Musculoskeletal Research Center, Division of Bone and Mineral Diseases, Department of Medicine.
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110.
Microbiol Spectr. 2016 Jun;4(3). doi: 10.1128/microbiolspec.MCHD-0011-2015.
The differentiation of osteoclasts (OCs) from early myeloid progenitors is a tightly regulated process that is modulated by a variety of mediators present in the bone microenvironment. Once generated, the function of mature OCs depends on cytoskeletal features controlled by an αvβ3-containing complex at the bone-apposed membrane and the secretion of protons and acid-protease cathepsin K. OCs also have important interactions with other cells in the bone microenvironment, including osteoblasts and immune cells. Dysregulation of OC differentiation and/or function can cause bone pathology. In fact, many components of OC differentiation and activation have been targeted therapeutically with great success. However, questions remain about the identity and plasticity of OC precursors and the interplay between essential networks that control OC fate. In this review, we summarize the key principles of OC biology and highlight recently uncovered mechanisms regulating OC development and function in homeostatic and disease states.
破骨细胞 (OC) 由早期髓系前体分化而来,这是一个受到骨微环境中多种介质严格调控的过程。一旦生成,成熟 OC 的功能取决于受骨侧膜上含有 αvβ3 的复合物控制的细胞骨架特征,以及质子和酸性蛋白酶组织蛋白酶 K 的分泌。OC 还与骨微环境中的其他细胞(包括成骨细胞和免疫细胞)有重要的相互作用。OC 分化和/或功能的失调可导致骨病理学。事实上,OC 分化和激活的许多成分已被成功地作为治疗靶点。然而,OC 前体的身份和可塑性以及控制 OC 命运的基本网络之间的相互作用仍存在疑问。在这篇综述中,我们总结了 OC 生物学的关键原则,并强调了最近发现的在稳态和疾病状态下调节 OC 发育和功能的机制。