首页> 外文期刊>Osteoarthritis and cartilage >The effects of TIMP-1 and -2 on canine chondrocytes cultured in three-dimensional agarose culture system.
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The effects of TIMP-1 and -2 on canine chondrocytes cultured in three-dimensional agarose culture system.

机译:TIMP-1和-2对三维琼脂糖培养系统中培养的犬软骨细胞的影响。

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OBJECTIVE: To investigate the effects of tissue inhibitor of metalloproteinase (TIMP)-1 and -2 on chondrocytes cultured with or without interleukin (IL)-1 beta. DESIGN: Canine articular chondrocytes were cultured in three-dimensional (3-D) agarose constructs. Cells were distributed into each of the two groups, those without IL-1 beta and those with IL-1 beta added to the liquid media. Each group was subdivided into three groups, based on the presence of TIMP-1 or -2. IL-1 beta and TIMPs were added to liquid media bathing the 3-D constructs beginning on day 3. The liquid media and the 3-D constructs were collected on days 9, 15, and 24, and analyzed histologically, biochemically, and immunohistochemically. RESULTS: Addition of TIMP-1 or -2 resulted in decreases in matrix metalloproteinase (MMP)-3 concentrations of 37 and 41%, and MMP-1 immunoreactivity of 32 and 36%, respectively, compared with the IL-1 beta group, on day 9. Chondrocytes in groups without IL-1 beta maintained viability and produced abundant extracellular matrix (ECM). Chondrocytes in IL-1 beta groups appeared less viable and produced less ECM compared with those without IL-1 beta. Glycosaminoglycan (GAG) concentrations in 3-D constructs (GAG/weight) were significantly (P<0.001) higher in groups without IL-1 beta than in those with IL-1 beta, on days 15 and 24. CONCLUSIONS: The addition of TIMP was not detrimental to chondrocytes, as used in this study. Despite evidence of decreased MMP levels, TIMPs did not prevent IL-1 beta-associated changes in cellular or ECM characteristics. Further study is necessary before clinically relevant conclusions can be drawn regarding the use of TIMPs in the treatment of osteoarthritis.
机译:目的:探讨组织金属蛋白酶抑制剂(TIMP)-1和-2对有或无白介素(IL)-1β培养的软骨细胞的影响。设计:将犬关节软骨细胞培养在三维(3-D)琼脂糖构建物中。将细胞分配到两组中的每组中,将没有IL-1β的细胞和具有IL-1β的细胞添加到液体培养基中。根据TIMP-1或-2的存在,将每组分为三组。从第3天开始,将IL-1 beta和TIMPs添加到液体培养基中,浸泡3-D构建体。在第9、15和24天收集液体培养基和3-D构建体,并进行组织学,生化和免疫组化分析。结果:与IL-1 beta组相比,添加TIMP-1或-2导致基质金属蛋白酶(MMP)-3浓度分别降低37%和41%,MMP-1免疫反应性分别降低32%和36%,在第9天。没有IL-1β的组中的软骨细胞保持活力并产生丰富的细胞外基质(ECM)。与没有IL-1 beta的软骨细胞相比,IL-1 beta组的软骨细胞似乎较不活跃,产生的ECM更少。在第15天和第24天,没有IL-1 beta的组中3-D构建体中的糖胺聚糖(GAG)浓度(GAG /重量)显着(P <0.001)。结论:结论:如本研究中所使用的,TIMP对软骨细胞无害。尽管有证据表明MMP水平降低,但TIMP并不能阻止IL-1β相关的细胞或ECM特征改变。在就使用TIMPs治疗骨关节炎得出临床相关结论之前,需要进一步研究。

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