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原代人成骨样细胞与hFOB 1.19细胞的比较:促炎细胞因子的对比作用

Comparison of Primary Human Osteoblast-like Cells and hFOB 1.19 Cells: Contrasting Effects of Proinflammatory Cytokines.

作者信息

Bousch Juliana Franziska, Beyersdorf Christoph, Schultz Katharina, Schnitker Matthis, Suschek Christoph Viktor, Maus Uwe

机构信息

Department for Orthopedics and Trauma Surgery at the University Hospital, Medical Faculty, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.

出版信息

Cells. 2025 Aug 15;14(16):1264. doi: 10.3390/cells14161264.

Abstract

Proinflammatory cytokines such as IL-1β, IL-6, and TNF-α are key mediators of inflammatory bone loss and are commonly described as inhibitors of osteoblast function. However, their effects on osteogenesis remain controversial, likely due to the differences in the cell models and experimental settings in in vitro studies. We recently showed that these cytokines significantly enhanced the mineralization of primary human osteoblast-like cells (OBs). Here, we provide the first analysis of cytokine effects on the osteogenesis of the widely used human osteoblastic cell line hFOB 1.19 and compare them to primary OBs. Unexpectedly, all three cytokines significantly inhibited mineralization in hFOB 1.19 cells without affecting the proliferation. IL-1β and TNF-α also suppressed ALP activity, whereas IL-6 acted ALP-independent but increased the osteogenic marker expression despite the reduced mineralization, indicating a possible uncoupled differentiation and mineralization. Morphological and transcriptional analyses indicated that hFOB 1.19 cells represent an earlier osteogenic differentiation stage, while primary OBs show phenotypic heterogeneity and donor-dependent expression profiles. These data demonstrate that proinflammatory cytokines can have severely different effects on the osteogenesis of different cell models, supported by the highly contradictory findings reported in the literature. Nevertheless, elucidating the mechanisms underlying the inhibition of osteogenesis in hFOB 1.19 cells may provide important insights into the cell model and differentiation-stage-specific cytokine effects.

摘要

白细胞介素-1β、白细胞介素-6和肿瘤坏死因子-α等促炎细胞因子是炎性骨丢失的关键介质,通常被描述为成骨细胞功能的抑制剂。然而,它们对成骨作用的影响仍存在争议,这可能是由于体外研究中细胞模型和实验设置的差异所致。我们最近发现,这些细胞因子能显著增强原代人成骨样细胞(OBs)的矿化作用。在此,我们首次分析了细胞因子对广泛使用的人成骨细胞系hFOB 1.19成骨作用的影响,并将其与原代OBs进行比较。出乎意料的是,所有三种细胞因子均显著抑制hFOB 1.19细胞的矿化作用,而不影响其增殖。白细胞介素-1β和肿瘤坏死因子-α也抑制碱性磷酸酶(ALP)活性,而白细胞介素-6的作用不依赖于ALP,尽管矿化减少,但却增加了成骨标志物的表达,这表明可能存在分化与矿化的解偶联。形态学和转录分析表明,hFOB 1.19细胞代表了更早的成骨分化阶段,而原代OBs表现出表型异质性和供体依赖性表达谱。这些数据表明,促炎细胞因子对不同细胞模型的成骨作用可能有截然不同的影响,文献中报道的高度矛盾的研究结果也支持了这一点。尽管如此,阐明hFOB 1.19细胞中抑制成骨作用的机制,可能会为细胞模型和分化阶段特异性细胞因子效应提供重要的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ec2/12384873/b000cde81cad/cells-14-01264-g001.jpg

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