Localisation of the high-affinity choline transporter-1 in the rat skeletal motor unit

被引:33
作者
Lips, KS [1 ]
Pfeil, U [1 ]
Haberberger, RV [1 ]
Kummer, W [1 ]
机构
[1] Univ Giessen, Inst Anat & Cell Biol, D-35385 Giessen, Germany
关键词
acetylcholine; choline transporter; motoneuron; motor endplate; vesicular acetylcholine transporter; rat (Wistar);
D O I
10.1007/s00441-002-0520-4
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The rate-limiting step in neuronal acetylcholine (ACh) synthesis is the uptake of choline via a high-affinity transporter. We have generated antisera against the recently identified transporter CHT1 to investigate its distribution in rat motor neurons and skeletal muscle and have used these antisera in combination with (1) antisera against the vesicular acetylcholine transporter (VAChT) to identify cholinergic synapses and (2) Alexa-488-labelled alpha-bungarotoxin to identify motor endplates. In the motor unit, immunohistochemistry and RT-PCR have demonstrated that CHT1 is restricted to motoneurons and absent from the non-neuronal ACh-synthesizing elements, e.g. skeletal muscle fibres. In addition, CHT1 is also present in parasympathetic neurons of the tongue, as evidenced by immunohistochemistry and RT-PCR. CHT1 immunoreativity is principally found at all segments (perikaryon, dendrites, axon) of the motoneuron but is enriched at neuro-neuronal and neuro-muscular synapses. This preferential localisation matches well with its anticipated pivotal role in synaptic transmitter recycling and synthesis.
引用
收藏
页码:275 / 280
页数:6
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