Cellbricks GmbH, Berlin, Germany.
Department of Medical Biotechnology, Technische Universität Berlin, Berlin, Germany.
Sci Rep. 2021 Oct 6;11(1):19833. doi: 10.1038/s41598-021-99323-8.
Radiotherapy of head and neck squamous cell carcinoma can lead to long-term complications like osteoradionecrosis, resulting in severe impairment of the jawbone. Current standard procedures require a 6-month wait after irradiation before dental reconstruction can begin. A comprehensive characterization of the irradiation-induced molecular and functional changes in bone cells could allow the development of novel strategies for an earlier successful dental reconstruction in patients treated by radiotherapy. The impact of ionizing radiation on the bone-forming alveolar osteoblasts remains however elusive, as previous studies have relied on animal-based models and fetal or animal-derived cell lines. This study presents the first in vitro data obtained from primary human alveolar osteoblasts. Primary human alveolar osteoblasts were isolated from healthy donors and expanded. After X-ray irradiation with 2, 6 and 10 Gy, cells were cultivated under osteogenic conditions and analyzed regarding their proliferation, mineralization, and expression of marker genes and proteins. Proliferation of osteoblasts decreased in a dose-dependent manner. While cells recovered from irradiation with 2 Gy, application of 6 and 10 Gy doses not only led to a permanent impairment of proliferation, but also resulted in altered cell morphology and a disturbed structure of the extracellular matrix as demonstrated by immunostaining of collagen I and fibronectin. Following irradiation with any of the examined doses, a decrease of marker gene expression levels was observed for most of the investigated genes, revealing interindividual differences. Primary human alveolar osteoblasts presented a considerably changed phenotype after irradiation, depending on the dose administered. Mechanisms for these findings need to be further investigated. This could facilitate improved patient care by re-evaluating current standard procedures and investigating faster and safer reconstruction concepts, thus improving quality of life and social integrity.
头颈部鳞状细胞癌的放射治疗可导致骨坏死等长期并发症,从而严重损害颌骨。目前的标准程序要求在照射后等待 6 个月才能开始进行牙齿重建。对骨细胞中放射诱导的分子和功能变化进行全面描述,可以为接受放射治疗的患者开发出更早成功进行牙齿重建的新策略。然而,电离辐射对成骨细胞(即牙槽骨骨细胞)的影响仍然难以捉摸,因为以前的研究依赖于基于动物的模型和胎儿或动物源性细胞系。本研究首次提供了从原代人牙槽骨骨细胞获得的体外数据。从健康供体中分离和扩增原代人牙槽骨骨细胞。在接受 2、6 和 10 Gy 的 X 射线照射后,将细胞在成骨条件下培养,并分析其增殖、矿化以及标记基因和蛋白的表达。骨细胞的增殖呈剂量依赖性下降。虽然用 2 Gy 照射的细胞恢复了,但 6 和 10 Gy 剂量的应用不仅导致增殖永久受损,而且还导致细胞形态改变和细胞外基质结构紊乱,这通过胶原 I 和纤连蛋白的免疫染色得到证实。在接受任何检查剂量照射后,大多数研究基因的标记基因表达水平均下降,显示出个体间的差异。原代人牙槽骨骨细胞在照射后表现出明显的表型改变,这取决于所给予的剂量。需要进一步研究这些发现的机制。这可以通过重新评估当前的标准程序并研究更快、更安全的重建概念来改善患者护理,从而提高生活质量和社会完整性。