摘要
目的制备大鼠坐骨神经离断后的腓肠肌萎缩模型,研究人脐血单个核细胞(CB-MNCs)肌肉多点注射对损伤的治疗效果。方法采集并制备新鲜人CB-MNCs;将30只4~6周龄Wistar大鼠随机分为正常对照组(Normal组,n=10)、CB-MNCs治疗组(Therapy组,n=10)和生理盐水治疗组(NS组,n=10),Therapy组和NS组大鼠离断坐骨神经,建立腓肠肌萎缩模型;在造模后第7天、第14天和第21天,分3次将CB-MNCs或等体积生理盐水多点注射到腓肠肌损伤局部,观察大鼠行动能力改变和足弓坏疽发展情况,并于第28天取样测定腓肠肌湿重比、肌肉横截面积,以及血液和腓肠肌中氧化应激相关指标、炎性因子水平和凋亡相关基因的表达,观察肌肉组织中血管内皮生长因子-α(VEGF-α)、α-肌动蛋白(α-actin)和肌营养不良蛋白(Dystrophin)的表达变化。结果 Therapy组大鼠足部坏疽面积和水肿程度明显比NS组减轻(P=0. 002),而且Therapy组中腓肠肌湿重比较NS组升高(P <0. 001);病理切片显示,Normal组、NS组和Therapy组肌肉横截面积分别为(12 452. 0±202. 8)、(6 287. 0±142. 2)和(8 193. 0±115. 5)μm2,差异有统计学意义(P <0. 001)。与NS组相比,Therapy组血清和肌肉肌酸激酶(CK)、丙二醛(MDA)含量明显降低,超氧化物歧化酶(SOD)和过氧化氢酶(CAT)含量明显增高(P <0. 001)。Therapy组较NS组半胱天冬酶-3(Caspase-3)、促凋亡基因Bax、肿瘤坏死因子-α(TNF-α)的mRNA表达量降低,抑凋亡基因Bcl-2、白细胞介素-10 (IL-10)、α-actin、Dystrophin和VEGF-α的mRNA表达量增高(P <0. 05)。与NS组相比,Therapy组α-actin、Dystrophin和VEGF-α蛋白表达均增高(P <0. 05)。免疫组化发现,NS组和Therapy组Dystro-phin表达均增加,但Therapy组明显高于NS组(P <0. 05)。结论肌肉注射CB-MNCs可有效促进腓肠肌失神经损伤的伤口愈合,缓解萎缩、促进肌肉修复,并降低凋亡细胞比例。
Objective To explore the effect of human cord blood mononuclear cells(CB-MNCs)on relieving the gastrocnemius muscle atrophy and promoting the damage repair in the isolated sciatic nerve rats after intramuscular administration.Methods CB-MNCs were isolated from healthy term infants and cultured in vitro.Thirty juvenile Wistar rats weighting about 200 g were randomized into three groups:CB-MNCs intramuscular administration group(Therapy group,n=10),saline intramuscular administration group(NS group,n=10)and healthy group(Normal group,n=10).The animal model of denervated gastrocnemius muscles were formed by cutting both sides of the sciatic nerve of rats which resulted in the nerve disconnection about 1 cm in the first two groups.One million of CB-MNCs were injected into the gastrocnemius muscles of rats in d7,d14,and d21 after despairing the nerves of Therapy group.The rats in Normal and NS groups were only injected saline with equal volume at the same time.Hind limb movements and gangrenous area ratios of rats were observed.The both sides of gastrocnemius muscles of each rat were weighed to measure wet weight ratios and HE staining was taken to determine cross-sectional area of muscle fiber at the end of the forth week.Peripheral blood serum and bilateral gastrocnemius muscles were taken to measure creatine kinase(CK),catalase(CAT),malondialdehyde(MDA),and superoxide dismutase(SOD)levels.The mRNA expressions of Bax,B-cell lymphoma-2(Bcl-2),Caspase-3,vascular endothelial growth factor-α(VEGF-α),tumor necrosis factor-α(TNF-α),interleukin-10(IL-10),α-actin and Dystrophin were tested by qRT-PCR.The expressions ofα-actin,Dystrophin and VEGF-αprotein were detected by Western blotting.The expression of Dystrophin in cells was also observed by immunohistochemistry.Results The gangrenous area ratio of the Therapy group was lower than that of the NS group(P=0.002)and the wet weight of the gastrocnemius muscle in the Therapy group was higher than that in the NS group(P<0.001).The HE staining results showed that the muscle cross-sectional areas of the Normal group,NS group and Therapy group were respective(12 452.0±202.8),(6 287.0±142.2),and(8 193.0±115.5)μm2 with a statistical difference(P<0.001).Compared with the NS group,the CK and MDA contents of the serum and muscles in the Therapy group were significantly decreased,and the SOD and CAT contents were significantly increased(all P<0.001).In contrast to the NS group,the mRNA levels of Caspase-3,Bax and TNF-αdecreased while the mRNA levels of Bcl-2,IL-10,α-actin,Dystrophin and VEGF-αincreased in the Therapy group(all P<0.05).Compared with the NS group,the expressions ofα-actin,Dystrophin and VEGF-αprotein in the Therapy group were increased(all P<0.05).IHC analysis showed that the expression of Dystrophin was increased in both NS and Therapy groups,but the expression of Dystrophin in the Therapy group was significantly higher than that in the NS group(all P<0.05).Conclusion Injecting CB-MNCs into the paralyzed gastrocnemius can reduce the proportion of apoptotic cells,promote the wound healing,prevent muscle atrophy,and improve muscle functions.
作者
刘子琳
李栋
时庆
李聪
黄金献
朱华甦
鞠秀丽
LIU Zilin;LI Dong;SHI Qing;LI Cong;HUANG Jinxian;ZHU Huasu;JU Xiuli(Childrens Medical Center,Qilu Hospital of Shandong University,Jinan 250012,Shandong,China;Research Center of Stem Cell and Regenerative Medicine,Shandong University,Jinan 250012,Shandong,China)
出处
《山东大学学报(医学版)》
CAS
北大核心
2019年第2期61-69,共9页
Journal of Shandong University:Health Sciences
基金
山东省重点研发计划(2017GSF18155
2017GSF218015)
济南市科技发展计划(201704066)