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首页> 外文期刊>International journal of biological sciences >Identification of TmemlO as a Novel Late-stage Oligodendrocytes Marker for Detecting Hypomyelination
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Identification of TmemlO as a Novel Late-stage Oligodendrocytes Marker for Detecting Hypomyelination

机译:鉴定TMEMLO作为一种用于检测低髓鞘化的新型后阶oligodendrocytes标志物

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Oligodendrocytes ensheath axons to form compact insulating multilamellar structures known as myelin. TmemlO is a novel type I transmembrane glycoprotein that is highly expressed in oligodendrocytes and whose biological function remains largely unknown. Furthermore, the expression pattern of Tmem 10 remains a matter of some controversy. Given the inconsistency of its expression pattern and the lack of validated specific antibodies, Tmem 10 is not widely accepted as a marker for mature oligodendrocytes. As a means to solve these problems and to aid future studies of oligodendrocyte-associated diseases, we have generated a highly specific Tmem 10 antibody. Using this TmemlO antibody, we clarify that TmemlO protein is firstly expressed at 2 weeks in the postnatal mouse brain with age-related increase, only in the central nervous system (CNS). We also reveal that TmemlO is expressed specifically in late stage oligodendrocytes and later than MAG, a late-stage myelin marker. Finally, we show that Tmem 10 co-expresses with MOG- and MBP-positive myelin fibers and is dramatically reduced in a hypomyelination mouse model. In conclusion, our study demonstrates that Tmem 10 can be used as a specific marker for myelinating oligodendrocytes and perhaps for the evaluation of myelination diseases, such as multiple sclerosis.
机译:Oligodendrocytes eNsheath轴突,形成紧凑的绝缘多样子结构,称为髓鞘。 TMEMLO是一种新型I型跨膜糖蛋白,其在少突胶质细胞中高度表达,其生物学功能仍然很大程度上未知。此外,TMEM 10的表达式模式仍然是一些争议的问题。鉴于其表达模式的不一致和缺乏验证的特异性抗体,TMEM 10不被广泛接受为成熟少突胶质细胞的标志物。作为解决这些问题的手段并帮助未来对少突胶质细胞相关疾病的研究,我们已经产生了高度特异性的TMEM 10抗体。使用该TMEMLO抗体,我们阐明了在后期小鼠脑中的2周内表达TMEMLO蛋白,其年龄与中枢神经系统(CNS)中有效地增加。我们还揭示了TMEMLO在晚期的少突卵细胞晚期表达,而不是MAG,这是一个晚期髓质标记。最后,我们表明TMEM 10与萌芽和MBP阳性髓蛋白纤维共表达,并且在低聚鼠模型中显着降低。总之,我们的研究表明,TMEM 10可以用作髓鞘寡核细胞的特定标志物,并且可能用于评估髓鞘疾病,例如多发性硬化症。

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