Varela-Echevarría Alfredo, Vargas-Barroso Víctor, Lozano-Flores Carlos, Larriva-Sahd Jorge
Department of Developmental Biology and Neurophysiology, Instituto de Neurobiología Universidad Nacional Autónoma de MéxicoQuerétaro, Mexico.
Front Neuroanat. 2017 Sep 4;11:75. doi: 10.3389/fnana.2017.00075. eCollection 2017.
A set of astrocytic process associated with altered myelinated axons is described in the forebrain of normal adult rodents with confocal, electron microscopy, and 3D reconstructions. Each process consists of a protuberance that contains secretory organelles including numerous lysosomes which polarize and open next to disrupted myelinated axons. Because of the distinctive asymmetric organelle distribution and ubiquity throughout the forebrain neuropil, this enlargement is named paraxial process (PAP). The myelin envelope contiguous to the PAP displays focal disruption or disintegration. In routine electron microscopy clusters of large, confluent, lysosomes proved to be an effective landmark for PAP identification. In 3D assemblies lysosomes organize a series of interconnected saccules that open up to the plasmalemma next to the disrupted myelin envelope(s). Activity for acid hydrolases was visualized in lysosomes, and extracellularly at the PAP-myelin interface and/or between the glial and neuronal outer aspects. Organelles in astrocytic processes involved in digesting pyknotic cells and debris resemble those encountered in PAPs supporting a likewise lytic function of the later. Conversely, processes entangling tripartite synapses and glomeruli were devoid of lysosomes. Both oligodendrocytic and microglial processes were not associated with altered myelin envelopes. The possible roles of the PAP in myelin remodeling in the context of the oligodendrocyte-astrocyte interactions and in the astrocyte's secretory pathways are discussed.
利用共聚焦显微镜、电子显微镜和三维重建技术,在正常成年啮齿动物的前脑中描述了一组与髓鞘轴突改变相关的星形胶质细胞突起。每个突起由一个包含分泌细胞器的突出物组成,这些细胞器包括许多溶酶体,它们在受损的有髓轴突旁极化并开放。由于细胞器独特的不对称分布以及在前脑神经毡中的普遍存在,这种增大被命名为近轴突起(PAP)。与PAP相邻的髓鞘包膜显示出局灶性破坏或解体。在常规电子显微镜下,大的、融合的溶酶体簇被证明是识别PAP的有效标志。在三维组装中,溶酶体组织一系列相互连接的囊泡,这些囊泡在受损的髓鞘包膜旁通向质膜。在溶酶体中以及在PAP - 髓鞘界面的细胞外和/或神经胶质细胞与神经元外部之间观察到酸性水解酶的活性。星形胶质细胞突起中参与消化固缩细胞和碎片的细胞器与PAP中遇到的细胞器相似,这支持了PAP同样具有溶解功能。相反,缠绕三联突触和肾小球的突起没有溶酶体。本文讨论了PAP在少突胶质细胞 - 星形胶质细胞相互作用背景下的髓鞘重塑以及星形胶质细胞分泌途径中的可能作用。