期刊文献+

功能矫形后退大鼠下颌后髁突软骨改建的分子机制 被引量:1

Molecule mechanism of growth rat condylar cartilage remodeling after functional retraction of mandible
下载PDF
导出
摘要 目的:探讨功能矫形后退大鼠下颌后髁突软骨改建的分子调控机制。方法:SD大鼠40只,实验组配戴模拟临床功能矫治器,强制大鼠下颌后退,对照组不戴模拟矫治器,实验后3天、1、2、3周处死大鼠取髁突,HE染色观察组织学变化,免疫组织化学方法结合图像分析检测TGF-β1、TGF-βR1、IGF-1在髁突中的表达及分布。结果:实验组大鼠下颌后退1~2mm,镜下见颞下颌关节髁突软骨厚度增加,以生发层和过渡层增加明显,细胞数增多,细胞体积增大,核肥大深染。髁突各层软骨细胞均有TGF-β1、TGF-βR1和IGF-1的表达,免疫组织化学阳性染色相对面积和积分灰度的比较显示:在功能矫形后退下颌后,实验组TGF-β1、TGF-βR1和IGF-1的表达较对照组明显增强,其差异具有统计学意义(P<0.05)。结论:功能矫形后髁突软骨表现为增生改建、分化功能增强,其发生与TGF-β1、TGF-βR1和IGF-1的表达密切相关。 Objective: To investigate the molecule mechanism of growth rat condylar cartilage remodeling after functional retraction of mandible, neth .ods:Forty SD rats were randomly divided into experiment group and control group. The mimic functional appliances were used in experiment group to back off the mandible. The rats were killed for condylars after 3 days, 1 week, 2 weeks or 3 weeks. HE staining was used to detect the histological changes and immunohistochemical technique was used to detect the expression of TGF-β1,TGF-β R1 and IGF-I in condylar. Results:In experimental group,the rat mandibles fell back for 1-2 mm,and incrassation of condylar cartilage was detected in procreative layers and transitional layers. The amount and volume of the cells was aug- mented,and the karyon was increscent and fuscous, while the cytoplasm was reduced. TGF-β1,TGF-βR1 and IGF-1 were expressed throughout the condylar cartilage and the immunostain levels of experiment group were higher than those of control groups(P 〈 0.05). Conclusion: The condylar cartilage remodeling and enhanced differentiation are related with the expression of TGF-β1 ,TGF- β R1 and IGF-1.
出处 《南京医科大学学报(自然科学版)》 CAS CSCD 北大核心 2006年第8期702-705,F0003,共5页 Journal of Nanjing Medical University(Natural Sciences)
关键词 β转化生长因子-1 受体 胰岛素样生长因子-1 髁突软骨 transforming growth factor beta-1 receptor insulin-like growth factor 1 condylar cartilage
  • 相关文献

参考文献11

二级参考文献21

  • 1Oshima Y, Sakamoto T, Hisatomi T, et al. Gene transfer of soluble TGF-beta type Ⅱ receptor inhibits experimental proliferative vitreoretinopathy [J]. Gene Therapy,2002,Sep ,9( 18):1214-1220. 被引量:1
  • 2Enzmann V, Hollborn M, Wiedemann P, et al. Minor influence of the immunosuppressive cytokines IL-10 and TGF-beta on the proliferation and apoptosis of human retinal pigment epithelial (RPE) cells in vitro [J]. Ocul Immunol Inflamm, 2001,9 (4): 259-266. 被引量:1
  • 3Frank F, Zeisberg M, Renziehausen A, et al. TGF-β1induces proliferation in human renal fibroblast via induction of basic fibroblast growth factor (FGF-2) [J].Kidney Int, 2001,59 (2): 579-592. 被引量:1
  • 4Martin F, Pastor JC. Proliferative vitreoretinopathy:cytologic finding in vitreous samples [J]. Ophthalmic Res, 2003,35 (4): 232-238. 被引量:1
  • 5Kon OH, Occleston NL, Aylward GW, et al. Expression of vitreous cytokines in proliferative vitreoretinopathy:a prospective study [J]. Invest Ophthalmol Vis Sci,1999,40(3) :705-771. 被引量:1
  • 6Leung WK,Kim JJ,Kim JG,et al.Microsatellite instability in gastric intestinal metaplasia in patients with and without gastic cancer[J].Am J Pathol,2000,156:537-543. 被引量:1
  • 7Kim HS,Lee BL,Woo DK,et al.Assesment of markers for the identification of microsatellite instability phenotype in gastric neoplasmas[J] .Cancer Letters,2001,164:61-68. 被引量:1
  • 8Kim HS,Woo DK,Bae S,et al.Microsatellite instability in the adenoma-carcinoma sequence of the stomach[J].Laboratory Investigation,2000,18(1):57-64. 被引量:1
  • 9Kim J J,Baek M,Kim L,et al.Accumulated frameshift mutations at coding nucleotide repeats during the progression of gastric carcinoma with microsatellite instability[J].Laboratory Investigation,1999,79(9):1113-1120. 被引量:1
  • 10Schneider BG,Bravo JC,Roa JC,et al.Microsatellite instability,prognosis and metastasis in gastric cancers from a low-risk population [J].Int J Cancer,2000,89(5):444-452. 被引量:1

共引文献23

同被引文献8

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