Janetzko A, Zimmermann H, Volknandt W
AK Neurochemie, Zoologisches Institut der J. W. Goethe-Universität, Frankfurt am Main, F.R.G.
Neuroscience. 1989;32(1):65-77. doi: 10.1016/0306-4522(89)90108-5.
The distribution of a cholinergic synaptic vesicle-specific transmembrane glycoprotein (Buckley and Kelly, 1985, J. Cell Biol. 100, 1284-1294) was investigated in the entire electromotor neuron of Torpedo marmorata using a monoclonal antibody and immunocytochemistry at the light- and electron-microscopical level (immunoperoxidase, colloidal gold). In the nerve, terminal binding of immunogold particles is restricted to synaptic vesicles. In the axon a number of additional membrane compartments like multivesicular bodies, vesiculotubular structures, lamellar bodies and electron-dense granules share the surface located synaptic vesicle-specific transmembrane glycoprotein-epitope. Membranous structures likely to represent the axoplasmic reticulum inside axons and nerve terminals are not labelled. Antibody-binding membrane compartments are accumulated at nodes of Ranvier. In the perikaryon the tubules of the trans-Golgi network as well as multivesicular bodies, lamellar bodies, electron-lucent vesicles, granules with electron-dense core and peroxisomes are labelled. Immunotransfer blots of isolated synaptic vesicles and tissue extracts of electric organ display a 100,000 mol. wt band of broad electrophoretic mobility typical of the synaptic vesicle-specific transmembrane glycoprotein. Extracts of electromotor nerve and electric lobe contain in addition a strong band at 85,000 mol. wt and a few lower molecular weight bands. We suggest that the synaptic vesicle originates directly from the trans-Golgi network. The endoplasmic reticulum is not involved in vesicle formation or retrieval. On retrograde transport the vesicle membrane compartment is likely to fuse with other intra-axonal (endosomal?) organelles.
利用单克隆抗体和光镜及电镜水平的免疫细胞化学技术(免疫过氧化物酶、胶体金),研究了一种胆碱能突触小泡特异性跨膜糖蛋白(Buckley和Kelly,1985年,《细胞生物学杂志》100卷,1284 - 1294页)在多纹电鳐整个电运动神经元中的分布情况。在神经中,免疫金颗粒的末端结合仅限于突触小泡。在轴突中,一些其他的膜性区室,如多泡体、囊泡管状结构、板层体和电子致密颗粒,也具有位于表面的突触小泡特异性跨膜糖蛋白表位。可能代表轴突和神经末梢内轴浆网的膜性结构未被标记。抗体结合的膜性区室在郎飞结处聚集。在胞核中,反式高尔基体网络的小管以及多泡体、板层体、电子透亮小泡、具有电子致密核心的颗粒和过氧化物酶体被标记。分离的突触小泡和电器官组织提取物的免疫印迹显示出一条100,000道尔顿分子量的宽带,具有突触小泡特异性跨膜糖蛋白典型的宽电泳迁移率。电运动神经和电叶的提取物中还含有一条85,000道尔顿分子量的强带和几条较低分子量的带。我们认为突触小泡直接起源于反式高尔基体网络。内质网不参与小泡的形成或回收。在逆行运输过程中,小泡膜区室可能与其他轴突内(内体样?)细胞器融合。