Knapp P E
Department of Anatomy and Neurobiology, University of Kentucky College of Medicine, Lexington, USA.
Dev Neurosci. 1996;18(4):297-308. doi: 10.1159/000111420.
Proteolipid protein (PLP) is the most abundant protein of central nervous system (CNS) myelin. Because of its predicted topography, PLP has been assumed to function as a structural component of myelin, providing stability and maintaining the compact lamellar structure. However, developmental studies have shown that the PLP gene is active long before myelination begins. This and other evidence from various PLP mutants and transgenic models has fueled speculation that PLP or other products of the gene have additional, nonstructural roles both within and outside the CNS. PLP is structurally related to a family of ion channel proteins which includes the connexins, synaptophysins and various neurotransmitter receptors, and there is some experimental evidence which supports a role for PLP in ion gating. Other provocative ideas are that the PLP gene may influence autocrine signaling within oligodendrocytes or that PLP mRNAs have a function apart from protein coding.
蛋白脂蛋白(PLP)是中枢神经系统(CNS)髓鞘中含量最丰富的蛋白质。由于其预测的拓扑结构,PLP被认为作为髓鞘的结构成分发挥作用,提供稳定性并维持紧密的层状结构。然而,发育研究表明,PLP基因早在髓鞘形成开始之前就已活跃。来自各种PLP突变体和转基因模型的这一证据及其他证据引发了人们的猜测,即PLP或该基因的其他产物在中枢神经系统内外具有额外的非结构作用。PLP在结构上与一类离子通道蛋白相关,其中包括连接蛋白、突触囊泡蛋白和各种神经递质受体,并且有一些实验证据支持PLP在离子门控中的作用。其他引人关注的观点是,PLP基因可能影响少突胶质细胞内的自分泌信号传导,或者PLP mRNA具有除蛋白质编码之外的功能。