Patzig Julia, Kusch Kathrin, Fledrich Robert, Eichel Maria A, Lüders Katja A, Möbius Wiebke, Sereda Michael W, Nave Klaus-Armin, Martini Rudolf, Werner Hauke B
Department of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.
Center for Nanoscale Microscopy and Molecular Physiology of the Brain, Göttingen, Germany.
Glia. 2016 Jan;64(1):155-74. doi: 10.1002/glia.22922. Epub 2015 Sep 22.
Protein zero (P0) is the major structural component of peripheral myelin. Lack of this adhesion protein from Schwann cells causes a severe dysmyelinating neuropathy with secondary axonal degeneration in humans with the neuropathy Dejerine-Sottas syndrome (DSS) and in the corresponding mouse model (P0(null)-mice). In the mammalian CNS, the tetraspan-membrane protein PLP is the major structural myelin constituent and required for the long-term preservation of myelinated axons, which fails in hereditary spastic paraplegia (SPG type-2) and the relevant mouse model (Plp(null)-mice). The Plp-gene is also expressed in Schwann cells but PLP is of very low abundance in normal peripheral myelin; its function has thus remained enigmatic. Here we show that the abundance of PLP but not of other tetraspan myelin proteins is strongly increased in compact peripheral myelin of P0(null)-mice. To determine the functional relevance of PLP expression in the absence of P0, we generated P0(null)*Plp(null)-double-mutant mice. Compared with either single-mutant, P0(null)*Plp(null)-mice display impaired nerve conduction, reduced motor functions, and premature death. At the morphological level, axonal segments were frequently non-myelinated but in a one-to-one relationship with a hypertrophic Schwann cell. Importantly, axonal numbers were reduced in the vital phrenic nerve of P0(null)*Plp(null)-mice. In the absence of P0, thus, PLP also contributes to myelination by Schwann cells and to the preservation of peripheral axons. These data provide a link between the Schwann cell-dependent support of peripheral axons and the oligodendrocyte-dependent support of central axons.
蛋白零(P0)是外周髓鞘的主要结构成分。施万细胞中缺乏这种黏附蛋白会导致严重的脱髓鞘性神经病变,并伴有继发性轴突变性,在患有德热里纳 - 索塔斯综合征(DSS)的人类以及相应的小鼠模型(P0基因敲除小鼠)中均如此。在哺乳动物的中枢神经系统中,四跨膜蛋白PLP是髓鞘的主要结构成分,对于有髓轴突的长期保存是必需的,而在遗传性痉挛性截瘫(2型SPG)及相关小鼠模型(Plp基因敲除小鼠)中则无法发挥该作用。Plp基因也在施万细胞中表达,但PLP在正常外周髓鞘中的丰度非常低;因此其功能一直成谜。在此我们表明,在P0基因敲除小鼠的致密外周髓鞘中,PLP的丰度显著增加,而其他四跨膜髓鞘蛋白的丰度并未增加。为了确定在缺乏P0的情况下PLP表达的功能相关性,我们构建了P0基因敲除Plp基因敲除双突变小鼠。与任一单突变小鼠相比,P0基因敲除Plp基因敲除小鼠表现出神经传导受损、运动功能减退和过早死亡。在形态学水平上,轴突节段常常无髓鞘包裹,但与肥大的施万细胞呈一对一关系。重要的是,P0基因敲除*Plp基因敲除小鼠的膈神经中轴突数量减少。因此,在缺乏P0的情况下,PLP也有助于施万细胞的髓鞘形成以及外周轴突的保存。这些数据为施万细胞对外周轴突的依赖性支持与少突胶质细胞对中枢轴突的依赖性支持之间建立了联系。