Brenner H R, Herczeg A, Slater C R
Department of Physiology, University of Basel, Switzerland.
Development. 1992 Sep;116(1):41-53. doi: 10.1242/dev.116.1.41.
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.
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。