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首页> 外文期刊>Journal of pharmacological sciences. >Expression of microsomal prostaglandin E synthase-1 in the spinal cord in a transgenic mouse model of amyotrophic lateral sclerosis
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Expression of microsomal prostaglandin E synthase-1 in the spinal cord in a transgenic mouse model of amyotrophic lateral sclerosis

机译:肌萎缩侧索硬化转基因小鼠模型中脊髓微粒体前列腺素E合酶-1的表达

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Prostaglandin E 2 (PGE 2) is a key molecule involved in the neuroinflammatory processes that characterize amyotrophic lateral sclerosis (ALS). Although PGE 2 synthesis is regulated by PGE 2 synthases (PGESs), the pathological role of PGESs in ALS still remains unknown. Experiments were performed to elucidate the expression of PGESs and the localization of microsomal PGES-1 (mPGES-1) in neurons and glial cells in the spinal cord of ALS model (G93A) mice. Neurological symptom was observed in G93A mice from 14 weeks by the tail suspension test, and rotarod performances were decreased at 16 weeks and older. Western blotting revealed that the level of mPGES-1 was increased in G93A mice at 15 weeks and older. In contrast, the levels of cytosolic PGES and mPGES-2 did not change at any age. Immunohistochemical analysis demonstrated that age-dependent expression of mPGES-1 was found in motor neurons in G93A mice at 11 and 15 weeks. Immunoreactivity of mPGES-1 was also co-localized in Iba1-positive microglia in G93A mice at 15 weeks. These results suggest that mPGES-1 in motor neurons may play a role in the pathogenesis of ALS and that mPGES-1 may work sequentially in motor neurons and activated microglia to produce ALS symptoms in G93A mice.
机译:前列腺素E 2(PGE 2)是参与神经炎性过程的关键分子,其特征是肌萎缩性侧索硬化症(ALS)。尽管PGE 2合成受PGE 2合酶(PGES)调控,但PGES在ALS中的病理作用仍然未知。进行实验以阐明ALS模型(G93A)小鼠脊髓中神经元和神经胶质细胞中PGES的表达和微粒体PGES-1(mPGES-1)的定位。通过尾部悬吊测试,从第14周开始在G93A小鼠中观察到神经系统症状,而在16周及以上时,旋转杆性能下降。蛋白质印迹显示,在15周及以上的G93A小鼠中,mPGES-1的水平升高。相比之下,胞浆中PGES和mPGES-2的水平在任何年龄都没有变化。免疫组织化学分析表明,在11周和15周时,在G93A小鼠的运动神经元中发现了mPGES-1的年龄依赖性表达。 15周时,mPGES-1的免疫反应性也共定位在G93A小鼠的Iba1阳性小胶质细胞中。这些结果表明,运动神经元中的mPGES-1可能在ALS的发病机理中起作用,并且mPGES-1可能在运动神经元和活化的小胶质细胞中顺序发挥作用,从而在G93A小鼠中产生ALS症状。

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