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中华口腔医学研究杂志(电子版) ›› 2020, Vol. 14 ›› Issue (05) : 294 -301. doi: 10.3877/cma.j.issn.1674-1366.2020.05.004

所属专题: 文献

基础研究

血管内皮生长因子对临界下颌骨缺损纳米骨块移植的影响
杜兵1, 刘伟珍2, 杜钺3,()   
  1. 1. 佛山第二人民医院口腔医学中心 528000
    2. 南方医科大学附属口腔医院牙周科,广州 511400
    3. 大连医科大学基础医学院病理学教研室 116044
  • 收稿日期:2020-06-14 出版日期:2020-10-01
  • 通信作者: 杜钺

The effect of vascular endothelial growth factor on the healing of nano block bone grafting in critical-sized mandibular defects

Bing Du1, Weizhen Liu2, Yue Du3,()   

  1. 1. Center of Stomatology, The Second People′s Hospital of Foshan, Foshan 528000, China
    2. Department of Periodontics, Affiliated Stomatological Hospital of Southern Medical University, Guangzhou 511400, China
    3. Department of Pathology, Dalian Medical University, Dalian 116044, China
  • Received:2020-06-14 Published:2020-10-01
  • Corresponding author: Yue Du
  • About author:
    Corresponding author: Du Yue, Email:
  • Supported by:
    Natural Science Foundation of Guangdong Province(2016A030310240); Medical and Technological Key project of Foshan(2018AB002711)
引用本文:

杜兵, 刘伟珍, 杜钺. 血管内皮生长因子对临界下颌骨缺损纳米骨块移植的影响[J]. 中华口腔医学研究杂志(电子版), 2020, 14(05): 294-301.

Bing Du, Weizhen Liu, Yue Du. The effect of vascular endothelial growth factor on the healing of nano block bone grafting in critical-sized mandibular defects[J]. Chinese Journal of Stomatological Research(Electronic Edition), 2020, 14(05): 294-301.

目的

研究血管内皮生长因子(VEGF)对临界下颌骨缺损块状骨移植骨愈合的影响。

方法

4只比格犬,于每侧下颌骨建立4个标准化临界骨缺损。利用半口对照设计将单纯纳米羟基磷灰石珊瑚骨块(nHA/coral)和复合VEGF的nHA/coral植于缺损中,VEGF/nHA/coral组为实验组,nHA/coral组为对照组。3、8周后处死动物,通过Masson和vWF免疫组化染色观察新生血管和骨组织生长情况;通过双荧光标记观察钙化骨组织新生情况。采用SPSS 18.0统计分析软件,对vWF免疫组化染色的新生血管密度和荧光标记的钙化新生骨面积比数据进行独立样本t检验统计分析。

结果

3周时,Masson染色可见蓝染的胶原蛋白表达活跃,结构尚未成熟,与nHA/coral组相比,VEGF/nHA/coral组新生骨胶原纤维相对成熟整齐,局部可见骨陷窝、有钙盐沉积的骨细胞以及与伴行的血管系统。8周时,两组均可见蓝色的骨细胞和骨样组织以及成熟的骨性胶原纤维排列整齐而致密,新生骨胶原分布均明显增宽增多,有编织骨形成,红蓝相间。免疫组化染色结果显示:3周时,nHA/coral组和VEGF/nHA/coral组的新生血管密度分别为(105 ± 31)和(146 ± 33)个/mm2,实验组明显高于对照组(P<0.05)。8周时,两组的新生血管数量均有显著增加至(269 ± 67)和(341 ± 71)个/mm2,差异无统计学意义(P>0.05)。荧光标记组织形态测量结果显示:3周时,nHA/coral组和VEGF/nHA/coral组的钙化新生骨面积比分别为(0.79 ± 0.21)%和(1.08 ± 0.29)%,组间差异有统计学意义(P<0.05);8周时,两组的钙化新生骨面积比分别为增长至(4.25 ± 1.13)%和(5.21 ± 1.07)%,组间差异无统计学意义(P>0.05)。

结论

局部应用血管内皮生长因子可在骨愈合早期阶段显著提高血管新生和新生骨矿化程度。

Objective

To study the effect of vascular endothelial growth factor on the healing of nano block bone grafting in critical-sized mandibular defects.

Methods

Four critical-sized defects in each side of mandible of four Beagle dogs were built. There were two groups in our study, i.e., the VEGF/nHA/coral group acted as the experimental group, and the nHA/coral group as the control group. Pure nano-hydroxyapatite/coralline blocks and VEGF-coated blocks were implanted into the above defects in a split-mouth design. In three and eight weeks, the animals were euthanized, and the angiogenesis and bone regeneration in both groups were histologically observed by Masson′s trichrome and vWF staining technique. Newly formed calcified bone was evaluated by two fluorescents labeling technique. Neovascular density of vWF immunohistochemical stained blood vessels and the percentage of fluorescent marked calcified new bone area were statistically analyzed in two independent sample t-test in SPSS 18.0.

Results

At three weeks in two groups, from the Masson stained images, newly formed trabecular bone was obvious with immature collagen fibers disorderly arranged and blue stained. Compared to the newly-formed bone in nHA/coral group, collagen fibers in VEGF/nHA/coral group were relatively more mature and regular arranged; Osteoblasts were surrounded by osteoid bone, which evoluted into bone cells and bone lacuna; Calcium salt deposited bone cells and bone lacuna structure were blue stained. At eight weeks in both groups, blue stained bone cells and mature bone with better aligned and wider collagen fibers were observed; Mature collagen matrix secretion was significantly increased, and some woven bone formation can be easily found. In addition, immunohistochemical analysis revealed that compared to the nHA/coral samples (105 ± 31 vessels/mm2) , the VEGF/nHA/coral samples showed an increase in the neovascular density (146 ± 33 vessels/mm2) at three weeks, with a significant difference between the two groups (P< 0.05) . At eight weeks, with the increasement of bone healing time, the quantity of new blood vessels in the two groups significantly increased. The neovascular density innHA/coral group and VEGF/nHA/coral group increased to 269 ± 67 and 341 ± 71, respectively, without significant difference (P>0.05) . Fluorescence analysis results indicated that at three weeks, the percentage of calcified new bone area was (0.79 ± 0.21) % for the nHA/coral group and (1.08 ± 0.29) % for the VEGF/nHA/coral group, with a significant difference between two groups (P<0.05) . At eight weeks, fluorescence labeled new bone in periphery and internal of scaffolds was significantly increased, and yellow tetracycline fluorescence can be easily observed in the different parts of blocks in two groups. PMBF in both groups increased to (4.25 ± 1.13) % and (5.21 ± 1.07) %, respectively, with no significant difference (P>0.05) .

Conclusion

The local delivery of VEGF can significantly improve neovascularization and mineralization of newly formed bone at the early stage of block bone healing in this dog implantation model.

图1 纳米羟基磷灰石珊瑚骨块的外貌和规格
图2 临界慢性兔下颌骨缺损模型建立及纳米羟基磷灰石/珊瑚(nHA/coral)骨块植入骨缺损过程 A:全麻加局麻下采用分根法拔除兔双侧下颌第二、三、四前磨牙以及第一和第二磨牙(P2-M2),分别在双侧下颌骨制备出4个标准化箱型临界慢性骨缺损;B:一期手术后8周获得的慢性骨缺损面观;C:对箱型骨缺损进行重新塑形,将nHA/coral骨块和血管内皮细胞生长因子(VEGF)/nHA/coral骨块组分别植入骨缺损内
图3 骨块-骨组织样本不脱钙切片荧光标记的新生骨的ZEN 2009 Light Edition软件测量和分析示意图 A:通过ZEN 2009 Light Edition软件打开图片,此界面为split界面,展示不同通道所有图片;B:点击2D所呈现的界面;C:纳米羟基磷灰石/珊瑚(nHA/coral)和血管内皮细胞生长因子(VEGF)/nHA/coral骨块-骨组织样本颊舌向切割并制作不脱钙硬组织切片,激光共聚焦显微镜下拍摄数码整体图;D:使用IPP软件测量支架总面积和钙化新生骨组织面积,白线代表支架边框
图4 纳米羟基磷灰石/珊瑚(nHA/coral)骨块的大体观察和表面形貌观察分析 A:nHA/coral骨块大体观表面晶体和多孔结构;B:nHA/coral骨块具有和天然珊瑚一样的不规则连通多孔结构,且表面呈灰白色,利用nano measurer软件画出孔结构横切直径(SEM);C:利用nano measurer软件查看报告,并导出测量的孔径数据;D:nHA/coral骨块表面均匀排列着指状纳米级白色晶体,部分晶体在基底部融合为一体,利用nano measurer软件画出纳米羟基磷灰石晶体横直径(SEM);E:利用nano measurer软件查看报告,并导出测量的晶体直径数据
图5 不同时间点两组样本Masson染色脱钙切片的组织学观察 A:3周时纳米羟基磷灰石/珊瑚(nHA/coral)组可见新骨生成,蓝染的胶原蛋白表达活跃;B:3周时血管内皮细胞生长因子(VEGF)/nHA/coral组可见蓝染骨陷窝,相伴行的血管系统较为丰富;C:8周时nHA/coral组可见蓝色的骨细胞和骨样组织以及成熟的骨性胶原纤维排列整齐而相对致密;D:VEGF/nHA/coral组8周时成熟的新生骨组织胶原分布均明显增宽增多,钙盐沉积明显,红蓝相间;蓝染结构为骨基质胶原,nv代表新生血管,nb代表新生编织骨,黑色箭头所示为线性排列的成骨细胞
图6 vWF染色免疫组化脱钙切片的组织学观察和组织形态测量分析 A:vWF染色的脱钙切片;B:vWF染色的脱钙切片放大;C:vWF免疫组织化学染色的新生血管密度对比分析( ± sn = 8),aP<0.05,bP<0.01;箭头所指的深棕色着色结构为vWF染色阳性的新生血管
图7 双荧光标记的硬组织切片激光共聚焦观察 A:纳米羟基磷灰石/珊瑚(nHA/coral)组绿色钙黄绿素荧光明显呈现网状,主要分布在支架周边尤其是近宿主骨-支架界面处;B:3周时血管内皮细胞生长因子(VEGF)/nHA/coral组绿色钙黄绿素荧光带相对较多,部分进入到网孔状骨块内部;C:8周时nHA/coral组黄色和绿色荧光标记的新骨在支架周边和内部均有明显显现;D:8周时VEGF/nHA/coral组的荧光带尤其是黄色荧光明显更多。蓝色箭头所指的是钙黄绿素标记的绿色荧光带,白色箭头所指的是盐酸四环素标记的黄色荧光带,O代表宿主骨(旧骨),S代表支架(骨块)
表1 不同时间点钙化新生骨面积比的组间比较(%, ± s
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