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纳米 HA/胶原复合水凝胶对间充质干细胞成骨行为的影响。

Effect of Nano-HA/Collagen Composite Hydrogels on Osteogenic Behavior of Mesenchymal Stromal Cells.

机构信息

Department of Biomaterials, Radboudumc, Ph van Leijdenlaan 25, 6525 ex, Nijmegen, The Netherlands.

出版信息

Stem Cell Rev Rep. 2016 Jun;12(3):352-64. doi: 10.1007/s12015-016-9644-x.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c092/4879177/650a8dabf73c/12015_2016_9644_Fig1_HTML.jpg

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