Ulrike Steffen, Fabian T. Andes, Georg Schett
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引用次数: 11
Abstract
Osteoclasts are the only bone-resorbing cells in the body. Together with bone-forming osteoblasts, they are responsible for bone homeostasis and constant bone remodeling. Aberrant activation of osteoclasts leads to bone loss, as seen in postmenopausal osteoporosis or in autoimmune diseases like rheumatoid arthritis. Although much research has been performed to understand and prevent osteoclast-mediated bone loss, the mechanisms of osteoclast hyperactivation are not completely understood. This unit describes several protocols for ex vivo generation of murine and human osteoclasts, allowing study of the effects of specific cells, cytokines, or chemical substances on osteoclast formation and activity without the need for expensive and time-consuming animal experiments. In addition, we provide protocols for specific staining of osteoclasts and for analysis of resorption activity using calcium phosphate–coated surfaces or bone slices. © 2019 by John Wiley & Sons, Inc.
人与鼠破骨细胞的生成与分析
破骨细胞是人体内唯一的骨吸收细胞。它们与成骨细胞一起负责骨稳态和持续的骨重塑。破骨细胞的异常激活导致骨质流失,如绝经后骨质疏松症或自身免疫性疾病,如风湿性关节炎。尽管已经进行了大量研究来了解和预防破骨细胞介导的骨质流失,但破骨细胞过度活化的机制尚未完全了解。本单元描述了几种体外生成小鼠和人类破骨细胞的方案,允许研究特定细胞,细胞因子或化学物质对破骨细胞形成和活性的影响,而无需昂贵且耗时的动物实验。此外,我们还提供了破骨细胞特异性染色和使用磷酸钙涂层表面或骨片分析吸收活性的方案。©2019 by John Wiley &儿子,Inc。
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