Bando Yasuhiko, Sakashita Hide, Taira Fuyoko, Miyake Genki, Ogasawara Yudai, Sakiyama Koji, Owada Yuji, Amano Osamu
Division of Anatomy, Meikai University School of Dentistry, 1-1 Keyakidai, Sakado, Saitama, 3500283, Japan.
Division of Maxillofacial Surgery II, Meikai University School of Dentistry, 1-1 Keyakidai, Sakado, Saitama, 3500283, Japan.
Histochem Cell Biol. 2018 Jun;149(6):645-654. doi: 10.1007/s00418-018-1653-1. Epub 2018 Feb 20.
Septoclasts are mononuclear spindle-shaped phagocytes with their long processes in uncalcified cartilage matrices and locate adjacent to the capillary endothelium at the chondro-osseous junction of the growth plate. We have previously revealed a selective expression of epidermal-type fatty acid-binding protein (E-FABP/FABP5) in septoclasts. Although, pericytes are known to distribute along capillaries and directly surround their endothelial cells in a situation similar to septoclasts, no clear evidence is available on the relationship between septoclasts and pericytes. We investigated the chronological localization and morphological change of septoclasts during development of the tibia of mice to clarify the development of septoclasts and the immune-localization of pericyte markers in septoclasts to clarify the origin of septoclasts. E-FABP-immunoreactive septoclasts emerged at the perichondrium in the middle of the cartilaginous templates of the tibia in prenatal development. Septoclasts migrated to the surface of the cartilage adjacent to invading blood vessels. Processes of septoclasts became longer and their apexes attached to Von Kossa-negative uncalcified matrices during the formation process of the primary ossification center. Not only platelet-derived growth factor receptor beta, but also neuron-glial antigen 2 was localized in septoclasts of mice from E15 (embryonic day 15) to P6w (postnatal 6 week). Our results suggest that septoclasts are originated from pericytes and involved in the blood vessel invasion during formation of the primary ossification center.
破骨细胞是单核梭形吞噬细胞,其长突起位于未钙化的软骨基质中,并位于生长板软骨-骨交界处的毛细血管内皮附近。我们之前已经揭示了表皮型脂肪酸结合蛋白(E-FABP/FABP5)在破骨细胞中的选择性表达。尽管已知周细胞沿毛细血管分布,并在类似于破骨细胞的情况下直接围绕其内皮细胞,但关于破骨细胞与周细胞之间的关系尚无明确证据。我们研究了小鼠胫骨发育过程中破骨细胞的时间定位和形态变化,以阐明破骨细胞的发育以及破骨细胞中周细胞标志物的免疫定位,从而阐明破骨细胞的起源。在产前发育过程中,E-FABP免疫反应性破骨细胞出现在胫骨软骨模板中部的软骨膜处。破骨细胞迁移到与侵入血管相邻的软骨表面。在初级骨化中心形成过程中,破骨细胞的突起变长,其顶端附着于冯·科萨阴性未钙化基质。从胚胎第15天(E15)到出生后第6周(P6w),血小板衍生生长因子受体β和神经胶质抗原2均定位于小鼠的破骨细胞中。我们的结果表明,破骨细胞起源于周细胞,并参与初级骨化中心形成过程中的血管侵入。