Corporate Affiliated Research Institute, Feagle Co., Ltd., Yangsan 50561, Republic of Korea.
Department of Dental Hygiene, Kyungnam College of Information & Technology, Busan 47011, Republic of Korea.
Medicina (Kaunas). 2024 Aug 14;60(8):1318. doi: 10.3390/medicina60081318.
: Enhanced osteoblast differentiation may be leveraged to prevent and treat bone-related diseases such as osteoporosis. No-ozone cold plasma (NCP) treatment is a promising and safe strategy to enhance osteoblast differentiation. Therefore, this study aimed to determine the effectiveness of direct and indirect NCP treatment methods on osteoblast differentiation. Mouse osteoblastic cells (MC3T3-E1) were treated with NCP using different methods, i.e., no NCP treatment (NT group; control), direct NCP treatment (DT group), direct NCP treatment followed by media replacement (MC group), and indirect treatment with NCP-treated media only (PAM group). : The MC3T3-E1 cells were subsequently assessed for cell proliferation, alkaline phosphatase (ALP) activity, calcium deposition, and ALP and osteocalcin mRNA expression using real-time polymerase chain reaction. : Cell proliferation significantly increased in the NCP-treated groups (DT and PAM; MC and PAM) compared to the NT group after 24 h ( < 0.038) and 48 h ( < 0.000). ALP activity was increased in the DT and PAM groups at 1 week ( < 0.115) and in the DT, MC, and PAM groups at 2 weeks ( < 0.000) compared to the NT group. Calcium deposition was higher in the NCP-treated groups than in NT group at 2 and 3 weeks ( < 0.000). ALP mRNA expression peaked in the MC group at 2 weeks compared to the NP group ( < 0.014). Osteocalcin mRNA expression increased in the MC group at 2 weeks ( < 0.000) and was the highest in the PAM group at 3 weeks ( < 0.000). Thus, the effects of direct (DT and MC) and indirect (PAM) treatment varied, with MC direct treatment showing the most significant impact on osteoblast activity. : The MC group exhibited enhanced osteoblast differentiation, indicating that direct NCP treatment followed by media replacement is the most effective method for promoting bone formation.
增强成骨细胞分化可能被利用来预防和治疗与骨骼相关的疾病,如骨质疏松症。无臭氧冷等离子体(NCP)治疗是一种有前途且安全的策略,可以增强成骨细胞分化。因此,本研究旨在确定直接和间接 NCP 处理方法对成骨细胞分化的有效性。使用不同方法用 NCP 处理小鼠成骨细胞(MC3T3-E1),即无 NCP 处理(NT 组;对照)、直接 NCP 处理(DT 组)、直接 NCP 处理后更换培养基(MC 组)和仅用 NCP 处理的培养基间接处理(PAM 组)。随后使用实时聚合酶链反应评估 MC3T3-E1 细胞的细胞增殖、碱性磷酸酶(ALP)活性、钙沉积以及 ALP 和骨钙素 mRNA 表达。与 NT 组相比,NCP 处理组(DT 和 PAM;MC 和 PAM)在 24 小时( < 0.038)和 48 小时( < 0.000)后细胞增殖显著增加。在 1 周时,DT 和 PAM 组的 ALP 活性增加( < 0.115),在 2 周时,DT、MC 和 PAM 组的 ALP 活性增加( < 0.000)与 NT 组相比。在 2 周和 3 周时,NCP 处理组的钙沉积均高于 NT 组( < 0.000)。与 NP 组相比,MC 组的 ALP mRNA 表达在 2 周时达到峰值( < 0.014)。在 2 周时,MC 组的骨钙素 mRNA 表达增加( < 0.000),在 3 周时,PAM 组的骨钙素 mRNA 表达最高( < 0.000)。因此,直接(DT 和 MC)和间接(PAM)处理的效果不同,MC 直接处理对成骨细胞活性的影响最大。MC 组表现出增强的成骨细胞分化,表明直接 NCP 处理后更换培养基是促进骨形成最有效的方法。