›› 2013, Vol. 4 ›› Issue (1): 35-39.

• 论著 • 上一篇    下一篇

Runx蛋白在不同发育时期小鼠髁状突中的表达

张渊岫1,李强2,王震东2,许衍2,邵胜1,李琥1,马俊青3,胡佳艺4,尹璐5,陈文静2   

  1. 1. 南京医科大学附属口腔医院
    2. 南京医科大学口腔医学研究所
    3. 南京医科大学
    4. 江苏省口腔医院
    5. 南京市陆军指挥学院
  • 收稿日期:2012-11-02 修回日期:2013-01-22 出版日期:2013-03-25 发布日期:2013-03-30
  • 通讯作者: 陈文静 E-mail:chenwenjing_orth@163.com

Expression of Runx Family in the Development of the Mice Mandibular Condyle

  • Received:2012-11-02 Revised:2013-01-22 Online:2013-03-25 Published:2013-03-30

摘要: 目的 探索小鼠髁状突形态发育及此过程中RUNX蛋白的表达变化及意义。方法 取胚胎14.5 d(E14.5)至出生后7.5 d(P7.5)的小鼠下颌骨,制备髁突矢状位切片,苏木素—伊红(HE)染色观察。免疫组化方法检测RUNX蛋白表达分布。结果 E14.5开始,髁突间充质细胞聚集,而后逐渐分化出完整的软骨细胞分层,髁突逐渐由半圆变扁平。免疫组化示RUNX1、2阳性信号主要位于增殖层、前软骨细胞层及部分肥大层细胞,RUNX3阳性信号主要位于前软骨细胞层及肥大层。髁突前后部,RUNX1、2在前软骨细胞层的信号强度较肥大层更高。RUNX 的表达呈现双峰曲线。结论 髁突前后部成熟较晚,更易发生改建。RUNX1、2协同作用于软骨细胞分化早期,RUNX3调节作用于软骨细胞成熟期。

Abstract: Objective: To investigate the normal development of mandibular condylar cartilage in the mice, and to clarify the change of RUNX expression and its meaning. Methods: Mandibular condyle of Balb/c mice were fixed from embryonic day 14.5 (E14.5) through Postnatal day 7.5(P7.5). Samples were cut at the sagittal plane. The histomorphology were examined using Hematoxylin-eosin staining(HE). The RUNX protein levels and distribution were detected using immunohistochemistry (IHC). Results: The mesenchymal cell aggregation began at E14.5, followed by the appearance of full-layer differentiated chondrocytes. The condylar morphology developed from semicircular into flat form. IHC showed the expressions of RUNX1, 2 focused in the proliferation, prechondrocyte and part of the hypertrophic layer, while the RUNX3 mainly expressed in the prechondrocyte and hypertrophic layer. The RUNX1, 2 expressions, both in condyles’ anterior (ant) and posterior (post) segments, were relatively higher in the prechondrocyte layer than the hypertrophic layer. The expression level of all RUNX presented as bimodal curve. Conclusion: The anterior (ant) and posterior (post) segment of condyle remained in premature stage, which suggested its remodeling potential. RUNX1 cooperated with RUNX2 in mediating the early stage of chondrogenesis. RUNX3 played an important role in chondrocyte maturation.

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