Marino Silvia, Logan John G, Mellis David, Capulli Mattia
Academic Unit of Bone Biology, Department of Human Metabolism, Mellanby Centre for Bone Research, University of Sheffield , Sheffield, UK.
Department of Molecular Endocrinology, Imperial College London, Hammersmith Hospital , London, UK.
Bonekey Rep. 2014 Sep 10;3:570. doi: 10.1038/bonekey.2014.65. eCollection 2014.
Osteoclasts are highly specialized cells of haematopoietic lineage that are uniquely responsible for bone resorption. In the past, osteoclasts were isolated as mature cells from chicken long bones, or were generated using osteoblasts or stromal cells to induce osteoclast formation in total bone marrow from mice or rabbits. The Copernican revolution in osteoclast biology began with the identification of macrophage-colony stimulating factor (M-CSF) and receptor activator NFκB-ligand (RANKL ) as the key regulators of osteoclast formation, fusion and function. The availability of recombinant human and mouse M-CSF and RANKL has enabled researchers to reliably generate osteoclasts from primary monocyte/macrophage cells as well as from cell lines such as RAW 264.7. This article summarizes the most commonly used procedures for the isolation, generation and characterization of human, rodent and chicken osteoclasts in vitro. Lists of further reading and recommendations are included to facilitate a successful application by the reader.
破骨细胞是造血谱系中高度特化的细胞,唯一负责骨吸收。过去,破骨细胞是从鸡的长骨中分离出成熟细胞,或者使用成骨细胞或基质细胞诱导小鼠或兔子全骨髓中的破骨细胞形成。破骨细胞生物学的哥白尼式革命始于巨噬细胞集落刺激因子(M-CSF)和核因子κB受体活化因子配体(RANKL)被确定为破骨细胞形成、融合和功能的关键调节因子。重组人源和鼠源M-CSF以及RANKL的可得性使研究人员能够可靠地从原代单核细胞/巨噬细胞以及RAW 264.7等细胞系中生成破骨细胞。本文总结了体外分离、生成和鉴定人、啮齿动物和鸡破骨细胞的最常用方法。还列出了进一步阅读的文献和建议,以方便读者成功应用。