Department of Biomaterials, Radboudumc, Ph van Leijdenlaan 25, 6525 ex, Nijmegen, The Netherlands.
Stem Cell Rev Rep. 2016 Jun;12(3):352-64. doi: 10.1007/s12015-016-9644-x.
This study aimed to comparatively evaluate the in vitro effect of nanosized hydroxyapatite and collagen (nHA/COL) based composite hydrogels (with different ratios of nHA and COL) on the behavior of human mesenchymal stromal cells (MSCs), isolated from either adipose tissue (AT-MSCs) or bone marrow (BM-MSCs). We hypothesized that (i) nHA/COL composite hydrogels would promote the osteogenic differentiation of MSCs in an nHA concentration dependent manner, and that (ii) AT-MSCs would show higher osteogenic potential compared to BM-MSCs, due to their earlier observed higher proliferation and osteogenic differentiation potential in 2D in vitro cultures [1]. The obtained results indicated that AT-MSCs show indeed high proliferation, differentiation and mineralization capacities in nHA/COL constructs compared to BM-MSCs, but this effect was irrespective of nHA concentration. Based on the results of alkaline phosphatase (ALP) activity and osteocalcin (OCN) protein level, the osteogenic differentiation of BM-MSCs started in the beginning of the culture period and for AT-MSCs at the end of the culture period. At a molecular level, both cell types showed high expression of osteogenic markers (bone morphogenic protein 2 [BMP2], runt-related transcription factor 2 [RUNX2], OCN or COL1) in both an nHA concentration and time dependent manner. In conclusion, AT-MSCs demonstrated higher osteogenic potential in nHA/COL based 3D micro-environments compared to BM-MSCs, in which proliferation and osteogenic differentiation were highly promoted in a time dependent manner, irrespective of nHA amount in the constructs. The fact that AT-MSCs showed high proliferation and mineralization potential is appealing for their application in future pre-clinical research as an alternative cell source for BM-MSCs.
本研究旨在比较评价纳米羟基磷灰石和胶原(nHA/COL)基复合水凝胶(具有不同 nHA 和 COL 比例)对来源于脂肪组织(AT-MSCs)或骨髓(BM-MSCs)的人间充质基质细胞(MSCs)行为的体外影响。我们假设:(i)nHA/COL 复合水凝胶将以 nHA 浓度依赖的方式促进 MSCs 的成骨分化,并且(ii)由于在二维体外培养中观察到的更高增殖和更早的成骨分化潜力,AT-MSCs 与 BM-MSCs 相比将显示出更高的成骨潜能[1]。所得结果表明,与 BM-MSCs 相比,AT-MSCs 在 nHA/COL 构建体中确实具有更高的增殖、分化和矿化能力,但这种作用与 nHA 浓度无关。基于碱性磷酸酶(ALP)活性和骨钙素(OCN)蛋白水平的结果,BM-MSCs 的成骨分化在培养期开始时开始,而 AT-MSCs 的成骨分化在培养期末开始。在分子水平上,两种细胞类型均以 nHA 浓度和时间依赖性方式高度表达成骨标志物(骨形态发生蛋白 2 [BMP2]、 runt 相关转录因子 2 [RUNX2]、OCN 或 COL1)。总之,与 BM-MSCs 相比,AT-MSCs 在基于 nHA/COL 的 3D 微环境中表现出更高的成骨潜能,其中增殖和成骨分化在时间依赖性方式下得到高度促进,而与构建体中的 nHA 量无关。AT-MSCs 表现出高增殖和矿化潜力的事实,为其作为 BM-MSCs 的替代细胞来源在未来的临床前研究中的应用提供了吸引力。