de Waegh S M, Lee V M, Brady S T
Department of Cell Biology and Neuroscience, University of Texas Southwestern Medical Center, Dallas 75235.
Cell. 1992 Feb 7;68(3):451-63. doi: 10.1016/0092-8674(92)90183-d.
Studies in Trembler and control mice demonstrated that myelinating Schwann cells exert a profound influence on axons. Extensive contacts between myelin and axons have been considered structural. However, demyelination decreases neurofilament phosphorylation, slow axonal transport, and axonal diameter, as well as significantly increasing neurofilament density. In control sciatic nerves with grafted Trembler nerve segments, these changes were spatially restricted: they were confined to axon segments without normal myelination. Adjacent regions of the same axons had normal diameters, neurofilament phosphorylation, cytoskeletal organization, and axonal transport rates. Close intercellular contacts between myelinating Schwann cells and axons modulate a kinase-phosphatase system acting on neurofilaments and possibly other substrates. Myelination by Schwann cells sculpts the axon-altering functional architecture, electrical properties, and neuronal morphologies.
对震颤小鼠和对照小鼠的研究表明,形成髓鞘的施万细胞对轴突有深远影响。髓鞘与轴突之间广泛的接触一直被认为是结构性的。然而,脱髓鞘会降低神经丝磷酸化、减缓轴突运输和轴突直径,同时显著增加神经丝密度。在移植了震颤神经节段的对照坐骨神经中,这些变化在空间上受到限制:它们局限于没有正常髓鞘形成的轴突节段。同一轴突的相邻区域具有正常的直径、神经丝磷酸化、细胞骨架组织和轴突运输速率。形成髓鞘的施万细胞与轴突之间紧密的细胞间接触调节着作用于神经丝及可能其他底物的激酶-磷酸酶系统。施万细胞形成髓鞘塑造了轴突,改变了其功能结构、电特性和神经元形态。