Mikura Ayako, Okuhara Shigeru, Saito Masahiro, Ota Masato, Ueda Koichi, Iseki Sachiko
Section of Molecular Craniofacial Embryology, Tokyo Medical and Dental University Graduate School of Medical and Dental Sciences, Tokyo, Japan.
Congenit Anom (Kyoto). 2009 Jun;49(2):77-84. doi: 10.1111/j.1741-4520.2009.00227.x.
Tenascin-W is a tenascin family member that forms part of a complex extracellular matrix, and previous studies have suggested its association with osteogenesis. In the present study we investigated the roles of tenascin-W in osteogenesis. We found that tenascin-W is expressed in osteoblasts at the edge of the developing bone domain prior to mineralization in mouse fetuses. Expression of tenascin-W was induced during the course of mineralization of the Kusa-A1 osteoblast cell line. In the interfrontal suture of postnatal mice, the anterior portion remains patent and the posterior portion closes by 4 weeks of age. Tenascin-W expression was downregulated at 1 week of age in the posterior frontal suture, whereas in the anterior suture, expression was maintained until the mice reached 4 weeks of age. Fibroblast growth factor 2 (FGF2)-bead application to the mouse fetal skull by ex-utero surgery accelerated osteoblast differentiation, but inhibited mineralization with a downregulation of tenascin-W expression. These results suggest that tenascin-W is involved in osteoblast maturation (i.e. mineralization).
腱生蛋白-W是腱生蛋白家族的一员,构成复杂细胞外基质的一部分,先前的研究表明它与骨生成有关。在本研究中,我们调查了腱生蛋白-W在骨生成中的作用。我们发现,在小鼠胎儿矿化之前,腱生蛋白-W在发育中骨区域边缘的成骨细胞中表达。腱生蛋白-W的表达在久佐-A1成骨细胞系矿化过程中被诱导。在出生后小鼠的额间缝中,前部保持开放,而后部在4周龄时闭合。在额后缝中,腱生蛋白-W的表达在1周龄时下调,而在前缝中,表达一直维持到小鼠4周龄。通过宫外手术将成纤维细胞生长因子2(FGF2)珠应用于小鼠胎儿颅骨可加速成骨细胞分化,但会抑制矿化,并下调腱生蛋白-W的表达。这些结果表明,腱生蛋白-W参与成骨细胞成熟(即矿化)。