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不同死后间隔时间小鼠大脑皮质蛋白质表达变化的蛋白质组学特征:法医生物标志物鉴定的初步研究。

Proteomic Characterization of Changes in Mouse Brain Cortex Protein Expression at Different Post-Mortem Intervals: A Preliminary Study for Forensic Biomarker Identification.

机构信息

Department of Medicine and Aging Sciences, University "G. d'Annunzio" of Chieti-Pescara, Via dei Vestini 31, 66100 Chieti, Italy.

Center for Advanced Studies and Technologies (CAST), University "G. d'Annunzio" of Chieti-Pescara, Via Luigi Polacchi 13, 66100 Chieti, Italy.

出版信息

Int J Mol Sci. 2024 Aug 10;25(16):8736. doi: 10.3390/ijms25168736.

DOI:10.3390/ijms25168736
PMID:39201424
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11354345/
Abstract

Accuracy in the evaluation of death-induced tissue degradation for thanato-chronological purposes is strictly dependent on the condition of the biological source as well as on the precision of post-mortem interval (PMI) estimation. Thus, the optimization of tissue handling and identification of sensitive post-mortem biomarkers could help establish a timeline for post-mortem events. To this aim, we investigated the proteome changes in cortex samples of 6-week-old female SAMR1 mice over a post-mortem time course. After death, brain tissue was removed immediately (T0), and after 4, 8, 12, 24, and 32 h, four mice were used for each time period, and animals were maintained at 4 °C until brain removal. Dissected tissues were frozen at -80 °C until processed. Proteomic analysis, performed on samples related to early and late PMIs (<24 h and >24 h post-mortem, respectively) showed protein level changes as compared to T0 samples, with a remarkable increase in Calpain11 in the early PMI, as well as in Caspases 7 and 8 together with Gasdermin 3 in late PMI. These findings were confirmed by LIFT mass spectrometry technology and western blot analysis and, although requiring further investigation in other biological samples, suggest that these proteins could be considered as putative biomarkers of different PMIs.

摘要

为了达到法医年代学的目的,准确评估死亡导致的组织降解严格依赖于生物样本的状况以及死后间隔时间(PMI)估计的精度。因此,优化组织处理和鉴定敏感的死后生物标志物可以帮助建立死后事件的时间轴。为此,我们研究了在死后时间过程中,6 周龄雌性 SAMR1 小鼠大脑皮层样本中的蛋白质组变化。死后,立即取出脑组织(T0),然后在 4、8、12、24 和 32 小时时,每个时间点使用 4 只小鼠,将动物保持在 4°C 直至脑组织取出。解剖组织在-80°C 下冷冻直至处理。与 T0 样本相比,对与早期和晚期 PMI(分别为死后<24 小时和>24 小时)相关的样本进行蛋白质组分析显示出蛋白质水平的变化,在早期 PMI 中钙蛋白酶 11 显著增加,而在晚期 PMI 中 Caspases 7 和 8 以及 Gasdermin 3 共同增加。这些发现通过 LIFT 质谱技术和 Western blot 分析得到了证实,尽管需要在其他生物样本中进一步研究,但这些蛋白质可能被认为是不同 PMI 的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b53f/11354345/83245b5244d8/ijms-25-08736-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b53f/11354345/1e686a2b7e09/ijms-25-08736-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b53f/11354345/6c810bf01fb5/ijms-25-08736-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b53f/11354345/12b81e5cc9a9/ijms-25-08736-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b53f/11354345/37b489532fa0/ijms-25-08736-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b53f/11354345/83245b5244d8/ijms-25-08736-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b53f/11354345/1e686a2b7e09/ijms-25-08736-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b53f/11354345/6c810bf01fb5/ijms-25-08736-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b53f/11354345/12b81e5cc9a9/ijms-25-08736-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b53f/11354345/37b489532fa0/ijms-25-08736-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b53f/11354345/83245b5244d8/ijms-25-08736-g005a.jpg

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