期刊文献+

PMA诱导C6细胞rPer1,rDbp基因的近日节律表达 被引量:1

PMA-induced Circadian Gene Expression of rPer1,rDbp in C6 Cells
下载PDF
导出
摘要 目的寻找一种新的体外节律诱导剂以研究C6神经胶质瘤细胞近日节律基因的表达情况。方法采用PMA(phorbol12-myristate13-acetate),100nmol/L)及50%的马血清刺激体外培养的小鼠NIH-3T3细胞,RT-PCR检测不同时间点mPer1mRNA的表达水平,比较两者的诱导效率;PMA刺激体外培养的大鼠C6神经胶质瘤细胞,RT-PCR检测不同时间点rPer1,rDbpmRNA的表达水平。结果PMA及50%的马血清均能诱导NIH-3T3细胞mPer1的近日节律表达且诱导效率近似;并首次发现C6细胞的rPer1,rDbp基因存在着近日节律振荡。结论PMA是一种有效的体外节律诱导剂;经PMA诱导后,C6细胞的节律基因存在近日振荡,为体外研究授时因子对近日节律的导引机制提供依据。 Objective To investigate the expression level of circadian gene in C6 glioma cells by searching for a novel rhythm-inductor in vitro. Method In order to compare the induction efficiency of PMA with horse serum,the cultured NIH-3T3 cells were stimulated by PMA( phorbol 12-myristate 13-acetate , 100 nmol/L) and 50% horse serum respectively and performed RT-PCR to examine the expression of mPerl mRNAs at the indicated times. The cultured C6 glioma cells were also stimulated by PMA and examined the expression of rPerl, rObp mRNAs at the indicated times by RT-PCR. Result Both PMA and 50% horse serum could induce the circadian gene expression of mPerl in NIH- 3T3 cells and achieved similar induction efficiency ,and it was confirmed that circadian oscillation of rPerl ,rDbp existed in C6 glioma cells. Conclusion PMA is an effective rhythm inductor in vitro, and elicit the circadian oscillation of clock genes in C6 glioma cells, which confer an advantage to the investigation of circadian entrainment mechanisms in vitro.
出处 《航天医学与医学工程》 CAS CSCD 北大核心 2006年第6期462-464,共3页 Space Medicine & Medical Engineering
基金 国家自然科学基金资助项目(30470623 30470684)
关键词 近日节律 PMA period1基因 D6p基因 C6神经胶质瘤细胞 circadian PMA periodl gene Dbp gene C6 glioma cells
  • 相关文献

参考文献9

二级参考文献38

  • 1王跃锜,华慧,朱彬,尹华虎,刘延友,杨春蕾,王正荣.节律基因mPeriod2对Lewis肺癌细胞生长的影响[J].航天医学与医学工程,2005,18(3):222-223. 被引量:7
  • 2李光明,刘延友,朱彬,文世民,郎锦义,王正荣.鼻咽癌时辰放疗与常规放疗的比较[J].航天医学与医学工程,2006,19(3):225-227. 被引量:10
  • 3Camacho F,Cilio M,Guo Y,et al.Human casein kinase Idelta phosphorylation of human circadian clock proteins Period 1 and 2[J].FEBS Lett,2001,489(2-3):159-165. 被引量:1
  • 4Keesler GA,Camacho F,Guo Y,et al.Phosphorylation and destabilization of human Period I clock protein by human casein kinase I epsilon[J].NeuroReport,2000,11 (5):951-955. 被引量:1
  • 5Guillemot F,Billault A,Auffray C.Physical linkage of a guanine nucleotide-binding protein-related gene to the chicken major histocompatibility complex[J].Proc Nat Acad Sci USA,1989,86(12):4594 -4598. 被引量:1
  • 6Ron D,Chen CH,Caldwell J,et al.Cloning of an intracellular receptor for protein kinase C:a homolog of the beta subunit of G proteins[J].Proc Nat Acad Sci USA,1994,91(3):839-843. 被引量:1
  • 7Ceci M,Gaviraghi C,Gorrini C,et al.Release of elF6 (p27-BBP) from the 60S subunit allows 80S ribosome assembly[J].Nature,2003,426(6966):579-584. 被引量:1
  • 8Gerbasi VR,Weaver CM,Hill S,et al.Yeast Asc1p and mammalian RACK1 are functionally orthologous core 40S ribosomal proteins that repress gene expression[J].Molec Cell Biol,2004,24(18):8276-8287. 被引量:1
  • 9Mamidipudi V,Zhang J,Lee KC,et al.RACK1 regulates G1/S progression by suppressing Src kinase activity[J].Mol Cell Biol,2004,24(15):6788-6798. 被引量:1
  • 10Kiely PA,Leahy M,O'Gorman D,et al.RACK1-mediated integration of adhesion and insulin-like growth factor I (IGF-I) signaling and cell migration are defective in cells expressing an IGF-I receptor mutated at tyrosines 1250 and 1251[J].J Biol Chem,2005,280(9):7624-7633. 被引量:1

共引文献22

同被引文献2

引证文献1

二级引证文献1

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