期刊文献+

siRNA干扰CLEC2B基因沉默对黑素细胞的影响

Effects of RNA Interference Inducing CLEC2B Gene Silence on Melanocytes
下载PDF
导出
摘要 目的探讨小干扰RNA(small interfering RNA,siRNA)诱导淋巴细胞中CLEC2B(C-type lectin domain family 2,member B)基因沉默后,其淋巴细胞上清液对黑素细胞增殖活性的影响,从而揭示CLEC2B基因参与白癜风发病的免疫学机制。方法选用Jurkat淋巴瘤细胞及B16黑素瘤细胞为研究对象,应用RNA干扰技术沉默淋巴细胞CLEC2B mRNA的表达,MTT法检测CLEC2B基因沉默后淋巴细胞增殖情况及其上清液作用后对黑素细胞增殖情况。结果CLEC2B基因沉默后淋巴细胞增殖无明显影响,CLEC2B基因沉默后淋巴细胞上清液对黑素细胞的抑制作用降低,黑素细胞存活率增加(P<0.05)。结论 CLEC2B基因表达下调后减弱对黑素细胞的抑制作用,提示CLEC2B基因影响黑素细胞增殖活性,从而参与白癜风发病。 Objective To observe effect on that whether lymphocytes' supernatant could influence melanocytes proliferation or not when CLEC2B gene expression is silenced by establishing the lymphocytes transient silencing system, representing CLEC2B participation path in the immunity mechanism of vitiligo. Methods The lymphocytes lines Jurkat and melanocytes lines B16 were selected. CLEC2B gene was silenced by RNA interference technique, the proliferation of melanocytes and lymphocytes were detected by MTF. Results The lymphocyte proliferation had no significantly change, lymphocytes' supernatant could decrease the suppression to melanocytes proliferation (P〈0.05), so as to create beneficial environment for melanocytes living rate. Conclusion Silencing CLEC2B gene could influence melanocytes proliferation by the way of affecting lymphocytesI function. It shows that CLEC2B is participated in the immune-pathogenesis.
出处 《中国中西医结合皮肤性病学杂志》 CAS 2013年第1期17-19,共3页 Chinese Journal of Dermatovenereology of Integrated Traditional and Western Medicine
基金 天津市自然科学基金(09JCYBJC09600)
关键词 白癜风 CLEC2B基因 黑素细胞 Vitiligo CLEC2B gene Melanocyte
  • 相关文献

参考文献7

  • 1张峻岭,徐士福,柳君如,程琳,ZHOU Youwen.CLEC2B基因过表达的Jurkat细胞培养上清液对黑素瘤细胞B16的影响[J].中国中西医结合皮肤性病学杂志,2012,11(6):348-350. 被引量:4
  • 2杨萍,严金川,刘培晶.siRNA反向转染法提高原代悬浮细胞转染效率的应用[J].江苏大学学报(医学版),2010,20(3):267-269. 被引量:9
  • 3Pfaffl MW. A new mathematical model for relative quantification in real-time RT-PCR[J]. Nucleic Acids Res, 2001, 29: e45.
  • 4Holmskov U, Malhotra R, Sim RB, et al. Collectins: collagenous C- type lectins of the innate immune defense system[J]. Immunol Today, 1994, 15: 67-74.
  • 5Ljunggren HG. Cancer immunosurveillanee: NKG2D breaks cover [J]. Immunity, 2008, 28: 492-494.
  • 6Kuttruff S, Koch S, Kelp A, et al. NKp80 defines and stimulates a reactive subset of CD8 T cells[J]. Blood, 2009, 113: 358-369.
  • 7Eichler W, Ruschpler P, Wobus M, et al. Differentially induced expression of C-type lectins in activated lymphocytes[J], J Cell Biochem Suppl, 2001, Supp136: 201-208.

二级参考文献12

  • 1Bi F,Liu N,Fan D.Small interfering RNA:a new tool for gene therapy[J].Curr Gene Ther,2003,3(5):411-417.
  • 2Elbashir SM,Harborth J,Lendeckel W,et al.Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells[J].Nature,2001,411(6836):494-498.
  • 3Echeverri CJ,Perrimon N.High-throughput RNAi screening in cultured cells:a user's guide[J].Nat Rev Genet,2006,7(5):373-384.
  • 4LaPan P,Zhang J,Pan J.et al.Quantitative optimization of reverse transfection conditions for 384-well siRNA library screening[J].Assay Drug Dev Technol,2008,6(5):683-691.
  • 5Erfle H,Simpson JC,Bastiaens PI,et al.siRNA cell arrays for high-content screening microscopy[J].Biotechniques,2004,37(3):454-458.
  • 6Erfle H,Neumann B,Liebel U,et al.Reverse transfection on cell arrays for high content screening microscopy[J].Nat Protoc,2007,2(2):392-399.
  • 7Brummelkamp TR,Bernards R,Agami R.Stable suppression of tumorigenicity by virus mediated RNA interference[J].Cancer Cell,2002,2(3):243-247.
  • 8Fujita S,Ota E,Sasakia C,et al.Highly efficient reverse transfection with siRNA in multiple wells of microtiter plates[J].J Biosci Bioeng,2007,104(4):329-333.
  • 9Hamann J,Montgomery KT,Lau S. AICL:a new activationinduced antigen encoded by the human NK gene complex[J].Immunogenetics,1997.295-300.
  • 10Eichler W,Ruschpler P,Wobus M. Differentially induced expression of C-type lectins in activated lymphocytes[J].Journal of Cellular Biochemistry Supplement,2001,(Suppl 36):201-208.

共引文献10

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