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诱导颅神经嵴细胞向第一鳃弓外胚间充质细胞分化的实验研究
引用本文:江宏兵,田卫东,汤炜,刘磊,李晓东. 诱导颅神经嵴细胞向第一鳃弓外胚间充质细胞分化的实验研究[J]. 中华口腔医学杂志, 2005, 40(4): 319-322
作者姓名:江宏兵  田卫东  汤炜  刘磊  李晓东
作者单位:610041,成都,四川大学华西口腔医学院口腔颌面外科
基金项目:国家科学技术部重大基础研究前期研究专项基金资助项目(2002CCC00700)
摘    要:目的 研究体外成纤维细胞生长因子8(FGF-8)对颅神经嵴细胞向第一鳃弓表型分化的影响,并确立其时相效应,为进一步探讨颅神经嵴细胞的牙颌向分化诱导提供实验依据。方法 组织块法无血清条件培养颅神经嵴细胞,通过同源盒基因Hoxa2原位杂交及波形蛋白免疫细胞化学染色,观察不同剂量FGF-8对颅神经嵴细胞迁出前、后及其向第一鳃弓外胚间充质细胞表型分化的影响。结果 迁出前颅神经嵴细胞在100μg/LFGF-8作用下,呈现Hoxa2阴性表达、波形蛋白阳性表达,迁出后颅神经嵴细胞诱导组及对照组Hoxa2、波形蛋白表达均为阳性。结论 FGF-8可诱导颅神经嵴细胞向第一鳃弓外胚间充质细胞表型分化,具有早期诱导时相性特征。

关 键 词:颅神经嵴细胞 实验研究 细胞分化 外胚间充质细胞 成纤维细胞生长因子 免疫细胞化学染色 表型分化 波形蛋白 同源盒基因 分化诱导 条件培养 组织块法 原位杂交 不同剂量 阴性表达 阳性表达 细胞诱导 蛋白表达 无血清 对照组
修稿时间:2004-10-27

In vitro study on cranial neural crest differentiating into ectomesenchymal cell of the first branchial arch by FGF-8
JIANG Hong-bing,TIAN Wei-dong,TANG Wei,LIU Lei,LI Xiao-dong. In vitro study on cranial neural crest differentiating into ectomesenchymal cell of the first branchial arch by FGF-8[J]. Chinese journal of stomatology, 2005, 40(4): 319-322
Authors:JIANG Hong-bing  TIAN Wei-dong  TANG Wei  LIU Lei  LI Xiao-dong
Affiliation:Department of Oral and Maxillofacial Surgery, West China School of Stomatology, Sichuan University, Chengdu 610041, China.
Abstract:Objective To investigate the effects of FGF-8 on cranial neural crest cell(CNCC) differentiating into ectomesenchymal cell of the first branchial arch , and determine the appropriate dose and stage of CNCC exposure to FGF-8.Methods Cranial neural crest explants were cultured in free-serum medium containing modified DMEM/F12 and different doses of FGF-8.The differentiation type of CNCC were determined by in situ hybridization for Hoxa2 and immunocytochemistry for vimentin. Results Pre-emigrating CNCC demonstrated the negative Hoxa2 stain and positive vimentin stain after treated by 100 ug/ FGF-8 . Both post-emigrating CNCC group and contral group were positive for Hoxa2 and vimentin stain.Conclusions On the early stage of CNCC emigration, the first branchial arch phenotype of CNCC could be induced by FGF-8.This experiment could provide in vitro model for study on the mechanism of tooth-jaw regeneration.
Keywords:Cranial nerves  Branchial region  Ectoderm  Cell differentiation
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