Anderson C C, Cook J L, Kreeger J M, Tomlinson J L, Wagner-Mann C C
Department of Veterinary Medicine and Surgery, College of Veterinary Medicine, University of Missouri, Columbia 65211, USA.
Am J Vet Res. 1999 Dec;60(12):1546-51.
To determine effects of glucosamine and acetylsalicylate on canine chondrocytes in 3-dimensional culture.
Chondrocytes isolated from articular cartilage of 2 adult female dogs recently euthanatized for reasons unrelated to orthopedic abnormalities.
Chondrocytes were cultured in a 3-dimensional agarose-based medium alone (control), with glucosamine (100 microg/ml; GL), or with acetylsalicylate (18 microg/ml; AS). Supernatant and agarose plugs from 4 wells/group/d were collected on days 3, 6, and 12 of culture. Agarose plugs were evaluated for percentage of viable cells, percentage of cells producing pericellular or territorial matrix, glycosaminoglycan (GAG) concentration, and type-II collagen production. Prostaglandin E2 concentration in supernatants was determined.
Chondrocytes in all groups had characteristics indicative of viability and differentiation; however, on day 12, a lower percentage of viable cells was detected in the AS group, compared with the other 2 groups. On day 6, GAG concentration in the AS group was significantly greater than concentrations in the other 2 groups. On day 12, GAG concentrations in the GL and AS groups were significantly less than in the control group. Within the GL and AS groups, cell viability was significantly less on day 12, compared with day 3. Significant differences in PGE2 concentration among or within groups and evidence of type II collagen production were not detected.
3-dimensional culture of canine chondrocytes allows for production of hyaline cartilage matrix constituents and growth of cells with morphologic characteristics similar to those of articular cartilage. Acetylsalicylate and glucosamine, at the single concentration evaluated, had detrimental effects on chondrocyte viability, GAG production, or both.
确定氨基葡萄糖和乙酰水杨酸对三维培养的犬软骨细胞的影响。
从2只因与骨科异常无关的原因近期实施安乐死的成年雌性犬的关节软骨中分离出的软骨细胞。
软骨细胞分别在仅含三维琼脂培养基(对照)、含氨基葡萄糖(100微克/毫升;GL)或含乙酰水杨酸(18微克/毫升;AS)的条件下培养。在培养的第3、6和12天,从每组4个孔/天收集上清液和琼脂糖栓。对琼脂糖栓进行活细胞百分比、产生细胞周围或区域基质的细胞百分比、糖胺聚糖(GAG)浓度及II型胶原蛋白产生情况的评估。测定上清液中前列腺素E2的浓度。
所有组的软骨细胞均具有表明活力和分化的特征;然而,在第12天,与其他两组相比,AS组检测到的活细胞百分比更低。在第6天,AS组的GAG浓度显著高于其他两组。在第12天,GL组和AS组的GAG浓度显著低于对照组。在GL组和AS组内,与第3天相比,第12天的细胞活力显著降低。未检测到组间或组内PGE2浓度的显著差异以及II型胶原蛋白产生的证据。
犬软骨细胞的三维培养能够产生透明软骨基质成分,并使细胞生长,其形态学特征与关节软骨相似。在所评估的单一浓度下,乙酰水杨酸和氨基葡萄糖对软骨细胞活力、GAG产生或两者均有不利影响。