Meats J E, McGuire M K, Ebsworth N M, Englis D J, Russell R G
Rheumatol Int. 1984;4(4):143-9. doi: 10.1007/BF00541204.
We have examined the way in which products of cultured human blood mononuclear cells activate human articular chondrocytes. Conditioned medium from mononuclear cells enhanced the production of prostaglandin E by cultured human chondrocytes and also stimulated fibrinolytic activity in these cultures. These two effects may be interrelated, since the increased fibrinolysis in response to products of mononuclear cells was partially inhibited by indomethacin, an inhibitor of prostaglandin biosynthesis. The increased fibrinolysis is probably attributable to plasminogen activator, since it was strongly dependent on the presence of plasminogen. Increased amounts of PGE and chondroitin sulphate were also released from intact fragments of cartilage exposed to medium from cultured mononuclear cells. The time course and dose dependence of these effects were studied. The addition of exogenous arachidonic acid markedly enhanced production of PGE2. Ultrogel AcA54 was used to fractionate medium from cultured mononuclear cells and the chondrocyte-stimulating activity eluted with an apparent molecular weight between 12 000 and 25 000 daltons. Adherent and non-adherent mononuclear blood cells were also partially separated and conditioned medium from each was assayed for chondrocyte-stimulating factors. Both populations released factor(s) which increased the production of prostaglandin E by chondrocytes, but more activity came from the adherent mononuclear cells. The possible interrelationship between the chondrocyte activating factor studied here and others described in the literature is discussed.
我们研究了培养的人血单核细胞产物激活人关节软骨细胞的方式。单核细胞的条件培养基增强了培养的人软骨细胞中前列腺素E的产生,并且还刺激了这些培养物中的纤溶活性。这两种作用可能相互关联,因为对单核细胞产物的纤溶增加部分被吲哚美辛(一种前列腺素生物合成抑制剂)抑制。纤溶增加可能归因于纤溶酶原激活剂,因为它强烈依赖于纤溶酶原的存在。暴露于培养的单核细胞培养基中的完整软骨碎片也释放出更多量的前列腺素E和硫酸软骨素。研究了这些作用的时间进程和剂量依赖性。添加外源性花生四烯酸显著增强了前列腺素E2的产生。使用Ultrogel AcA54对培养的单核细胞培养基进行分级分离,软骨细胞刺激活性在表观分子量为12000至25000道尔顿之间洗脱。还对贴壁和非贴壁单核血细胞进行了部分分离,并测定了每种细胞的条件培养基中的软骨细胞刺激因子。两种细胞群体都释放出增加软骨细胞前列腺素E产生的因子,但更多的活性来自贴壁单核细胞。本文研究的软骨细胞激活因子与文献中描述的其他因子之间可能的相互关系进行了讨论。