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Molecular Dynamics during Osteoclast Formation: Implication for Osteoclast Biology

机译:破骨细胞形成期间的分子动力学:骨质骨糖生物学的含义

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Osteoclasts are specialized in bone resorption and most skeletal diseases are due to excess osteoclastic activity causing pain and fracture. Scientists often use cells of monocyte-macrophage lineage (precursors) and receptor activator of nuclear factor kappa B ligand (RANKL) to understand molecular mechanism of osteoclast formation and function in order to control the osteoclast activity. However, two sets of cell types (osteoclasts and tartrate resistant acid phosphatase (TRAP) positive mononucleated cells) are generated upon RANKL treatment hindering scientists from obtaining accurate information about osteoclasts (Figure 1).
机译:骨核苷酸在骨吸收中专门从事骨吸收,大多数骨骼疾病都是由于骨质细胞体积过多,导致疼痛和骨折。科学家们经常使用单核细胞 - 巨噬细胞谱系(前体)和核因子Kappa B配体(RANKL)的受体激活剂来了解骨细胞形成和功能的分子机制,以控制破骨细胞活性。然而,在RANKL治疗中妨碍科学家获得关于骨酸骨胶的准确信息,产生两组细胞类型(骨壳抗性酸性磷酸酶(捕获)阳性单核细胞),从而获得了关于破骨细胞的准确信息(图1)。

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