首页> 美国卫生研究院文献>Journal of the Japanese Physical Therapy Association >Effects of the Thermal Environment on Articular Chondrocyte Metabolism: A Fundamental Study to Facilitate Establishment of an Effective Thermotherapy for Osteoarthritis
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Effects of the Thermal Environment on Articular Chondrocyte Metabolism: A Fundamental Study to Facilitate Establishment of an Effective Thermotherapy for Osteoarthritis

机译:热环境对关节软骨细胞代谢的影响:基础研究以促进建立有效的骨关节炎的热疗法

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摘要

Aim: To facilitate establishment of an effective thermotherapy for osteoarthritis (OA), we investigated the effects of the thermal environment on articular chondrocyte metabolism in vitro. Methods: Chondrocytes were isolated from porcine knee joints, and cultured at 32°C, 37°C and 41°C. Cell proliferation and viability were assessed at Days 2, 4 and 8. In addition, TdT-mediated dUTP nick end labeling (TUNEL) assay was performed at Day 3 to determine the proportion of apoptotic chondrocytes. Analysis of genes specific for factors related to the cartilage extracellular matrix (ECM), cartilage destruction, and cartilage protection was performed at Day 2. Furthermore, evaluation of heat stress tolerance, and heat shock protein 70 (HSP70) mRNA expression and protein synthesis was performed at Day 2 and 3, respectively. Results: Cell proliferation was more at 37°C than at 32°C and 41°C. Cell viability and the number of TUNEL-positive cells were not affected until Day 8 and 3, respectively. The expression of the ECM-related genes was up-regulated at higher temperature. The expression of MMP13, a type II collagen destructive enzyme, and that of TIMP1 and TIMP2, which are MMP inhibitors, were up-regulated at higher temperatures. Finally, the chondrocytes cultured at 41°C may acquire heat stress tolerance, in part, due to the up-regulation of HSP70, and may inhibit apoptosis induced by various stresses, which is observed in OA. Conclusions: The thermal environment affects articular chondrocyte metabolism, and a heat stimulus of approximately 41°C could enhance chondrocyte anabolism and induce heat stress tolerance.
机译:目的:为了促进建立有效的骨关节炎(OA)热疗法,我们研究了热环境对体外关节软骨细胞代谢的影响。方法:从猪膝关节中分离软骨细胞,并分别在32℃,37℃和41℃下培养。在第2、4和8天评估细胞增殖和活力。此外,在第3天进行TdT介导的dUTP缺口末端标记(TUNEL)分析,以确定凋亡的软骨细胞比例。在第2天对与软骨细胞外基质(ECM),软骨破坏和软骨保护相关的因子进行了特异性基因分析。此外,评估了热应激耐受性和热休克蛋白70(HSP70)mRNA表达和蛋白合成。分别在第2天和第3天进行。结果:在37°C时,细胞增殖比在32°C和41°C时更高。直到第8天和第3天,细胞活力和TUNEL阳性细胞的数量才受到影响。 ECM相关基因的表达在较高温度下被上调。 II型胶原破坏性酶MMP13的表达以及MMP抑制剂TIMP1和TIMP2的表达在较高温度下被上调。最后,在41°C下培养的软骨细胞可能部分由于HSP70的上调而获得了热应激耐受性,并且可能抑制了在OA中观察到的各种应激诱导的细胞凋亡。结论:热环境影响关节软骨细胞的代谢,大约41°C的热刺激可以增强软骨细胞的合成代谢并诱导热应激耐受性。

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