中国临床解剖学杂志 ›› 2017, Vol. 35 ›› Issue (1): 48-51.doi: 10.13418/j.issn.1001-165x.2017.01.010

• 实验研究 • 上一篇    下一篇

施万样细胞对大鼠脊神经节NGF 和BDNF 表达的影响

付秀美1, 王荣良2, 杨振江1, 付文亮1, 王小杰3   

  1. 1.承德医学院解剖教研室; 2.承德市妇幼保健院; 3.承德医学院基础所,  河北   承德    067000
  • 收稿日期:2016-11-07 出版日期:2017-01-25 发布日期:2017-02-22
  • 作者简介:付秀美(1980-),女,讲师,博士, 主要从事周围神经再生修复及人体解剖学研究,Tel:0314-2291137,E-mail:fuxiumei 2012@163.com
  • 基金资助:

    河北省教育厅资助项目(QN2014138); 河北省重点发展学科“人体解剖与组织胚胎学”建设资助项目

Effects of Schwann-like cells on the expression of NGF and BDNF in spinal ganglia of rats with sciatic nerve injury

FU Xiu-mei1, WANG Rong-liang2, YANG Zhen-jiang1, FU Wen-liang1, WANG Xiao-jie3   

  1. 1. Department of Anatomy, Chengde Medical College;  2. Chengde Maternal and Child Health Hospital;  3. Institute of Basic Medicine, Chengde Medical College, Chengde Hebei 067000, China
  • Received:2016-11-07 Online:2017-01-25 Published:2017-02-22

摘要:

目的 观察施万样细胞对坐骨神经损伤(sciatic nerve injury,SNI)大鼠脊神经节NGF 和BDNF 表达的影响,初步探讨施万样细胞对脊神经节的保护作用。   方法 先将脂肪源性干细胞(adipose-derived stem cells,ADSCs)诱导分化为施万样细胞并对后者进行鉴定,后将二者分别植入脱细胞神经移植物(ANA)中,构建组织工程神经。大鼠随机分为正常对照组、ADSC 组和施万样细胞组。后两组建立SNI 模型并用相应的组织工程神经桥接损伤的神经。术后4 周采用Western Blot 和Real-time PCR 检测各组大鼠脊神经节神经生长因子(nerve growth factor,NGF)和脑源性神经营养因子(brain-derived neurotrophic factor,BDNF)蛋白和mRNA 的表达。   结果 ADSCs 能够诱导分化为施万样细胞并表达施万细胞标记物S100β 和GFAP 蛋白。施万样细胞组大鼠脊神经节内NGF 和BDNF 蛋白及mRNA 表达量均高于ADSC 组(P<0.05)。   结论 施万样细胞可上调脊神经节NGF 和BDNF 的表达,对SNI 所致的脊神经节内神经元损伤有保护作用。

关键词: 施万样细胞, 脊神经节, NGF, BDNF

Abstract:

Objective To investigate the effects of Schwann-like cells on the expression of NGF and BDNF in spinal ganglia of rats with sciatic nerve injury (SNI) and explore the protective effects of Schwann-like cells on spinal ganglion. Methods Firstly,the adipose derived stem cells (ADSCs) were differentiated into Schwann-like cells and the phenotype of the differentiated cells were identified, then the ADSCs and Schwann-like cells were implanted into the acellular nerve grafts (ANA), so the tissue engineering nerves were constructed. The rats were randomly divided into 3 groups: normal control group, ADSC group and Schwann-like cells group. The SNI model was established in rats of the latter two groups, and then the corresponding tissue engineering nerves were used to bridge the injured sciatic nerves. 4 Weeks after operation, Western Blot and Real-time PCR were used to detect the expression of NGF and BDNF protein and mRNA in spinal ganglia. Results ADSCs can be induced to differentiate into Schwann-like cells and expression of S100β and GFAP protein (markers of Schwann cells). In contrast with ADSC group, the expressions of NGF and BDNF protein and mRNA in Schwann-like cells group rats increased (P<0.05). Conclusion  Schwann-like cells can enhance the expression of NGF and BDNF in the spinal ganglia, so they can have protective effects on the spinal ganglia in rats with SNI.

Key words: Schwann-like cells, Spinal ganglia, Nerve growth factor, Brain-derived neurotrophic factor