Department of Molecular Genetics, The Weizmann Institute of Science, Rehovot, Israel.
Methods Mol Biol. 2024;2743:57-79. doi: 10.1007/978-1-0716-3569-8_4.
Osteoclasts are specialized cells that degrade bone and are essential for bone formation and maintaining bone homeostasis. Excess or deficient activity of these cells can significantly alter bone mass, structure, and physical strength, leading to significant morbidity, as in osteoporosis or osteopetrosis, among many other diseases. Protein phosphorylation in osteoclasts plays critical roles in the signaling pathways that govern the production of osteoclasts and regulate their bone-resorbing activity. In this chapter, we describe the isolation of mouse splenocytes and their differentiation into mature osteoclasts on resorptive (e.g., bone) and non-resorptive (e.g., plastic or glass) surfaces, examining matrix resorption by osteoclasts, immunofluorescence staining of these cells, and knocking out genes by CRISPR in the mouse osteoclastogenic cell line RAW264.7.
破骨细胞是专门降解骨骼的细胞,对于骨骼的形成和维持骨骼内稳态至关重要。这些细胞的过度或不足活动会显著改变骨量、结构和物理强度,导致骨质疏松症或石骨症等多种疾病的发生。破骨细胞中的蛋白磷酸化在调控破骨细胞生成和调节其骨吸收活性的信号通路中发挥着关键作用。在本章中,我们描述了从小鼠脾脏细胞中分离并在有(如骨)和无(如塑料或玻璃)吸收表面上将其分化为成熟破骨细胞的方法,检测破骨细胞对基质的吸收、这些细胞的免疫荧光染色,以及在小鼠破骨细胞生成细胞系 RAW264.7 中通过 CRISPR 敲除基因。