Yang Xinlin, Shang Hulan, Katz Adam, Li Xudong
Orthopedic Research Laboratory, Department of Orthopedic Surgery, University of Virginia , Charlottesville, Virginia.
Biores Open Access. 2013 Aug;2(4):258-65. doi: 10.1089/biores.2013.0014.
Adipose-derived stem cells (ADSCs) are an attractive cell source for tissue engineering, and recently a modified aggregate culture of human ADSCs (hADSCs) was established based on preparation of three-dimensional (3D) cell aggregates in growth factor-enriched low serum medium using the hanging droplet method. Growth and differentiation factor 5 (GDF5) plays a critical role in chondrogenesis and cartilage development. In the present study, we examine (1) whether the modified aggregate culture is feasible for chondrogenic induction of hADSCs, (2) whether overexpressed GDF5 can promote chondrogenesis, and (3) the gene expression profile during chondrogenesis in this aggregate culture. hADSCs were infected with an adenovirus carrying the GDF5 gene (Ad-GDF5). Cells were cultured with chondrogenic media either in a modified aggregate culture or in an attached micromass culture that served as a control. The chondrogenic phenotype was assessed by morphology (n=8), biochemistry (n=3), and histology (n=2). Expression of 12 genes was determined by quantitative real-time polymerase chain reaction (n=3). We found that ADSCs cultured in the modified aggregates exhibited denser pellets and higher content of sulfated glycosaminoglycan (sGAG) compared with those cultured in the micromass. Infection of cells with Ad-GDF5 increased the aggregate size and sGAG content. It also up-regulated expression of GDF5, aggrecan, and leptin and down-regulated expression of COL I, while expression of COL II and COL 10 remained unchanged. We concluded that the modified aggregate culture is feasible for chondrogenic induction of human ADSCs. Infection with Ad-GDF5 appears to promote the chondrogenesis. These findings suggest that genetic modification of ADSCs with GDF5 in the modified aggregate culture could be useful for treating diseases with cartilage defects.
脂肪来源干细胞(ADSCs)是组织工程中一种有吸引力的细胞来源,最近基于使用悬滴法在富含生长因子的低血清培养基中制备三维(3D)细胞聚集体,建立了人ADSCs(hADSCs)的改良聚集体培养方法。生长和分化因子5(GDF5)在软骨形成和软骨发育中起关键作用。在本研究中,我们研究了(1)改良聚集体培养对于hADSCs软骨形成诱导是否可行,(2)过表达的GDF5是否能促进软骨形成,以及(3)这种聚集体培养中软骨形成过程中的基因表达谱。用携带GDF5基因的腺病毒(Ad-GDF5)感染hADSCs。细胞在改良聚集体培养或作为对照的贴壁微团培养中用软骨形成培养基培养。通过形态学(n = 8)、生物化学(n = 3)和组织学(n = 2)评估软骨形成表型。通过定量实时聚合酶链反应测定12个基因的表达(n = 3)。我们发现,与在微团中培养的细胞相比,在改良聚集体中培养的ADSCs表现出更致密的微球和更高的硫酸化糖胺聚糖(sGAG)含量。用Ad-GDF5感染细胞增加了微球大小和sGAG含量。它还上调了GDF5、聚集蛋白聚糖和瘦素的表达,下调了COL I的表达,而COL II和COL 10的表达保持不变。我们得出结论,改良聚集体培养对于人ADSCs的软骨形成诱导是可行的。用Ad-GDF5感染似乎促进了软骨形成。这些发现表明,在改良聚集体培养中用GDF5对ADSCs进行基因修饰可能有助于治疗软骨缺损疾病。