期刊文献+

LIF诱导小鼠胚胎后肾间充质细胞分化形成肾上皮细胞

LIF on Induced Mesenchymal-epithial Conversion in Mouse Metanephros
下载PDF
导出
摘要 目的观察白血病抑制因子(Leukemia inhibitory factor,LIF)能否诱导后肾间充质细胞(metanephric mesenchymal cells,MMCS)分化形成肾上皮细胞,并探讨其机制。方法取孕11.5天的小鼠胚胎,分离后肾间充质组织,去除输尿管芽,Pax-2染色鉴定。对鉴定后的肾间充质细胞进行体外培养,并在培养液中加入细胞因子成纤维细胞生长因子(FGF2)、转化生长因子(TGF-α)和LIF进行诱导,用免疫荧光染色和RT-PCR检测后肾间充质细胞分化形成肾上皮细胞过程中的形态学和基因表达变化。结果经细胞因子LIF处理,后肾间充质细胞由排列杂乱无序的细胞发育形成有连续基底膜的肾小球。RT-PCR检测发现上皮细胞标记因子(E-caderin、CollagenⅣ、podocalyxin)的表达逐渐增高。结论 LIF能诱导后肾间充质细胞分化形成肾上皮细胞,可为肾脏疾病的细胞治疗提供实验依据。 Objective To investigate the biological characteristic in mesenchymal-epithial conversion. Methods We isolated the metanephric mesenchyme cells from E11.5 embryo without Ureteric Bud and identified it with Pax-2 staining. Results The isolated metanephric mesenchyme cells developed from a disorganised array into small chains with continuous basement membranes in the presence of Leukemia inhibitory factor (LIF).And RT-PCR results showed the expression of the marker protein of epithelial cell,such as E-cadherin,Collagen Ⅳ,and podocalyxin were also affected. Conclusion LIF induced mesenchymal-epithial conversion in mouse metanephros.
出处 《中南医学科学杂志》 CAS 2014年第1期31-35,共5页 Medical Science Journal of Central South China
基金 湖南省自然科学衡阳市联合基金(10JJ9016)资助
关键词 后肾间充质细胞 上皮细胞 白血病抑制因子 诱导 metanephric mesenchyme cells epithelial cells Leukemia inhibitory factor induce
  • 相关文献

参考文献1

二级参考文献37

  • 1苟永禧.自体脾组织移植的研究[J].临床军医杂志,2000,28(4):29-30. 被引量:3
  • 2Clarke JC, Pate SR, Raymond RM Jr, Andrew S, Robinson BG, Dressler GR, Brophy PD. Regulation of c-Ret in the developing kidney is responsive to Pax2 gene dosage. Human Mol Genet, 2006, 15(23): 3420-3428.
  • 3Li X, Oghi KA, Zhang J, Krones A, Bush KT, Glass CK, Nigam SK, Aggarwal AK, Maas R, Rose DW, Rosenfeld MG. Eya protein phosphatase activity regulates Six1-Dach-Eya transcriptional effects in mammalian organogenesis. Nature, 2003, 426(6964): 247-254.
  • 4Sajithlal G, Zou D, Silvius D, Xu PX. Eya1 acts as a critical regulator for specifying the metanephric mesenchyme. Dev Biol, 2005, 284(2): 323-336.
  • 5Gong KQ, Yallowitz AR, Sun HS, Dressler GR, Wellik DM. A Hox-Eya-Pax complex regulates early kidney developmental gene expression. Mol Cell Biol, 2007, 27(21): 7661-7668.
  • 6Dziarmaga A, Hueber PA, Iglesias D, Hache N, Jeffs A, Gendron N, Mackenzie A, Eccles M, Goodyer P. Neuronal apoptosis inhibitory protein is expressed in developing kidney and is regulated by Pax2. Am J Physiol Renal Physiol, 2006, 291(4): F913-F920.
  • 7Dziarmaga A, Eccles M, Goodyer P. Suppression of ureteric bud apoptosis rescues nephron endowment and adult renal function in Pax2 mutant mice. J Am Soc Nephrol, 2006, 17(6): 1568-1575.
  • 8Hu MC, Mo R, Bhella S, Wilson CW, Chuang PT, Hui CC, Rosenblum ND. Gli3-dependent transcriptional repression of Gli1, Gli2 and kidney patterning genes disrupts renal morphogenesis. Development, 2005, 13(3): 569-578.
  • 9Narlis M, Grote D, Gaitan Y, Boualia SK, bouchard M. Pax2 and Pax8 regulate branching morphogenesis and nephron differentiation in the developing kidney. J Am Soc Nephrol, 2007, 18(4): 1121-1129.
  • 10Torban E, Dziarmaga A, Iglesias D, Chu LL, Vassilieva T, Little M, Eccles M, Discenza M, Pelletier J, Goodyer P. Pax2 activates WNT4 expression during mammalian kidney development. J Biol Chem, 2005, 281(18): 12705-12712.

共引文献9

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