Melendez-Vasquez C V, Rios J C, Zanazzi G, Lambert S, Bretscher A, Salzer J L
Department of Cell Biology, New York University School of Medicine, New York, NY 10016, USA.
Proc Natl Acad Sci U S A. 2001 Jan 30;98(3):1235-40. doi: 10.1073/pnas.98.3.1235.
In the adult peripheral nerve, microvillous processes of myelinating Schwann cells project to the nodes of Ranvier; their composition and physiologic function have not been established. As the ezrin-radixin-moesin (ERM) proteins are expressed in the microvilli of many epithelial cells, we have examined the expression and distribution of these proteins in Schwann cells and neurons in vitro and in vivo. Cultured Schwann cells express high levels of all three proteins and the ezrin-binding protein 50, whereas neurons express much lower, although detectable, levels of radixin and moesin. Ezrin is specific for Schwann cells. All three ERM proteins are expressed predominantly at the membrane of cultured Schwann cells, notably in their microvilli. In vivo, the ERM proteins are concentrated strikingly in the nodal processes of myelinating Schwann cells. Because these processes are devoid of myelin proteins, they represent a unique compartment of the myelinating Schwann cell. During development, the ERM proteins become concentrated at the ends of Schwann cells before myelin basic protein expression, demonstrating that Schwann cells are polarized longitudinally at the onset of myelination. ERM-positive Schwann cell processes overlie and are associated closely with nascent nodes of Ranvier, identified by clusters of ankyrin G. Ankyrin accumulation at the node precedes that of Caspr at the paranodes and therefore does not depend on the presence of mature paranodal junctions. These results demonstrate that nodes of Ranvier in the peripheral nervous system form in contact with specialized processes of myelinating Schwann cells that are highly enriched in ERM proteins.
在成人外周神经中,髓鞘形成雪旺细胞的微绒毛突起伸向郎飞结;其组成和生理功能尚未明确。由于埃兹蛋白-根蛋白-膜突蛋白(ERM)在许多上皮细胞的微绒毛中表达,我们研究了这些蛋白在体外和体内雪旺细胞及神经元中的表达和分布。培养的雪旺细胞表达所有三种蛋白以及埃兹蛋白结合蛋白50的高水平,而神经元表达的根蛋白和膜突蛋白水平低得多,尽管可检测到。埃兹蛋白对雪旺细胞具有特异性。所有三种ERM蛋白主要在培养的雪旺细胞膜上表达,特别是在其微绒毛中。在体内,ERM蛋白显著集中在髓鞘形成雪旺细胞的结状突起中。由于这些突起不含髓鞘蛋白,它们代表了髓鞘形成雪旺细胞的一个独特区域。在发育过程中,ERM蛋白在髓鞘碱性蛋白表达之前集中在雪旺细胞的末端,表明雪旺细胞在髓鞘形成开始时沿纵向极化。ERM阳性的雪旺细胞突起覆盖并与新生的郎飞结紧密相关,郎飞结由锚蛋白G簇识别。锚蛋白在结处的积累先于紧密连接蛋白在 paranodes 处的积累,因此不依赖于成熟 paranodal 连接的存在。这些结果表明,外周神经系统中的郎飞结与富含ERM蛋白的髓鞘形成雪旺细胞的特化突起接触形成。