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细胞死亡蛋白作为早期死后间隔时间的标志物。

Cell death proteins as markers of early postmortem interval.

作者信息

C Zapico Sara, Menéndez Sofía T, Núñez Paula

机构信息

Department of Anthropology, National Museum of Natural History (NMNH), MRC 112, Smithsonian Institution, 10th and Constitution Avenue, NW, Washington, DC, 20560, USA,

出版信息

Cell Mol Life Sci. 2014 Aug;71(15):2957-62. doi: 10.1007/s00018-013-1531-x. Epub 2013 Dec 3.

Abstract

Estimation of time since death is one of the challenges in forensic science. There are many approaches to estimate the postmortem interval, including both physical and thanatochemistry methods. Decomposition is triggered by a process called autolysis, which induces destructive changes in the cell leading to cell death. Based on the process of cell death signaling, this study analyzed the early postmortem interval (2-8 h since death) using the study of the mRNA expression of Fas Ligand (FasL) and phosphatase and tensin homologue deleted on chromosome 10 (PTEN) by Quantitative-PCR. Results of the study indicate a time-dependent increase in the mRNA levels of both proteins up until 6 h after death. Using a regression analysis in these first 6 h, a positive linear correlation was found between the mRNA expression of these proteins and the time since death. Since PTEN and FasL are implicated in signaling pathways, both proteins are potential candidates to analyze the time since death in time intervals of 6 h or less. Further research is needed to find additional cell death markers and expand the time period for time since death estimation.

摘要

死亡时间的估计是法医学中的挑战之一。有许多方法可用于估计死后间隔时间,包括物理方法和死后化学方法。分解是由一个称为自溶的过程引发的,该过程会导致细胞发生破坏性变化,从而导致细胞死亡。基于细胞死亡信号传导过程,本研究通过定量聚合酶链反应研究Fas配体(FasL)和10号染色体缺失的磷酸酶和张力蛋白同源物(PTEN)的mRNA表达,分析了死后早期间隔时间(死亡后2至8小时)。研究结果表明,直到死亡后6小时,这两种蛋白质的mRNA水平均呈时间依赖性增加。在这最初的6小时内进行回归分析,发现这些蛋白质的mRNA表达与死亡时间之间存在正线性相关。由于PTEN和FasL参与信号通路,这两种蛋白质都是在6小时或更短时间间隔内分析死亡时间的潜在候选物。需要进一步研究以找到更多的细胞死亡标志物,并扩大死亡时间估计的时间段。

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