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山东大学学报 (医学版) ›› 2019, Vol. 57 ›› Issue (2): 61-69.doi: 10.6040/j.issn.1671-7554.0.2018.1442

• • 上一篇    

人脐血单个核细胞对大鼠腓肠肌失神经损伤的治疗作用

刘子琳1,李栋2,时庆2,李聪1,黄金献1,朱华甦1,鞠秀丽1,2   

  1. 1. 山东大学齐鲁医院儿童医疗中心, 山东 济南 250012;〓〓2. 山东大学干细胞与再生医学研究中心, 山东 济南250012
  • 发布日期:2022-09-27
  • 通讯作者: 鞠秀丽. E-mail:jxlqlyy@163.com
  • 基金资助:
    山东省重点研发计划(2017GSF18155,2017GSF218015);济南市科技发展计划(201704066)

Therapy of rat denervated gastrocnemius muscles damage using human cord blood mononuclear cells

LIU Zilin1, LI Dong2, SHI Qing2, LI Cong1, HUANG Jinxian1, ZHU Huasu1, JU Xiuli1,2   

  1. 1. Childrens Medical Center, Qilu Hospital of Shandong University, Jinan 250012, Shandong, China;
    2. Research Center of Stem Cell and Regenerative Medicine, Shandong University, Jinan 250012, Shandong, China
  • Published:2022-09-27

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Dystrophin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。

关键词: 干细胞治疗, 人脐血单个核细胞, 去神经支配, 骨骼肌萎缩

Abstract: 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 山 东 大 学 学 报 (医 学 版)57卷2期 -刘子琳,等.人脐血单个核细胞对大鼠腓肠肌失神经损伤的治疗作用 \=-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 of α-actin, Dystrophin and VEGF-α protein 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-α decreased while the mRNA levels of Bcl-2, IL-10, α-actin, Dystrophin and VEGF-α increased in the Therapy group(all P<0.05). Compared with the NS group, the expressions of α-actin, Dystrophin and VEGF-α protein 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.

Key words: Stem cell therapy, Human cord blood mononuclear cells, Denervation, Muscular atrophy

中图分类号: 

  • R332
[1] Mu LC, Sobotka S, Su H. Nerve-muscle-endplate band grafting: a new technique for muscle reinnervation[J]. Neurosurgery, 2011, 69(2 Suppl Operative): ons208-ons224; discussion ons224.
[2] Kern H, Carraro U. Home-based functional electrical stimulation for long-term denervated human muscle: history, basics, results and perspectives of the vienna rehabilitation strategy[J]. Eur J Transl Myol, 2014, 24(1): 3296. doi:10.4081/ejtm.2014.3296.
[3] Biazar E. Use of umbilical cord and cord blood-derived stem cells for tissue repair and regeneration[J]. Expert Opin Biol Ther, 2014, 14(3): 301-310.
[4] Tang HB, Inoki K, Lee M, et al. mTORC1 promotes denervation-induced muscle atrophy through a mechanism involving the activation of FoxO and E3 ubiquitin ligases[J]. Sci Signal, 2014, 7(314): ra18. doi:10.1126/sci-signal.2004809.
[5] Rudolf R, Deschenes MR, Sandri M. Neuromuscular junction degeneration in muscle wasting[J]. Curr Opin Clin Nutr Metab Care, 2016, 19(3): 177-181.
[6] 赵志强, 刘强, 李钢. 骨骼肌卫星细胞移植对延缓失神经肌肉萎缩的作用[J]. 中华骨科杂志, 2006, 26(1): 51-55. ZHAO Zhiqiang, LIU Qiang, LI Gang. The effect of transplantation of skeletal muscle satellite cell on retard the denervated muscles atrophy[J]. Chinese Journal of Orthopaedics, 2006, 26(1): 51-55.
[7] Kim S, Kim K. The effects of exercise and conjugated linoleic acid intake on IGF-1 and pro-inflammatory cytokines in atrophied skeletal muscle of rats[J]. Integr Med Res, 2013, 2(4): 166-173.
[8] Arakawa T, Katada A, Shigyo H, et al. Electrical stimulation prevents apoptosis in denervated skeletal muscle[J]. NeuroRehabilitation, 2010, 27(2): 147-154.
[9] 裴艳宏, 刘坤祥. 黄芪丹参联合应用可延缓大鼠失神经骨骼肌萎缩[J]. 解剖学报, 2014, 45(2): 278-282. PEI Yanhong, LIU Kunxiang. Role of Huangqi combined with Danshen in the denervated skeletal muscle atrophy[J]. Acta Anatomica Sinica, 2014, 45(2): 278-282.
[10] Reza MM, Subramaniyam N, Sim CM, et al. Irisin is a pro-myogenic factor that induces skeletal muscle hypertrophy and rescues denervation-induced atrophy[J]. Nat Commun, 2017, 8(1): 1104. doi:10.1038/s41467-017-01131-0.
[11] Farjah GH, Fazli F, Karimipour M, et al. The effect of bone marrow mesenchymal stem cells on recovery of skeletal muscle after neurotization surgery in rat[J]. Iran J Basic Med Sci, 2018, 21(3): 236-243.
[12] Pimentel-Coelho PM, Rosado-de-Castro PH, da Fonseca LM, et al. Umbilical cord blood mononuclear cell transplantation for neonatal hypoxic-ischemic encephalopathy[J]. Pediatr Res, 2012, 71(4 Pt 2): 464-473.
[13] 练诗梅, 王晓波, 薛祖光, 等. 脐血与外周血树突状细胞及细胞组成的比较[J]. 临床和实验医学杂志, 2005, 4(2): 71-73. LIAN Shimei, WANG Xiaobo, XUE Zuguang, et al. Analysis of dendritic cells and cellular component of umbilical cord blood and peripheral blood[J]. Journal of Clinical and Experimental Medicine, 2005, 4(2): 71-73.
[14] Galieva LR, Mukhamedshina YO, Arkhipova SS, et al. Human umbilical cord blood cell transplantation in neuroregenerative strategies[J]. Front Pharmacol, 2017, 8: 628. doi:10.3389/fphar.2017.00628.
[15] Hosseini SR, Kaka G, Joghataei MT, et al. Assessment of neuroprotective properties of melissa officinalis in combination with human umbilical cord blood stem cells after spinal cord injury[J]. ASN Neuro, 2016, 8(6): 1759091416674833. doi:10.1177/1759091416674833.
[16] Correa A, Ottoboni GS, Senegaglia AC, et al. Expanded CD133+ cells from human umbilical cord blood improved heart function in rats after severe myocardial infarction[J]. Stem Cells Int, 2018, 2018: 5412478. doi:10.1155/2018/5412478.
[17] Bertaggia E, Scabia G, Dalise S, et al. Haptoglobin is required to prevent oxidative stress and muscle atrophy[J]. PLoS One, 2014, 9(6): e100745. doi:10.1371/journal.pone.0100745.
[18] Reid MB, Moylan JS. Beyond atrophy: redox mechanisms of muscle dysfunction in chronic inflammatory disease[J]. J Physiol(Lond), 2011, 589(Pt 9): 2171-2179.
[19] Marzetti E, Privitera G, Simili V, et al. Multiple pathways to the same end: mechanisms of myonuclear apoptosis in sarcopenia of aging[J]. Scientific World Journal, 2010, 10: 340-349. doi:10.1100/tsw.2010.27.
[20] Iwakura T, Fujimoto S, Kagimoto S, et al. Sustained enhancement of Ca(2+)influx by glibenclamide induces apoptosis in RINm5F cells[J]. Biochem Biophys Res Commun, 2000, 271(2): 422-428.
[21] Shehata AS, Al-Ghonemy NM, Ahmed SM, et al. Effect of mesenchymal stem cells on induced skeletal muscle chemodenervation atrophy in adult male albino rats[J]. Int J Biochem Cell Biol, 2017, 85: 135-148. doi:10.1016/j.biocel.2017.01.016.
[22] Kuchroo P, Dave V, Vijayan A, et al. Paracrine factors secreted by umbilical cord-derived mesenchymal stem cells induce angiogenesis in vitro by a VEGF-independent pathway[J]. Stem Cells Dev, 2015, 24(4): 437-450.
[23] Sun HL, Liu J, Ding F, et al. Investigation of differentially expressed proteins in rat gastrocnemius muscle during denervation-reinnervation[J]. J Muscle Res Cell Motil, 2006, 27(3/4): 241-250.
[24] Pallafacchina G, Blaauw B, Schiaffino S. Role of satellite cells in muscle growth and maintenance of muscle mass[J]. Nutr Metab Cardiovasc Dis, 2013, 23(Suppl 1): S12-S18.
[25] 刘晓蓉, 张成, 张为西, 等. 骨髓移植治疗Duchenne型肌营养不良模型鼠的实验研究[J]. 中国病理生理杂志, 2005, 21(8): 1462-1466. LIU Xiaorong, ZHANG Cheng, ZHANG Weixi, et al. Experimental treatment of the model mice of Duchenne muscular dystrophy by bone marrow transplantation[J]. Chinese Journal of Pathophysiology, 2005, 21(8): 1462-1466.
[26] Witt R, Weigand A, Boos AM, et al. Mesenchymal stem cells and myoblast differentiation under HGF and IGF-1 stimulation for 3D skeletal muscle tissue engineering[J]. BMC Cell Biol, 2017, 18(1): 15. doi:10.1186/s12860-017-0131-2.
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