The experimental study on the effect calcitonin gene-related peptide on bone resorption mediated by interleukin-1.

K Lian, J Du, Z Rao, H Luo
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Abstract

To investigate the effect of calcitonin gene-related peptide (CGRP) on bone resorption mediated by interleukin-1 beta(IL-1 beta) in vitro, the osteoclasts isolated from the long bones of newborn SD rats were co-cultured with osteoblasts on ivory slices placed in 24-well plates. 24 h later, conditioned media containing CGRP and/or IL-1 beta were added to the wells respectively, and continued culturing for 48 h. After the cells were stripped off by ultrasonication, the ivory slices were stained in toludine blue. The number and the total area of resorption lacunae on each slice were measured by computer imaging analysis system. Our results showed that IL-1 beta significantly stimulated bone resorption, but CGRP inhibited the effect mediated by IL-1 beta in a dose-dependent manner. It is suggested that CGRP may inhibit osteoclastic bone resorption through two ways: One is that CGRP functions directly on osteoclasts to block their activation; the other is that CGRP regulates the release of cytokines by osteoblasts and indirectly affects the function of osteoclasts.

降钙素基因相关肽对白细胞介素-1介导的骨吸收作用的实验研究。
为了研究降钙素基因相关肽(CGRP)对白细胞介素-1 beta(IL-1 beta)介导的体外骨吸收的影响,研究人员将从新生 SD 大鼠长骨中分离的破骨细胞与成骨细胞共同培养在 24 孔板中的象牙切片上。24 小时后,向培养孔中分别加入含有 CGRP 和/或 IL-1 beta 的条件培养基,继续培养 48 小时。通过计算机成像分析系统测量每张切片上吸收裂隙的数量和总面积。我们的研究结果表明,IL-1 beta 能明显刺激骨吸收,但 CGRP 能以剂量依赖的方式抑制 IL-1 beta 介导的骨吸收效应。这表明 CGRP 可通过两种途径抑制破骨细胞的骨吸收:一种是 CGRP 直接作用于破骨细胞,阻止其活化;另一种是 CGRP 调节成骨细胞释放细胞因子,间接影响破骨细胞的功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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