Department of Orthopaedics and Trauma Surgery, Musculoskeletal University Center Munich (MUM), University Hospital, Ludwig Maximilian University (LMU) Munich, Munich, Germany.
Gene Center, Laboratory for Functional Genome Analysis, University Hospital, Ludwig Maximilian University (LMU) Munich, Munich, Germany.
Front Immunol. 2022 Feb 11;13:820843. doi: 10.3389/fimmu.2022.820843. eCollection 2022.
Endoprosthetic loosening still plays a major role in orthopaedic and dental surgery and includes various cellular immune processes within peri-implant tissues. Although the dental and orthopaedic processes vary in certain parts, the clinical question arises whether there are common immune regulators of implant loosening. Analyzing the key gene expressions common to both processes reveals the mechanisms of osteoclastogenesis within periprosthetic tissues of orthopaedic and dental origin.
Donor peripheral blood mononuclear cells (PBMCs) and intraoperatively obtained periprosthetic fibroblast-like cells (PPFs) were (co-)cultured with [± macrophage-colony stimulating factor (MCSF) and Receptor Activator of NF-κB ligand (RANKL)] in transwell and monolayer culture systems and examined for osteoclastogenic regulations [MCSF, RANKL, osteoprotegerin (OPG), and tumor necrosis factor alpha (TNFα)] as well as the ability of bone resorption. Sequencing analysis compared dental and orthopaedic (co-)cultures.
Monolayer co-cultures of both origins expressed high levels of OPG, resulting in inhibition of osteolysis shown by resorption assay on dentin. The high OPG-expression, low RANKL/OPG ratios and a resulting inhibition of osteolysis were displayed by dental and orthopaedic PPFs in monolayer even in the presence of MCSF and RANKL, acting as osteoprotective and immunoregulatory cells. The osteoprotective function was only observed in monolayer cultures of dental and orthopaedic periprosthetic cells and downregulated in the transwell system. In transwell co-cultures of PBMCs/PPFs profound changes of gene expression, with a significant decrease of OPG (20-fold dental versus 100 fold orthopaedic), were identified. Within transwell cultures, which offer more like conditions, RANKL/OPG ratios displayed similar high levels to the original periprosthetic tissue. For dental and orthopaedic implant loosening, overlapping findings in principal component and heatmap analysis were identified.
Thus, periprosthetic osteoclastogenesis may be a correlating immune process in orthopaedic and dental implant failure leading to comparable reactions with regard to osteoclast formation. The transwell cultures system may provide an like model for the exploration of orthopaedic and dental implant loosening.
内假体松动仍然是矫形和牙科手术中的一个主要问题,包括种植体周围组织中的各种细胞免疫过程。尽管牙科和矫形过程在某些方面有所不同,但临床上出现了一个问题,即是否存在假体松动的共同免疫调节剂。分析这两个过程中共同的关键基因表达可以揭示骨科和牙科来源的假体周围组织中破骨细胞形成的机制。
将供体外周血单核细胞(PBMCs)和术中获得的假体成纤维细胞样细胞(PPFs)与(±巨噬细胞集落刺激因子(MCSF)和核因子 kappaB 配体受体激活剂(RANKL))在 Transwell 和单层培养系统中共同培养,并检测破骨细胞生成调节因子[MCSF、RANKL、骨保护素(OPG)和肿瘤坏死因子 alpha(TNFα)]以及骨吸收能力。测序分析比较了牙科和矫形(共)培养物。
两种来源的单层共培养物均表达高水平的 OPG,导致牙本质吸收测定中骨溶解的抑制。在单层培养中,即使存在 MCSF 和 RANKL,牙科和矫形 PPFs 也表现出高水平的 OPG 表达、低 RANKL/OPG 比值和骨溶解抑制作用,表现为成骨保护和免疫调节细胞。成骨保护功能仅在牙科和矫形假体周围细胞的单层培养中观察到,并在 Transwell 系统中下调。在 PBMCs/PPFs 的 Transwell 共培养中,发现基因表达发生了深刻变化,OPG 显著减少(牙 20 倍,矫形 100 倍)。在更类似于条件的 Transwell 培养物中,RANKL/OPG 比值显示出与原始假体组织相似的高水平。对于牙科和矫形种植体松动,主成分和热图分析中发现了重叠的发现。
因此,假体周围的破骨细胞形成可能是矫形和牙科种植体失败的一个相关免疫过程,导致破骨细胞形成的类似反应。Transwell 培养系统可能为探索矫形和牙科种植体松动提供一个更类似于体内的模型。