Chang Mei-Chi, Tsai Yi-Ling, Liou Eric Jein-Wein, Tang Chia-Mei, Wang Tong-Mei, Liu Hsin-Cheng, Liao Ming-Wei, Yeung Sin-Yuet, Chan Chiu-Po, Jeng Jiiang-Huei
Biomedical Science Team, Chang Gung University of Science and Technology, Kwei-Shan, Taoyuan City, Taiwan.
Department of Dentistry, Chang Gung Memorial Hospital, Taipei, Taiwan.
PLoS One. 2016 Nov 28;11(11):e0165438. doi: 10.1371/journal.pone.0165438. eCollection 2016.
Butyric acid is one major metabolic product generated by anaerobic Gram-negative bacteria of periodontal and root canal infection. Butyric acid affects the activity of periodontal cells such as osteoblasts. The purposes of this study were to investigate the effects of butyrate on MG-63 osteoblasts.
MG-63 cells were exposed to butyrate and cell viability was estimated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The mRNA and protein expression of type I collagen and cell cycle-related proteins were measured by reverse-transcriptase polymerase chain reaction (RT-PCR), western blotting or immunofluorescent staining. Cellular production of reactive oxygen species (ROS) was analyzed by 2',7'-dichlorofluorescein (DCF) fluorescence flow cytometry.
Exposure to butyrate suppressed cell proliferation, and induced G2/M (8 and 16 mM) cell cycle arrest of MG-63 cells. Some cell apoptosis was noted. The mRNA expression of cdc2 and cyclin-B1 decreased after exposure to butyrate. The protein expression of type I collagen, cdc2 and cyclin B1 were decreased, whereas the expression of p21, p27 and p57 was stimulated. Under the treatment of butyrate, ROS production in MG-63 cells markedly increased.
The secretion of butyric acid by periodontal and root canal microorganisms may inhibit bone cell growth and matrix turnover. This is possibly due to induction of cell cycle arrest and ROS generation and inhibition of collagen expression. These results suggest the involvement of butyric acid in the pathogenesis of periodontal and periapical tissue destruction by impairing bone healing responses.
丁酸是牙周和根管感染的厌氧革兰氏阴性菌产生的一种主要代谢产物。丁酸会影响成骨细胞等牙周细胞的活性。本研究的目的是探讨丁酸盐对MG-63成骨细胞的影响。
将MG-63细胞暴露于丁酸盐中,通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法评估细胞活力。通过逆转录聚合酶链反应(RT-PCR)、蛋白质印迹法或免疫荧光染色检测I型胶原蛋白和细胞周期相关蛋白的mRNA和蛋白质表达。通过2',7'-二氯荧光素(DCF)荧光流式细胞术分析细胞活性氧(ROS)的产生。
暴露于丁酸盐会抑制MG-63细胞的增殖,并诱导其G2/M期(8和16 mM)细胞周期停滞。观察到一些细胞凋亡。暴露于丁酸盐后,cdc2和细胞周期蛋白B1的mRNA表达降低。I型胶原蛋白、cdc2和细胞周期蛋白B1的蛋白质表达降低,而p21、p27和p57的表达受到刺激。在丁酸盐处理下,MG-63细胞中的ROS产生显著增加。
牙周和根管微生物分泌的丁酸可能会抑制骨细胞生长和基质周转。这可能是由于诱导细胞周期停滞和ROS生成以及抑制胶原蛋白表达所致。这些结果表明丁酸通过损害骨愈合反应参与牙周和根尖周组织破坏的发病机制。