Friedrich-Alexander-University Erlangen-Nürnberg (FAU), Department of Internal Medicine 3 - Rheumatology and Immunology, Universitätsklinikum Erlangen, Erlangen, Germany.
Friedrich-Alexander-University Erlangen-Nürnberg (FAU), Department of Internal Medicine 3 - Rheumatology and Immunology, Universitätsklinikum Erlangen, Erlangen, Germany; Department of Radiation Oncology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
Bone. 2017 Dec;105:35-41. doi: 10.1016/j.bone.2017.08.013. Epub 2017 Aug 16.
Bone tissue undergoes permanent and lifelong remodeling with a concerted action of bone-building osteoblasts and bone-resorbing osteoclasts. A precise cooperation between those two cell types is critical in the complex process of bone renewal. Galectin-3 is a member of the β-galactoside-binding lectin family playing multiple roles in cell growth, differentiation and aggregation. As it has been described to be expressed in bone, galectin-3 might influence bone homeostasis by regulating the function and/or interplay of osteoblasts and osteoclasts. Here, we investigated the role of galectin-3 in osteoclastogenesis and osteoblast-osteoclast interactions. Bone histomorphometric analysis and μCT measurements revealed a decreased trabecular bone volume and an increased osteoclast number in 12weeks old male galectin-3 knockout mice compared to wildtype littermates. Galectin-3 deficient bone marrow cells displayed a higher osteoclastogenic capacity in ex vivo differentiation assays, associated with elevated TRAF6 mRNA levels, suggesting an intrinsic inhibition of osteoclastogenesis by galectin-3 interfering with RANKL-mediated signaling. Furthermore, the addition of extracellular galectin-3 to murine or human osteoclastogenesis assays inhibited osteoclast formation and osteoclast numbers were higher in co-culture assays with galectin-3 deficient osteoblasts. In conclusion, our data suggest the secretion of galectin-3 as a novel mechanism for osteoblasts to control osteoclastogenesis and to maintain trabecular bone homeostasis independently of the RANKL/OPG-axis.
骨组织通过协同作用的成骨细胞和破骨细胞进行永久性和终身重塑。这两种细胞类型之间的精确合作对于骨更新的复杂过程至关重要。半乳糖凝集素-3 是β-半乳糖苷结合凝集素家族的一员,在细胞生长、分化和聚集中发挥多种作用。由于它被描述为在骨中表达,半乳糖凝集素-3 可能通过调节成骨细胞和破骨细胞的功能和/或相互作用来影响骨稳态。在这里,我们研究了半乳糖凝集素-3 在破骨细胞生成和破骨细胞-成骨细胞相互作用中的作用。骨组织形态计量学分析和 μCT 测量显示,与野生型同窝仔相比,12 周龄雄性半乳糖凝集素-3 敲除小鼠的小梁骨体积减少,破骨细胞数量增加。体外分化实验显示,半乳糖凝集素-3 缺陷的骨髓细胞具有更高的破骨细胞生成能力,与 TRAF6 mRNA 水平升高相关,表明半乳糖凝集素-3 通过干扰 RANKL 介导的信号转导,对内源性抑制破骨细胞生成。此外,将细胞外半乳糖凝集素-3 添加到鼠或人破骨细胞生成实验中,抑制破骨细胞形成,并且与半乳糖凝集素-3 缺陷型成骨细胞共培养时破骨细胞数量增加。总之,我们的数据表明,半乳糖凝集素-3 的分泌是成骨细胞控制破骨细胞生成并维持小梁骨稳态的一种新机制,而不依赖于 RANKL/OPG 轴。