期刊文献+

酶消化法培养Balb/c胎鼠下颌突未分化外胚间充质细胞 被引量:9

Culture of undifferentiated ectomesenchymal cells of mandibular process of Balb/c fetal mice by enzymatic cell separation method
下载PDF
导出
摘要 目的 :用酶消化法培养Balb/c胎鼠下颌突外胚间充质细胞 ,并与组织块法相比较 ,研究其形态和生长特性。方法 :采用 1.2 5 g/L的胰酶消化法获取E 12 .5dBalb/c胎鼠下颌突外胚间充质细胞 ,用含 10 6U/LLIF的D/F12 培养细胞 ,倒置显微镜下观察细胞形态和生长情况 ,免疫组化鉴定细胞来源及分化状况。结果 :培养的细胞呈单层生长 ,长梭形 ,有 2~ 4个突起 ,抗HNK - 1、Vimentin、S - 10 0、NSE染色阳性 ,抗GFAP、NF、MA染色阴性 ,证实为未分化外胚间充质细胞。结论 :用酶消化法可在短期内获得大量的未分化外胚间充质细胞。 AIM:Primary ectomesenchymal cells of Balb/c fetal mandibular process were got by trypsin. Then their morphology and growth rate was studied. METHODS: The primary ectomesenchymal cells of E 12.5 Balb/c fetal mice mandibular process were isolated by 1.25 g/L trypsin and cultured with D/F 12 with 10 6U/L LIF. Their morphology and growth rate were observed by phase-contrast microscope. Immunohistochemistry was used to identify the characteristics of cells. RESULTS: The cultured cells displayed monolayer growth and were fibroblast-like with 2~4 processes. Cells were anti-HNK-1?Vimentin?S-100?NSE positive and anti-GFAP?NF?MA negative in immunohistochemistry. CONCLUSION: A large number of undifferentiated ectomesenchymal cells could be obtained by 1.25 g/L trypsin in a short time.
出处 《牙体牙髓牙周病学杂志》 CAS 2002年第8期403-406,I001,共5页 Chinese Journal of Conservative Dentistry
关键词 酶消化法 外胚间充质细胞 细胞培养 组织工程 ectomesenchymal cells trypsin method cell culture
  • 相关文献

参考文献2

二级参考文献5

共引文献7

同被引文献81

  • 1邓蔓菁,金岩,史俊南,董蕊,何大为.端粒酶在面突外胚间充质细胞干细胞中的表达[J].第四军医大学学报,2003,24(19):1739-1741. 被引量:5
  • 2中华人民共和国科学技术部.关于善待实验动物的指导性意见.2006.09-30 被引量:704
  • 3[3]Zhao M, Xiao GZ,Berry EB, et al. Bone morphologetic protein 2 induces dental follicle cells to differentiate toward a cementoblast/osteoblast phenotype. J Bone Miner Res. 2002,7(12)∶1441 被引量:1
  • 4[4]Laura C, Howard CP, Charles L, et al. Emdogain regulation of cellular differentiation in wounded rat periodontium. J Periodont Res, 2003,38(2)∶164-174 被引量:1
  • 5[5]Marriko O, Naoto S, Yoko Y, et al. Effect of enamel matrix derivative on the differentiation of C2C12 cells. J Periodontol, 2002,73(5)∶543 被引量:1
  • 6[6]Pitaru S, Pritzki A, Bar-Kana I, et al. Bone morphogenetic protein 2 induces the expression of cementum attachment protein in human periodontal ligament clones. Connect Tissue Res,2002,43(2-3)∶257-64 被引量:1
  • 7[9]Margarita ZD. Is there more to enamel matrix proteins than biomineralization? Matrix Biology, 2001, 20 (2)∶307-316 被引量:1
  • 8Sharpe PT.Neural crest and tooth morphogenesis.Adv Dent Res.2001;15:4-7. 被引量:1
  • 9Mitsiadis TA,Graf D.Cell fate determination during tooth development and regeneration.Birth Defects Res C Embryo Today.2009;87(3):199-211. 被引量:1
  • 10Trainor PA,Sobieszczuk D,Wilkinson D,et al.Signalling between the hindbrain and paraxial tissues dictates neural crest migration pathways.Development.2002;129(2):433-442. 被引量:1

引证文献9

二级引证文献17

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部