Miyamoto Takeshi
Takeshi Miyamoto, Department of Orthopedic Surgery, Keio University School of Medicine, 35 Shinano-machi, Shinjuku-ku, Tokyo 160-8582, Japan.
World J Orthop. 2013 Oct 18;4(4):198-206. doi: 10.5312/wjo.v4.i4.198.
Bone marrow (BM) cavities are utilized for hematopoiesis and to maintain hematopoietic stem cells (HSCs). HSCs have the ability to self-renew as well as to differentiate into multiple different hematopoietic lineage cells. HSCs produce their daughter cells throughout the lifespan of individuals and thus, maintaining HSCs is crucial for individual life. BM cavities provide a specialized microenvironment termed "niche" to support HSCs. Niches are composed of various types of cells such as osteoblasts, endothelial cells and reticular cells. Osteoclasts are unique cells which resorb bones and are required for BM cavity formation. Loss of osteoclast function or differentiation results in inhibition of BM cavity formation, an osteopetrotic phenotype. Osteoclasts are also reportedly required for hematopoietic stem and progenitor cell (HSPC) mobilization to the periphery from BM cavities. Thus, lack of osteoclasts likely results in inhibition of HSC maintenance and HSPC mobilization. However, we found that osteoclasts are dispensable for hematopoietic stem cell maintenance and mobilization by using three independent osteoclast-less animal models. In this review, I will discuss the roles of osteoclasts in hematopoietic stem cell maintenance and mobilization.
骨髓腔用于造血并维持造血干细胞(HSC)。造血干细胞具有自我更新以及分化为多种不同造血谱系细胞的能力。造血干细胞在个体的整个生命周期中产生其子代细胞,因此,维持造血干细胞对个体生命至关重要。骨髓腔提供了一个称为“龛位”的特殊微环境来支持造血干细胞。龛位由多种类型的细胞组成,如成骨细胞、内皮细胞和网状细胞。破骨细胞是独特的细胞,可吸收骨骼,是骨髓腔形成所必需的。破骨细胞功能或分化的丧失会导致骨髓腔形成受到抑制,即骨质石化表型。据报道,破骨细胞也是造血干祖细胞(HSPC)从骨髓腔动员到外周所必需的。因此,缺乏破骨细胞可能会导致造血干细胞维持和造血干祖细胞动员受到抑制。然而,我们通过使用三种独立的无破骨细胞动物模型发现,破骨细胞对于造血干细胞的维持和动员是可有可无的。在这篇综述中,我将讨论破骨细胞在造血干细胞维持和动员中的作用。