Stanescu R, Stanescu V
Unité de Recherches de Génétique Médicale (INSERM U.12), Hôpital des Enfants-Malades, Paris, France.
J Rheumatol. 1988 Nov;15(11):1677-82.
The effects of cross-linking agents on the resistance of the articular surface to digestion with clostridial collagenase were studied using a described in vitro system. Mouse femoral heads were treated with various concentrations of glutaraldehyde, with osmium tetraoxide and with dithiobis (succinimydil propionate), digested with the enzyme, labeled with cationized ferritin and examined by electron microscopy. Collagenase alone caused disruption of the articular surface with penetration of the large marker into the cartilage matrix. After treatment of the femoral heads with the cross-linking agents, no effects on the morphology and on the labeling of the articular surface and no penetration of the label into the cartilage matrix were observed. Increasing cross-linking at the articular surface might be a new route for therapeutic intervention. However, experiments would be needed to assess the effect of the procedure on the viability and nutrition of chondrocytes and on the functional properties of the tissue.
使用一种已描述的体外系统,研究了交联剂对关节表面抵抗梭菌胶原酶消化的影响。用不同浓度的戊二醛、四氧化锇和二硫代双(琥珀酰亚胺丙酸酯)处理小鼠股骨头,用该酶消化,用阳离子化铁蛋白标记并通过电子显微镜检查。单独的胶原酶会导致关节表面破坏,大标记物渗透到软骨基质中。用交联剂处理股骨头后,未观察到对关节表面形态和标记的影响,也未观察到标记物渗透到软骨基质中。增加关节表面的交联可能是一种新的治疗干预途径。然而,需要进行实验来评估该程序对软骨细胞活力和营养以及组织功能特性的影响。