Dadon-Nachum M, Ben-Zur T, Srugo I, Shamir H M, Melamed E, Yaffe D, Offen D
Felsenstein Medical Research Center and Sackler School of Medicine , Tel-Aviv University.
Koret School of Veterinary Medicine, The Hebrew University of Jerusalem , Rehovot.
J Stem Cells Regen Med. 2012 Apr 14;8(1):21-7. doi: 10.46582/jsrm.0801004. eCollection 2012.
Sciatic nerve injury may cause neurological deficits, particularly muscle weakness. Previous studies have shown that administration of neurotrophic factors (NTFs), naturally occurring proteins that support the development and survival of neurons, partially protected the damaged motor neuron in the injured sciatic nerve. In the current study, we have examined whether the administration of various combinations of transfected muscle progenitor cells (MPCs) populations, each expressing a single NTF (BDNF, GDNF, IGF-1 or VEGF) or conditioned media of such culture are capable of rescuing motor neurons in culture or in vivo. We have found that the mixture of conditioned media collected from cultured myogenic cells (MPCs- MIX(+)) alleviated the toxic effect of exposure of the motor neuron cell line NSC34 to hypoxic environment. Furthermore, NTFs secreting cells transplantation, protected motor neurons in a unilateral rat sciatic nerve injury model: One day after the crush, rats underwent transplantation at the lesion site with rat myogenic cells expressing one of the four NTFs; a mixture of cells expressing all four NTFs (MPCs- MIX(+)), MPCs-GFP or PBS. We found that in rats injected with MPCs- MIX(+) the motor function was markedly preserved, compared to groups injected with cells secreting a single NTF, GFP or PBS. Transplantation of the MPCs- MIX(+) significantly inhibited the degeneration of the neuromuscular junctions and enhanced the survival of the myelinated motor axons. The injection of MPCs- MIX(+) preserved the compound muscle action potential (CMAP) as was demonstrated by motor nerve conduction studies. Our findings suggest that MPCs induced to secrete several NTFs can synergistically alleviate symptoms of sciatic nerve injury and perhaps other motor neuron disorders..
坐骨神经损伤可能导致神经功能缺损,尤其是肌肉无力。先前的研究表明,给予神经营养因子(NTFs),即支持神经元发育和存活的天然存在的蛋白质,可部分保护受损坐骨神经中的运动神经元。在本研究中,我们检测了给予转染的肌肉祖细胞(MPCs)群体的各种组合(每个群体表达一种单一的神经营养因子(BDNF、GDNF、IGF-1或VEGF))或此类培养物的条件培养基是否能够挽救培养物或体内的运动神经元。我们发现,从培养的成肌细胞收集的条件培养基混合物(MPCs-MIX(+))减轻了运动神经元细胞系NSC34暴露于低氧环境的毒性作用。此外,分泌神经营养因子的细胞移植在单侧大鼠坐骨神经损伤模型中保护了运动神经元:挤压后一天,大鼠在损伤部位接受表达四种神经营养因子之一的大鼠成肌细胞移植;表达所有四种神经营养因子的细胞混合物(MPCs-MIX(+))、MPCs-GFP或PBS。我们发现,与注射分泌单一神经营养因子的细胞、GFP或PBS的组相比,注射MPCs-MIX(+)的大鼠运动功能得到明显保留。MPCs-MIX(+)的移植显著抑制了神经肌肉接头的退化,并提高了有髓运动轴突的存活率。运动神经传导研究表明,注射MPCs-MIX(+)可保留复合肌肉动作电位(CMAP)。我们的研究结果表明,诱导分泌多种神经营养因子的MPCs可协同减轻坐骨神经损伤以及可能的其他运动神经元疾病的症状。