华西口腔医学杂志

• 基础研究 • 上一篇    下一篇

牙髓干细胞向神经细胞方向的诱导分化实验

贺慧霞1, 2, 金岩1, 史俊南3, 罗玉庆4, 周艳妮2, 彭智2, 许玉和2   

  1. 1.第四军医大学口腔医院病理科组织工程中心, 陕西西安710032; 2.武警甘肃总队医院口腔科, 甘肃兰州730050; 3.第四军医大学口腔医院牙体牙髓科, 陕西西安710032; 4.兰州军区临潼疗养院三区门诊部, 陕西西安710600
  • 收稿日期:2007-08-25 修回日期:2007-08-25 出版日期:2007-08-20 发布日期:2007-08-20
  • 通讯作者: 金岩,Tel:029- 84776147
  • 作者简介: 贺慧霞(1970-),女,甘肃人,副主任医师,博士
  • 基金资助:

    甘肃省自然科学基金资助项目(3ZS061- A25- 112);国家“八六三”计划资助项目(2002AA205041)

Exper iment on inducing human dental pulp stem cells into neur al - like cells

HE Hui - xia1,2, JIN Yan1, SHI Jun- nan3, LUO Yu- qing4, ZHOU Yan- ni2, PENG Zhi2, XU Yu- he2   

  1. 1. Research and Development Center for Tissue Engineering,Dept. of Oral Histology and Pathology, School of Stomatology, The Fourth Military Medical University, Xi′an 710032, China; 2. Dept. of Stomatology, Gansu Provincial Corps Hospital, Chinese People′s Armed Police Force, Lanzhou 730050, China; 3. Dept. of Conservative Dentistry, School of Stomatology, The Fourth Military Medical University, Xi′an 710032, China; 4. Outpatient Department, The Third Region of Lintong Convalescent Hospital, Lanzhou Military Area Command of Chinese PLA, Xi′an 710600, China
  • Received:2007-08-25 Revised:2007-08-25 Online:2007-08-20 Published:2007-08-20
  • Contact: JIN Yan,Tel:029- 84776147

摘要:

目的探讨克隆化培养分离的人牙髓干细胞是否具有向神经细胞方向分化的潜能,并确定其诱导条件。方法克隆化培养的人牙髓干细胞预诱导24 h,然后换含一定浓度二甲基亚砜(DMSO)、丁羟基茴香醚(BHA)、forskolin、β- 巯基乙醇(β-ME)和氢化可的松(hydrocortisone)的联合诱导液连续诱导4 d,对诱导细胞进行形态学观察,神经胶质酸性蛋白(GFAP)、非特异性酯酶(NSE)免疫组化染色和GFAP mRNA RT- PCR检测。同时,以未诱导细胞为对照。结果诱导12 h时细胞形态开始改变,24 h时分化为较为典型的神经细胞样细胞,继续诱导分化细胞数量增多;诱导细胞表达神经元细胞特异性标志NSE和GFAP蛋白;RT- PCR检测诱导细胞表达GFAP mRNA,而未诱导细胞均无上述改变和表达。结论人牙髓干细胞在一定的诱导条件下可横向分化为神经元样细胞。

关键词: 牙髓干细胞, 诱导, 分化

Abstract:

Objective To explore the multi - differentiated capability of human dental pulp stem cells(hDPSCs) obtained by cell - clone culture approach and to determine the appropriate induced medium. Methods The cloned isolation and expansion of hDPSCs were preinduced for 24 h, and were subsequently replaced with neural- inductive medium containing certain concentration of dimethylsulfoxide(DMSO), butylated hydroxyanisode(BHA), forskolin, β- mercaptoethanol(β-ME) and hydrocortisone for 4 days. Then induced cells were analyzed by morphological observation, immnocytochemical staining for non- specific esterase(NSE) and glial fibrillary acidic protein(GFAP) expression, RT- PCR for GFAP mRNA. Meanwhile, the uninduced hDPSCs were used as negative control. Results The morphology of induced cells changed at the initial 12 h, and displayed a typical neuron- like cells at 24 h. There was a gradual increase in the number of these neuronal differentiated cells with continuous induction. Furthermore, immnocytochemical staining showed that the induced cell expressed NSE and GFAP, two marked enzymes of neuron cell. The GFAP mRNA was also detected in induced cells by RT- PCR assay. In contrast, the uninduced cells maintained its original appearance and had no expression on them. Conclusion hDPSCs may possess potential of multiple- differentiation and may differentiate into neuron- like cells on certain inductive condition.

Key words: dental pulp stem cells, induction, differentiation