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首页> 外文期刊>Cell death & disease. >Neuropilin-1-mediated pruning of corticospinal tract fibers is required for motor recovery after spinal cord injury
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Neuropilin-1-mediated pruning of corticospinal tract fibers is required for motor recovery after spinal cord injury

机译:脊髓损伤后运动恢复需要Neuropilin-1介导的皮质脊髓束纤维修剪

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摘要

Following incomplete spinal cord injury (SCI), reorganization of the corticospinal tract (CST) contributes to spontaneous motor recovery. Axotomized CST fibers form collaterals and make synapses with interneurons, followed by pruning of excess fibers. Although axonal pruning is involved in refinement of neural circuits, its molecular mechanisms and functional roles remain poorly understood. To address these questions, we performed dorsal hemisections of mouse thoracic spinal cord. We observed that Neuropilin-1 (Nrp1) mRNA was upregulated in layer 5 pyramidal neurons in the motor cortex 14 days after SCI, when the pruning occurred. Nrp1 knockdown using adeno-associated virus (AAV) vector encoding Nrp1 shRNA in the hindlimb motor area impaired the pruning of collaterals after SCI. Nrp1 knockout by injecting AAV vector encoding Cre recombinase into Nrp1 floxed mice also suppressed axonal pruning. Propriospinal neurons, interneurons that connect CST and motoneurons, expressed Semaphorin 3A (Sema3A), the ligand of Nrp1. Furthermore, the genetic deletion of Nrp1 specifically in the hindlimb motor area suppressed the recovery of skilled movement at 21 and 28 days after SCI. The present findings demonstrate that the pruning of collaterals mediated by Nrp1 is required for motor recovery after SCI, and suggest that refinement of the neuronal network facilitates motor recovery.
机译:脊髓不完全损伤(SCI)后,皮质脊髓束(CST)的重组有助于自发运动恢复。切开的CST纤维形成侧支并与神经元形成突触,然后修剪多余的纤维。尽管轴突修剪涉及神经回路的完善,但其分子机制和功能作用仍然知之甚少。为了解决这些问题,我们进行了小鼠胸脊髓的背部半切。我们观察到,当修剪发生后14天,运动皮层的5层锥体神经元中Neuropilin-1(Nrp1)mRNA上调。在后肢运动区使用编码Nrp1 shRNA的腺相关病毒(AAV)载体进行Nrp1敲低会损害SCI后对侧枝的修剪。通过将编码Cre重组酶的AAV载体注射到Nrp1的小鼠体内,Nrp1基因敲除也抑制了轴突修剪。脊髓前神经元(连接CST和运动神经元的中间神经元)表达Semaphorin 3A(Sema3A),即Nrp1的配体。此外,在SCI后21天和28天,Nrp1的基因缺失特别是在后肢运动区抑制了熟练运动的恢复。目前的发现表明,SCI后运动恢复需要Nrp1介导的侧枝修剪,并且表明神经元网络的细化有助于运动恢复。

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