Division of Forensic Pathology and Science, Unit of Social Medicine, Course of Medical and Dental Sciences, Graduate School of Biomedical Sciences, Nagasaki University School of Medicine, 1-12-4 Sakamoto, Nagasaki, Nagasaki, 852-8523, Japan.
Forensic Science Laboratory, Nagasaki Prefectural Police Headquarters, Nagasaki, Nagasaki, Japan.
Sci Rep. 2020 Sep 22;10(1):15432. doi: 10.1038/s41598-020-71931-w.
Forensic diagnosis of fatal hypothermia is considered difficult because there are no specific findings. Accordingly, exploration of novel fatal hypothermia-specific findings is important. To elucidate the molecular mechanism of homeostasis in hypothermia and identify novel molecular markers to inform the diagnosis of fatal hypothermia, we focused on microRNA expression in skeletal muscle, which plays a role in cold-induced thermogenesis in mammals. We generated rat models of mild, moderate, and severe hypothermia, and performed body temperature-dependent microRNA expression analysis of the iliopsoas muscle using microarray and quantitative real-time PCR (qRT-PCR). The results show that rno-miR-374-5p expression was significantly induced only by severe hypothermia. Luciferase reporter assay and qRT-PCR results indicated that Mex3B expression was regulated by rno-miR-374-5p and decreased with decreasing body temperature. Gene ontology analysis indicated the involvement of Mex3B in positive regulation of GTPase activity. siRNA analysis showed that Mex3B directly or indirectly regulated Kras expression in vitro, and significantly changed the expression of apoptosis-related genes and proteins. Collectively, these results indicate that rno-miR-374-5p was activated by a decrease in body temperature, whereby it contributed to cell survival by suppressing Mex3B and activating or inactivating Kras. Thus, rno-miR-374-5p is a potential supporting marker for the diagnosis of fatal hypothermia.
法医学诊断致命性低体温较为困难,因为没有特定的发现。因此,探索新的致命性低体温特异性发现非常重要。为了阐明低体温时体内平衡的分子机制并确定可用于致命性低体温诊断的新分子标志物,我们专注于骨骼肌中的 microRNA 表达,其在哺乳动物的冷诱导产热中发挥作用。我们生成了轻度、中度和重度低体温的大鼠模型,并使用微阵列和定量实时 PCR(qRT-PCR)对髂腰肌进行了依赖体温的 microRNA 表达分析。结果表明,仅严重低体温可显著诱导 rno-miR-374-5p 的表达。荧光素酶报告基因检测和 qRT-PCR 结果表明,Mex3B 的表达受 rno-miR-374-5p 调控,且随体温降低而降低。基因本体分析表明 Mex3B 参与 GTPase 活性的正向调节。siRNA 分析表明,Mex3B 在体外直接或间接调节 Kras 的表达,并且显著改变了与凋亡相关的基因和蛋白的表达。总之,这些结果表明,rno-miR-374-5p 因体温降低而被激活,从而通过抑制 Mex3B 并激活或失活 Kras 来促进细胞存活。因此,rno-miR-374-5p 是致命性低体温诊断的潜在支持性标志物。