Hardy R J, Friedrich V L
Brookdale Center for Molecular Biology, Mount Sinai Medical School, New York, NY 10029, USA.
Dev Neurosci. 1996;18(4):243-54. doi: 10.1159/000111414.
Myelin sheaths develop in the central nervous system (CNS) as elaborations of the processes of oligodendrocytes. Although many details of the spiral wrapping of oligodendrocyte processes around axons and their subsequent transformation into myelin sheaths are known from thin-section electron-microscopic studies, the three-dimensional architecture of the myelin-forming cells is incompletely understood. To characterize this aspect of oligodendrocyte development, we labeled thick (100- to 300-microns) sections of developing murine CNS with oligodendrocyte marker antibodies, recorded individual cells in serial optical sections by confocal microscopy, and created whole-cell reconstructions of oligodendrocytes before and during the initiation of myelination. We distinguish three stages in the maturation of oligodendrocytes, which at all three stages are labeled by the O4, O1 and Ranscht monoclonals and by antibodies against the myelin-specific proteins CNP and myelin basic protein. Premyelinating oligodendrocytes, present before axonal ensheathment begins, emit multiple irregular processes which have predominant radial orientation. These processes, which generally terminate within 50 microns of the cell body, have a surface area 3-8 times or more that of the cell body itself and may represent a mechanism for sampling the local environment of each cell and for identifying target axons. Transitional cells have initiated one or more myelin sheaths; these cells progressively reduce the number of their radial processes as they increase the number of their myelin internodes. The radial processes of each transitional cell are most reduced in parts of the process arbor where ensheathment has begun, suggesting directional control in the elaboration or stability of the radial processes. Mature myelin-bearing oligodendrocytes entirely lack the radial processes and instead emit a few sparsely branching processes which connect cell bodies with myelin internodes. Three-dimensional analysis of the earliest stages in myelin sheath formation reveals two distinct phases. The initiating event in the formation of myelin internodes is the growth of thin unbranched processes, termed 'initiator processes', along axons. The second phase, spiral ensheathment of target axons, begins through the elaboration from each initiator process of lamellar extensions which extend circumferentially around the target axon and thereby form the first turn of its myelin sheath.
髓鞘在中枢神经系统(CNS)中作为少突胶质细胞突起的精细结构而发育形成。尽管通过薄切片电子显微镜研究已经了解到少突胶质细胞突起围绕轴突进行螺旋缠绕以及随后转变为髓鞘的许多细节,但对形成髓鞘细胞的三维结构仍未完全理解。为了表征少突胶质细胞发育的这一方面,我们用少突胶质细胞标记抗体标记发育中小鼠CNS的厚切片(100至300微米),通过共聚焦显微镜在连续光学切片中记录单个细胞,并在髓鞘形成开始之前和期间创建少突胶质细胞的全细胞重建。我们区分了少突胶质细胞成熟的三个阶段,在所有这三个阶段,少突胶质细胞都被O4、O1和Ranscht单克隆抗体以及针对髓鞘特异性蛋白CNP和髓鞘碱性蛋白的抗体标记。在轴突被包裹开始之前出现的前髓鞘形成少突胶质细胞发出多个不规则突起,这些突起主要呈径向取向。这些突起通常在细胞体50微米范围内终止,其表面积是细胞体本身的3至8倍或更多,可能代表了一种对每个细胞局部环境进行采样和识别靶轴突的机制。过渡细胞已经开始形成一个或多个髓鞘;随着髓鞘节段数量的增加,这些细胞逐渐减少其径向突起的数量。每个过渡细胞的径向突起在包裹开始的突起树突部分减少最多,这表明在径向突起的形成或稳定性方面存在方向控制。成熟的带有髓鞘的少突胶质细胞完全没有径向突起,而是发出一些稀疏分支的突起,这些突起将细胞体与髓鞘节段连接起来。对髓鞘形成最早阶段的三维分析揭示了两个不同的阶段。髓鞘节段形成的起始事件是沿着轴突生长出细的无分支突起,称为“起始突起”。第二阶段,即靶轴突的螺旋包裹,通过从每个起始突起延伸出的层状延伸开始,这些层状延伸围绕靶轴突周向延伸,从而形成其髓鞘的第一圈。