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小龙虾节段性巨神经元的超微结构

Ultrastructure of the segmental giant neuron of crayfish.

作者信息

Heitler W J, Cobb J L, Fraser K

出版信息

J Neurocytol. 1985 Dec;14(6):921-41. doi: 10.1007/BF01224805.

Abstract

The ultrastructure of the crayfish segmental giant (SG) neuron is described, and compared to other identified and unidentified crayfish neurons. The SG was specifically stained by intracellular injection of horseradish peroxidase and is divided into four regions of interest. In the dorsal region, finger-like dendrites of the SG make contact with the through-conducting giant fibres (GF). These contacts are physiologically defined rectifying electrical synapses. They are characterized by the presence of 30-95 nm agranular vesicles in the presynaptic GFs, some postsynaptic density in the SG, and a narrowing of the intermembrane cleft to approximately 5 nm. There is little evidence for connecting cytoplasmic bridges. Unidentified neurons make chemical input with either round or elliptical vesicle types onto SG bottlenecks close to the electrical synapses. Ventral to the GFs, dendritic profiles of the SG make three sorts of contact with unidentified neurons. (a) Regions of close membrane apposition (approximately 5 nm) are presumed to be electrical output synapses, but there are no vesicles such as at the input synapses, and, again, little sign of connecting bridges. (b) Chemical input is received from unidentified presynaptic neurons containing either round or elliptical vesicles. These synapses are characterized by 30-75 nm presynaptic agranular vesicles, widened cleft (approximately 20 nm), granular cleft material and postsynaptic density. There is no sign of any presynaptic density. (c) Very occasional SG profiles containing vesicles and making output synapses to unidentified neurons occur. In the lateral neuropil at the edge of the ganglion the SG gives rise to a small tuft of very fine dendrites. These are nearly all laden with vesicles and ramify in a complex region of neuropil containing many small profiles which are also vesicle-laden. The SG axon diminishes in diameter as it progresses along its peripheral nerve root, and finally terminates at a blind ending near the base of the swimmerets. It is sheathed along its entire length, and there is no sign of vesicles within it. We conclude that the SG axon makes no peripheral output.

摘要

描述了小龙虾节段性巨神经元(SG)的超微结构,并与其他已鉴定和未鉴定的小龙虾神经元进行了比较。通过细胞内注射辣根过氧化物酶对SG进行特异性染色,并将其分为四个感兴趣区域。在背侧区域,SG的指状树突与传导性巨纤维(GF)接触。这些接触在生理上被定义为整流电突触。其特征是突触前GF中存在30 - 95纳米的无颗粒小泡,SG中有一些突触后致密物质,以及膜间裂隙变窄至约5纳米。几乎没有证据表明存在连接细胞质桥。未鉴定的神经元通过圆形或椭圆形小泡类型对靠近电突触的SG瓶颈进行化学输入。在GF的腹侧,SG的树突轮廓与未鉴定的神经元有三种接触方式。(a)紧密的膜贴附区域(约5纳米)被认为是电输出突触,但此处没有输入突触处那样的小泡,同样也几乎没有连接桥的迹象。(b)从含有圆形或椭圆形小泡的未鉴定突触前神经元接收化学输入。这些突触的特征是突触前有30 - 75纳米的无颗粒小泡、裂隙增宽(约20纳米)、裂隙中有颗粒物质和突触后致密物质。没有任何突触前致密物质的迹象。(c)偶尔会出现含有小泡并与未鉴定神经元形成输出突触的SG轮廓。在神经节边缘的外侧神经毡中,SG产生一小束非常细的树突。这些树突几乎都充满了小泡,并在一个复杂的神经毡区域分支,该区域包含许多也充满小泡的小轮廓。SG轴突在沿着其外周神经根延伸时直径逐渐减小,最终在游泳足基部附近终止于一个盲端。它在整个长度上都有鞘包裹,且内部没有小泡的迹象。我们得出结论,SG轴突没有外周输出。

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