Loring R H, Dahm L M, Zigmond R E
Neuroscience. 1985 Feb;14(2):645-60. doi: 10.1016/0306-4522(85)90316-1.
Binding sites for [125I]alpha-bungarotoxin were localized in the chick ciliary ganglion by light and electron microscopic autoradiography. Groups of four ganglia were incubated for 4 h with 20 nM [125I]alpha-bungarotoxin alone or with radioactive alpha-bungarotoxin plus either 1 microM unlabeled alpha-bungarotoxin or 100 microM d-tubocurarine. Specific binding to various morphological regions was determined by subtracting the densities of autoradiographic grains in the presence of competing nonradioactive ligands from the densities in the absence of those ligands. Most of the specific binding in the ganglion (91%) was associated with neurons. Seventy-four per cent was found within 1.2 micron of neuronal plasma membranes and 17% was found overlying neuronal cell bodies. Analysis of the specific binding associated with neurons, but not with the neuronal plasma membranes, revealed that lysosomes and multivesicular bodies were 9- and 32-fold more heavily labeled than other cellular organelles. The grain density over choroid cell bodies was significantly higher than that over ciliary neurons. Most (greater than 75%) of the autoradiographic grains within 0.25 micron of neuronal plasma membranes were found in "complex" contact regions of the membranes, which are characterized by extensive membrane evaginations. However, after correcting for the amount of plasma membrane present in the various regions of the membrane studied, alpha-bungarotoxin binding was found to be uniform. Few (less than 10%) of the specialized membranes between pre- and postsynaptic neurons were found in these "complex" contact regions suggesting that the bulk of alpha-bungarotoxin binding to neuronal membranes is located at some distance from the sites of transmitter release. The density of alpha-bungarotoxin binding sites in the neuronal plasma membrane was low (approximately 100-200 sites/micron 2 of neuronal membrane) compared to published values of the density of binding sites at the neuromuscular junction. Since alpha-bungarotoxin does not bind preferentially to specialized synaptic membranes, it seems unlikely that the binding sites for this toxin are the neuronal nicotinic receptors.
通过光学显微镜和电子显微镜放射自显影术,将[125I]α-银环蛇毒素的结合位点定位在鸡睫状神经节中。将四组神经节分别与20 nM [125I]α-银环蛇毒素单独孵育4小时,或与放射性α-银环蛇毒素以及1 μM未标记的α-银环蛇毒素或100 μM d-筒箭毒碱一起孵育。通过从不存在竞争性非放射性配体时的放射自显影片颗粒密度中减去存在这些配体时的密度,来确定与各种形态区域的特异性结合。神经节中的大多数特异性结合(91%)与神经元相关。74%的结合位点位于距神经元质膜1.2微米范围内,17%位于神经元细胞体上方。对与神经元相关但与神经元质膜无关的特异性结合进行分析发现,溶酶体和多泡体的标记程度比其他细胞器分别高9倍和32倍。脉络膜细胞体上的颗粒密度明显高于睫状神经元上的颗粒密度。在距神经元质膜0.25微米范围内的大多数(超过75%)放射自显影片颗粒位于膜的“复杂”接触区域,其特征是广泛的膜内陷。然而,在对所研究膜的各个区域中存在的质膜量进行校正后,发现α-银环蛇毒素结合是均匀的。在这些“复杂”接触区域中,很少(不到10%)能发现突触前和突触后神经元之间的特化膜,这表明与神经元膜结合的大部分α-银环蛇毒素位于距递质释放位点一定距离处。与已发表的神经肌肉接头处结合位点密度值相比,神经元质膜中α-银环蛇毒素结合位点的密度较低(约100 - 200个位点/微米2神经元膜)。由于α-银环蛇毒素不会优先结合特化的突触膜,因此这种毒素的结合位点似乎不太可能是神经元烟碱受体。