Simões Gustavo F, Benitez Suzana U, Oliveira Alexandre L R
Departament of Structural and Functional Biology, Institute of Biology, University of Campinas (UNICAMP) CP 6109, CEP 13083-907, Campinas, SP, Brazil.
Brain Behav. 2014 Sep;4(5):738-53. doi: 10.1002/brb3.250. Epub 2014 Aug 5.
G-CSF has been shown to decrease inflammatory processes and to act positively on the process of peripheral nerve regeneration during the course of muscular dystrophy.
The aims of this study were to investigate the effects of treatment of G-CSF during sciatic nerve regeneration and histological analysis in the soleus muscle in MDX mice.
Six-week-old male MDX mice underwent left sciatic nerve crush and were G-CSF treated at 7 days prior to and 21 days after crush. Ten and twenty-one days after surgery, the mice were euthanized, and the sciatic nerves were processed for immunohistochemistry (anti-p75(NTR) and anti-neurofilament) and transmission electron microscopy. The soleus muscles were dissected out and processed for H&E staining and subsequent morphologic analysis. Motor function analyses were performed at 7 days prior to and 21 days after sciatic crush using the CatWalk system and the sciatic nerve index.
Both groups treated with G-CSF showed increased p75(NTR) and neurofilament expression after sciatic crush. G-CSF treatment decreased the number of degenerated and regenerated muscle fibers, thereby increasing the number of normal muscle fibers.
The reduction in p75(NTR) and neurofilament indicates a decreased regenerative capacity in MDX mice following a lesion to a peripheral nerve. The reduction in motor function in the crushed group compared with the control groups may reflect the cycles of muscle degeneration/regeneration that occur postnatally. Thus, G-CSF treatment increases motor function in MDX mice. Nevertheless, the decrease in baseline motor function in these mice is not reversed completely by G-CSF.
已表明粒细胞集落刺激因子(G-CSF)可减少炎症过程,并在肌肉营养不良过程中对周围神经再生过程产生积极作用。
本研究的目的是调查在MDX小鼠坐骨神经再生过程中G-CSF治疗的效果以及比目鱼肌的组织学分析。
六周龄雄性MDX小鼠接受左侧坐骨神经挤压,并在挤压前7天和挤压后21天接受G-CSF治疗。手术后10天和21天,对小鼠实施安乐死,并对坐骨神经进行免疫组织化学处理(抗p75神经营养因子受体(NTR)和抗神经丝)以及透射电子显微镜检查。解剖出比目鱼肌并进行苏木精-伊红(H&E)染色及随后的形态学分析。在坐骨神经挤压前7天和挤压后21天,使用CatWalk系统和坐骨神经指数进行运动功能分析。
两组接受G-CSF治疗的小鼠在坐骨神经挤压后p75(NTR)和神经丝表达均增加。G-CSF治疗减少了退化和再生肌纤维的数量,从而增加了正常肌纤维的数量。
p75(NTR)和神经丝的减少表明MDX小鼠在周围神经损伤后再生能力下降。与对照组相比,挤压组运动功能的降低可能反映了出生后发生的肌肉退化/再生周期。因此,G-CSF治疗可提高MDX小鼠的运动功能。然而,这些小鼠的基线运动功能降低并未被G-CSF完全逆转。