Coleman Rhima M, Case Natasha D, Guldberg Robert E
Parker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Biomaterials. 2007 Apr;28(12):2077-86. doi: 10.1016/j.biomaterials.2007.01.010. Epub 2007 Jan 24.
The aim of this study was to investigate the effects of alginate and agarose on the response of bone marrow stromal cells (BMSCs) to chondrogenic stimuli. Rat BMSCs were expanded in monolayer culture with or without FGF-2 supplementation. Cells were then seeded in 2% alginate and agarose gels and cultured in media with or without TGF-beta1 or dexamethasone (Dex). Sulfated glycosaminoglycans (sGAGs), collagen type II, and aggrecan were expressed in all groups that received TGF-beta1 treatment during hydrogel culture. Expansion of rat BMSCs in the presence of FGF-2 increased production of sGAG in TGF-beta1-treated groups over those cultures that were treated with TGF-beta1 alone in alginate cultures. However, in agarose, cells exposed to FGF-2 during expansion produced less sGAG within TGF-beta1-supplemented groups over those cultures treated with TGF-beta1 alone. Dex was required for optimal matrix synthesis in both hydrogels, but was found to decrease cell viability in agarose constructs. These results indicate that the response of BMSCs to a chondrogenic growth factor regimen is scaffold dependent.
本研究的目的是探讨藻酸盐和琼脂糖对骨髓基质细胞(BMSCs)软骨形成刺激反应的影响。将大鼠BMSCs在添加或不添加FGF-2的单层培养中进行扩增。然后将细胞接种到2%的藻酸盐和琼脂糖凝胶中,并在添加或不添加转化生长因子-β1(TGF-β1)或地塞米松(Dex)的培养基中培养。在水凝胶培养期间接受TGF-β1处理的所有组中均表达了硫酸化糖胺聚糖(sGAGs)、II型胶原和聚集蛋白聚糖。与在藻酸盐培养中仅用TGF-β1处理的培养物相比,在FGF-2存在下扩增大鼠BMSCs增加了TGF-β1处理组中sGAG的产生。然而,在琼脂糖中,与仅用TGF-β1处理的培养物相比,在扩增过程中暴露于FGF-2的细胞在添加TGF-β1的组中产生的sGAG较少。在两种水凝胶中,Dex都是最佳基质合成所必需的,但发现它会降低琼脂糖构建体中的细胞活力。这些结果表明,BMSCs对软骨形成生长因子方案的反应取决于支架。