Xu Haiwei, Xu Baoshan, Yang Qiang, Li Xiulan, Zhang Yang, Zhang Chunqiu, Wu Yaohong, Cui Li
Department of Spinal Surgery, Tianjin Hospital, Tianjin, 300211, P.R.China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2013 Feb;27(2):193-8.
To observe the chondrogenic differentiation of adipose-derived stem cells (ADSCs) by co-culturing chondrocytes and ADSCs.
ADSCs and chondrocytes were isolated and cultured from 8 healthy 4-month-old New Zealand rabbits (male or female, weighing 2.2-2.7 kg). ADSCs and chondrocytes at passage 2 were used. The 1 mL chondrocytes at concentration 2 x 10(4)/mL and 1 mL ADSCs at concentration 2 x 10(4)/mL were seeded on the upper layer and lower layer of Transwell 6-well plates separately in the experimental group, while ADSCs were cultured alone in the control group. The morphology changes of the induced ADSCs were observed by inverted phase contrast microscope. The glycosaminoglycan and collagen type II synthesized by the induced ADSCs were detected with toluidine blue staining and immunohistochemistry staining. The mRNA expressions of collagen type II, aggrecan, and SOX9 were detected with real-time fluorescent quantitative PCR.
ADSCs in the experimental group gradually became chondrocytes-like in morphology and manifested as round; while ADSCs in the control group manifested as long spindle in morphology with whirlool growth pattern. At 14 days after co-culturing, the results of toluidine blue staining and immunohistochemistry staining were positive in the experimental group, while the results were negative in the control group. The results of real-time fluorescent quantitative PCR indicated that the expression levels of collagen type II, aggrecan, and SOX9 mRNA in the experimental group (1.43 +/- 0.07, 2.13 +/- 0.08, and 1.08 +/- 0.08) were significantly higher than those in the control group (0.04 +/- 0.03, 0.13 +/- 0.04, and 0.10 +/- 0.02) (P < 0.05).
ADSCs can differentiate into chondrocytes-like after co-culturing with chondrocytes.
通过软骨细胞与脂肪来源干细胞(ADSCs)共培养,观察ADSCs的软骨分化情况。
从8只健康的4月龄新西兰兔(雌雄不限,体重2.2 - 2.7 kg)分离并培养ADSCs和软骨细胞。使用第2代的ADSCs和软骨细胞。实验组将浓度为2×10⁴/mL的1 mL软骨细胞和浓度为2×10⁴/mL的1 mL ADSCs分别接种于Transwell 6孔板的上层和下层,而对照组单独培养ADSCs。用倒置相差显微镜观察诱导后ADSCs的形态变化。用甲苯胺蓝染色和免疫组织化学染色检测诱导后ADSCs合成的糖胺聚糖和Ⅱ型胶原。用实时荧光定量PCR检测Ⅱ型胶原、聚集蛋白聚糖和SOX9的mRNA表达。
实验组ADSCs形态逐渐变为类软骨细胞样,呈圆形;而对照组ADSCs形态呈长梭形,呈漩涡状生长模式。共培养14天后,实验组甲苯胺蓝染色和免疫组织化学染色结果为阳性,而对照组结果为阴性。实时荧光定量PCR结果显示,实验组Ⅱ型胶原、聚集蛋白聚糖和SOX9 mRNA的表达水平(1.43±0.07、2.13±0.08和1.08±0.08)显著高于对照组(0.04±0.03、0.13±0.04和0.10±0.02)(P < 0.05)。
ADSCs与软骨细胞共培养后可分化为类软骨细胞。