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Expression of Fas receptor and apoptosis in vertebral endplates with degenerative disc diseases categorized as Modic type I or II.

机译:Fas受体的表达和椎间盘退变伴椎间盘退变疾病的I型或II型分类。

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STUDY DESIGN: Vertebral endplate tissues were obtained from patients with degenerated lumbar disc classified as Modic type 1 or type 2 and investigated with immunohistochemical staining and the DNA nick end labelling techniques. OBJECTIVE: To examine the expression of fas receptor (FasR) and apoptosis in the endplate cells isolated from patients with degenerative disc disease and to see whether they are associated with the pathological change of endplate. METHODS: Fifty-six degenerated lumbar endplate specimens were obtained from the patients with degenerative disc disease categorized as type Modic I or II in magnetic resonance imaging (MRI) and eight nondegenerated specimens as control (vertebra burst fracture patients without degenerative change in MRI) during surgical procedures. Immunohistochemical staining was performed to determine the presence of FasR and apoptosis in sections of those endplate tissues. To investigate whether the FasR expression and apoptosis in endplate were influenced by degeneration and ageing of the discs, the level of FasR expression and apoptosis in the changed and unchanged endplates was analysed. RESULTS: FasR were expressed in the cytoplasm of the endplate cells. A higher degree of FasR expression and apoptosis in endplate cells in degenerated discs was found than that in nondegenerated discs. In cell culture, the level of FasR expression and apoptosis in cells from the degenerative endplates was higher than those in unchanged endplates. The percentage of FasR-positive endplate and apoptotic endplate cells correlated significantly with the patient's age (r=0.301, p<0.05; r=0.307, p<0.05. respectively), but not with the degree of disc degeneration in MRI (r=0.047, p>0.05; r=0.066, p>0.05, respectively). CONCLUSION: This is the first study to compare the expression of FasR and apoptosis on vertebral endplate cells in degenerated disc with in nondegenerated disc. The results show that the endplate in degenerated disc may undergo fas-mediated apoptosis and vice versa, endplate degenerative changes may promotes apoptosis of the endplate cells within degenerated disc.
机译:研究设计:椎间盘终末组织是从腰椎间盘退变患者分类为Modic 1型或2型的,并通过免疫组织化学染色和DNA缺口末端标记技术进行研究。目的:检测退行性椎间盘疾病患者终板细胞中fas受体(FasR)的表达和细胞凋亡,并探讨其是否与终板病理变化有关。方法:在磁共振成像(MRI)中,将退行性椎间盘疾病的患者分类为Modic I或II型,将56例退行性腰椎终板标本作为对照,将8例未退变的腰椎终板标本作为对照(椎体爆裂性骨折,但无退行性改变的MRI患者)外科手术。进行免疫组织化学染色以确定那些终板组织切片中FasR的存在和凋亡。为了研究椎间盘的变性和老化是否影响终板中FasR的表达和凋亡,分析了改变后的和未改变的终板中FasR的表达和凋亡水平。结果:FasR在终板细胞的细胞质中表达。发现在退化的椎间盘中终板细胞中FasR表达和凋亡的程度高于未退化的椎间盘中。在细胞培养中,来自变性终板的细胞中FasR表达和细胞凋亡的水平高于未改变终板的细胞。 FasR阳性终板和凋亡终板细胞的百分比与患者年龄显着相关(r = 0.301,p <0.05; r = 0.307,p <0.05),但与MRI椎间盘退变的程度无关(r = 0.047,p> 0.05; r = 0.066,p> 0.05)。结论:这是第一个比较FasR在退化性椎间盘和非退化性椎间盘中在椎终板细胞中的表达和凋亡的研究。结果表明,退变椎间盘中终板可能经历由fas介导的凋亡,反之亦然,终板退行性改变可能促进退变椎间盘中终板细胞的凋亡。

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