Lee Jin-Ha, Jung Ji-Yeon, Jeong Yeon-Jin, Park Jae-Hong, Yang Kyu-Ho, Choi Nam-Ki, Kim Sun-Hun, Kim Won-Jae
Dental Science Research Institute, 2nd Stage of Brain Korea 21 for School of Dentistry, Chonnam National University, Gwang Ju 500-757, South Korea.
Toxicology. 2008 Jan 20;243(3):340-7. doi: 10.1016/j.tox.2007.10.026. Epub 2007 Nov 4.
Sodium fluoride (NaF) has been shown to be cytotoxic and produces inflammatory responses in humans. However, the cellular mechanisms underlying the NaF-induced cytotoxicity in periodontal tissues are unclear. This study examined whether or not NaF induces apoptosis in human gingival fibroblasts (HGF), and its underlying mechanisms by monitoring various apoptosis-associated processes. NaF reduced the cell viability of HGF in a dose- and time-dependent manner. NaF increased TUNEL-positive cell and induced apoptosis with concomitant chromatin condensation and DNA fragmentation in HGF. In addition, NaF increased the level of cytochrome c released from the mitochondria into the cytosol, enhanced the caspase-9, -8 and -3 activities, the cleavage of poly (ADP-ribose) polymerase (PARP), and up-regulated the voltage-dependent anion channel (VDAC) 1. However, NaF did not affect the production of reactive oxygen species (ROS) which is a strong apoptotic inducer. Furthermore, NaF up-regulated the Fas-ligand (Fas-L), a ligand of death receptor. Bcl-2, a member of the anti-apoptotic Bcl-2 family, was down-regulated, whereas the expression of Bax, a member of the pro-apoptotic Bcl-2 family, was unaffected in the NaF-treated HGF. These results suggest that NaF induces apoptosis in HGF through both the mitochondria-mediated pathways regulated by the Bcl-2 family and death receptor-mediated pathway.
已证实氟化钠(NaF)具有细胞毒性,并可在人体引发炎症反应。然而,NaF诱导牙周组织细胞毒性的细胞机制尚不清楚。本研究通过监测各种凋亡相关过程,检测NaF是否诱导人牙龈成纤维细胞(HGF)凋亡及其潜在机制。NaF以剂量和时间依赖性方式降低HGF的细胞活力。NaF增加了HGF中TUNEL阳性细胞数量,并诱导凋亡,同时伴有染色质浓缩和DNA片段化。此外,NaF增加了从线粒体释放到细胞质中的细胞色素c水平,增强了半胱天冬酶-9、-8和-3的活性、聚(ADP-核糖)聚合酶(PARP)的裂解,并上调了电压依赖性阴离子通道(VDAC)1。然而,NaF不影响作为强凋亡诱导剂的活性氧(ROS)的产生。此外,NaF上调了死亡受体的配体Fas配体(Fas-L)。抗凋亡Bcl-2家族成员Bcl-2被下调,而促凋亡Bcl-2家族成员Bax的表达在NaF处理的HGF中未受影响。这些结果表明,NaF通过Bcl-2家族调节的线粒体介导途径和死亡受体介导途径诱导HGF凋亡。