Im Gun-Il, Jung Nam-Hee, Tae Suk-Kee
Department of Orthopedics, Dongguk University International Hospital, Goyang, Korea.
Tissue Eng. 2006 Mar;12(3):527-36. doi: 10.1089/ten.2006.12.527.
There is a controversy about the capacity of the mesenchymal stem cells (MSCs) from aged individuals to proliferate and differentiate into cartilage. The purpose of this study was to investigate the optimal condition to culture human MSCs from the aged individuals (>50 years) for cartilage tissue engineering. We tested the hypothesis that effective proliferation and chondrogenesis can be achieved with human MSCs from aged individuals under appropriate conditions. To investigate the best condition for proliferation, MSCs were cultured in medium containing four concentrations subsets (0, 0.05, 0.5, 5 ng/mL) of recombinant human TGF-beta2 and FGF-2, either with or without fetal calf serum. The cell numbers were counted 0, 1, 3, and 7 days after growth factors were given. For the induction of chondrogenesis in 3-dimensional (3-D) culture, cells were cultured in pellets with chondrogenic medium containing combinations of various growth factors. After 4 weeks of culture, the pellets were fixed and evaluated with Safranin-O staining for proteoglycan and immunohistochemical staining for type II collagen. RT-PCR was also performed for the mRNAs of type I collagen, type II collagen, and cartilage oligomeric protein (COMP). In a monolayer culture, TGF-beta2 in concentrations of 0.5 and 5 ng/mL caused significant reduction in cell number irrespective of the presence of serum. FGF-2 of 5 ng/mL most effectively increased cell number even in the absence of serum. In a pellet culture, remarkable chondrocyte-like differentiation of cells was induced around the peripheral areas of a pellet with 5 ng/mL of TGF-beta2, accompanied by increased proteoglycan and type II collagen production. The addition of 100 ng/mL of IGF-I induced notable increase in proteoglycan contents. The results of RT-PCR mirrored those of histological studies. This study shows that an effective proliferation and chondrogenesis may be obtained with proper combinations of growth factors and mesenchymal stem cells from aged individuals.
关于老年个体间充质干细胞(MSCs)增殖及分化为软骨的能力存在争议。本研究旨在探究培养老年个体(>50岁)人MSCs用于软骨组织工程的最佳条件。我们检验了如下假设:在适当条件下,老年个体的人MSCs可实现有效增殖和成软骨分化。为研究增殖的最佳条件,将MSCs培养于含有重组人转化生长因子-β2(TGF-β2)和碱性成纤维细胞生长因子-2(FGF-2)四个浓度亚组(0、0.05、0.5、5 ng/mL)的培养基中,添加或不添加胎牛血清。给予生长因子后0、1、3和7天对细胞进行计数。为在三维(3-D)培养中诱导成软骨分化,将细胞培养于含有多种生长因子组合的软骨形成培养基的微团中。培养4周后,固定微团,用番红O染色评估蛋白聚糖,用免疫组织化学染色评估II型胶原。还对I型胶原、II型胶原和软骨寡聚基质蛋白(COMP)的mRNA进行了逆转录聚合酶链反应(RT-PCR)。在单层培养中,无论有无血清,浓度为0.5和5 ng/mL的TGF-β2均导致细胞数量显著减少。即使在无血清的情况下,5 ng/mL的FGF-2最有效地增加了细胞数量。在微团培养中,5 ng/mL的TGF-β2可在微团周边区域诱导细胞显著向软骨细胞样分化,同时蛋白聚糖和II型胶原生成增加。添加100 ng/mL的胰岛素样生长因子-I(IGF-I)可使蛋白聚糖含量显著增加。RT-PCR结果与组织学研究结果一致。本研究表明,通过生长因子与老年个体间充质干细胞的适当组合,可实现有效增殖和成软骨分化。