Hashimoto Yoshiya, Adachi Seita, Matsuno Tomonori, Omata Kazuhiko, Yoshitaka Yamauchi, Ozeki Yasuyuki, Umezu Yoshikazu, Satoh Tazuko, Nakamura Masaaki
Department of Biomaterials, Osaka Dental University, Osaka, Hirakata, Osaka, Japan.
Biomed Mater Eng. 2009;19(6):391-400. doi: 10.3233/BME-2009-0604.
The objective of this study was to evaluate the effect of beta-tricalcium phosphate (beta-TCP) bead size on the behavior of KUSA/A1 mouse osteoblasts when the beta-TCP beads are used as the solid phase of a scaffold in which alginate was used as the gel phase. KUSA/A1 cells were loaded onto a three-dimensional (3D) scaffold fabricated from beta-TCP beads with diameters ranging from 300 to 500 microm (small beads), 500-700 microm (medium beads) and 700-850 microm (large beads); cells were cultured for 3, 7 and 14 days. Scanning electron microscope observations showed that each bead was connected in a network consisting of the alginate gel and KUSA/A1 cellular matrix that was tightly bonded to form a 3D structure. After 3 days, cells in the 3D scaffold with medium beads had a significantly higher alkaline phosphatase activity (ALP) than cells in the other scaffolds. However, by 7 and 14 days in culture there was no significant difference in DNA levels, ALP activity or osteocalcin expression. At 8 weeks, only the composite containing small beads and KUSA/A1 cells had turned completely into bone in vivo. Thus, bead size may influence the success of bone formation in this context.
本研究的目的是评估当β-磷酸三钙(β-TCP)珠粒用作支架的固相(其中藻酸盐用作凝胶相)时,β-TCP珠粒大小对KUSA/A1小鼠成骨细胞行为的影响。将KUSA/A1细胞接种到由直径范围为300至500微米(小珠粒)、500 - 700微米(中珠粒)和700 - 850微米(大珠粒)的β-TCP珠粒制成的三维(3D)支架上;细胞培养3、7和14天。扫描电子显微镜观察表明,每个珠粒都连接在由藻酸盐凝胶和紧密结合形成3D结构的KUSA/A1细胞基质组成的网络中。3天后,含有中珠粒的3D支架中的细胞碱性磷酸酶活性(ALP)明显高于其他支架中的细胞。然而,培养7天和14天后,DNA水平、ALP活性或骨钙素表达没有显著差异。在8周时,只有含有小珠粒和KUSA/A1细胞的复合材料在体内完全变成了骨。因此,在这种情况下,珠粒大小可能会影响骨形成的成功与否。