|本期目录/Table of Contents|

[1]潘大宇,宁广智,冯世庆.雪旺细胞外泌体影响胶质瘢痕形成修复小鼠脊髓损伤的实验研究[J].天津医科大学学报,2020,26(05):397-400.
 PAN Da-yu,NING Guang-zhi,FENG Shi-qing.Schwann cell-derived exosomes promote functional recovery of spinal cord injury in mice via affecting glial scar formation[J].Journal of Tianjin Medical University,2020,26(05):397-400.
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雪旺细胞外泌体影响胶质瘢痕形成修复小鼠脊髓损伤的实验研究(PDF)
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《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]

卷:
26卷
期数:
2020年05期
页码:
397-400
栏目:
基础医学
出版日期:
2020-09-20

文章信息/Info

Title:
Schwann cell-derived exosomes promote functional recovery of spinal cord injury in mice via affecting glial scar formation
文章编号:
1006-8147(2020)05-0397-04
作者:
潘大宇宁广智冯世庆
(天津医科大学总医院骨科,天津市神经科学院,中枢神经系统神经损伤后神经修复和再生教育部重点实验室,天津300052)
Author(s):
PAN Da-yu NING Guang-zhi FENG Shi-qing
(Department of Orthopedics, General Hospital, Tianjin Medical University, Tianjin Neurological Institute, Key Laboratory of Post-Neuroinjury Neuro-Repair and Regeneration in Central Nervous System, Ministry of Education and Tianjin City, Tianjin 300052, China)
关键词:
脊髓损伤雪旺细胞外泌体胶质瘢痕
Keywords:
spinal cord injury schwann cells exosomes glial scar
分类号:
R68
DOI:
-
文献标志码:
A
摘要:
目的:探讨雪旺细胞外泌体(SCDEs)对小鼠脊髓损伤的修复作用。方法:从小鼠坐骨神经中提取原代雪旺细胞,并将雪旺细胞培养上清分次超速离心得到雪旺细胞外泌体。透射电镜鉴定外泌体 ,尾静脉注射外泌体,每周2次,每次3 μL/只,BMS评分观察小鼠行为学功能恢复,免疫荧光染色观察外泌体神经保护作用和胶质瘢痕变化情况。结果:SCDEs的直径范围为40~100 nm;与PBS组相比, SCDEs组行为学BMS评分增加(P<0.05),神经学功能指标有所恢复(P<0.01),胶质瘢痕增加(P<0.01)。结论:SCDEs可以促进损伤后胶质瘢痕的增加,修复脊髓损伤。
Abstract:
Objective: To investigate the repair effect of schwann cell-derived exosomes(SCDEs) on spinal cord injury in mice. Methods: Primary schwann cells were extracted from the sciatic nerve of mice, and the schwann cell culture supernatant was subjected to ultracentrifugation to obtain SCDEs. Transmission electron microscopy was used to identify exosomes, and exosomes were injected via tail vein 2 times a week, 3 μL each mouse. Basso mouse scale(BMS) was used to observe the behavioral function, nerve function recovery and changes scar were observed by immunofluorescence staining. Results: SCDEs ranged in size from 40 to 100 nm. Compared with the PBS group, BMS was increased(P<0.05), neurological functional recovery was induced(P<0.001), glial scar formation was increased in the SCDEs group (P<0.001). Conclusion: SCDEs can promote the increase of glial scar and repairing spinal cord injuries.

参考文献/References:

[1] McDonald J W, Sadowsky C. Spinal-cord injury[J]. Lancet, 2002, 359(9304):417
[2] Holmes D. Spinal-cord injury: spurring regrowth[J]. Nature, 2017, 552(7684):S49
[3] Kucera K L, Yau R K, Register-Mihalik J, et al. Traumatic brain and spinal cord fatalities among high school and college football players -united states, 2005-2014[J]. MMWR Morb Mortal Wkly Rep,2017, 65(52):1465
[4] Stower H. Cell therapy for spinal cord injury[J]. Nat Med, 2018, 24(8):1088
[5] Chhabra H S, Sarda K. Clinical translation of stem cell based interventions for spinal cord injury - Are we there yet?[J]. Adv Drug Deliv Rev, 2017(120):41
[6] Mothe A J, Tator C H. Advances in stem cell therapy for spinal cord injury[J]. J Clin Invest,2012,122(11): 3824
[7] Fang X, Zhang C, Zhang C, et al. Reactivation of denervated schwann cells by embryonic spinal cord neurons to promote axon regeneration and remyelination[J]. Stem Cells Int,2019,(2019):7378594
[8] Fu X M, Wang Y, Fu W L, et al. The combination of adipose-derived schwann-like cells and acellular nerve allografts promotes sciatic nerve regeneration and repair through the JAK2/STAT3 signaling pathway in rats[J]. Neuroscience, 2019,(422):134
[9] Mousavi M, Hedayatpour A, Mortezaee K, et al. Schwann cell transplantation exerts neuroprotective roles in rat model of spinal cord injury by combating inflammasome activation and improving motor recovery and remyelination[J]. Metab Brain Dis, 2019, 34(4):1117
[10] Marquardt L M, Doulames V M, Wang A T, et al. Designer, injectable gels to prevent transplanted Schwann cell loss during spinal cord injury therapy[J]. Sci Adv, 2020, 6 (14): eaaz1039
[11] Yang B, Chen Y, Shi J. Exosome biochemistry and advanced nanotechnology for next-generation theranostic platforms[J]. Adv Mater,2019, 31(2): e1802896
[12] Hyder A A, Wunderlich C A, Puvanachandra P, et al. The impact of traumatic brain injuries: a global perspective[J]. NeuroRehabilitation, 2007, 22(5):341
[13] Lopez-Verrilli M A, Picou F, Court F A. Schwann cell-derived exosomes enhance axonal regeneration in the peripheral nervous system[J]. Glia, 2013, 61(11):1795
[14] Aryani A, Denecke B. Exosomes as a nanodelivery system: a key to the future of neuromedicine?[J]. Mol Neurobiol, 2016, 53(2): 818
[15] Marklund N, Bakshi A, Castelbuono D J, et al. Evaluation of pharmacological treatment strategies in traumatic brain injury[J]. Curr Pharm Des, 2006, 12(13):1645
[16] Blesch A, Tuszynski M H. Spinal cord injury: plasticity, regeneration and the challenge of translational drug development[J]. Trends Neurosci, 2009, 32(1):41
[17] Filbin M T. Myelin-associated inhibitors of axonal regeneration in the adult mammalian CNS[J]. Nat Rev Neurosci, 2003, 4(9):703
[18] Court F A, Coleman M P. Mitochondria as a central sensor for axonal degenerative stimuli[J]. Trends Neurosci, 2012, 35(6):364
[19] Lopez-Verrilli M A, Court F A. Transfer of vesicles from schwann cells to axons: a novel mechanism of communication in the peripheral nervous system[J]. Front Physiol, 2012.(3):205
[20] Klingeborn M, Dismuke W M, Bowes Rickman C, et al. Roles of exosomes in the normal and diseasedeye[J]. Prog Retin Eye Res,2017(59): 158

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备注/Memo

备注/Memo:
基金项目 国家自然科学基金国际合作与交流项目(81620108018);国家自然科学基金资助项目(81930070)
作者简介 潘大宇(1993-),男,硕士在读,研究方向:骨外科学;
通信作者:宁广智,E-mail: ningguangzhi@foxmail.com;冯世庆,E-mail:sqfeng@tmu.edu.cn。
更新日期/Last Update: 2020-09-18