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Leukocytes Enhance Inflammatory and Catabolic Degenerative Changes in the Intervertebral Disc After Endplate Fracture In Vitro Without Infiltrating the Disc

机译:终板体外破裂后白细胞增强椎间盘的炎症性和分解代谢性退行性变化,而不会渗入椎间盘

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Study Design.An established rabbit intervertebral disc (IVD)/endplate explant fracture model was extended with physiologic post-traumatic dynamic loading (PTDL) and coculturing of peripheral blood mononuclear cells (PBMCs).Objective.The aim of this study was to quantify the effects of PTDL and of cocultured PBMCs on post-traumatic disc degeneration (DD) and to determine whether PTDL facilitates homing of PBMC to fractured IVD/endplates.Summary of Background Data.DD is associated with endplate fracture. In vivo studies suggest a key role of immune cells in the pathogenesis of DD. However, the complexity of in vivo systems impedes the investigation of single factors governing the pathogenesis.Methods.Seventy-two IVD/endplate specimens were divided into 4 groups. In group A, endplate fractures were induced with a high-velocity axial load and exposed to PTDL in coculture with PBMCs for 14 days. Group A was compared with 3 control groups, with single-factor removal, in order to assess the relative contribution of PTDL (group B), PBMCs (group C), and endplate fracture (group D) to the biological response of the IVD. Disc gene transcription and serum nitric oxide (NO) serum concentration were measured to investigate differences in anabolism, catabolism, and inflammatory response between the groups. Changes in matrix composition and disc structure were assessed histologically.Results.PBMCs did not home to fractured IVDs, with or without PTDL. Group A compared with group D showed an enhanced transcription of anabolic, catabolic, and pro-inflammatory genes during the entire experiment, and an increased NO concentration for the first 3 days. Changes typical for DD were also found in histological sections. Group A compared with group C showed significant increases in catabolic and pro-inflammatory gene transcription after at least 7 days. No differences were found between groups A and B.Conclusion.Trauma induces degenerative changes; PTDL neither aggravates nor ameliorates this response. Although PBMCs do not infiltrate the disc, they aggravate the degenerative changes.Level of Evidence: N/A
机译:研究设计:采用创伤后生理学动态负荷(PTDL)和外周血单个核细胞(PBMC)共同培养的方法,建立了已建立的兔椎间盘(IVD)/终板外植体骨折模型。 PTDL和共培养的PBMC对创伤后椎间盘退变(DD)的影响,并确定PTDL是否有助于将PBMC归巢至破裂的IVD /终板。背景数据摘要DD与终板骨折相关。体内研究表明免疫细胞在DD的发病机理中起着关键作用。然而,体内系统的复杂性阻碍了对控制发病机理的单一因素的研究。方法:将72例IVD /终板标本分为4组。在A组中,在高速轴向载荷下诱发终板骨折,并与PBMC共培养14天,暴露于PTDL中。为了评估PTDL(B组),PBMC(PBC)(C组)和终板骨折(D组)对IVD生物学反应的相对贡献,将A组与3个对照组进行了单因素去除比较。测量了椎间盘基因转录和血清一氧化氮(NO)的浓度,以研究两组之间代谢,分解代谢和炎症反应的差异。通过组织学评估基质成分和椎间盘结构的变化。与D组相比,A组在整个实验过程中均显示出合成代谢,分解代谢和促炎基因的转录增强,并且前3天NO浓度升高。在组织学切片中也发现了典型的DD改变。与C组相比,A组在至少7天后显示出分解代谢和促炎基因转录的显着增加。结论:创伤引起的退行性改变; PTDL既不会加重也不会改善这种反应。尽管PBMC不会渗入椎间盘,但会加剧退化性变化。证据级别:N / A

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