Fioravanti A, Cantarini L, Chellini F, Manca D, Paccagnini E, Marcolongo R, Collodel G
Rheumatology Unit, Department of Clinical Medicine and Immunological Sciences, University of Siena, Le Scotte Policlinico, Siena, Italy.
Osteoarthritis Cartilage. 2005 Aug;13(8):688-96. doi: 10.1016/j.joca.2005.03.006.
This study investigated the in vitro effects of hyaluronic acid (HA) of molecular weight (MW) 500-730 kDa on human articular chondrocytes cultivated for 48 h in the presence of interleukin-1beta (IL-1beta) with and without hydrostatic cyclical pressure.
The effects of 10 and 100 microg/ml HA with and without IL-1beta were assessed in the culture medium of cells exposed to pressurization cycles in the form of sinusoidal waves (minimum pressure 1MPa, maximum pressure 5MPa) at a frequency of 0.25Hz for 3h, by the immunoenzymatic method on microplates for the quantitative measurement of human proteoglycans (PG) and by the Griess method for nitrites (NO). Morphological analyses were performed by transmission electron microscopy (TEM) and scanning electron microscopy (SEM).
The presence of IL-1beta determines a significant decrease in PG and a significant increase in NO concentrations measured in the culture medium. When the cells are cultured in the presence of IL-1beta and HA at the two concentrations, a statistically significant restoration of PG and a decrease in NO levels are observed. Under pressurization conditions, we observed that the PG concentration in the medium of cells presented a very significant increase in all the conditions used in the study, except for IL-1beta alone. NO production decreased very significantly in the presence of IL-1beta+HA 10 and IL-1beta+HA 100. The results of metabolic evaluation are confirmed by morphological findings obtained by TEM and SEM.
These in vitro studies confirm both the protective role of HA (MW 500-730 kDa), which counteracts the IL-1beta-induced effects, and the importance of pressure on chondrocyte metabolism and morphology.
本研究调查了分子量为500 - 730 kDa的透明质酸(HA)在有和没有静水压循环压力的情况下,对在白细胞介素 - 1β(IL - 1β)存在下培养48小时的人关节软骨细胞的体外作用。
通过酶免疫法在微孔板上定量测量人蛋白聚糖(PG),并通过格里斯法测量亚硝酸盐(NO),评估在以正弦波形式(最小压力1MPa,最大压力5MPa)、频率为0.25Hz的加压循环下暴露3小时的细胞培养基中,10和100μg/ml HA在有和没有IL - 1β情况下的作用。通过透射电子显微镜(TEM)和扫描电子显微镜(SEM)进行形态学分析。
IL - 1β的存在导致培养基中测量的PG显著减少,NO浓度显著增加。当细胞在两种浓度的IL - 1β和HA存在下培养时,观察到PG有统计学意义的恢复,NO水平降低。在加压条件下,我们观察到除单独使用IL - 1β外,在本研究使用的所有条件下,细胞培养基中的PG浓度都有非常显著的增加。在IL - 1β + HA 10和IL - 1β + HA 100存在下,NO产生非常显著地减少。代谢评估结果通过TEM和SEM获得的形态学发现得到证实。
这些体外研究证实了HA(分子量500 - 730 kDa)的保护作用,其抵消了IL - 1β诱导的作用,以及压力对软骨细胞代谢和形态的重要性。