中文摘要：

目的观察分析胚胎脊髓细胞悬液（fetal spinal cord cell suspension，FSCS）联合自体激活雪旺细胞（autologus activated Schwann cells，AASCs）在损伤脊髓移植区中的突触发育过程。方法42只Wistar成年大鼠结扎单侧隐神经，1周后取出结扎远端神经组织，分离、培养、纯化AASCs。以改良Allen法（10g×5cm）打击脊髓，3天后将孕14天（E14）FSCS20μl联合AASCs植入损伤空腔，移植后2、4、6、8、10和12周，以光学显微镜、电镜、免疫组织化学观察移植物成活、分化及其与宿主之间关系。结果移植区AASCs生长分化良好，胶质瘢痕少。成神经细胞最先展示了胞质突起，随之出现低电子密度的突触前、后膜，突触前、后膜电子密度逐渐增高形成良好的致密突起。突触小泡数量和种类逐渐增多，突触小泡有圆形清亮小泡、椭圆形小泡、颗粒状小泡和扁平小泡-f型。突触的连接方式由单个的胞体-树突突触，出现多个的胞体-树突和树突-树突突触。同时，移植成神经细胞、成少突胶质细胞、成星形细胞的细胞器日渐完善，细胞功能活跃。血脑屏障也随之出现。移植区可见神经微丝、组织胺、降钙素基因相关肽、胶原纤维酸性蛋白阳性纤维。结论（1）AASCs辅助下FSCS在成年大鼠损伤脊髓内可发育为成熟的突触；（2）FSCS与宿主脊髓重建突触方式的信息交换具有潜在可行性。

英文摘要：

Objective To observe and analyze the synapses developing process of newly generated connections of autologus activated Schwann cells （AASCs） in combination with fetal spinal cord cell suspension （FSCS） in the surrounding area of the spinal cord injury site. Methods A total of 42 Wistar rats underwent unilateral ligation of the saphenous nerve. The portion of nerve tissues distal to the ligation site were harvested 1 week after operation. AASCs were isolated, cultured and purified. Spinal cord injury model pro- duced in 42 Wistar rats on T7 by modified Allen impact method. Three days after injury, 20 txl FSCS with a density of l~105/trl prepared from pregnant rats （El4） in combination with AASCs were injected into the epi- center of the traumatized cavity. Animals were sacrificed at 2, 4, 6, 8, 10, 12 weeks post transplantation. Light and electronmicroscopic studies as well as immunohistochemical assay were carried out to evaluate the graft survival, its differentation and integration with the host. Results In the transplantation area, AASCs showed good growth and differentiation, and glial scarring surrounding the lesions was less. The neuroblast stretched out the terminal endings 4 weeks after implantation, followed by the presenting of the pre- and post-synaptic membrane. Eight weeks post transplantation, the dense or developed projections were observed in the pre- and post-synaptic membrane, the high electron dense substance full filled the synaptic cleft. All the spherical cleat vesicles, granular vesicles, elliptical vesicles and flattened-f type vesicles were discovered under the electron microscope. Ten weeks after injury, the axosomatic, dendrosomatic, dendro-dendritic, axo- axonic, and dendro-axonic synapses coexisted. Light microscopy showed that the graft cell grew gradually. Immunohistochemical assay showed that NF, 5-HT, CGRP and GFAP positive fibers were in the graft. Synapses, glia fibers and blood brain barrier integrated each other. Conclusion 1） The transplanted FSCS combined with