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Osteogenic potential of cultured marrow stromal stem cells on the surface of zinc-containing bioceramics

机译:培养骨髓基质干细胞对含锌生物陶瓷表面的成骨潜力

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We prepared zinc-containing TCP/HAp ceramics (Zn-TCP/HAp) in the shape of disk, and examined the effect of zinc on the osteogenic differentiation of cultured marrow cells on the surface of Zn-TCP/HAp. Fresh marrow cells were obtained from the femora of Fischer rats and cultured in a medium containing 15percent fetal bovine serum to reach confluent. After trypsinization, the cells were seeded at 20 x 10~3 cells/16 mm PHI on Falcon tissue wells with the ceramic disk for subculture. Just before the cell seeding, three different disks (TCP/HAp containing 0, 0.126, or 0.316 wtpercent Zn) were placed in the wells. After 2 weeks of subculture in the presence of beta -glycerophosphate, vitamin C phosphate, and dexamethasone, the cells were stained for alkaline phosphatase (ALP). The ALP positive area on the Zn-TCP/HAp disk was expanded with an increase in Zn content, as covering almost the entire surface of the Zn-TCP/HAp disk of 0.316 Zn wtpercent. The results indicate that the Zn doped TCP/HAp ceramics stimulate osteoblastic differentiation in cultured marrow stromal cells.
机译:我们在盘的形状中制备含锌的TCP / HAP陶瓷(Zn-TCP / HAP),并检查了锌对Zn-TCP / Hap表面培养骨髓细胞的成骨细胞的影响。从费城大鼠的股票中获得新鲜骨髓细胞,并在含有15个胎儿牛血清的培养基中培养以达到汇合。在胰蛋白酶化之后,将细胞在与陶瓷盘上以20×10〜3个细胞/ 16mM pHI接种,用陶瓷盘进行亚培培。就在细胞播种之前,将三个不同的盘(包含0,0.126或0.316次WTPercent Zn)的三种不同的盘(将0.126或0.316℃)放置在孔中。在β-甘油磷酸盐存在2周后2周培养后,将细胞染色碱性磷酸酶(ALP)。 Zn-TCP / HAP盘上的ALP正区域随着Zn含量的增加而扩展,因为覆盖了0.316 Zn WTPercent的Zn-TCP / HAP盘的整个表面。结果表明,Zn掺杂的TCP / HAP陶瓷刺激培养骨髓基质细胞中的骨细胞分化。

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