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Migration of Marrow Stromal Cells in Response to Sustained Release of Stromal-Derived Factor-1α from Poly(lactide ethylene oxide fumarate) Hydrogels

机译:骨髓基质细胞迁移响应于聚(丙交酯环氧乙烷富马酸盐)水凝胶的基质衍生因子-1α的持续释放

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Stromal derived factor-1α (SDF-1α) is an important chemokine in stem cell trafficking and plays a critical role in the homing, osteogenesis as well as angiogenesis of bone marrow stromal (BMS) cells. The objective of this work was to investigate the release characteristics of SDF-1α from the degradable poly(lactide ethylene oxide fumarate) (PLEOF) hydrogels and to determine the effect of sustained release of SDF-1α on migration of BMS cells. Three PLEOF macromers with PLA content of 6, 9, and 24 by weight were synthesized by condensation polymerization. The cumulative amount of biologically-active SDF-1α released from the PLEOF hydrogels after 3 weeks was between 20-25% of the initial loading and was independent of PLA/PEG ratio in the hydrogel. The migration of BMS cells in response to the time-release SDF-1α from PLEOF hydrogels closely followed the release kinetics of SDF-1α from the hydrogels. Results demonstrate that migration of BMS cells was significantly increased by the sustained release of SDF-1α from PLEOF hydrogels.
机译:基质衍生因子-1α(SDF-1α)是干细胞运输中的重要趋化因子,并在归巢,骨发生以及骨髓基质(BMS)细胞的血管生成中起着关键作用。该作品的目的是研究来自可降解聚(丙交酯环氧乙烷富马酸盐)(Pleof)水凝胶的SDF-1α的释放特性,并确定SDF-1α缓释对BMS细胞迁移的影响。通过缩合聚合合成具有PLA含量为6,9和24重量的PLA含量的三种碎片碎片。在3周后,从水凝胶中释放的生物活性SDF-1α的累积量在初始载荷的20-25%之间,与水凝胶中的PLA / PEG比无关。 BMS细胞响应于来自水凝胶的时间释放SDF-1α的迁移,紧密遵循来自水凝胶的SDF-1α的释放动力学。结果表明,通过来自水凝胶的持续释放SDF-1α的持续释放,BMS细胞的迁移显着增加。

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