期刊文献+

阻遏蛋白β-TrCP在小鼠牙胚不同发育时期的表达与意义 被引量:1

β-transduction Repeat Containing Protein Expressed in Tooth Germs and Ameloblast and Odontoblast of Different Stage of Tooth Development
下载PDF
导出
摘要 目的观察Sonic hedgehog(shh)信号转导通路的阻遏蛋白-βTrCP在小鼠牙胚发育不同时期的表达情况,探讨-βTrCP在晚期牙胚发育中的作用与意义。方法取不同发育时期的鼠胚、乳鼠鼠头标本,用标记生物素链亲和素LsAB法观察β-TrCP蛋白在不同发育时期牙胚组织的表达情况。结果β-TrCP在胚胎10.5、13.5、14.5、16.5、18.5 d的小鼠牙胚上皮层与间充质层,以及出生后0、3、6 d的小鼠成釉细胞与成牙本质细胞胞浆呈特征性表达。结论-βTrCP在正常发育小鼠牙胚及成釉细胞与成牙本质细胞特征性表达,提示-βTrCP在牙胚发育中维持/限定shh信号通路的正常信号转导具有重要意义。 Objective The Sonic hedgehog signalling peptide has been demonstrated to play important roles in the growth and patterning of the tooth development. This study aims on whether the antagonist β-transduction repeat containing protein of Sonic hedgehog signal transduction expressed in tooth germs ameloblast and odontoblast or not. Methods The mouse embryo heads of different developmental stages of E10.5, E13.5, E14.5, E16.5, E18.5 and P0, P3, P6 after birth were acquired fixed with 4% paraformaldehyde for 48 hours, embeded with Paraffin and examined using LsAB (labelled streptavidin-biotin) method to observe the β-TrCP expression pattern in tooth germs, ameloblast and edontoblast. Results It was demonstrated that β-TrCP expressed in oral epithelium, tooth bud, mesenchymal cell cytoplasm of ameloblast and edontoblast of different stage of tooth development. Conclusion β-TrCP expressed from early stage to later stage of murine tooth development. And these findings provide the evidence of antagonist regulatory pathways for shh in teeth development.
出处 《华西口腔医学杂志》 CAS CSCD 北大核心 2007年第2期195-197,共3页 West China Journal of Stomatology
基金 国家自然科学基金资助项目(30471904和30572051) 教育部重点资助项目(106134)
关键词 牙胚 成釉细胞 成牙本质细胞 tooth germs ameloblast edontoblast
  • 相关文献

参考文献9

  • 1Cohen MM Jr.The hedgehog signaling network[J].Am J Med Genet A,2003,123 (1):5-28.
  • 2Miletich I,Cobourne MT,Abdeen M,et al.Expression of the hedgehog antagonists Rab23 and slimb/beta-TrCP during mouse tooth development[J].Arch Oral Biol,2005,50(2):147-151.
  • 3Ballarino M,Marchioni M,Carnevali F.The Xenopus laevis betaTrCP gene:Genomic organization,alternative splicing,5'and 3'region characterization and comparison of its structure with that of human beta-TrCP genes[J].Biochim Biophys Acta,2002,1577(1):81-92.
  • 4Wang B,Li Y.Evidence for the direct involvement of beta-TrCP in Gli3 protein processing[J].Proc Natl Acad Sci U S A,2006,103 (1):33-38.
  • 5Jiang J,Struhl G.Regulation of the hedgehog and wingless signalling pathways by the F-box/WD40-repeat protein slimb[J].Nature,1998,391 (6666):493-496.
  • 6Wang G,Wang B,Jiang J.Protein kinase A antagonizes hedgehog signaling by regulating both the activator and repressor forms of cubitus interruptus[J].Genes Dev,1999,13 (21):2828-2837.
  • 7Pan Y,Bai CB,Joyner AL,et al.Sonic hedgehog signaling regulates Gli2 transcriptional activity by suppressing its processing and degradation[J].Mol Cell Biol,2006,26(9):3365-3377.
  • 8Smelkinson MG,Kalderon D.Processing of the drosophila hedgehog signaling effector Ci-155 to the repressor Ci-75 is mediated by direct binding to the SCF component slimb[J].Curr Biol,2006,16(1):110-116.
  • 9Bhatia N,Thiyagarajan S,Elcheva I,et al.Gli2 is targeted for ubiquitination and degradation by beta-TrCP ubiquitin ligase[J].J Biol Chem,2006,281 (28):19320-19326.

同被引文献18

  • 1潘克清,杨丕山,李纾,戚向敏.Runt相关基因2/核心结合因子a1在小鼠牙周组织发育中的免疫组化定位研究[J].口腔医学,2005,25(3):172-175. 被引量:5
  • 2郑莉琴,戴银清,张彦定.牙齿发育与再生[J].组织工程与重建外科杂志,2007,3(1):1-6. 被引量:8
  • 3Li L, Kwon HJ, Harada H, et al. Expression patterns of ABCG2, Bmi-l, Oct-3/4, and Yap in the develo?ping mouse incisor[J]. Gene Expr Patterns, 2011, 11 (3/4): 163-170.
  • 4Buttitta LA, Edgar BA. How size is controlled: From Hippos to Yorkies[J]. Nat Cell BioI, 2007, 9(11): 1225-1227.
  • 5Pan D. Hippo signaling in organ size control[J]. Genes Dev, 2007, 21(8):886-897.
  • 6Dong J, Feldmann G, Huang J, et al. Elucidation of a universal size-control mechanism in Drosophila and mammals[J]. Cell, 2007, 130(6):1120-1133.
  • 7Kanai F, Marignani PA, Sarbassova D, et al. TAZ: A novel transcriptional co-activator regulated by in?teractions with 14-3-3 and PDZ domain proteins[J]. EMBO J, 2000, 19(24):6778-6791.
  • 8Komuro A, Nagai M, Navin NE, et al. WW domain?containing protein YAP associates with ErbB-4 and acts as a co-transcriptional activator for the carboxyl?terminal fragment of ErbB-4 that translocates to the nuc1eus[J]. J BioI Chem, 2003, 278(35):33334-33341.
  • 9Basu S, Totty NF, Irwin MS, et al. Akt phosphory?lates the Yes-associated protein, YAP, to induce interaction with 14-3-3 and attenuation of p73- mediated apoptosis[J]. Mol Cell, 2003, 11(1): 11-23.
  • 10Espinosa JF, Syud FA, Gellman SH. An autono?mously folding beta-hairpin derived from the human Y AP65 WW domain: Attempts to define a minimum ligand-binding motif[J]. Biopolymers, 2005, 80(2/3):303-311.

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