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首页> 外文期刊>The Journal of Comparative Neurology >Promotion of motoneuron survival and branching in rapsyn-deficient mice.
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Promotion of motoneuron survival and branching in rapsyn-deficient mice.

机译:在rapsyn缺陷型小鼠中促进运动神经元存活和分支。

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摘要

Inhibition of programmed cell death of motoneurons during embryonic development requires the presence of their target muscle and coincides with the initial stages of synaptogenesis. To evaluate the role of synapse formation on motoneuron survival during embryonic development, we counted the number of motoneurons in rapsyn-deficient mice. Rapsyn is a 43 kDa protein needed for the formation of postsynaptic specialisations at vertebrate neuromuscular synapses. Here we show that the rapsyn-deficient mice have a significant increase in the number of motoneurons in the brachial lateral motor column during the period of naturally occurring programmed cell death compared to their wild-type littermates. In addition, we observed an increase in intramuscular axonal branching in the rapsyn-deficient diaphragms compared to their wild-type littermates at embryonic day 18.5. These results suggest that deficits in the formation of the postsynaptic specialisation at the neuromuscular synapse, brought about by the absence of rapsyn, are sufficient to induce increases in both axonal branching and the survival of the innervating motoneuron. Moreover, these results support the idea that skeletal muscle activity through effective synaptic transmission and intramuscular axonal branching are major mechanisms that regulate motoneuron survival during development. Copyright 2001 Wiley-Liss, Inc.
机译:抑制运动神经元在胚胎发育过程中的程序性细胞死亡需要其靶标肌肉的存在,并且与突触形成的初始阶段相吻合。为了评估突触形成对胚胎发育过程中运动神经元存活的作用,我们计算了rapsyn缺陷小鼠中运动神经元的数量。 Rapsyn是在脊椎动物神经肌肉突触中形成突触后专长所需的43 kDa蛋白。在这里,我们显示,与野生型同窝仔相比,rapsyn缺陷型小鼠在自然发生的程序性细胞死亡期间,臂外侧运动列中运动神经元的数量显着增加。此外,我们观察到rapsyn缺乏的diaphragm肌肌轴突分支在胚胎第18.5天与其野生型同窝仔相比有所增加。这些结果表明,由于缺少rapsyn而导致的神经肌肉突触中突触后专业化的形成不足,足以引起轴突分支的增加和神经支配的运动神经元的存活。此外,这些结果支持这样的想法,即通过有效的突触传递和肌内轴突分支而产生的骨骼肌活动是调节发育过程中运动神经元存活的主要机制。版权所有2001 Wiley-Liss,Inc.

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