Zhu Yi, Wu Yuan, Liang Yu, Tan Wenfu, Liu Zhuoran, Xiao Jianhua
Department of Orthopaedics, the Second Hospital Affiliated to the University of South China, Hengyang, China.
Department of Laboratory, the Second Hospital Affiliated to the University of South China, Hengyang, China.
Arch Med Sci. 2016 Jun 1;12(3):502-6. doi: 10.5114/aoms.2015.55821. Epub 2015 Nov 30.
The aim of this study is to determine whether regulation of the expression level of fms-like tyrosine kinase-4 (Flt-4) is related to osteoclast differentiation.
Osteoclast formation and differentiation of mouse bone marrow cells and RAW264.7 cells were performed. To induce osteoclast differentiation, RANKL (50 ng/ml) with or without vascular endothelial growth factor-C (VEGF-C) and vascular endothelial growth factor-D (VEGF-D) was added to mouse bone marrow cells and RAW264.7 cells. Then cells were examined under a microscope. TRAP-positive cells with 3 nuclei or more were considered as osteoclasts and counted. The Flt-4 gene was knocked down by transfection of siRNAs against Flt-4. Immunoblot analyses were performed.
The osteoclast formation assay indicated that VEGF-C resulted in 500 or 450 vs. 100 (p < 0.05) of osteoclasts in mouse bone marrow cells and RAW264.7 cells, respectively. Vascular endothelial growth factor-D resulted in about 600 or 630 vs. 100 (p < 0.05) of osteoclasts for both mouse bone marrow cells and RAW264.7 cells. The knock-down of Flt-4 expression abolished the induction by VEGF-C or VEGF-D, resulting in induction similar to that of the negative control PBS.
Both VEGF-C and VEGF-D can induce osteoclast differentiation in the presence of the receptor activator of nuclear factor κB ligand. Down-regulation of expression level of Flt-4 protein abolishes osteoclast differentiation induced by VEGF-C or VEGF-D.
本研究旨在确定fms样酪氨酸激酶4(Flt-4)表达水平的调节是否与破骨细胞分化有关。
进行小鼠骨髓细胞和RAW264.7细胞的破骨细胞形成与分化实验。为诱导破骨细胞分化,将含或不含血管内皮生长因子C(VEGF-C)和血管内皮生长因子D(VEGF-D)的核因子κB受体活化因子配体(RANKL,50 ng/ml)添加到小鼠骨髓细胞和RAW264.7细胞中。然后在显微镜下观察细胞。将具有3个或更多细胞核的抗酒石酸酸性磷酸酶(TRAP)阳性细胞视为破骨细胞并进行计数。通过转染针对Flt-4的小干扰RNA(siRNA)敲低Flt-4基因。进行免疫印迹分析。
破骨细胞形成实验表明,VEGF-C分别导致小鼠骨髓细胞和RAW264.7细胞中破骨细胞数量为500个或450个,而对照组为100个(p < 0.05)。血管内皮生长因子D使小鼠骨髓细胞和RAW264.7细胞中的破骨细胞数量分别约为600个或630个,而对照组为100个(p < 0.05)。Flt-4表达的敲低消除了VEGF-C或VEGF-D的诱导作用,导致诱导情况与阴性对照磷酸盐缓冲液(PBS)相似。
在核因子κB受体活化因子配体存在的情况下,VEGF-C和VEGF-D均可诱导破骨细胞分化。Flt-4蛋白表达水平的下调消除了VEGF-C或VEGF-D诱导的破骨细胞分化。