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首页> 外文期刊>Dental Materials Journal >Differentiation behavior of iPS cells cultured on PLGA with osteoinduction medium
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Differentiation behavior of iPS cells cultured on PLGA with osteoinduction medium

机译:骨诱导培养基在PLGA上培养的iPS细胞的分化行为

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摘要

In the present report, we have generated osteoblast-like cells derived from mouse induced-pluripotent stem (iPS) cells on PLGA with osteoinduction medium in vitro and in vivo . The cell culture period was 2 weeks. At 2 weeks, mRNA level of type I collagen was significantly higher than at 1 week. Osteocalcin mRNA level at 2 weeks was tendency to increase compared with at 1 week. And the cells cultured on PLGA were positive for immunofluorescent staining of osteocalcin and alizarin red S staining. The scaffold and osteogenic-like cells induced in vitro were implanted subcutaneously into SCID mice. In resected teratoma, hard tissues resembling bone were observed mixed with other tissues on the scaffold. The sum of these findings suggests that PLGA does not disturb the osteogenesis of iPS cells.
机译:在本报告中,我们已经在体外和体内用骨诱导培养基在PLGA上产生了源自小鼠诱导多能干(iPS)细胞的成骨样细胞。细胞培养期为2周。在2周时,I型胶原的mRNA水平显着高于1周时。与第1周相比,第2周的骨钙素mRNA水平有增加的趋势。 PLGA培养的细胞对骨钙素的免疫荧光染色和茜素红S染色呈阳性。将体外诱导的支架和成骨样细胞皮下植入SCID小鼠。在切除的畸胎瘤中,观察到类似于骨骼的硬组织与支架上的其他组织混合。这些发现的总和表明PLGA不会干扰iPS细胞的成骨作用。

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