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在无神经支配情况下再生的大鼠比目鱼肌纤维中,乙酰胆碱受体基因及其产物在原始突触部位的突触特异性表达。

Synapse-specific expression of acetylcholine receptor genes and their products at original synaptic sites in rat soleus muscle fibres regenerating in the absence of innervation.

作者信息

Brenner H R, Herczeg A, Slater C R

机构信息

Department of Physiology, University of Basel, Switzerland.

出版信息

Development. 1992 Sep;116(1):41-53. doi: 10.1242/dev.116.1.41.

DOI:10.1242/dev.116.1.41
PMID:1282861
Abstract

To test the hypothesis that synaptic basal lamina can induce synapse-specific expression of acetylcholine receptor (AChR) genes, we examined the levels mRNA for the alpha- and epsilon-subunits of the AChR in regenerating rat soleus muscles up to 17 days of regeneration. Following destruction of all muscle fibres and their nuclei by exposure to venom of the Australian tiger snake, new fibres regenerated within the original basal lamina sheaths. Northern blots showed that original mRNA was lost during degeneration. Early in regeneration, both alpha- and epsilon-subunit mRNAs were present throughout the muscle fibres but in situ hybridization showed them to be concentrated primarily at original synaptic sites, even when the nerve was absent during regeneration. A similar concentration was seen in denervated regenerating muscles kept active by electrical stimulation and in muscles frozen 41-44 hours after venom injection to destroy all cells in the synaptic region of the muscle. Acetylcholine-gated ion channels with properties similar to those at normal neuromuscular junctions were concentrated at original synaptic sites on denervated stimulated muscles. Taken together, these findings provide strong evidence that factors that induce the synapse-specific expression of AChR genes are stably bound to synaptic basal lamina.

摘要

为了验证突触基底层能够诱导乙酰胆碱受体(AChR)基因的突触特异性表达这一假说,我们检测了再生17天内的大鼠比目鱼肌中AChR α亚基和ε亚基的mRNA水平。在暴露于澳大利亚虎蛇毒液破坏所有肌纤维及其细胞核后,新的肌纤维在原来的基底层鞘内再生。Northern印迹显示,在退变过程中原有的mRNA丢失。再生早期,α亚基和ε亚基的mRNA均存在于整个肌纤维中,但原位杂交显示它们主要集中在原来的突触部位,即使在再生过程中神经缺失时也是如此。在通过电刺激保持活性的去神经支配再生肌肉以及在注射毒液破坏肌肉突触区域所有细胞后41 - 44小时冷冻的肌肉中也观察到类似的集中分布。具有与正常神经肌肉接头相似特性的乙酰胆碱门控离子通道集中在去神经支配刺激肌肉的原来突触部位。综上所述,这些发现提供了有力证据,表明诱导AChR基因突触特异性表达的因子稳定地结合于突触基底层。

相似文献

1
Synapse-specific expression of acetylcholine receptor genes and their products at original synaptic sites in rat soleus muscle fibres regenerating in the absence of innervation.在无神经支配情况下再生的大鼠比目鱼肌纤维中,乙酰胆碱受体基因及其产物在原始突触部位的突触特异性表达。
Development. 1992 Sep;116(1):41-53. doi: 10.1242/dev.116.1.41.
2
The influence of basal lamina on the accumulation of acetylcholine receptors at synaptic sites in regenerating muscle.基底层对再生肌肉突触部位乙酰胆碱受体聚集的影响。
J Cell Biol. 1984 Apr;98(4):1453-73. doi: 10.1083/jcb.98.4.1453.
3
Synaptic basal lamina contains a signal for synapse-specific transcription.突触基底层包含一个用于突触特异性转录的信号。
Development. 1992 Jul;115(3):673-80. doi: 10.1242/dev.115.3.673.
4
Neural factors regulate AChR subunit mRNAs at rat neuromuscular synapses.神经因素调节大鼠神经肌肉突触处的乙酰胆碱受体亚基mRNA。
J Cell Biol. 1991 Jul;114(1):125-41. doi: 10.1083/jcb.114.1.125.
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The clustering of acetylcholine receptors and formation of neuromuscular junctions in regenerating mammalian muscle grafts.再生哺乳动物肌肉移植物中乙酰胆碱受体的聚集及神经肌肉接头的形成。
Am J Anat. 1986 Jun;176(2):191-205. doi: 10.1002/aja.1001760208.
6
Basal lamina directs acetylcholinesterase accumulation at synaptic sites in regenerating muscle.基膜指导再生肌肉突触部位乙酰胆碱酯酶的积累。
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The roles of the synaptic basal lamina and of innervation in directing the accumulation of a synaptic molecule, mAb 3B6 antigen, in regenerating skeletal muscles.
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Neurotrophic control of channel properties at neuromuscular synapses of rat muscle.大鼠肌肉神经肌肉突触处通道特性的神经营养控制。
J Physiol. 1983 Apr;337:159-71. doi: 10.1113/jphysiol.1983.sp014617.
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Acetylcholine receptor distribution on regenerating mammalian muscle fibers at sites of mature and developing nerve-muscle junctions.乙酰胆碱受体在成熟和发育中的神经肌肉接头部位的再生哺乳动物肌纤维上的分布。
J Physiol (Paris). 1985;80(4):238-46.
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Control of number and distribution of synapses during ectopic synapse formation in adult rat soleus muscles.成年大鼠比目鱼肌异位突触形成过程中突触数量和分布的控制。
Neuroscience. 1988 Feb;24(2):673-86. doi: 10.1016/0306-4522(88)90360-0.

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J Neurosci. 1997 Sep 1;17(17):6534-44. doi: 10.1523/JNEUROSCI.17-17-06534.1997.
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