期刊文献+

先天性腭裂形成中胚胎腭器官的电镜观察 被引量:1

Electron Microscopic Study of the Embryonic Palate during Cleft Palate Formation
下载PDF
导出
摘要 背景与目的:建立先天性腭裂模型观察其形成过程中胚胎腭突细胞的超微结构改变。材料与方法:于NIH雌性小鼠受孕第12.5d(GD12.5)通过腹腔注射磷酸地塞米松(50mg/kg)诱发NIH小鼠胚胎先天性腭裂模型,同时设正常对照组注射生理盐水相同条件下饲养。实验组和对照组母鼠分别于GD13.5、GD14.5、GD15.5脱颈处死,剖腹取出胎鼠,切取胎鼠头部制作光镜和电镜样本,采用扫描电镜和透射电镜观察胚胎腭发育及先天性腭裂形成过程中腭突细胞的超微结构。结果:随着胚胎发育,对照组腭突双侧裂隙逐渐变小,上皮基底膜破坏,腭突中嵴上皮细胞(MEE)细胞核染色质呈块状并边集,并可见上皮细胞内出现分泌物质,胚腭间充质细胞(EPM)细胞之间基质丰富,胚胎GD15.5腭突完全融合;实验组腭突生长缓慢,体积较同期对照组小,随着腭突的发育,腭突表层MEE细胞仍然连接紧密,基底膜完整,上皮细胞多层化,细胞表面出现纤毛,EPM细胞之间基质较少,在GD15.5形成裂隙。结论:地塞米松作用后胚胎腭突细胞的正常发育分化受到影响,从而导致腭裂形成。 BACKGROUND AND AIM: To observe the ultrastructure of embryonic palate cells during cleft palate formation using the model of congenital cleft palate. MATERIALS AND METHODS: The model of congenital cleft palate was induced in NIH mice by intraperitoneaL injection of dexamethasone on GD12.5. The control group was raised under the same condition except the injection of dexamethasone. The mice was sacrificed by cervical dislocation on GD13.5, GD14.5 and GD15.5. The fetal mice were removed and the heads were cut for light and electron microscopic studies.The embryonic palate and the palatal cells were examined by SEM and TEM during the process of the palate development and congenital cleft palate formation. RESULTS: In the control group, with the embryonic development, the cleft was diminished, basal epithelial membrane was broken down, pieces of nuclear chromatin became marginated, excretion appeared in the MEE cell, the matrix was abundant between EPM cells, palatine shelves were fused completely on GD15.5. In the experimental group, palatine shelf grew slowly, and was smaller than the control group at the same time point, MEE cells on the palatine shelf surface were connected tightly yet with the development of palatine shelves, basal membrane remained intact, epithelial cell became multiplayer, cilia appeared on the cell surface, the matrix was less between EPM cells, the cleft was formed on GD15.5. CONCLUSION: The development and differentiation of embryonic palatal cells were affected after being exposed to dexamethasone, which was associated with cleft palate formation.
出处 《癌变.畸变.突变》 CAS CSCD 2008年第3期175-177,共3页 Carcinogenesis,Teratogenesis & Mutagenesis
关键词 先天性腭裂 胚胎 电镜观察 congenital cleft palate embryo electron microscope
  • 相关文献

参考文献6

  • 1傅豫川.腭裂发生机制的生物学基础[M]//樊明文.口腔医学新进展.武汉:武汉科学技术出版社,2000:129-144.
  • 2Ferguson MJ. Palate development[ J ] . Development, 1990, 103 (suppl) :41 - 60
  • 3Reddy CS, ltanumaiah B, Hayes TG, et al. Developmental stage specificity and dose response of secalonic acid D-induced cleft palate and the absence of cytotoxicity in developing mouse palate[ J ]. Toxicol Appl Pharmacol, 1986, 84 (2) : 346 - 354.
  • 4Abbott BD, Harris MW, Birnbaum LS. Comparisons of the effects of TCDD anti hydrocortisone on growth factor expression provide in sight into their interaction in the embryonic palate [J]. Teratology, 1992, 45(1) :35 - 47.
  • 5邓末宏,龙星,李宏礼,董红梅.地塞米松诱发先天性腭裂对TGF-β_1、TGF-β_2表达的影响[J].实用口腔医学杂志,2003,19(6):598-600. 被引量:2
  • 6黄磊,石冰,孙晋虎,王.地塞米松对体外培养A系小鼠腭突腭中嵴上皮融合的影响[J].华西口腔医学杂志,2005,23(2):103-105. 被引量:5

二级参考文献9

  • 1[1]Gehris AL,D'Angelo M,Greene RM,et al.Immunodetection of the transforming growth factors beta 1 and beta 2 in the developing murine palate.Int J Dev Biol,1991,35(1):17
  • 2[2]Gehris AL,Greene RM.Regulation of murine embryonic epithelial cell differentiation by transforming growth factors beta.Differentiation,1992,49(3):167
  • 3[3]Sharpe PM,Foreman DM,Carette MJ,et al.The effects of transforming growth factor-beta 1 on protein production by mouse embryonic palate mesenchymal cells in the presence or absence of serum.Arch Oral Biol,1992,37(3):39
  • 4[4]Foreman DM,Sharpe PM,Ferguson MW.Comparative biochemistry of mouse and chick secondary-palate development in vivo and vitro with particular emphasis on extracellular matrix moleculars and the effects of growth factor on their synthesis.Arch Oral Biol,1991,36(6):457
  • 5Hassell JR. The development of rat palatal shelves in vitro. An ultrastructural analysis of the inhibition of epithelial cell death and palate fusion by the epidermal growth factor[J]. Dev Biol, 1975,45(1) :90-102.
  • 6Bulleit RF, Zimmerman EF. The influence of the epithelium on palate shelf reorientation [J]. J Embryol Exp Morphol, 1985,88 (8): 265-279.
  • 7邓末宏,董红梅,李宏礼,傅豫川.地塞米松在诱发先天性腭裂发病中对表皮生长因子受体表达的影响[J].口腔颌面外科杂志,2000,10(3):225-227. 被引量:4
  • 8石冰,孙晋虎,王大章,左晖.地塞米松和维生素B_(12)对A系小鼠胚胎腭突细胞生长因子基因表达的影响[J].四川大学学报(医学版),2003,34(1):27-30. 被引量:5
  • 9石冰,左晖,毛祖彝.地塞米松诱发小鼠腭裂时AnnexinⅠ、cPLA_2和PCNA表达的研究[J].中华口腔医学杂志,2003,38(3):188-191. 被引量:6

共引文献4

同被引文献170

引证文献1

二级引证文献14

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