Hayashi Mikihito, Nakashima Tomoki, Takayanagi Hiroshi
Department of Cell Signaling, Tokyo Medical and Dental University, Japan.
Clin Calcium. 2012 Nov;22(11):1693-9.
Bone is continuously remodeled by osteoclastic bone resorption and osteoblastic bone formation to maintain the structural integrity and mineral homeostasis. This process is called "bone remodeling" . These bone cells are regulated by mechanical stimulation and systemic (hormonal) factors in addition to autocrine, paracrine factors and cell-cell interactions. Recently, we reported that two semaphorin molecules Sema4D and Sema3A have a crucial role in the regulation of bone remodeling. Sema4D derived from osteoclasts inhibits osteoblast differentiation not to hamper osteoclastic bone resorption. Sema3A derived from osteoblast lineage cells inhibits osteoclast differentiation and promotes osteoblast differentiation synchronously to increase bone mass. These studies provide a scientific basis for future therapeutic approaches to bone diseases.
骨骼通过破骨细胞的骨吸收和成骨细胞的骨形成不断重塑,以维持结构完整性和矿物质稳态。这个过程称为“骨重塑”。除了自分泌、旁分泌因子和细胞间相互作用外,这些骨细胞还受机械刺激和全身(激素)因素的调节。最近,我们报道了两种信号素分子Sema4D和Sema3A在骨重塑调节中起关键作用。破骨细胞衍生的Sema4D抑制成骨细胞分化,以免妨碍破骨细胞的骨吸收。成骨细胞谱系细胞衍生的Sema3A抑制破骨细胞分化,并同步促进成骨细胞分化以增加骨量。这些研究为未来骨疾病的治疗方法提供了科学依据。