Todhunter P G, Kincaid S A, Todhunter R J, Kammermann J R, Johnstone B, Baird A N, Hanson R R, Wright J M, Lin H C, Purohit R C
Department of Large Animal Surgery and Medicine, College of Veterinary Medicine, Auburn University, AL 36849, USA.
Am J Vet Res. 1996 Jul;57(7):1080-93.
To use lipopolysaccharide (LPS) to create synovitis in the midcarpal joint of ponies, and to assess the morphologic, histochemical, and immunohistochemical effects of synovitis on articular cartilage of the third carpal bone.
2- to 3-year-old ponies, 6 control (group 1) and 6 treated (group 2).
Synovitis was induced in 1 midcarpal joint of group-2 ponies by intra-articular injections of LPS (0.02 micrograms/kg of body weight), morphine (0.1 mg/kg), and saline solution (group 2a) and a morphine and saline solution alone in the contralateral midcarpal joint (group 2b). Articular cartilage sections and attached synovial membrane from the third carpal bones were examined by immunohistochemical distribution of interleukin 1 beta, tumor necrosis factor (TNF)-alpha, TNF receptors (P55, P75) and 3-B-3(-) epitopes, and by localization of proteoglycans (metachromatic staining). Proteoglycan extracts were assessed by metachromatic staining or western blotting and immunohistochemical staining, using anti-3-B- antibodies.
Enhanced immunoreactivity for the cytokines and receptors was found in inflamed synovial membrane and noncalcified cartilage (group 2a more than 2b). Metachromasia of the noncalcified cartilage was greater in group-1 than in group-2a and group-2b specimens. In group 2a, chondrocyte hypertrophy and enhanced immunoreactivity for 3-B-3(-) epitope in areas of increased cytokine immunoreactivity suggested possible phenotypic change of the chondrocytes in response to synovitis. Immunohistochemical analysis by western blotting of proteoglycan extracts indicated strong 3-B-3(-) epitope immunolocalization in group-2a, weaker staining in group-2b, and barely detectable stain in group-1 specimens, which correlated with in situ immunolocalization.
Intra-articular administration of LPS may be used to induce a synovial environment conductive to increased immunoreactivity of interleukin 1 beta, TNF-alpha, and its receptors in equine synovial membrane and articular cartilage. These cytokines may be involved in the early phenotypic change of chondrocytes that is believed to occur in osteoarthritis and is characterized in this study by enhanced 3-B-3(-) epitope immunoreactivity and chondrocyte hypertrophy.
使用脂多糖(LPS)在小马腕中关节诱发滑膜炎,并评估滑膜炎对第三腕骨关节软骨的形态学、组织化学和免疫组织化学影响。
2至3岁小马,6匹作为对照组(第1组),6匹作为治疗组(第2组)。
给第2组小马的1个腕中关节内注射LPS(0.02微克/千克体重)、吗啡(0.1毫克/千克)和生理盐水(第2a组),对侧腕中关节仅注射吗啡和生理盐水(第2b组),诱导滑膜炎。通过白细胞介素1β、肿瘤坏死因子(TNF)-α、TNF受体(P55、P75)和3-B-3(-)表位的免疫组织化学分布,以及蛋白聚糖的定位(异染性染色),检查第三腕骨的关节软骨切片和附着的滑膜。使用抗3-B-抗体,通过异染性染色或蛋白质印迹法及免疫组织化学染色评估蛋白聚糖提取物。
在炎症滑膜和未钙化软骨中发现细胞因子和受体的免疫反应性增强(第2a组比第2b组更明显)。第1组未钙化软骨的异染性比第2a组和第2b组标本更强。在第2a组中,细胞因子免疫反应性增加区域的软骨细胞肥大和3-B-3(-)表位免疫反应性增强表明,软骨细胞可能因滑膜炎而发生表型变化。通过蛋白聚糖提取物的蛋白质印迹法进行的免疫组织化学分析表明,第2a组有强烈的3-B-3(-)表位免疫定位,第2b组染色较弱,第1组标本中几乎检测不到染色,这与原位免疫定位相关。
关节内注射LPS可用于诱导一种滑膜环境,这种环境有利于马滑膜和关节软骨中白细胞介素1β、TNF-α及其受体的免疫反应性增加。这些细胞因子可能参与软骨细胞的早期表型变化,这种变化被认为发生在骨关节炎中,在本研究中其特征是3-B-3(-)表位免疫反应性增强和软骨细胞肥大。