Institute of Radiation Medicine, Fudan University, Shanghai 200032, China.
Food Chem Toxicol. 2011 Sep;49(9):2392-7. doi: 10.1016/j.fct.2011.06.053. Epub 2011 Jun 24.
The mechanism of cadmium effects on bone is not fully understood. In this study, we investigated the effects of cadmium on osteoclasts differentiation and the probable mechanism. RAW264.7 cells were exposed to cadmium (0-60 nmol/L) in the presence or absence of receptor-activated nuclear factor κ B ligand (RANKL) for 5 days. Then, the viability, tartrate-resistant acid phosphatase (TRAP) activity and the formation of TRAP positive multinucleated osteoclasts were observed. Receptor activator of nuclear factor κ B (RANK), tumor necrosis factor receptor associated factor 6 (TRAF6), c-src, c-fos, fos-related antigen 1 (Fra1) expression were determined by reverse transcription polymerase chain reaction. Cadmium increased TRAP activity (20-40%) and TRAP positive cell formation in the presence of RANKL, but had no obvious influence on them without RANKL. RANK, TRAF6, Fra1, c-src and c-fos (at 15-30 nmol/L) expression were enhanced (30-70%) by cadmium in the presence of RANKL, but cadmium had little influence on them in the absence of RANKL. This study demonstrated that cadmium could induce differentiation of osteoclasts precursor into osteoclasts in the presence of RANKL. Even though the changes of gene expression were small, RANKL/RANK and downstream genes may play an important role in cadmium effects on osteoclasts.
镉对骨骼的作用机制尚未完全阐明。本研究旨在探讨镉对破骨细胞分化的影响及其可能的机制。将 RAW264.7 细胞用不同浓度(0-60nmol/L)的镉在存在或不存在核因子κ B 受体激活物配体(RANKL)的情况下培养 5 天。然后,观察细胞活力、抗酒石酸酸性磷酸酶(TRAP)活性和 TRAP 阳性多核破骨细胞的形成。采用逆转录聚合酶链反应检测核因子κ B 受体激活物(RANK)、肿瘤坏死因子受体相关因子 6(TRAF6)、c-src、c-fos、fos 相关抗原 1(Fra1)的表达。结果显示,在 RANKL 存在的情况下,镉可增加 TRAP 活性(20-40%)和 TRAP 阳性细胞的形成,但在无 RANKL 时,其无明显影响。在 RANKL 存在的情况下,镉(15-30nmol/L)可增强 RANK、TRAF6、Fra1、c-src 和 c-fos(30-70%)的表达,但在无 RANKL 时,镉对其影响较小。本研究表明,在 RANKL 存在的情况下,镉可诱导破骨细胞前体向破骨细胞分化。尽管基因表达的变化较小,但 RANKL/RANK 和下游基因可能在镉对破骨细胞的作用中发挥重要作用。