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大鼠脊髓损伤后神经元再生研究 被引量:3

Neuron regeneration after spinal cord injury in rats
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摘要 目的 观察成年大鼠脊髓损伤后是否存在神经元再生. 方法 36只Wistar成年雌性大鼠按随机数字表法分为正常对照组(6只)和脊髓损伤组(30只).采用Allen打击模型(25 g·cm)在T10段造成急性脊髓损伤,于损伤后3d、1,2,3,4周进行取材.取材前72 h开始经腹腔注射BrdU (300 mg·kg^-1·d^-1),每12 h注射1次.取距离损伤中心10 mm内脊髓行NF-200和BrdU免疫荧光双标,观察其表达阳性细胞数量. 结果 正常对照组可见少量BrdU阳性细胞,未发现BrdU和NF-200双标阳性细胞.脊髓损伤组伤后3d可见大量BrdU阳性细胞出现;1周时BrdU阳性细胞数量达到高峰,并可见少量BrdU和NF-200双标阳性细胞;2周时BrdU和NF-200双标阳性细胞最多见,主要集中在距离损伤区约3~5 mm处;3周时BrdU和NF-200双标阳性细胞罕见;4周时均未发现BrdU和NF-200双标阳性细胞. 结论 大鼠脊髓损伤后在损伤部位附近存在神经元再生,为干细胞修复脊髓损伤提供新的思路. Objective To observe the neuronal regeneration after spinal cord injury in adult rats.Methods Thirty-six adult Wistar rats were randomly divided into normal control group (n =6) and spinal cord injury group (n =30).Allen's weight-drop method (25 g/cm) was adopted to produce acute spinal cord injury at T10 segment.Rats were sacrificed at 3 days and 1,2,3,and 4 weeks postinjury.BrdU was administered intraperitoneally to the rats 72 hours before operation,once per 12 hours.Double immunofluorescence staining of NF-200 and BrdU was performed at spinal sites within 10 mm away from the injury to detect the positive cells in both groups.Results A few BrdU-positive cells were founded in the normal control group,with no BrdU/NF-200 positive cells.In spinal cord injury group,BrdU-positive cells were abundant at day 3 and peaked at week 1 along with few Brdu/NF-200 positive cells ; Brdu/NF-200 positive cells showed a peak increase at week 2 with majority accumulated at area 3-5 mm away from the injury,were rare at week 3 and none at week 4.Conclusion Neuronal regeneration is detected in the vicinity of the injury,which provides new ideas for induction of endogenous stem cells to treat spinal cord injury.
出处 《中华创伤杂志》 CAS CSCD 北大核心 2015年第2期164-168,共5页 Chinese Journal of Trauma
基金 国家自然科学基金资助项目(81272172) 国家临床重点专科建设资助项目(2013544)
关键词 脊髓损伤 神经元 干细胞 大鼠 Spinal cord injuries Neurons Stem cells Rats
作者简介 通信作者:南国新,电话:13608397992,Email:ngx1215@126.com
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参考文献22

  • 1Gage FH. Mammalian neural stem cells [ J ]. Science, 2000, 287(5457) :1433-1438.
  • 2Huang H, Liu L, Li B, et al. Ketamine interferes with the prolif-eration and differentiation of neural stem cells in the subventricularzone of neonatal rats[ J ]. Cell Physiol Biochem, 2015 , 35 (1 ):315-325.
  • 3Gage FH, Coates PW, Palmer TD, et al. Survival and dilerentia-tion of adult neuronal progenitor cells transplanted to the adultbrain[J]. J Proc Nat Acad Sci USA, 1995, 92(25) :11879-11883.
  • 4Weiss S, Dunne C, Hewson J, et al. Multipotent CNS stem cellsare present in the adult mammalian spinal cord and ventricularneuroaxis[ J]. J Neurosci, 1996,16(23):7599-7609.
  • 5Okano H, Sakaguchi M, Ohki K, et al. Regeneration of the cen-tral nervous system using endogenous repair mechanisms [ J ]. JNeurochem, 2007,102(5) : 1459-1465.
  • 6Beattie MS, Bresnahan JC, Komon J, et al. Endogenous repair af-ter spinal cord contusion injuries in the rat [ J ]. Exp Neurol,1997,148(2) :453463.
  • 7Vaquero J, Ramiro MJ, Oya S, et al. Ependymal reaction afterexperimental spinal cord injury [ J ]. Acta Neurochir ( Wien ),1981,55(34):295-302.
  • 8Stenudd M,Sabelstrom H,Fris6n J. role of endogenous neuralstem cells in spinal cord injury and repair [ J ]. JAMA Neurol,2014,Dec. 22. [ Epub ahead of print].
  • 9Johansson CB, Momma S, Clarke DL, et al. Identification of aneural stem cell in the adult mammalian central nervous system[ J].Cell, 1999, 96(1).,25-34.
  • 10Okano H, Okada S, Nakamura M, et al. Neural stem cells andregeneration of injured spinal cord [ J ]. Kidney Int,2005,68(5);1927-1931.

二级参考文献14

  • 1[1]Gage FH,Coates PW,Palmer TD,et al.Survival and differentiation of adult neuronal progenitor cells transplanted to the adult brain.Proc Natl Acad Sci U S A,1995,92:11879-11883
  • 2[2]Young W.Spinal cord contusion models.Prog Brain Res,2002,137:231-255
  • 3[3]Rossi F,Cattaneo E.Opinion:neural stem cell therapy for neurological diseases:dreams and reality.Nat Rev Neurosci,2002,3:401-409
  • 4[4]Johansson CB,Momma S,Clarke DL,et al.Identification of a neural stem cell in the adult mammalian central nervous system.Cell,1999,96:25-34
  • 5[5]Doetsch F,Caille I,Lim DA,et al.Subventricular zone astrocytes are neural stem cells in the adult mammalian brain.Cell,1999,97:703-716
  • 6[6]McMahon SS,McDermott KW.Morphology and differentiation of radial glia in the developing rat spinal cord.J Comp Neurol,2002,454:263-271
  • 7[7]Doetsch F.The glial identity of neural stem cells.Nat Neurosci,2003,6:1127-1134
  • 8[8]Pevny L,Rao MS.The stem-cell menagerie.Trends Neurosci,2003,26:351-359
  • 9[9]Lendahl U,Zimmerman LB,McKay RD.CNS stem cells express a new class of intermediate filament protein.Cell,1990,60:585-595
  • 10[10]Malatesta P,Hartfuss E,Gotz M.Isolation of radial glial cells by fluorescent-activated cell sorting reveals a neuronal lineage.Development,2000,127:5253-5263

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  • 1Parfitt AM. Osteonal and hemi-osteonal remodeling: the spatial and temporal framework for signal traffic in adult human bone[ J]. J Cell Biochem, 1994, 55 (3) :273-286. DOI : 10. 1002/jeb. 240 550303.
  • 2Demulder A, Guns M, Ismail A, et al. Increased osteoelast-like cells formation in long-term bone marrow cultures from patients with a spinal cord injury[J]. Calcif Tissue Int, 1998, 63(5) : 396-400. DOI : 10. 1007/s002239900547.
  • 3Smith CB, Smith DA. Relations between age, mineral density and mechanical properties of human moral compacta [ J]. Acta Onhop Scand, 1976, 47(5):496-502. DOI:10.3109/17453677 608988727.
  • 4Edwards WB, Schnitzer TJ, Troy KL. Bone mineral loss at the proximal femur in acute spinal cord injury [ J]. Osteoporos Int, 2013, 24(9) :2461-2469. DOI:10. 1007/s00198-013-2323-8.
  • 5Hammond ER, Metcalf HM, Mcdonald JW, et at. Bone mass in individuals with chronic spinal cord injury: associations with activity-based therapy, neorologic and functional status, a retro- spective study [ J]. Arch Phys Med Rehabil, 2014, 95 (12): 2342-2349. DOI : 10. 1016/j. apmr. 2014.07. 395.
  • 6Yan J, Li B, Chen J, et al. Spinal cord injury causes bone loss through peroxisome proliferator-activated receptor-'y and Wnt signalling[ J]. J Cellul Molecul Med, 2012, 16 ( 12 ) : 2968- 2977. DOI: 10.1111/j. 1582-4934. 2012. 01624.
  • 7Mach DB, Rogers SD, Sabino MC, et al. Origins of skeletal pain : sensory and sympathetic innervation of the mouse femur[ J]. Neu- roscience, 2002, 113 ( 1 ) : 155-166. DOI: 10. 1016/S0306-4522 (02)00165-3.
  • 8Chang KV, Hung CY, Chen WS, et al. Effectiveness of bisphosphonate analogues and functional electrical stimulation on attenuating post-injury osteoporosis in spinal cord injury patients- a systematic review and meta-analysis [ J]. PLoS One, 2013, 8 ( 11 ) : e81124. DOI : 10. 1371/journal. pone. 0081124.
  • 9Suzue N, Nikawa T, Onishi Y, et al. Ubiquitin ligase Cbl-b downregulates bone formation through suppression of IGF-I signa- ling in osteoblasts during denervation [ J]. J Bone Miner Res, 2006, 21 (5) :722-734. DOI : 10. 1359/jbmr. 060207.
  • 10Peake MA, Cooling LM, Magnay JL, et al. Selected contribu- tion: regulatory pathways involved in mechanical induction of c- los gene expression in bone cells[J]. J Appl Physiol, 2000, 89 ( 6 ) : 2498-2507.

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