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Synaptic development in the injured spinal cord cavity following co-transplantation of fetal spinal cord cells and autologous activated Schwann cells 被引量:4

Synaptic development in the injured spinal cord cavity following co-transplantation of fetal spinal cord cells and autologous activated Schwann cells
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摘要 Transplantation of activated transgenic Schwann cells or a fetal spinal cord cell suspension has been widely used to treat spinal cord injury. However, little is known regarding the effects of co-transplantation. In the present study, autologous Schwann cells in combination with a fetal spinal cord cell suspension were transplanted into adult Wistar rats with spinal cord injury, and newly generated axonal connections were observed ultrastructurally. Transmission electron microscopic observations showed that the neuroblast first presented cytoplasmic processes, followed by pre- and postsynaptic membranes with low electron density forming a dense projection. The number and types of synaptic vesicles were increased. Synaptic connections developed from single cell body-dendritic synapses into multiple cell body-dendritic and dendrite-dendritic synapses. In addition, the cell organs of the transplanted neuroblast, oligodendroblast and astroblast matured gradually. The blood-brain barrier appeared subsequently. Moreover, neurofilament, histamine, calcitonin-gene-related peptides, and glial fibrillary acidic protein positive fibers were observed in the transplant region. These findings demonstrate that fetal spinal cord cells in the presence of autologous activated Schwann cells can develop into mature synapses in the cavity of injured spinal cords, suggesting the possibility of information exchange through the reconstructed synapse between fetal spinal cord cells and the host. Transplantation of activated transgenic Schwann cells or a fetal spinal cord cell suspension has been widely used to treat spinal cord injury. However, little is known regarding the effects of co-transplantation. In the present study, autologous Schwann cells in combination with a fetal spinal cord cell suspension were transplanted into adult Wistar rats with spinal cord injury, and newly generated axonal connections were observed ultrastructurally. Transmission electron microscopic observations showed that the neuroblast first presented cytoplasmic processes, followed by pre- and postsynaptic membranes with low electron density forming a dense projection. The number and types of synaptic vesicles were increased. Synaptic connections developed from single cell body-dendritic synapses into multiple cell body-dendritic and dendrite-dendritic synapses. In addition, the cell organs of the transplanted neuroblast, oligodendroblast and astroblast matured gradually. The blood-brain barrier appeared subsequently. Moreover, neurofilament, histamine, calcitonin-gene-related peptides, and glial fibrillary acidic protein positive fibers were observed in the transplant region. These findings demonstrate that fetal spinal cord cells in the presence of autologous activated Schwann cells can develop into mature synapses in the cavity of injured spinal cords, suggesting the possibility of information exchange through the reconstructed synapse between fetal spinal cord cells and the host.
出处 《Neural Regeneration Research》 SCIE CAS CSCD 2010年第19期1445-1450,共6页 中国神经再生研究(英文版)
基金 the Tianjin Science and Technology Commission Key Project,No.07JCZDJC08000 the Natural Science Foundation of China, No.30772193,30571876 National High-Tech R&D Program of China (863 Program),No.2007AA04Z235
关键词 fetal spinal cord cell suspension SYNAPSE DEVELOPMENT autologous activated Schwann cells spinal cord injury peripheral nerve injury neural regeneration fetal spinal cord cell suspension synapse development autologous activated Schwann cells spinal cord injury peripheral nerve injury neural regeneration
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  • 1唐娟,于娜,吴亮生,杨磊,仙玲玲,黄延红,张树军,黄瑾.人Neuritin在原核表达系统的构建及表达纯化[J].中国生物工程杂志,2006,26(4):46-50. 被引量:6
  • 2张树军,仙玲玲,于娜,巴鹏飞,徐芬,杨磊,黄瑾.Neuritin在毕赤酵母中的分泌表达与鉴定[J].农垦医学,2006,28(5):321-324. 被引量:1
  • 3Dergham P, Ellezam B. Rho signaling pathway targeted to promote spinal cord repair. Neurosci, 2002, 22(15): 6570-6577.
  • 4Bulsara KR, Iskandar BJ, Villavicencio AT, et al. A new millennium for spinal cord regeneration: growth-associated genes. Spine, 2002, 27(17): 1946-1949.
  • 5Mcllvain VA, Robertson DR, Maimone MM, et al. Abnormal thalamocortical Pathfinding and terminal arbors lead to enlarged barrels in neonatal GAP-43 heterozygous mice. Comp Neurol, 2003, 462(2): 252-264.
  • 6Nomura T, Honmou O, Harada K, et al. I. V. Infusion of brain derived neurotrophic factor gene-modified human mesenchymal stem cells protects against injury in a cerebral ischemia model in adult rat. Neurosci, 2005, 136(1): 161-169.
  • 7Karamoysoyli E, Burnand RC, TomLinson DR, et al. Neuritin mediates nerve growth factor-induced axonal regeneration and is deficient in experimental diabetic neuropathy. Diabetes, 2008, 57( 1): 181-189.
  • 8Pahnke J, Mix E, Knoblich R, et al. Overexpression of glial cell linederived neurotrophic factor induces genes regulating migration and differentiation of neuronal progenitor cells. Exp Cell Res, 2004, 297(2): 484-494.
  • 9Wibrand K, Messaoudi E, Havik B, et al. Identification of genes coupregulated with Arc during BDNF-induced long-term potentiation in adult rat dentate gyrus in vivo. Eur J Neurosci, 2006, 23(6): 1501-1511.
  • 10Basso DM, Beattie MS, Bresnahan JC, et al. MASCIS evaluation of open field locomotor scores: effects of experience and teamwork on reliability. Multicenter Animal Spinal Cord Injury Study. J Neurotrauma, 1996, 13(7): 343-359.

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