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四氯二苯二噁英致胎鼠腭裂作用机制的初步探讨 被引量:8

Mechanism of cleft palate in mice induced by 2, 3, 7, 8-tetrachlorodibenzo-p-dioxin
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摘要 目的探讨四氯二苯二噁英(2,3,7,8-tetrachlorodibenzo-p-dioxin,TCDD)致胎鼠先天性腭裂的可能作用机制。方法12只C57BL/6J孕鼠于妊娠第10天随机分为实验组和对照组,每组6只,实验组以TCDD64μg/kg灌胃,对照组以等量玉米油灌胃,于妊娠第18.5天在解剖显微镜下观察胎鼠腭裂的发生率。另取18只C57BL/6J孕鼠,于妊娠第10天随机分为实验组和对照组,每组9只,处理方法同前,根据标本采集时间不同,每组又分为妊娠第13.5、14.5和15.5天3个亚组,每个亚组3只,分别于妊娠第13.5、14.5和15.5天剪取胎鼠腭突组织提取RNA和DNA,采用RT—PCR检测Smad2~4及Smad7mRNA的表达情况、甲基化特异性PCR(methylmion specific PCR,MSP)检测转化生长因子-β3(transforming growthfactor—β3,TGF—β3)基因启动子甲基化水平。两样本间均数比较采用t检验。结果TCDD成功诱导建立C57BL/6J胎鼠先天性腭裂模型,实验组腭裂发生率为100%,对照组无腭裂发生。在妊娠第13.5、14.5和15.5天,RT—PCR显示实验组Smad2mRNA的相对表达值分别为0.263±0.088、0.296±0.016和0.159±0.027,对照组为0.180±0.042、0.282±0.029和0.165±0.018,差异无统计学意义(t=-1.474、-0.762、0.321,P〉0.05);实验组Smad3mRNA的相对表达值分别为0.453±0.153、0.551±0.160和0.328±0.049,对照组为0.375±0.126、0.510±0.145和0.259±0.035,差异无统计学意义(t=-0.678、-0.336、-2.005,P〉0.05);实验组Smad4mRNA的相对表达值分别为0.675±0.174、0.577±0.070和0.396±0.066,对照组为0.557±0.138、0.587±0.080和0.441±0.054,差异无统计学意义(t=-0.926、0.161、0.927,P〉0.05);实验组Smad7mRNA的相对表达值分别为0.283±0.050、0.320±0.068和0.169±0.045,对照组为0.207±0.043、0.288±0.051和0.15 Objective To explm'e the mechanism of cleft palate in mice induced by 2, 3, 7, 8- Tetrachlorodibenzo pdioxin (TCDD). Methods On gestation day 10 (GD 10), 12 pregnant mice were randmnly divided into two groups as the treated group and the eontrol group with 6 mice in each group. The mice in the treated group received intragastric administration with 64 p,g TCDD/kg, while the mice in the control group received equivalent corn oil. The embryos were examined under stereomicroscope to detect the incidence of cleft palate on GD 18.5. Another 18 pregnant mice were randomly divided into two groups (treated group and control group) on GD 10 with 9 pregnant mice in each group. Then each group was divided into 3 subgroups: GD 13.5, GD 14.5 and GD 15.5, with 3 pregnant mice in each subgroup. The palatal shelves were dissected from the embryos for RNA and DNA extraction on GD 13.5, GD 14, 5 and GD 15.5. At last the expression of Smad 24 and Smad 7 mRNA was investigated by RT-PCR, and the TGF-153 promoter methylamine levels were investigated by methylmion specific PCR ( MSP). Results The cleft palate mice model was established successfully by exposing pregnant C57BL/6J mice to TCDD. Total frequency of clefts was 100% in TCDD group, and the frequency of clefts was 0 in the control group. The relative expression of Smad 2 mRNA was 0. 263 ± 0. 088, 0. 296± 0. 016 and 0. 159 ± 0. 027 in TCDD group, 0. 180 ±0. 042, 0. 282 ± 0. 029 and 0. 165 ± 0. 018 in control group. The relative expression of Smad 3 mRNA was 0. 453 ±0. 153, O. 551 ±0. 160 and 0. 328 ±0. 049 in TCDD group, 0. 375 ± 0. 126, 0. 510 ±0. 145 and 0. 259 ±0. 035 in control group. The relative expression of Smad 4 mRNA was 0. 675 ± 0. 174, 0. 577 ±0. 070 and 0. 396 ±0. 066 in TCDD group, 0. 557 ±0. 138, 0. 587 ±0. 080 and 0. 441 ± 0. 054 in control group. The relative expression of Smad 7 mRNA was 0. 283 ± 0. 050, 0. 320 ± 0. 068 and 0. 169 ±0.045 in TCDD group, 0.207 ±0.043, 0.288 ±0.051 and 0.155 ±0.040 in control group. Ther
出处 《中华整形外科杂志》 CAS CSCD 北大核心 2011年第6期448-453,共6页 Chinese Journal of Plastic Surgery
基金 重庆市自然科学基金重点项目(2009BA5085)
关键词 腭裂 四氯二苯二噁英 转化生长因子-Β3 Cleft palate Tetrachlorodibenzo-p-dioxin Transforming growth factor-β3
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参考文献19

  • 1Fujiwara K, Yamada T, Mishima K, et al. Morphological and immunohlsto-chemical studies on cleft palates induced by 2, 3, 7, 8-tetrachiorodibenzo-p-dioxin in mice. Congenit Anom (Kyote) , 2008, 48(2) :68-73. 被引量:1
  • 2Gan LQ, Fu YX, Liu X, et al. Transforming growth factor-β3 expression up-regulates on cleft palates induced by 2, 3, 7, 8- tetrachlorodibenzo-p-dioxin in mice. Toxicol Ind Health, 2009, 25 ( 7 ) :473-478. 被引量:1
  • 3李承浩,石冰,何苇,蒙田,卢胜军.TCDD和B6联合作用下小鼠腭板形态的扫描电镜观察[J].口腔医学研究,2010,26(1):1-3. 被引量:6
  • 4Yu W, Ruest LB, Svoboda KK. Regulation of epithelialmesenehymal transition in palatal fusion. Exp Biol Med (Maywood) , 2009, 234(5) :483-491. 被引量:1
  • 5Lamouille S, Derynck R. Emergence of the phosphoinositide 3- kinase-Akt-marnmalian target of rapamyein axis in transforming growth factor-β-indueed epithelial-mesenehymal transition. Cells Tissues Organs, 2011, 193(1-2) :8-22. 被引量:1
  • 6Dudas M, Nagy A, Laping N J, et al. Tgf-beta3-induced palatal fusion is mediated by Alk-5/Smad pathway. Dev Biol, 2004, 266( 1 ) :96-108. 被引量:1
  • 7Iordanskaia T, Nawshad A. Mechanisms of transforming growth factor 13 induced cell cycle arrest in palate development. J Cell Physiol, 2011, 226 ( 5 ) : 1415-1424. 被引量:1
  • 8Kuriyama M, Udagawa A, Yoshimoto S, et al. DNA methylation changes during cleft palate formation induced by retinoic acid in mice. Cleft Palate Craniofac J, 2008, 45 (5) :545-551. 被引量:1
  • 9Thomae TL, Stevens EA, Bradfield CA. Transforming growth factor-133 restores fusion in palatal shelves exposed to 2, 3, 7, 8- Tetra-chlorodlbenzo-p-dloxin. Biological Chemistry, 2005, 280 ( 13 ) : 12742-12746. 被引量:1
  • 10Fitzpatrick DR, Denhez F, Kondaiah P, et al. Differential expression of TGF beta isoforms in murine palatogenesis. Development, 1990, 109 (3) :585-595. 被引量:1

二级参考文献20

  • 1李志萍,孙宏晨,欧阳喈.TGFα和TGFβ3基因多态性与国人非综合征型唇腭裂发病关系的研究[J].实用口腔医学杂志,2006,22(5):667-671. 被引量:11
  • 2Ivkovic S, Yoon B S, Popoff S N, et al. Connective tissue growth factor coordinates chondrogenesis and angiogenesis during skeletal development [J]. Development, 2003,130 ( 12): 2779-2791. 被引量:1
  • 3Mao B,Niehrs C. Kremen2 modulates Dickkopf2 activity during Wnt/LRP6 signaling [J]. Gene, 2003, 302 ( 1-2 ): 179-183. 被引量:1
  • 4Gabriele P, Sharon A P, Michael V W, et al. Transforming grown factor β 3 is required for secondary palate fusion[J]. Nature Genetics Volumn, 1995,11 (4): 409-414. 被引量:1
  • 5Proetzel C,Pawlowaki S A,Wiles W V,et al. Transforming growth factor- β 3 is required for secondary palate fusion[J]. Nat Genet, 1995,11 (4): 409-414. 被引量:1
  • 6Lidral A C,Romitti P A,Basart A M. Association of MSX1 and TGF β 3 with nonsyndromic clefting in humans[J]. Am J Hum Genet, 1998, 63(2): 557-568. 被引量:1
  • 7Maestri N E, Beaty T H, Hetmanski J. Application of transmittion diseqilibrium tests to nonsysdromic oral clefts: Including candidate genes and environmental exposure in the models[J]. Am J Med Genet, 1997,73 ( 3 ):337-344. 被引量:1
  • 8Vieira A R, Orioli I M, Castilla E E, et al. MSX1 and TGF β 3 Contribute to clefiing in south America[J]. J Dent Res, 2003,82(4): 289-292. 被引量:1
  • 9Moreno L M,Arcos-Burgos M,Marazita M L,et al. Genetic analysis of candidate loci in nonsyndromic cleft lip families from Antioquia-Colombia and Ohio[J]. Am J Med Genet, 2004, 125 ( 2 ):135-144. 被引量:1
  • 10Beaty T H,Wang H,Hetmanski J B,et al. A case-control study of nonsyndromic oral clefts in Maryland[J]. Ann Epidemiol, 2001,11 (6): 434-442. 被引量:1

共引文献9

同被引文献53

  • 1黎燕,孙海鹏,苏放明.孕期服用叶酸预防和阻止小鼠腭裂的初步研究[J].中国妇幼保健,2006,21(17):2392-2393. 被引量:5
  • 2CHOPRA M, SCHRENK D. Dioxin toxicity, aryl hydrocarbon receptor signaling, and apoptosis-persistent pollutants affect programmed cell death [ J ]. Crit Rev Toxicol,2011,41 (4) :292-320. 被引量:1
  • 3PRATT R M,DENCKER L,DIEWERT V M. 2,3,7,8- tetrachlorodibenzo-p-dioxin induced cleft palate in the mouse: evidence for alterations in palatal shelf fusion [ J ]. Teratog Carcinog Mutagen, 1984,4 ( 5 ) :427-436. 被引量:1
  • 4FUJIWARA K, YAMADA T, MISHIMA K, et al. Morphological and immunohistochemical studies on cleft palates induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin in mice[J]. Congenit Anom,2008,48(2) :68-73. 被引量:1
  • 5GRITLI-LINDE A. Molecular control of secondary palate development [ J ]. Dev Biol, 2007,301 ( 2 ) : 309-326. 被引量:1
  • 6CUERVO R,COVARRUBIAS L. Death is the major fate of medial edge epithelial cells and the cause of basal lamina degradation during palatogenesis [ J ]. Development, 2004,131 ( 1 ) : 15 -24. 被引量:1
  • 7VAZIRI-SANI F, HALLBERG K, HARFE B D, et al. Fate-mapping of the epithelial seam during palatal fusion rules out epithelial-mesenchymal transformation [ J ]. Dev Biol,2005,285 (2) :490-495. 被引量:1
  • 8CARETTE M J, FERGUSON M W. The fate of medial edge epithelial cells during palatal fusion in vitro by DiI labelling and eonfocal microscopy [ J ]. Development, 1992,114 ( 2 ) : 379-388. 被引量:1
  • 9FERGUSON M W. Palate development [ J ]. Development, 1988,103:41-61. 被引量:1
  • 10YAMADA T, MISHIMA K, FUJIWARA K, et al. Cleft lip and palate in mice treated with 2, 3, 7, 8- tetrachlorodibenzo-p-dioxin: a morphological in vivo study[ J]. Congenit Anom ,2006,46( 1 ) :21-25. 被引量:1

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