Mala Supaporn, Buranapraditkun Supranee, Sooklert Kanidta, Sereemaspun Amornpun, Lapthanasupkul Puangwan, Rungraungrayabkul Dulyapong, Kitkumthorn Nakarin
Reseach Office, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.
Division of Allergy and Clinical Immunology, Department of Medicine, King Chulalongkorn Memorial Hospital, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Eur J Dent. 2025 May;19(2):464-471. doi: 10.1055/s-0044-1789269. Epub 2024 Dec 30.
Particulate matter 2.5 (PM2.5), an important air pollution particle, has been previously studied for its effects on various normal and cancer tissues. However, research on the impact of PM2.5, specifically on normal cavity tissue, is still limited. This study aimed to assess the effects of PM2.5 on cell vitality, cell cycle, and apoptosis in PGK (normal oral keratinocyte) and HGF (human gingival fibroblast) cell lines.
The effect of PM2.5 was examined through cell vitality using the Cell Counting Kit-8 (CCK8) assay, while cell cycle and apoptosis were determined via flow cytometry. Cells incubated with 0.05% dimethyl sulfoxide were used as the negative control.
In a concentration-dependent manner, PM2.5 inhibited the proliferation of HGF and PGK cells. The half-maximal inhibitory concentration (IC50) of PM2.5 after 24 hours of incubation was 400 ng/µL for HGF cells and 100 ng/µL for PGK cells. This particulate matter arrested the cell cycles of both HGF and PGK cells at the G0/G1 phase. Additionally, PM2.5 was found to trigger apoptosis in both HGF and PGK cell lines and also cause necrosis in the PGK cell line at higher concentrations.
Kruskal-Wallis tests were employed to evaluate all quantitative data.
The findings indicated that PM2.5 decreases cell viability, halts cell cycle progression, and triggers apoptosis in normal oral cavity cell lines. Therefore, it is advisable to avoid PM2.5 exposure in order to mitigate potential health risks. To understand PM2.5-induced oral cellular damage, more research is needed.
细颗粒物2.5(PM2.5)是一种重要的空气污染颗粒,此前已对其对各种正常组织和癌组织的影响进行了研究。然而,关于PM2.5的影响,特别是对正常腔道组织的影响的研究仍然有限。本研究旨在评估PM2.5对PGK(正常口腔角质形成细胞)和HGF(人牙龈成纤维细胞)细胞系的细胞活力、细胞周期和凋亡的影响。
通过细胞计数试剂盒-8(CCK8)检测法检测PM2.5对细胞活力的影响,同时通过流式细胞术测定细胞周期和凋亡情况。将用0.05%二甲基亚砜孵育的细胞用作阴性对照。
PM2.5以浓度依赖性方式抑制HGF和PGK细胞的增殖。孵育24小时后,PM2.5对HGF细胞的半数最大抑制浓度(IC50)为400 ng/µL,对PGK细胞为100 ng/µL。这种颗粒物使HGF和PGK细胞的细胞周期停滞在G0/G1期。此外,发现PM2.5在HGF和PGK细胞系中均引发凋亡,并且在较高浓度下还导致PGK细胞系坏死。
采用Kruskal-Wallis检验评估所有定量数据。
研究结果表明,PM2.5会降低正常口腔细胞系的细胞活力,阻止细胞周期进程并引发凋亡。因此,为降低潜在健康风险,建议避免接触PM2.5。为了解PM2.5诱导的口腔细胞损伤,还需要更多研究。