基础医学与临床 ›› 2012, Vol. 32 ›› Issue (5): 487-492.

• 研究论文 • 上一篇    下一篇

腺相关病毒介导的klotho基因表达对去势大鼠骨Runx2及MMP-13表达的影响

王艳娇1,马厚勋1,吴平2,李宝善1   

  1. 1. 重庆医科大学附属第一医院老年病科
    2. 重庆医科大学附属第一医院老年科 重庆
  • 收稿日期:2011-10-31 修回日期:2012-03-02 出版日期:2012-05-05 发布日期:2012-04-16
  • 通讯作者: 马厚勋 E-mail:mahouxun1966@yahoo.com.cn
  • 基金资助:
    klotho基因单核苷酸多态性及组合与衰老相关性疾病关系;klotho cDNA腺相关病毒载体及其在衰老相关性疾病与靶器官损害中的作用机制

Effects of adeno-associated virus-mediated klotho gene delivery on the expression of runx2 and mmp-13 gene in the bone of the ovariectomy rats

  • Received:2011-10-31 Revised:2012-03-02 Online:2012-05-05 Published:2012-04-16

摘要: 摘要:目的 探讨腺相关病毒介导的klotho(KL)基因表达对去势骨质疏松大鼠的调控作用。方法 SD雌性大鼠随机分为假手术组(S组)和手术组,外科去势术后12周再随机分为模型组(O组)、17β-雌二醇组(E组)、KL基因组(KO组)和空质粒组(GO组),实验12周后处死。取股骨、胫骨测骨密度;冰冻切片及免疫组化法观察肾KL荧光及KL蛋白表达;RT-PCR和免疫组化法检测骨Runx2、MMP-13 mRNA及蛋白表达;HE染色观察骨组织形态学变化。结果 KO组和E组骨密度高于O组和GO组(P<0.05);KO组大鼠肾有小鼠KL基因特异性表达;与O组相比,KO组Runx2 mRNA表达明显上调,MMP-13 mRNA表达显著下调(P<0.05);免疫组化分析KO组Runx2吸光度值为411±96,显著高于O组的353±50(P<0.05);KO组MMP-13 吸光度值为397±84,显著低于O组的656±89(P<0.05)。KO组、E组和S组大鼠骨小梁排列紧密,连接成网,形态结构较完整,明显优于O组和GO组。结论 KL基因表达上调可减缓去势大鼠骨质疏松症的发展及骨组织微结构的破坏,提示KL基因可能在骨质疏松症的发展中扮演重要角色。

关键词: 关键词:骨质疏松, klotho, Runx2, MMP-13, 骨代谢

Abstract: Abstract: Objective To research on the effect of the recombinant adeno-associated virus vector containing klotho gene delivery to regulate for ovariectomized rats.Methods Female SD rats were randomly divided into sham operation group (S group) and model group.Model was successfully constructed with ovariectomy after 12 weeks,they were randomly divided into model group (O group), 17β-estradiol (E group), klotho gene group (KO group), empty vector group (GO group), all were sacrificed after 12 weeks.Bone mineral density(BMD) of the femurs and tibia were measured. The fluorescent expression of renal klotho was observed by Cryo-sectioning Technique.The Runx2 and MMP-13 mRNA expression of bone tissue were detected by reverse transcription-polymerase chain reaction(RT-PCR).Expression of klotho protein in kidney and Runx2,MMP-13 protein in bone were detected by immunohistochemistry. Bone morphological changes of the different groups were observed by HE staining.Results BMD of KO and E groups were significantly higher than those in the O and GO groups(P<0.05). Specific expression of mouse klotho was seen only in KO group.Renal klotho protein in KO group were increased obviously by immunohistochemistry.Compared to O group,the expression of Runx2 mRNA increased greatly,but the expression of MMP-13 mRNA decreased in bone tissue of KO group (P<0.05). Immunohistochemistry analysis showed,the average absorbance of Runx2 was 411±96 in KO group,it was a significant higher than 353±50 of O group(P<0.05). The average absorbance of MMP-13 was 397±84 in KO group,the value of O group was 656±89,so KO group showed a significantly lower than those in O group (P<0.05).The trabecular bones in KO,E,S groups tightly packed, interconnected to form a network,had relatively complete histologic structure.Conclusion Klotho gene delivery attenuates the progression of osteoporosis and bone microstructure damage in ovariectomized rats, these results suggest that klotho gene may play a role in the progression of osteoporosis.

Key words: Key words: osteoporosis, klotho, Runx2, MMP-13, bone metabolism

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