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The expression of excitatory amino acid transporter 2 in traumatic brain injury.

机译:兴奋性氨基酸转运蛋白2在脑外伤中的表达。

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It is well recognized that glutamate is the major excitatory neurotransmitter, which is removed from the synaptic cleft by excitatory amino acid transporter 2 (EAAT2) located on the perisynaptic astrocytes and that neuronal death has been associated with an increased extracellular glutamate concentration. In this study, we have immunohistochemically demonstrated the expression of EAAT2 protein in the human brain after traumatic brain injury (TBI). The EAAT2 expression patterns can be divided into three types: continuous and highly extensive staining (E); continuous but sporadic staining (M); and sporadic pattern staining (S). In six of the nine short survival cases studied (1h to 1 day), continuous and highly extensive staining for EAAT2 (E type) was observed in the ipsilateral cerebral cortex. On the other hand, we were able to demonstrate weak staining (S and M types) in 5 of the 7 long survival cases (>/=1 day) and in 12 of the 14 very short survival cases (<1h) studied. Similar findings were obtained in the contralateral cerebral cortex and also in the ipsilateral hippocampus. In addition, positive staining for glial fibrillary acidic protein was detected around the cerebral contusion, but the EAAT2-positive expression was not observed in the same region for all of the six short and long survival cases (>/=1h) after TBI. These findings clearly showed the differences in EAAT2 expression in the cerebral cortex according to the survival time and severity of cerebral contusion after TBI. Therefore, we emphasized that EAAT2 might play an important role in contributing to extracellular glutamate concentrations and secondary brain injury after TBI.
机译:众所周知,谷氨酸是主要的兴奋性神经递质,可通过位于突触周围星形胶质细胞上的兴奋性氨基酸转运蛋白2(EAAT2)从突触间隙中去除,并且神经元的死亡与细胞外谷氨酸浓度的升高有关。在这项研究中,我们已经免疫组织化学证实了创伤性脑损伤(TBI)后人脑中EAAT2蛋白的表达。 EAAT2表达模式可分为三种类型:连续染色和高度广泛染色(E);连续但偶发的染色(M);和零星的图案染色(S)。在研究的九个短期生存病例中(六个小时)(1h至1天),有六个在同侧大脑皮层中观察到了连续且高度广泛的EAAT2染色(E型)。另一方面,我们能够在所研究的7个长期生存病例中的5个(> / = 1天)和14个非常短期生存病例中的12个(<1h)中证明弱染色(S和M型)。在对侧大脑皮层和同侧海马中也获得了类似的发现。此外,在脑挫裂伤周围检测到了胶质纤维酸性蛋白的阳性染色,但是在TBI后的6个短期和长期生存病例中,在同一区域中均未观察到EAAT2阳性表达。这些发现清楚地表明,根据TBI后存活时间和脑挫裂伤的严重程度,大脑皮层EAAT2表达的差异。因此,我们强调EAAT2可能在TBI后导致细胞外谷氨酸浓度和继发性脑损伤中起重要作用。

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