Kolambkar Yash M, Peister Alexandra, Soker Shay, Atala Anthony, Guldberg Robert E
Wallace H Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA.
J Mol Histol. 2007 Oct;38(5):405-13. doi: 10.1007/s10735-007-9118-1. Epub 2007 Aug 1.
For regenerating damaged articular cartilage, it is necessary to identify an appropriate cell source that is easily accessible, can be expanded to large numbers, and has chondrogenic potential. Amniotic fluid-derived stem (AFS) cells have recently been isolated from human and rodent amniotic fluid and shown to be highly proliferative and broadly pluripotent. The purpose of this study was to investigate the chondrogenic potential of human AFS cells in pellet and alginate hydrogel cultures. Human AFS cells were expanded in various media conditions, and cultured for three weeks with growth factor supplementation. There was increased production of sulfated glycosaminoglycan (sGAG) and type II collagen in response to transforming growth factor-beta (TGF-beta) supplementation, with TGF-beta1 producing greater increases than TGF-beta3. Modification of expansion media supplements and addition of insulin-like growth factor-1 during pellet culture further increased sGAG/DNA over TGF-beta1 supplementation alone. Compared to bone marrow-derived mesenchymal stem cells, the AFS cells produced less cartilaginous matrix after three weeks of TGF-beta1 supplementation in pellet culture. Even so, this study demonstrates that AFS cells have the potential to differentiate along the chondrogenic lineage, thus establishing the feasibility of using these cells for cartilage repair applications.
为了再生受损的关节软骨,有必要确定一种合适的细胞来源,这种来源应易于获取、能够大量扩增且具有软骨形成潜能。羊水来源的干细胞(AFS细胞)最近已从人和啮齿动物的羊水中分离出来,并显示出高度增殖和广泛的多能性。本研究的目的是探讨人AFS细胞在微球和藻酸盐水凝胶培养中的软骨形成潜能。人AFS细胞在各种培养基条件下进行扩增,并在添加生长因子的情况下培养三周。补充转化生长因子-β(TGF-β)后,硫酸化糖胺聚糖(sGAG)和II型胶原蛋白的产量增加,其中TGF-β1的增加幅度大于TGF-β3。在微球培养过程中,改变扩增培养基补充剂并添加胰岛素样生长因子-1,与单独补充TGF-β1相比,进一步增加了sGAG/DNA。在微球培养中补充TGF-β1三周后,与骨髓来源的间充质干细胞相比,AFS细胞产生的软骨基质较少。即便如此,本研究表明AFS细胞具有沿软骨形成谱系分化的潜能,从而确立了将这些细胞用于软骨修复应用的可行性。