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运动轴突的靶标识别与突触形成:对侧步蛋白的反应。

Target recognition and synaptogenesis by motor axons: responses to the sidestep protein.

作者信息

de Jong Samanta, Cavallo Jaime A, Rios Carl D, Dworak Heather A, Sink Helen

机构信息

Skirball Institute of Biomolecular Medicine, New York University School of Medicine, 540 First Avenue, New York, NY 10016, USA.

出版信息

Int J Dev Neurosci. 2005 Jun;23(4):397-410. doi: 10.1016/j.ijdevneu.2004.10.002. Epub 2004 Nov 21.

Abstract

Sidestep (Side) is a pivotal molecular player in embryonic motor axon pathfinding. But questions about its functional repertoire remain: (i) can Side permanently overturn targeting preferences? (ii) does it promote synaptogenesis, and (iii) can Side facilitate synaptic stabilization? To address these questions, Side was temporally and spatially misexpressed and the visible consequences for neuromuscular junction morphology were assessed. When Side was misexpressed either broadly or selectively in muscles during targeting in a wildtype background motor axon targeting preferences were permanently overturned. However the misexpression of Side in all muscles post-targeting neither changed synapse morphology, nor compensated for a lack of the synapse-stabilizing protein Fasciclin II (FasII). Rather Side appears to be dependent on FasII, instead of on intrinsic ability, for sustaining targeting changes. We propose that Side helps to bring motor axons to their correct muscle targets and promotes synaptogenesis, then FasII serves to stabilize the synaptic contacts.

摘要

旁步蛋白(Side)是胚胎运动轴突路径寻找过程中的关键分子。但其功能范围仍存在一些问题:(i)旁步蛋白能否永久性地改变靶向偏好?(ii)它是否促进突触形成,以及(iii)旁步蛋白能否促进突触稳定?为了解决这些问题,我们在时间和空间上对旁步蛋白进行了错误表达,并评估了其对神经肌肉接头形态的可见影响。当在野生型背景下的靶向过程中,旁步蛋白在肌肉中广泛或选择性地错误表达时,运动轴突的靶向偏好会被永久性地改变。然而,在靶向完成后在所有肌肉中错误表达旁步蛋白,既不会改变突触形态,也不能弥补突触稳定蛋白Fasciclin II(FasII)的缺失。相反,旁步蛋白似乎依赖于FasII来维持靶向变化,而不是其内在能力。我们认为,旁步蛋白有助于将运动轴突引导至其正确的肌肉靶点并促进突触形成,然后FasII用于稳定突触连接。

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