Li Xiao-Feng, Xue Chun-Chun, Zhao Yong-Jian, Cheng Shao-Dan, Zhao Dong-Feng, Liang Qian-Qian, Chen Lin, Wang Qiang, Lu Sheng, Shi Qi, Wang Yong-Jun, Shu Bing
Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Spine Research Institute, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Spine (Phila Pa 1976). 2017 Jan 1;42(1):E8-E14. doi: 10.1097/BRS.0000000000001701.
Neovascularization and expression of inflammatory cytokines were examined in Osteoprotegerin (Opg) knockout (KO) mice that show intervertebral disc (IVD) degeneration.
The aim of this study was to clarify the pathological changes in lumbar IVD degeneration in Opg KO mice.
Osteoporosis is a controversial risk factor for IVD degeneration. Deletion of Opg resulted in IVD degeneration in mice. Neovascularization and inflammatory cytokines are key factors in IVD degeneration.
Opg KO mice and their wild-type (WT) littermates were euthanized. Lumbar IVDs were harvested. Safranin O/Fast Green staining was performed to examine the pathological changes. Microcomputed tomographic (micro-CT) analysis was performed to determine the structural changes at the junction of lumbar IVD cartilage and vertebrae. Tartrate-resistant acid phosphatase (TRAP) staining was performed to evaluate osteoclast formation. Protein expression of vascular endothelial growth factor A (VEGF-A), CD31, VE-cadherin, CD 34, interleukin-1β (IL-1β), and tumor necrosis factors α (TNF-α) were analyzed by immunohistochemistry (IHC) assays. Gene expressions of IL-1β, IL-6, and TNF-α were analyzed by real-time polymerase chain reaction (RT-PCR).
In 12-week-old Opg KO mice, new bone was formed in the endplate cartilage of lumbar IVDs and this became more obvious in 24-week-old Opg KO mice. Three-dimensional (3D) μCT reconstruction analyses showed that the edges of the L4 and L5 vertebrae were rugged with bone marrow cavities in it. Protein expression of VEGF-A, CD31, VE-cadherin, and CD34 was increased in the endplate and growth plate of lumbar IVDs of Opg KO mice. Gene expression of IL-1β, IL-6, and TNF-α as well as protein expression of IL-1β and TNF-α were highly expressed in the lumbar IVDs of Opg KO mice.
Deletion of Opg leads to increased neovascularization and expression of inflammatory cytokines in the lumbar disc in Opg KO mice, which may play important roles in IVD degeneration.
N/A.
在表现出椎间盘(IVD)退变的骨保护素(Opg)基因敲除(KO)小鼠中检测新生血管形成及炎性细胞因子的表达。
本研究旨在阐明Opg基因敲除小鼠腰椎IVD退变的病理变化。
骨质疏松症是IVD退变的一个有争议的危险因素。Opg基因缺失导致小鼠IVD退变。新生血管形成和炎性细胞因子是IVD退变的关键因素。
对Opg基因敲除小鼠及其野生型(WT)同窝小鼠实施安乐死。采集腰椎IVD。进行番红O/固绿染色以检查病理变化。进行微型计算机断层扫描(micro-CT)分析以确定腰椎IVD软骨与椎体交界处的结构变化。进行抗酒石酸酸性磷酸酶(TRAP)染色以评估破骨细胞形成。通过免疫组织化学(IHC)检测分析血管内皮生长因子A(VEGF-A)、CD31、血管内皮钙黏蛋白、CD 34、白细胞介素-1β(IL-1β)和肿瘤坏死因子α(TNF-α)的蛋白表达。通过实时聚合酶链反应(RT-PCR)分析IL-1β、IL-6和TNF-α的基因表达。
在12周龄的Opg基因敲除小鼠中,腰椎IVD终板软骨中有新骨形成,在24周龄的Opg基因敲除小鼠中这种情况变得更加明显。三维(3D)μCT重建分析显示,L4和L5椎体边缘凹凸不平,内部有骨髓腔。Opg基因敲除小鼠腰椎IVD终板和生长板中VEGF-A、CD31、血管内皮钙黏蛋白和CD34的蛋白表达增加。Opg基因敲除小鼠腰椎IVD中IL-1β、IL-6和TNF-α的基因表达以及IL-1β和TNF-α的蛋白表达均高表达。
Opg基因缺失导致Opg基因敲除小鼠腰椎间盘新生血管形成增加和炎性细胞因子表达增加,这可能在IVD退变中起重要作用。
无。