Department of Orthopaedics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Cartilage. 2021 Dec;13(2_suppl):453S-464S. doi: 10.1177/1947603520978574. Epub 2020 Dec 3.
Excessive use of glucocorticoids (GCs) may cause adverse effects on the skeletal system in children. However, only a few studies have reported the effects of GCs on the epiphyseal cartilage. This study aimed to uncover the subsequent epiphyseal cartilage changes of immature femoral heads after excessive GC treatment in a mouse model and explain the pathological changes preliminarily.
Female C57BL/6 mice were divided into control and model (excessive GC treatment) groups. The structure of the femoral heads was evaluated by using micro-computed tomography, hematoxylin-eosin staining, and safranin staining analyses. Immunohistochemistry was used to detect angiogenesis and cartilage metabolism. Western blotting and TUNEL staining were used to examine epiphyseal cartilage chondrocyte apoptosis. Primary chondrocytes were isolated from the femoral heads of healthy mice for studies. The effects of GCs on chondrocyte apoptosis and metabolism were determined by flow cytometry and Western blotting.
The epiphyseal cartilage ossification had started at 4 weeks posttreatment in a portion of mice; the ossification presented as a sequential process in the model group, while the epiphyseal cartilage maintained an unossified state in the control group. Vascular invasion into the epiphyseal cartilage of the model mice was observed at 4 weeks posttreatment. GCs induced chondrocyte apoptosis and altered chondrocyte metabolism in the epiphyseal cartilage.
The epiphyseal cartilage ossification accelerated in the femoral heads of female C57BL/6 mice after excessive GC treatment. Increased chondrocyte apoptosis, altered chondrocyte metabolism, as well as increased vascular invasion, are the potential factors influencing epiphyseal cartilage ossification.
糖皮质激素(GCs)的过度使用可能会对儿童的骨骼系统造成不良影响。然而,仅有少数研究报道了 GCs 对骺软骨的影响。本研究旨在揭示在小鼠模型中,过量 GC 治疗后不成熟股骨头的骺软骨随后发生的变化,并初步解释其病理变化。
将雌性 C57BL/6 小鼠分为对照组和模型组(过度 GC 处理)。通过微计算机断层扫描、苏木精-伊红染色和番红 O 染色分析评估股骨头的结构。免疫组织化学用于检测血管生成和软骨代谢。Western blot 和 TUNEL 染色用于检测骺软骨软骨细胞凋亡。从小鼠的股骨头中分离原代软骨细胞进行研究。通过流式细胞术和 Western blot 确定 GCs 对软骨细胞凋亡和代谢的影响。
部分小鼠在治疗后 4 周时骺软骨开始骨化;模型组的骨化呈连续过程,而对照组的骺软骨保持未骨化状态。治疗后 4 周时观察到模型小鼠的血管侵入骺软骨。GCs 诱导骺软骨软骨细胞凋亡并改变骺软骨中的软骨细胞代谢。
在雌性 C57BL/6 小鼠的股骨头中,过量 GC 治疗后骺软骨骨化加速。增加的软骨细胞凋亡、改变的软骨细胞代谢以及增加的血管侵入是影响骺软骨骨化的潜在因素。