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Tau protein (MAPT) as a possible biochemical marker of traumatic brain injury in postmortem examination

机译:TAU蛋白(MAPT)作为后期检查中的创伤性脑损伤可能的生化标志

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Highlights ? Serum and CSF MAPT levels may be mTBI/TBI marker in postmortem examination. ? mTBI involve undiagnosed consequences in forensic autopsy and H&E examination. ? BBB opening, glymphatic system or macrophagal transport may be involved in MAPT exit. Abstract MAPT is a neuronal protein that plays an important role in axonal stabilization, neuronal development, and neuronal polarity. MAPT release into the CSF and blood has been interpreted as indicative of axonal injury as its elevated levels were observed in olympic boxers even after a mild head trauma suggesting minor CNS injuries. In our study we wanted to check the potential relevance of MAPT examination for forensic purposes. The study was carried out using cases of head injury group and cases of sudden death (cardiopulmonary failure, no injuries of the head — control group) provided by forensic pathologists at the Department of Forensic Medicine, Medical University of Warsaw. CSF and blood were collected within 24h after death using suboccipital puncture and femoral vein puncture. Serum and cerebrospinal fluid Tau protein concentrations were compared using an enzyme-linked immunosorbent assay (elisa). Brain specimens (frontal cortex) were collected during forensic autopsies. Sections were stained histologically (hematoxylin-eosin) and immunohistochemically with anti human Tau antibody, anti glial fibrillary acid protein (GFAP), anti human macrosialin (CD68) or anti human endothelial cells (CD34). In our study we documented that elevated levels of serum and CSF MAPT may also be considered a marker for mild traumatic brain injury and traumatic brain injury (mTBI and TBI). An increase in CSF and serum levels of MAPT in the absence of visible macroscopic traumatic CNS changes indicates that even minor head injuries may result in changes at the neuronal level that could remain undiagnosed during regular forensic autopsy and routine histopathological examination.
机译:强调 ?血清和CSF MAPT水平可以是后期检查中的MTBI / TBI标记。还MTBI涉及法医尸检和H&E检查的未确诊后果。还MAPT出口可能涉及BBB开放,甘蓝系统或巨噬丸运输。摘要MAPT是一种在轴突稳定,神经元发育和神经元极性中起重要作用的神经元蛋白。 MAPT释放到CSF和血液中被解释为表明轴突损伤,即使在奥运拳击员中观察到升级的水平,即使在轻度的头部创伤暗示轻微的CNS受伤后也是如此。在我们的研究中,我们希望检查MapT检查对法医目的的潜在相关性。法医院法医院法医院法医院法医院法医院疾病病理学家提供的头部损伤组和猝死病例(心肺尿动衰竭,主管衰竭伤,无伤害,无伤害,无伤害伤害。使用子可染色体穿刺和股静脉穿刺死亡后24小时内收集CSF和血液。使用酶联免疫吸附测定(ELISA)进行比较血清和脑脊髓液Tau蛋白浓度。在法医尸检期间收集脑标本(额相皮质)。将切片染色(苏木精 - eosin)和免疫组织化学,用抗人Tau抗体,抗胶质纤维酸蛋白(GFAP),抗人巨粒素(CD68)或抗人类内皮细胞(CD34)。在我们的研究中,我们记录了血清和CSF MAPT的升高,也可以被认为是轻度创伤性脑损伤和创伤性脑损伤的标志物(MTBI和TBI)。在没有可见的宏观创伤性CNS变化的情况下,MAPT的CSF和血清水平的增加表明,即使是次要头部损伤也可能导致神经元水平的变化,这在常规法医尸检和常规组织病理学检查期间可以保持未结合。

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