Laboratory of Cell Proliferation & Ageing, Institute of Biosciences & Applications, NCSR "Demokritos", 153 10, Athens, Greece.
Biogerontology. 2013 Dec;14(6):741-51. doi: 10.1007/s10522-013-9449-0. Epub 2013 Aug 10.
Loss of teeth increases with age or after genotoxic treatments, like head and neck radiotherapy, due to periodontium breakdown. Periodontal ligament fibroblasts represent the main cell type in this tissue and are crucial for the maintenance of homeodynamics and for its regeneration. Here, we have studied the characteristics of human periodontal ligament fibroblasts (hPDLF) that became senescent after replicative exhaustion or after exposure to ionizing radiation, as well as their ability for osteoblastic differentiation. We found that senescent hPDLF express classical markers of senescence, as well as a catabolic phenotype, as shown by the decrease in collagen type I and the increase of MMP-2 expression. In addition, we observed a considerably decreased expression of the major transcription factor for osteoblastic differentiation, i.e. Runx2, a down-regulation which was found to be p53-dependent. In accordance to the above, senescent cells have a significantly decreased alkaline phosphatase gene expression and activity, as well as a reduced ability for osteoblastic differentiation, as found by Alizarin Red staining. Interestingly, cells from both type of senescence express similar characteristics, implying analogous functions in vivo. In conclusion, senescent hPDLF express a catabolic phenotype and express a significantly decreased ability towards an osteoblastic differentiation, thus probably affecting tissue development and integrity.
随着年龄的增长或接受头部和颈部放射治疗等遗传毒性治疗,牙齿会脱落,这是由于牙周组织的破坏。牙周韧带成纤维细胞是该组织中的主要细胞类型,对于维持内稳态和组织再生至关重要。在这里,我们研究了复制性耗竭或暴露于电离辐射后衰老的人牙周韧带成纤维细胞(hPDLF)的特征,以及它们向成骨细胞分化的能力。我们发现衰老的 hPDLF 表达衰老的经典标志物,以及分解代谢表型,如 I 型胶原蛋白表达减少和 MMP-2 表达增加。此外,我们观察到成骨细胞分化的主要转录因子 Runx2 的表达明显下调,这与 p53 依赖性下调有关。根据上述结果,衰老细胞的碱性磷酸酶基因表达和活性显著降低,成骨细胞分化能力降低,通过茜素红染色可以发现。有趣的是,两种衰老类型的细胞均表现出相似的特征,暗示其在体内具有类似的功能。总之,衰老的 hPDLF 表达分解代谢表型,并且向成骨细胞分化的能力显著降低,因此可能会影响组织的发育和完整性。