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肌梭在单突触牵张反射发展中的作用。

The role of muscle spindles in the development of the monosynaptic stretch reflex.

机构信息

Department of Molecular Physiology and Pharmacology, Tufts University School of Medicine, Boston, MA 02111, USA.

出版信息

J Neurophysiol. 2012 Jul;108(1):83-90. doi: 10.1152/jn.00074.2012. Epub 2012 Apr 4.

DOI:10.1152/jn.00074.2012
PMID:22490553
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3434619/
Abstract

Muscle sensory axons induce the development of specialized intrafusal muscle fibers in muscle spindles during development, but the role that the intrafusal fibers may play in the development of the central projections of these Ia sensory axons is unclear. In the present study, we assessed the influence of intrafusal fibers in muscle spindles on the formation of monosynaptic connections between Ia (muscle spindle) sensory axons and motoneurons (MNs) using two transgenic strains of mice. Deletion of the ErbB2 receptor from developing myotubes disrupts the formation of intrafusal muscle fibers and causes a nearly complete absence of functional synaptic connections between Ia axons and MNs. Monosynaptic connectivity can be fully restored by postnatal administration of neurotrophin-3 (NT-3), and the synaptic connections in NT-3-treated mice are as specific as in wild-type mice. Deletion of the Egr3 transcription factor also impairs the development of intrafusal muscle fibers and disrupts synaptic connectivity between Ia axons and MNs. Postnatal injections of NT-3 restore the normal strengths and specificity of Ia-motoneuronal connections in these mice as well. Severe deficits in intrafusal fiber development, therefore, do not disrupt the establishment of normal, selective patterns of connections between Ia axons and MNs, although these connections require the presence of NT-3, normally supplied by intrafusal fibers, to be functional.

摘要

在发育过程中,肌梭内的感觉轴突诱导肌梭内特殊的肌纤维发育,但肌梭内纤维在 Ia 感觉轴突中枢投射发育中的作用尚不清楚。在本研究中,我们使用两种转基因小鼠品系,评估肌梭内纤维对 Ia(肌梭)感觉轴突与运动神经元(MNs)之间单突触连接形成的影响。发育中的肌管中 ErbB2 受体的缺失破坏了肌梭内纤维的形成,并导致 Ia 轴突与 MNs 之间几乎完全缺乏功能性突触连接。出生后给予神经营养因子-3(NT-3)可完全恢复单突触连接,且 NT-3 处理的小鼠中的突触连接与野生型小鼠一样具有特异性。Egr3 转录因子的缺失也会损害肌梭内纤维的发育并破坏 Ia 轴突与 MNs 之间的突触连接。出生后注射 NT-3 也能恢复这些小鼠中 Ia-运动神经元连接的正常强度和特异性。因此,严重的肌梭内纤维发育缺陷不会破坏 Ia 轴突与 MNs 之间正常的、选择性的连接模式的建立,尽管这些连接需要 NT-3 发挥功能,而 NT-3 通常由肌梭内纤维提供。

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本文引用的文献

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