期刊文献+

无血清无饲养层培养体系在绵羊胚胎干细胞分离中的应用

The Application of the Separation of Sheep Embryonic Stem Cells in Serum-and Feeder-free Conditions
原文传递
导出
摘要 目的:本文采用N2B27无血清无饲养层的完全已知成份的培养体系,通过机械分离法分离不同阶段的绵羊囊胚,观察不同阶段囊胚对分离绵羊类胚胎干细胞的影响。方法:本实验采用N2B27无血清无饲养层成份完全已知的培养体系,利用机械分离法对不同阶段的绵羊囊胚进行分离,观察其绵羊类胚胎干细胞的原代集落形成率,以及AKP染色,多潜能性候选基因Oct-4和Sox-2免疫荧光检测。结果:分离早期阶段绵羊囊胚获得的绵羊类胚胎干细胞的形成率显著低于扩张(孵化)阶段囊胚(19.6%(11/56)vs 36.9%(31/84))(P<0.05),同时早期和扩张(孵化)阶段绵羊囊胚的AKP染色和多潜能性候选基因Oct-4、Sox-2的表达呈阳性。结论:N2B27无血清无饲养层培养体系是一种有效分离绵羊类胚胎干细胞的培养基,同时分离绵羊扩张(孵化)阶段的囊胚可以显著的提高原代类胚胎干细胞的建系率,为提高绵羊类胚胎干细胞的建系奠定了基础。 Objective: To observe the influence of the separation of sheep embryonic stem cells in vitro culture blastocysts at different developmental stages by N2B27 serum- and feeder-flee conditions. Methods: Mechanical separation was used to isolate the in vitro culture blastocysts at different developmental stages by N2B27 serum- and feeder-free conditions, and then we observed the formation rates of primary oESC-like, AKP dying, expression of multipotent candidate genes Oct-4 and Sox-2. Results: The formation rates of oESC-like of early blastocysts was lower extended blastocysts (19.6% (11/56) vs 36.9%(31/84))(P 〈0.05). It was all positive for the assays of alkaline phosphatase and expression of multipotent candidate genes Oct-4 and Sox-2. Conclusion: This is an effective method that the separation of sheep embryonic stem cells in N2B27 serum- and feeder-flee conditions. The extended blastocysts can improve the formation rates of primary oESC-like.
出处 《现代生物医学进展》 CAS 2014年第6期1012-1016,共5页 Progress in Modern Biomedicine
基金 新疆自治区科技计划项目(20111113) 新疆自治区科技支疆项目(201291147) 国家转基因重大专项(2011ZX08008-003) 国家自然科学基金(U1203381)
关键词 胚胎干细胞 囊胚 绵羊胚胎 N2B27 Embryonic stem cells Blastocyst Sheep embryo N2B27
  • 相关文献

参考文献17

  • 1Evans M J, Kaufman MH. Establishment in culture of pluripotential cells from mouse embryos[J]. Nature, 1981,292:154-156.
  • 2Martin, GR. Isolation of a pluripotent cell line from early mouse embryos cultured in medium conditioned by teratocarcinoma stem cells[J]. Proc Natl Acad Sci, 1981, 78:7634-7638.
  • 3Thomson JA, ltskovitz-Eldor J, Shapiro SS, et al. Embryonic stem cell lines derived from human blastoeysts [J]. Science, 1998, 282(5391): 1145-1147.
  • 4Buehr M, Meek S, Blair K, et al. Capture of authentic embryonic stem cells from rat blastocysts [J]. Cell, 2008, 135(7): 1287-1298.
  • 5Talbot NC, Rexroad CE Jr, Pursel VG, et al. Alkaline phosphatase staining of pig and sheep epiblast cells in culture[J]. Mol Reprod Dev, 1993, 36(2): 139-147.
  • 6Zhu SX, Sun Z, Zhang JP. Ovine (Ovis aries) blastula from an in vitro production system and isolation of primary embryonicstem cell [J]. Zygote, 2007, 15(1): 35-41.
  • 7Dattena M, Pilichi S, Rocca S, et al. Sheep embryonic stem-like cells transplanted in full-thickness cartilage defects [J]. Tissue Eng Regen Med, 2009, 3(3): 175-187.
  • 8白昌明,刘丑生,王志刚,王新庄.不同培养体系对绵羊类胚胎干细胞分离、传代的影响[J].生物工程学报,2008,24(7):1268-1273. 被引量:4
  • 9Zhao Y, Lin J, Wang L,et al. Derivation and characterization of ovine embryonic stem-like cell lines in semi-defined medium without feeder cells [J]. Exp Zool A Ecol Genet Physiol, 2011, 315 (10): 639-648.
  • 10Pesce M, Scholer HR. Oct-4:control of totipotency and germ line determination [J]. Mol Reprod Dev, 2000, 55(4): 452-457.

二级参考文献7

共引文献3

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