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巨大海兔神经元R2具有远端树突:蛋白质分选及第二个动作电位起始位点的证据。

Giant Aplysia neuron R2 has distal dendrites: evidence for protein sorting and a second spike initiation site.

作者信息

Ambron R T, Rayport S G, Babiarz J

机构信息

Department of Anatomy, Columbia University College of Physicians and Surgeons, New York, New York.

出版信息

J Neurosci. 1988 Feb;8(2):722-31. doi: 10.1523/JNEUROSCI.08-02-00722.1988.

Abstract

Because of its anatomy, the neuron R2 of Aplysia has been used to study how proteins are distributed to their appropriate destinations within the cell. The R2 cell body resides in the abdominal ganglion, while its axons terminate on glands in the skin. Using intracellular injection of HRP and intraxonal recordings, we found that R2 has a dendritic (receptive) arborization in the pleural ganglion. The structure of these dendrites was examined after injecting the soma with 3H-L-fucose, thereby labeling glycoproteins that are transported to all regions of the cell. Light- and electron-microscope autoradiography show that the openings to the dendrites are not on the periphery, but are suspended inside the axon by glial cell infoldings. All of the organelles seen in the axon are found in the dendrites, including 2 types of vesicles. Neither the axon nor the dendrites contain ribosomes. Thus, R2 has 3 functionally distinct regions--cell body, dendrites, presynaptic terminals--that are separated from each other by at least 4 cm. This implies that pre- and postsynaptic proteins made in the cell body are transported along the axon to the pleural ganglion, where they are sorted. To investigate this idea, we exposed the abdominal ganglion to 35S-methionine to label R2's proteins. Analyses by SDS-PAGE of the rapidly transported labeled proteins from R2 consistently showed a 78 kDa band that accumulated in the pleural ganglion and did not move into the peripheral nerves. This then is a putative dendritic constituent.

摘要

由于其解剖结构,海兔的神经元R2已被用于研究蛋白质如何在细胞内被分配到其适当的目的地。R2细胞体位于腹神经节中,而其轴突终止于皮肤中的腺体。通过细胞内注射辣根过氧化物酶(HRP)和轴突内记录,我们发现R2在胸膜神经节中有一个树突状(感受性)分支。在用3H-L-岩藻糖注射细胞体后检查这些树突的结构,从而标记被运输到细胞所有区域的糖蛋白。光学显微镜和电子显微镜放射自显影显示,树突的开口不在周边,而是通过神经胶质细胞的褶皱悬浮在轴突内部。在轴突中看到的所有细胞器在树突中都能找到,包括2种类型的小泡。轴突和树突都不含有核糖体。因此,R2有3个功能上不同的区域——细胞体、树突、突触前终端——它们彼此之间至少相隔4厘米。这意味着在细胞体中产生的突触前和突触后蛋白质沿着轴突被运输到胸膜神经节,在那里它们被分类。为了研究这个想法,我们将腹神经节暴露于35S-甲硫氨酸中以标记R2的蛋白质。对来自R2的快速运输的标记蛋白质进行SDS-PAGE分析,始终显示出一条78 kDa的条带,该条带在胸膜神经节中积累,并且没有进入外周神经。那么这就是一种假定的树突成分。

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