Atanasoski S, Shumas S, Dickson C, Scherer S S, Suter U
Institute of Cell Biology, Department of Biology, Swiss Federal Institute of Technology, ETH-Hönggerberg, CH-8093 Zurich, Switzerland.
Mol Cell Neurosci. 2001 Dec;18(6):581-92. doi: 10.1006/mcne.2001.1055.
Neurons regulate Schwann cell proliferation, but little is known about the molecular basis of this interaction. We have examined the possibility that cyclin D1 is a key regulator of the cell cycle in Schwann cells. Myelinating Schwann cells express cyclin D1 in the perinuclear region, but after axons are severed, cyclin D1 is strongly upregulated in parallel with Schwann cell proliferation and translocates into Schwann cell nuclei. During development, cyclin D1 expression is confined to the perinuclear region of proliferating Schwann cells and the analysis of cyclin D1-null mice indicates that cyclin D1 is not required for this type of Schwann cell proliferation. As in the adult, injury to immature peripheral nerves leads to translocation of cyclin D1 to Schwann cell nuclei and injury-induced proliferation is impaired in both immature and mature cyclin D1-deficient Schwann cells. Thus, our data indicate that the molecular mechanisms regulating proliferation of Schwann cells during development or activated by axonal damage are fundamentally different.
神经元调节雪旺细胞的增殖,但对于这种相互作用的分子基础知之甚少。我们研究了细胞周期蛋白D1是否是雪旺细胞细胞周期的关键调节因子。形成髓鞘的雪旺细胞在核周区域表达细胞周期蛋白D1,但轴突切断后,细胞周期蛋白D1与雪旺细胞增殖同步强烈上调,并转移至雪旺细胞核内。在发育过程中,细胞周期蛋白D1的表达局限于增殖雪旺细胞的核周区域,对细胞周期蛋白D1基因敲除小鼠的分析表明,这种类型的雪旺细胞增殖不需要细胞周期蛋白D1。与成年期一样,未成熟外周神经损伤会导致细胞周期蛋白D1转移至雪旺细胞核内,且在未成熟和成熟的细胞周期蛋白D1缺陷型雪旺细胞中,损伤诱导的增殖均受损。因此,我们的数据表明,发育过程中或由轴突损伤激活的调节雪旺细胞增殖的分子机制存在根本差异。