Department of Forensic Medicine and Toxicology, Faculty of Veterinary Medicine, Cairo University, Cairo, Egypt.
Department of Pathology, Faculty of Veterinary Medicine, Cairo University, Cairo, Egypt.
Int Wound J. 2019 Dec;16(6):1416-1425. doi: 10.1111/iwj.13206. Epub 2019 Aug 25.
In forensic medicine, it is vital to verify with the best attainable accuracy once injuries occurred during vital or post-mortem conditions. An immunohistochemical study was carried out to examine the time-dependent expression of macrophage-specific gene CD68 (cluster of differentiation 68), alpha-smooth muscle actin (α-SMA), and vascular endothelial growth factor (VEGF) in different skin wound timings (0, 1, 3, 5, 7, and 14 days) in rats. Histopathological studies were performed to assess the wound age and vitality. Eighteen male albino Wister rats (weighing 170-200 g) were used for wound induction. Rats (n = 3) were euthanised at 0, 1, 3, 5, 7, and 14 days from the starting point of wound induction. Histopathological examination showed that the epidermal re-epithelialisation was completed 14 days after skin incision. The inflammatory phase was recorded during the first 3 days of healing and reached the maximum levels at 5 days, then declined after 7 days, and completely removed at 14 days. The beginning of the proliferative phase was dated to day 3 and the peak at days 5 and 7. The initiation of the granulation tissue formation and remodelling phase of the healing process was observed 5 days after wounding. By immunohistochemical staining, negative VEGF gene expressions at early stages (0-3 days) were observed, as well as neither CD68+ macrophages nor α-SMA+ myofibroblast cells were detected. By increasing the wound ages (5-7 days), granulation tissue and angiogenesis were observed, with the migration of macrophages and fibroblast, which expressed VEGF, CD68, and α-SMA positive reaction. Time-dependent expression of the above markers suggested that they would be useful indicators for the determination of wound age. Both VEGF and transforming growth factor-beta 1 (TGFb1) mRNA levels were determined in different skin wound ages. The transcription of TGFb1 and VEGF increased shortly after wounding, until post-wounding day 7. It then declined constantly, reaching minimal values on day 14.
在法医学中,准确验证创伤是在生前还是死后发生至关重要。本研究通过免疫组织化学方法,研究了不同皮肤创伤时间(0、1、3、5、7 和 14 天)下,大鼠皮肤中巨噬细胞特异性基因 CD68(分化群 68)、α-平滑肌肌动蛋白(α-SMA)和血管内皮生长因子(VEGF)的时间依赖性表达。通过组织病理学研究评估伤口的年龄和活力。实验使用 18 只雄性白化 Wistar 大鼠(体重 170-200g)诱导伤口。从伤口诱导开始,每组 3 只大鼠在 0、1、3、5、7 和 14 天处死。组织病理学检查显示,皮肤切开后 14 天完成表皮再上皮化。在愈合的前 3 天记录炎症期,第 5 天达到最高水平,然后在第 7 天下降,第 14 天完全消除。增殖期的开始日期为第 3 天,第 5 天和第 7 天达到高峰。在受伤后第 5 天观察到肉芽组织形成和愈合过程重塑阶段的开始。通过免疫组织化学染色,在早期(0-3 天)观察到 VEGF 基因表达阴性,也未检测到 CD68+巨噬细胞或 α-SMA+肌成纤维细胞。随着伤口年龄的增加(5-7 天),观察到肉芽组织和血管生成,以及表达 VEGF、CD68 和 α-SMA 的巨噬细胞和纤维母细胞的迁移。上述标志物的时间依赖性表达表明,它们可作为确定伤口年龄的有用指标。在不同的皮肤伤口年龄中,均检测到 VEGF 和转化生长因子-β 1(TGFb1)mRNA 水平。TGFb1 和 VEGF 的转录在创伤后不久增加,直到创伤后第 7 天。然后持续下降,在第 14 天达到最小值。