Department of Human Enhancement and Hand Surgery, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.
Department of Human Enhancement and Hand Surgery, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.
Neuroscience. 2024 Nov 1;559:113-122. doi: 10.1016/j.neuroscience.2024.08.039. Epub 2024 Aug 30.
Respiratory muscle paralysis due to trauma or neurodegenerative diseases can have devastating consequences. Only a few studies have investigated the reconstruction of motor function in denervated diaphragms caused by such conditions. Here, we studied the efficacy of transplanting E14 embryonic spinal motor neurons (SMNs) into peripheral nerve grafts for functionally reconstructing a denervated diaphragm in a rat model. The diaphragms of 8-week-old male Fischer 344 rats were first denervated by transecting the phrenic nerves. Subsequently, peripheral nerve grafts taken from the lower limb were used for neurotization of the denervated diaphragms. One week later, fetal E14 SMNs were transplanted into the peripheral nerve grafts. After 3 months, we observed functional contraction of the diaphragm following neuromuscular electrical stimulation (NMES) of the peripheral nerve graft. Additionally, we confirmed that SMN transplantation into the peripheral nerve graft had an inhibitory effect on diaphragm muscle atrophy. The SMNs transplanted into the peripheral nerve grafts formed a structure similar to the spinal cord, and the neuromuscular junction of the denervated diaphragm was reinnervated. These findings suggest the establishment of an ectopic motor neuron pool in the peripheral nerve graft. Free peripheral intra-nerve SMN transplantation in combination with NMES, which can be applied for diaphragmatic pacing, offers novel insights into the development of neuroregenerative therapies for treating life-threatening and intractable respiratory muscle paralysis caused by severe nerve damage and degenerative diseases.
创伤或神经退行性疾病引起的呼吸肌瘫痪可能会产生严重的后果。只有少数研究调查了此类疾病导致的失神经膈肌运动功能的重建。在这里,我们研究了将 E14 胚胎脊髓运动神经元 (SMN) 移植到周围神经移植物中,以在大鼠模型中功能性重建失神经膈肌的效果。首先通过横断膈神经使 8 周龄雄性 Fischer 344 大鼠的膈肌去神经支配。随后,使用来自下肢的周围神经移植物对失神经支配的膈肌进行神经化。1 周后,将胎儿 E14 SMN 移植到周围神经移植物中。3 个月后,我们观察到在对周围神经移植物进行神经肌肉电刺激 (NMES) 后,膈肌出现功能性收缩。此外,我们证实 SMN 移植到周围神经移植物中对膈肌萎缩具有抑制作用。移植到周围神经移植物中的 SMN 形成类似于脊髓的结构,并且失神经膈肌的运动终板被重新支配。这些发现表明在外周神经移植物中建立了异位运动神经元池。游离外周神经内 SMN 移植结合 NMES 可用于膈肌起搏,为治疗由严重神经损伤和退行性疾病引起的危及生命和难治性呼吸肌瘫痪的神经再生治疗的发展提供了新的思路。