Wang Yi, Fu Ying-Xiao, Gu Jian-Hong, Yuan Yan, Liu Xue-Zhong, Bian Jian-Chun, Liu Zong-Ping
College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, PR China; Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou 225009, PR China.
College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, PR China; Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou 225009, PR China; Department of Bioscience, Bengbu Medical College, Bengbu 233000, PR China.
Vet J. 2014 Apr;200(1):181-5. doi: 10.1016/j.tvjl.2014.02.004. Epub 2014 Feb 14.
This study aimed to determine the in vitro effect of cadmium on the differentiation of duck embryonic bone marrow cells into osteoclasts. Bone marrow cells were harvested from 23-day old Gaoyou duck embryos and were cultured with either 50 nmol/L cadmium alone or different cadmium concentrations (0, 5, 10, 20 and 50 nmol/L) in combination with macrophage colony stimulating factor (M-CSF) and receptor activator of nuclear factor κB ligand (RANKL). Tartrate-resistant acid phosphatase (TRAP) staining, pit formation assay with bovine cortical bone slices, and co-staining with tetramethyl rhodamine isothiocyanate (TRITC)-conjugated phalloidin and Hoechst 33258 were performed to determine the number of TRAP-positive cells and bone resorption activity. Cadmium at a concentration ⩾ 10 nmol/L in the presence of M-CSF and RANKL significantly increased in a concentration-dependent manner both the number of TRAP-positive cells (35-160%) and bone resorption activity (36-261%) (P<0.05). High cadmium concentrations in the presence of M-CSF and RANKL markedly promoted the formation of filamentous (F)-actin rings in differentiated osteoclasts. In conclusion, cadmium promotes in vitro the differentiation of duck embryonic osteoclasts in the presence of M-CSF and RANKL.
本研究旨在确定镉对鸭胚胎骨髓细胞向破骨细胞分化的体外作用。从23日龄的高邮鸭胚胎中采集骨髓细胞,分别单独用50 nmol/L镉或与巨噬细胞集落刺激因子(M-CSF)和核因子κB受体活化因子配体(RANKL)联合使用不同浓度(0、5、10、20和50 nmol/L)的镉进行培养。采用抗酒石酸酸性磷酸酶(TRAP)染色、用牛皮质骨切片进行陷窝形成试验以及用异硫氰酸四甲基罗丹明(TRITC)偶联的鬼笔环肽和Hoechst 33258进行共染色,以确定TRAP阳性细胞的数量和骨吸收活性。在M-CSF和RANKL存在的情况下,浓度⩾10 nmol/L的镉以浓度依赖性方式显著增加了TRAP阳性细胞的数量(35 - 160%)和骨吸收活性(36 - 261%)(P<0.05)。在M-CSF和RANKL存在的情况下,高浓度镉显著促进了分化破骨细胞中丝状(F)-肌动蛋白环的形成。总之,在M-CSF和RANKL存在的情况下,镉在体外促进鸭胚胎破骨细胞的分化。