染色模式,我们定义了细胞坏死的明显早期、中期和晚期病理特征,这可能有助于在体内阐明烧伤进展的因果机制关系。