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β-连环蛋白和腺瘤性结肠息肉病蛋白在小鼠牙胚发育中的表达及相互关系的研究 被引量:2

Expression of β-catenin and adenomatous polyposis coli protein and correlation between them in the development of mouse tooth germ
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摘要 目的观察β-连环蛋白(β-catenin)和腺瘤性结肠息肉病(APC)蛋白在胎鼠下颌第一磨牙牙胚中的表达,探讨两者的作用及相互关系。方法将昆明小鼠按雌雄比2∶1合笼,发现阴栓视为妊娠,定为E0.5d,制作E13.5d、E14.5d、E15.5d、E16.5d、E17.5d胎鼠下颌第一磨牙石蜡切片,免疫组化SP法检测β-catenin和APC蛋白的表达与分布。结果β-catenin在牙胚蕾状期、帽状期、钟状期上皮内均有表达,且随着发育的成熟,其表达逐渐增强,着色于细胞膜、质及核。APC蛋白在蕾状期牙蕾上皮呈强阳性表达,随着牙胚发育其表达逐渐减弱,着色在细胞膜、质。β-catenin与APC蛋白有显著的负相关性(P<0.01)。结论β-catenin表达于牙胚早期细胞核及细胞质内,提示其参与了牙胚早期的细胞增殖过程。β-catenin与APC蛋白的时空表达有重叠现象,并呈显著负相关,这符合WNT经典信号通路中两者的作用关系。 Objective To examine the distributions of β-catenin and adenomatous polyposis coli (APC) protein in the tooth germ, and obtain the messages of function of the two factors and the relationship between them. Methods Mice were selected and cohabited with the ratio of female mice to male ones being 2:1, and Embryo day 0.5 was confirmed based on the finding of vaginal plug. The distributions of β-catenin and APC protein in the Embryos on day 13.5, 14.5, 15.5, 16.5, 17.5 were examined in the paraffin-embedded sections by immunohistochemistry methods. Results During E13.5 d to E17.5 d, positive expression of β-catenin was found in the oral epithelium and the dental lamina, and became more and more strong. The staining were whole cell. During the bud stage, strong positive expression of APC protein was found in the oral epithelium and the dental lamina, but the expression displayed a down-regulation tendency. The staining was the cytomembrane and cytoplasm. There was negative correlation between β-catenin and APC protein(P〈0.01). Conclusion The result of β-catenin suggests its contribution in the early development of enamel organ and the proliferation of cell. Coincidance of the two factors staining site was found, according to the statistics.
出处 《华西口腔医学杂志》 CAS CSCD 北大核心 2009年第4期370-373,共4页 West China Journal of Stomatology
基金 国家自然科学基金资助项目(30700955/c03031102)
关键词 Β-连环蛋白 腺瘤性结肠息肉病蛋白 牙胚 免疫组化 β-catenin adenomatous polyposis coli protein tooth germ immunohistochemistry
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  • 1赵彤,朱梅刚,黄宗义,张亚历,张素娟,李梅芳.肺癌癌基因蛋白产物同步检测的对比分析[J].癌症,1995,14(1):13-15. 被引量:54
  • 2谷化平,冯和平,徐志勇,苏红.免疫组化在恶性黑色素瘤诊断中的作用[J].中国肿瘤临床,1996,23(8):599-600. 被引量:4
  • 3[1]Francis-West PH,Robson L,Evans DJR.Craniofacial Development:The tissue and molecular interactions that control development of the head.In:Beck F,Kriz W,Marani E,Sano Y,Schoenwolf GC,Zilles K.Eds.Advances in Anatomy Embryology and Cell Biology.Springer-Verlag:New York 2003. 被引量:1
  • 4[2]Mooney MP,Siegel MI,eds.Understanding craniofacial anomalies:The etiopathogenesis of craniosynostoses and facial clefting.New York:Wiley-Liss,2002 被引量:1
  • 5[3]Hill RE,Jones PF,Rees AR,et al.A new family of mouse homeo box-containing genes:molecular structure,chromosomal location,and developmental expression of Hox-7.1.Genes Dev 1989;3:26-37. 被引量:1
  • 6[4]Robert B,Sassoon D,Jacq B,Gehring W,Buckingham M.Hox7,a mouse homeobox gene with a novel pattern of expression during embryogenesis.EMBO J 1989;8:91-100. 被引量:1
  • 7[5]Holland PWH.Cloning and evolutionary analysis of msh-like homeobox genes from mouse,zebrafish and ascidian.Gene 1991;98:253-7. 被引量:1
  • 8[6]Ma L,Golden S,Wu L,Maxson R.The molecular basis of Boston-type craniosynostosis:the Pro148->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences.Hum Mol Genet 1996;5:1915-20. 被引量:1
  • 9[7]Dobias SL,Ma L,Wu H,Bell JR,Maxson R.The evolution of Msx gene function:expression and regulation of a sea urchin Msx class homeobox gene.Mech Dev 1997;61:37-48. 被引量:1
  • 10[8]Akimenko MA,Johnson SL,Westerfield M,Ekker M.Differential induction of four msx homeobox genes during fin development and regeneration in zebrafish.Development 1995;121:347-57. 被引量:1

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