Combined influence of basal media and fibroblast growth factor on the expansion and differentiation capabilities of adipose-derived stem cells

IF 4 Q2 CELL & TISSUE ENGINEERING
Mark Ahearne , Joanne Lysaght , Amy P Lynch
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引用次数: 1

Abstract

Background

Interest in adipose-derived stem cells (ASCs) has increased in recent years due to their multi-linage differentiation capabilities. While much work has been done to optimize the differentiation media, few studies have focused on examining the influence of different expansion media on cell behavior. In this study, three basal media (low glucose Dulbecco’s modified Eagle’s medium (DMEM), high glucose DMEM and DMEM-F12) supplemented with or without fibroblast growth factor 2 (FGF) were examined to assess their suitability for expanding ASCs.

Findings

Flow cytometry, colony-forming unit assays (CFU-Fs) and differentiation assays were utilized to study cell behavior. High glucose media CFU-Fs produced fewest colonies while the addition of FGF increased colony size. By passage 2, the majority of cells were positive for CD44, 45, 73, 90 and 105 and negative for CD14, 31 and 45, indicating a mesenchymal phenotype. A sub-population of CD34 positive cells was present among passage 2 cells; however, by passage 4 the cells were negative for CD34. FGF has a negative effective on passage 4 ASC adipogenesis and high glucose media plus FGF-enhanced osteogenic capacity of passage 4 ASCs. FGF supplemented basal media were most suitable for chondrogenesis. High glucose media plus FGF appeared to be the most beneficial for priming ASCs to induce a keratocyte phenotype.

Conclusions

These findings demonstrate the reciprocal effect FGF and basal media have on ASCs. This research has implications for those interested regenerating bone, cartilage, cornea or adipose tissues.

Abstract Image

Abstract Image

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基础培养基和成纤维细胞生长因子对脂肪源性干细胞增殖和分化能力的联合影响
近年来,由于脂肪干细胞具有多谱系分化能力,人们对其越来越感兴趣。虽然已经做了大量的工作来优化分化培养基,但很少有研究集中在检查不同的扩增培养基对细胞行为的影响。在本研究中,研究了添加或不添加成纤维细胞生长因子2 (FGF)的三种基础培养基(低糖Dulbecco 's modified Eagle 's medium, DMEM)、高糖DMEM和DMEM- f12),以评估它们对扩增ASCs的适用性。流式细胞术、集落形成单位测定(CFU-Fs)和分化测定用于研究细胞行为。高糖培养基CFU-Fs产生的菌落最少,而添加FGF使菌落大小增加。通过传代2,大多数细胞CD44、45、73、90和105表达阳性,CD14、31和45表达阴性,为间充质表型。在传代2细胞中存在CD34阳性细胞亚群;然而,通过传代4,细胞CD34表达为阴性。FGF对传代4代ASC的脂肪生成和高糖培养基以及FGF增强的传代4代ASC的成骨能力有负作用。FGF补充基础培养基最适合软骨形成。高糖培养基加FGF似乎最有利于启动ASCs诱导角质细胞表型。结论FGF和基础培养基对ASCs有相互作用。这项研究对那些对再生骨、软骨、角膜或脂肪组织感兴趣的人有启示意义。
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来源期刊
Cell Regeneration
Cell Regeneration Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
5.80
自引率
0.00%
发文量
42
审稿时长
35 days
期刊介绍: Cell Regeneration aims to provide a worldwide platform for researches on stem cells and regenerative biology to develop basic science and to foster its clinical translation in medicine. Cell Regeneration welcomes reports on novel discoveries, theories, methods, technologies, and products in the field of stem cells and regenerative research, the journal is interested, but not limited to the following topics: ◎ Embryonic stem cells ◎ Induced pluripotent stem cells ◎ Tissue-specific stem cells ◎ Tissue or organ regeneration ◎ Methodology ◎ Biomaterials and regeneration ◎ Clinical translation or application in medicine
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