Palagummi Sai, Harbison Sallyann, Fleming Rachel
School of Chemical Sciences, University of Auckland, Auckland, New Zealand.
Int J Legal Med. 2014 May;128(3):403-14. doi: 10.1007/s00414-013-0941-5. Epub 2013 Nov 22.
The determination of dermal injury age is important in forensic practice. It helps answer questions that are important to an investigation such as the timing of the injury and incident, the order of infliction (where there is more than one injury), the survival time after injury (post-infliction interval) and the relation of the injury to the incident. Despite the importance of injury age determination, there currently exists no reliable method to estimate dermal injury age. In this study, the expression of the following 14 mRNAs was studied in human dermal injuries and their usefulness in the estimation of human dermal injury age was evaluated: dual specificity phosphate 1 (DUSP1), interleukin 7 (IL7), vascular cell adhesion molecule 1, tenascin C, cluster of differentiation 14, interleukin 6, tumour necrosis factor alpha (TNFα), interleukin 1beta (IL1β), chymase 1 (CMA1), collagen type III alpha I, interleukin 2, collagen type I alpha I, collagen type I alpha II and vascular endothelial growth factor A (VEGFA). DUSP1, IL7, TNFα and VEGFA showed an initial decrease in expression during the early stages followed by an increase in expression towards the middle and late phases. IL1β and CMA1 expression was limited to specific time points. The remaining markers either showed inconsistent expression or were undetected in our samples. The expression patterns of the detected markers suggest they have potential to predict injury age, especially during the initial stages of injury healing, if used in combination with one another.
在法医实践中,确定皮肤损伤时间很重要。它有助于回答对调查至关重要的问题,如损伤和事件的时间、损伤顺序(存在多处损伤时)、损伤后的存活时间(损伤后间隔时间)以及损伤与事件的关系。尽管损伤时间确定很重要,但目前尚无可靠方法来估计皮肤损伤时间。在本研究中,对人类皮肤损伤中以下14种mRNA的表达进行了研究,并评估了它们在估计人类皮肤损伤时间方面的实用性:双特异性磷酸酶1(DUSP1)、白细胞介素7(IL7)、血管细胞黏附分子1、腱生蛋白C、分化簇14、白细胞介素6、肿瘤坏死因子α(TNFα)、白细胞介素1β(IL1β)、糜酶1(CMA1)、Ⅲ型胶原蛋白α1、白细胞介素2、Ⅰ型胶原蛋白α1、Ⅰ型胶原蛋白α2和血管内皮生长因子A(VEGFA)。DUSP1、IL7、TNFα和VEGFA在早期表达最初下降,随后在中期和后期表达增加。IL1β和CMA1的表达仅限于特定时间点。其余标志物要么表达不一致,要么在我们的样本中未检测到。检测到的标志物的表达模式表明,如果相互结合使用,它们有可能预测损伤时间,尤其是在损伤愈合的初始阶段。