Shih C, Huang M Y
Department of Biology and Anatomy, National Defense Medical Center, Taipei, Taiwan, R.O.C.
Zhonghua Yi Xue Za Zhi (Taipei). 1996 Feb;57(2):85-92.
Interleukin-1 (IL-1) is produced by monocytes and marrow stromal cells and can stimulate bone resorption in tissue culture. In addition, IL-1 can induce osteoclast-like cell formation in long-term bone marrow culture. However, whether IL-1 can increase osteoclast formation by stimulating fusion of peripheral blood monocytes is not clear. In addition, the precise effect of IL-1 on osteoclastic activity is still not well known.
Using the bioassay of osteoclast formation, osteoclast-free fetal calvariae were harvested from 14-day timed-pregnant Sprague-Dawley rats and cultured in BGJb medium for 10 days. On the 10th day, mononuclear cells were obtained from peripheral blood of 8-week-old female Sprague-Dawley rats through cardiac puncture and Ficoll-Paque density gradient separation method and co-cultured with osteoclast-free developing bone explant. On the same day, various concentrations of IL-1 alpha (1,10 or 100 U/ml) were added daily in the experimental dishes while only BGJb medium was added in the controls. In addition, 45Ca release assay and quantitation of nuclei per osteoclast were performed to evaluate the effect of IL-1 alpha on osteoclastic activity.
Ten days after adding monocytes, there were 14.25 osteoclasts in the control, without IL-1 alpha; with 1 U of IL-1 alpha, there were 14.75 osteoclasts; with 10 U of IL-1 alpha, there were 18.00 osteoclasts; with 100 U of IL-1 alpha, there were 20.75 osteoclasts. In addition, IL-1 alpha stimulated the release of 45Ca and increased the number of average nuclei per osteoclast dose-dependently, indicating a significant increase in bone resorption.
IL-1 alpha could increase osteoclast formation by stimulating the fusion of peripheral blood monocytes. In addition, IL-1 alpha is a potent stimulator of osteoclastic activity.
白细胞介素 -1(IL-1)由单核细胞和骨髓基质细胞产生,在组织培养中可刺激骨吸收。此外,IL-1能在长期骨髓培养中诱导破骨样细胞形成。然而,IL-1是否能通过刺激外周血单核细胞融合来增加破骨细胞形成尚不清楚。另外,IL-1对破骨细胞活性的确切作用仍不为人所知。
采用破骨细胞形成生物测定法,从14天定时妊娠的斯普拉格 - 道利大鼠中获取无破骨细胞的胎鼠颅骨,在BGJb培养基中培养10天。第10天,通过心脏穿刺和Ficoll-Paque密度梯度分离法从8周龄雌性斯普拉格 - 道利大鼠外周血中获取单核细胞,并与无破骨细胞的发育中的骨外植体共培养。同一天,在实验培养皿中每日添加不同浓度的IL-1α(1、10或100 U/ml),而对照组仅添加BGJb培养基。此外,进行45Ca释放测定和每个破骨细胞核的定量分析,以评估IL-1α对破骨细胞活性的影响。
添加单核细胞10天后,对照组(无IL-1α)有14.25个破骨细胞;添加1 U IL-1α时有14.75个破骨细胞;添加10 U IL-1α时有18.00个破骨细胞;添加100 U IL-1α时有20.75个破骨细胞。此外,IL-1α刺激45Ca释放,并剂量依赖性地增加每个破骨细胞的平均核数,表明骨吸收显著增加。
IL-1α可通过刺激外周血单核细胞融合来增加破骨细胞形成。此外,IL-1α是破骨细胞活性的有效刺激剂。