Department of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
Muscle Nerve. 2013 Mar;47(3):364-71. doi: 10.1002/mus.23526. Epub 2012 Nov 21.
Recovery after peripheral nerve lesions depends on guiding axons back to their targets. Polysialic acid upregulation by regrowing axons has been proposed recently as necessary for this target selectivity.
We reexamined this proposition using a cross-reinnervation model whereby axons from obturator motor neurons that do not upregulate polysialic acid regenerated into the distal femoral nerve. Our aim was to assess their target selectivity between pathways to muscle and skin.
After simple cross-repair, obturator motor neurons showed no pathway preference, but the same repair with a shortened skin pathway resulted in selective targeting of these motor neurons to muscle by a polysialic acid-independent mechanism.
The intrinsic molecular differences between motor neuron pools can be overcome by manipulation of their access to different peripheral nerve pathways such that obturator motor neurons preferentially project to a terminal nerve branch to muscle despite not upregulating the expression of polysialic acid.
周围神经损伤后的恢复依赖于引导轴突回到其靶标。最近提出,再生轴突上调多唾液酸是这种靶标选择性所必需的。
我们使用交叉再支配模型重新检验了这一假设,即在该模型中,来自不会上调多唾液酸的闭孔运动神经元的轴突再生到远端股神经中。我们的目的是评估它们在肌肉和皮肤通路之间的靶标选择性。
单纯交叉修复后,闭孔运动神经元没有表现出通路偏好,但在缩短皮肤通路的相同修复中,通过一种多唾液酸非依赖性机制,这些运动神经元选择性地靶向肌肉。
通过操纵它们进入不同的周围神经通路的方式,可以克服运动神经元池之间的内在分子差异,使得闭孔运动神经元尽管没有上调多唾液酸的表达,但仍优先投射到末梢神经分支到肌肉。