首页> 外文期刊>International journal of biological sciences >Alpha-Calcitonin Gene-Related Peptide Can Reverse The Catabolic Influence Of UHMWPE Particles On RANKL Expression In Primary Human Osteoblasts
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Alpha-Calcitonin Gene-Related Peptide Can Reverse The Catabolic Influence Of UHMWPE Particles On RANKL Expression In Primary Human Osteoblasts

机译:降钙素基因相关肽可以逆转UHMWPE颗粒对原代人成骨细胞RANKL表达的分解代谢影响。

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Background and purpose: A linkage between the neurotransmitter alpha-calcitonin gene-related peptide (alpha-CGRP) and particle-induced osteolysis has been shown previously. The suggested osteoprotective influence of alpha-CGRP on the catabolic effects of ultra-high molecular weight polyethylene (UHMWPE) particles is analyzed in this study in primary human osteoblasts. Methods: Primary human osteoblasts were stimulated by UHMWPE particles (cell/particle ratios 1:100 and 1:500) and different doses of alpha-CGRP (10-7 M, 10-9 M, 10-11 M). Receptor activator of nuclear factor-κB ligand (RANKL) and osteoprotegerin (OPG) mRNA expression and protein levels were measured by RT-PCR and Western blot. Results: Particle stimulation leads to a significant dose-dependent increase of RANKL mRNA in both cell-particle ratios and a significant down-regulation of OPG mRNA in cell-particle concentrations of 1:500. A significant depression of alkaline phosphatase was found due to particle stimulation. Alpha-CGRP in all tested concentrations showed a significant depressive effect on the expression of RANKL mRNA in primary human osteoblasts under particle stimulation. Comparable reactions of RANKL protein levels due to particles and alpha-CGRP were found by Western blot analysis. In cell-particle ratios of 1:100 after 24 hours the osteoprotective influence of alpha-CGRP reversed the catabolic effects of particles on the RANKL expression. Interpretation: The in-vivo use of alpha-CGRP, which leads to down-regulated RANKL in-vitro, might inhibit the catabolic effect of particles in conditions of particle induced osteolysis.
机译:背景与目的:先前已经显示了神经递质α降钙素基因相关肽(α-CGRP)与颗粒诱导的骨溶解之间的联系。这项研究在人类原代成骨细胞中分析了建议的α-CGRP对超高分子量聚乙烯(UHMWPE)颗粒的分解代谢作用的骨保护作用。方法:UHMWPE颗粒(细胞/颗粒比例为1:100和1:500)和不同剂量的α-CGRP(10-7 M,10-9 M,10-11 M)刺激人类原代成骨细胞。通过RT-PCR和Western blot检测核因子-κB配体(RANKL)和骨保护素(OPG)的mRNA表达和蛋白水平。结果:颗粒刺激导致RANKL mRNA在两个细胞颗粒比率中的剂量依赖性显着增加,并在细胞颗粒浓度为1:500时显着下调OPG mRNA。由于颗粒刺激,发现碱性磷酸酶明显降低。在颗粒刺激下,所有测试浓度的Alpha-CGRP均对人类成骨细胞中RANKL mRNA的表达具有显着的抑制作用。通过蛋白质印迹分析发现了由于颗粒和α-CGRP引起的RANKL蛋白水平的可比反应。 24小时后,细胞与细胞的比例为1:100,α-CGRP的骨保护作用逆转了颗粒对RANKL表达的分解代谢作用。解释:体内使用α-CGRP可导致RANKL体外下调,在颗粒诱导的骨溶解条件下可能会抑制颗粒的分解代谢作用。

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