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上调趋化吸引受体 ChemR23 与骨折跟骨骨软骨碎片分离的人软骨细胞凋亡的发生。

Up-regulation of the chemo-attractive receptor ChemR23 and occurrence of apoptosis in human chondrocytes isolated from fractured calcaneal osteochondral fragments.

机构信息

Department of Biomedical, Metabolic and Neural Sciences - Section of Human Morphology, University of Modena and Reggio Emilia, Modena, Italy.

出版信息

J Anat. 2014 Jun;224(6):659-68. doi: 10.1111/joa.12176. Epub 2014 Apr 1.

Abstract

To study the expression level of a panel of pro/anti-apoptotic factors and inflammation-related receptors in chondral fragments from patients undergoing surgical treatment for intra-articular calcaneal fractures, cartilage fragments were retrieved from calcaneal fractures of 20 patients subjected to surgical treatment. Primary cultures were performed using chondral fragments from fractured and control patients. Chondrocyte cultures from each patient of the fractured and control groups were subjected to immunofluorescence staining and quantitatively analyzed under confocal microscopy. Proteins extracted from the cultured chondrocytes taken from the fractured and control groups were processed for Western blot experiments and densitometric analysis. The percentage of apoptotic cells was determined using the cleaved PARP-1 antibody. The proportion of labelled cells was 35% for fractured specimens, compared with 7% for control samples. Quantification of caspase-3 active and Bcl-2 proteins in chondrocyte cultures showed a significant increase of the apoptotic process in fractured specimens compared with control ones. Fractured chondrocytes were positively stained for ChemR23 with statistically significant differences with respect to control samples. Densitometric evaluation of the immunoreactive bands confirmed these observations. Human articular chondrocytes obtained from patients with intra-articular calcaneal fractures express higher levels of pivotal pro-apoptotic factors, and of the chemo-attractive receptor ChemR23, compared with control cultures. On the basis of these observations, the authors hypothesize that consistent prolonged chondrocyte death, associated with the persistence of high levels of pro-inflammatory factors, could enhance the deterioration of cartilage tissue with consequent development of post-traumatic arthritis following intra-articular bone fracture.

摘要

为了研究在接受关节内跟骨骨折手术治疗的患者的软骨碎片中一组促凋亡/抗凋亡因子和炎症相关受体的表达水平,从接受手术治疗的 20 例关节内跟骨骨折患者中取出软骨碎片。使用骨折和对照患者的软骨碎片进行原代培养。将骨折和对照组中每位患者的软骨细胞培养物进行免疫荧光染色,并在共聚焦显微镜下进行定量分析。从骨折和对照组的培养软骨细胞中提取蛋白质,进行 Western blot 实验和密度分析。使用 cleaved PARP-1 抗体确定凋亡细胞的百分比。骨折标本的标记细胞比例为 35%,而对照标本为 7%。骨折标本中 caspase-3 活性和 Bcl-2 蛋白的定量显示,与对照标本相比,凋亡过程明显增加。与对照标本相比,骨折软骨细胞对 ChemR23 呈阳性染色,具有统计学意义。免疫反应性条带的密度评估证实了这些观察结果。与对照培养物相比,来自关节内跟骨骨折患者的人关节软骨细胞表达更高水平的关键促凋亡因子和趋化性受体 ChemR23。基于这些观察结果,作者假设持续延长的软骨细胞死亡,伴随着高水平促炎因子的持续存在,可能会加剧软骨组织的恶化,随后发生创伤后关节炎。

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