Farivar Shirin, Ramezankhani Roya, Mohajerani Ezedin, Ghazimoradi Mohammad Hosein, Shiari Reza
Department of Molecular and Cell Biology, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University, General Campus, Tehran, Iran.
Laser and Plasma Research Institute, Shahid Beheshti University, General Campus, Tehran, Iran.
J Lasers Med Sci. 2019 Summer;10(3):171-178. doi: 10.15171/jlms.2019.27. Epub 2019 Jul 6.
Regarding the limited ability of the damaged cartilage cells to self-renew, which is due to their specific tissue structure, subtle damages can usually cause diseases such as osteoarthritis. In this work, using laser photobiomodulation and an interesting source of growth factors cocktail called the synovial fluid, we analyzed the chondrogenic marker genes in treated hair follicle dermal papilla cells as an accessible source of cells with relatively high differentiation potential. Dermal papilla cells were isolated from rat whisker hair follicle (Rattus norvegicus) and established cell cultures were treated with a laser (gallium aluminum arsenide diode Laser (λ=780 nm, 30 mW) at 5 J/cm ), the synovial fluid, and a combination of both. After 1, 4, 7, and 14 days, the morphological changes were evaluated and the expression levels of four chondrocyte marker genes ( and ) were assessed by the quantitative real-time polymerase chain reaction. It was monitored that treating cells with laser irradiation can accelerate the rate of proliferation of cells. The morphology of the cells treated with the synovial fluid altered considerably as in the fourth day they surprisingly looked like cultured articular chondrocytes. The gene expression analysis showed that all genes were up-regulated until the day 14 following the treatments although not equally in all the cell groups. Moreover, the cell groups treated with both irradiation and the synovial fluid had a significantly augmented expression in gene markers. Based on the gene expression levels and the morphological changes, we concluded that the synovial fluid can have the potential to make the dermal papilla cells to most likely mimic the chondrogenic and/or osteogenic differentiation, although this process seems to be augmented by the irradiation of the low-level laser.
由于受损软骨细胞自身更新能力有限,这归因于其特定的组织结构,微小损伤通常会引发骨关节炎等疾病。在这项研究中,我们利用激光光生物调节作用以及一种名为滑液的有趣生长因子混合物,分析了经处理的毛囊真皮乳头细胞中的软骨生成标记基因,毛囊真皮乳头细胞是一种易于获取且具有较高分化潜能的细胞来源。从大鼠(褐家鼠)胡须毛囊中分离出真皮乳头细胞,对建立的细胞培养物分别用激光(砷化镓铝二极管激光(λ = 780 nm,30 mW),能量密度为5 J/cm²)、滑液以及两者的组合进行处理。在1天、4天、7天和14天后,评估细胞的形态变化,并通过定量实时聚合酶链反应评估四个软骨细胞标记基因(此处原文未给出具体基因名称)的表达水平。监测发现,用激光照射处理细胞可加速细胞增殖速率。用滑液处理的细胞形态发生了显著变化,在第4天时,它们令人惊讶地看起来像培养的关节软骨细胞。基因表达分析表明,在处理后的第14天之前,所有基因均上调,尽管在所有细胞组中上调程度并不相同。此外,同时接受照射和滑液处理的细胞组在基因标记物方面的表达显著增强。基于基因表达水平和形态变化,我们得出结论,滑液有可能使真皮乳头细胞最有可能模拟软骨生成和/或成骨分化,尽管这一过程似乎因低强度激光照射而增强。