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Essential Function of Protein 4.1G in Targeting of Membrane Protein Palmitoylated 6 into Schmidt-Lanterman Incisures in Myelinated Nerves

机译:蛋白质4.1G的本质功能在有髓神经的Schmidt-Lanterman发作靶向膜蛋白棕榈酰化6。

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摘要

Protein 4.1G is a membrane skeletal protein found in specific subcellular structures in myelinated Schwann cells and seminiferous tubules. Here, we show that in the mouse sciatic nerve, protein 4.1G colocalized at Schmidt-Lanterman incisures (SLI) and the paranodes with a member of the membrane-associated guanylate kinase (MAGUK) family, membrane protein palmitoylated 6 (MPP6). Coimmunoprecipitation experiments revealed that MPP6 was interacting with protein 4.1G. In contrast to wild-type nerves, in 4.1G knockout mice, MPP6 was found largely in the cytoplasm near Schwann cell nuclei, indicating an abnormal protein transport. Although the SLI remained in the 4.1G knockout sciatic nerves, as confirmed by E-cadherin immunostaining, their shape was altered in aged 4.1G knockout nerves compared to their shape in wild-type nerves. In the seminiferous tubules, MPP6 was localized similarly to protein 4.1G along cell membranes of the spermatogonium and early spermatocytes. However, in contrast to myelinated peripheral nerves, the specific localization of MPP6 in the seminiferous tubules was unaltered in the absence of protein 4.1G. These results indicate that 4.1G has a specific role in the targeting of MPP6 to the SLI and the assembly of these subcellular structures.
机译:蛋白质4.1G是在有髓雪旺细胞和生精小管的特定亚细胞结构中发现的膜骨架蛋白。在这里,我们显示在小鼠坐骨神经中,蛋白4.1G共定位于Schmidt-Lanterman损伤(SLI)和具有与膜相关的鸟苷酸激酶(MAGUK)家族成员的腹节,膜蛋白被棕榈酰化6(MPP6)。免疫共沉淀实验表明MPP6与4.1G蛋白相互作用。与野生型神经相反,在4.1G基因敲除小鼠中,MPP6主要在雪旺细胞核附近的细胞质中发现,表明蛋白质运输异常。尽管SLI保留在4.1G敲除的坐骨神经中,如E-cadherin免疫染色所证实,但与野生型神经的形状相比,在老年4.1G敲除的神经中它们的形状发生了变化。在生精小管中,MPP6与4.1G蛋白类似地沿着精原细胞和早期精母细胞的细胞膜定位。但是,与有髓神经末梢神经相反,在没有蛋白4.1G的情况下,生精小管中MPP6的特异性定位没有改变。这些结果表明4.1G在MPP6靶向SLI和这些亚细胞结构的组装中具有特定作用。

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