Jin Xiao-Bing, Sun Yong-Sheng, Zhang Ke, Wang Jing, Ju Xiao-Dong, Lou Si-Quan
Department of Orthopedics, Peking University, Third Hospital, Beijing 100083, China.
Acta Pharmacol Sin. 2007 May;28(5):663-71. doi: 10.1111/j.1745-7254.2007.00553.x.
To examine the chondrogenic potential of human adipose derived stem cells (hASC) induced by human transforming growth factor beta2 (hTGF beta2) in vitro, and to investigate if predifferentiated hASC can produce neocartilage in vivo.
hASC were isolated from subcutaneous adipose tissue and cultured in pellets with the addition of hTGF beta2. Chondrogenic differentiation was assayed by RT-PCR, Western blotting, toluidine blue staining, and immunohistochemistry staining for collagen type II. For the in vivo study, intact induced cell pellets or the released cells embedded in alginate gel with different concentrations were implanted subcutaneously in nude mice. Specimens were harvested at different time points and carried with histological and immunohistochemistry examination to evaluate the cartilage formation.
RT-PCR analysis revealed that hASC produced aggrecan and collagen type II after 7 d of induction and continued throughout the culture period. This was also demonstrated by the Western blot analysis, positive staining of toluidine blue, and immunohistochemistry for collagen type II. After reseeding in the monolayer, the cells isolated from the pellets displayed a polygonal morphology compared with the primary spindle shape. hASC were released from the induced cell pellets when embedded in alginate gel (implanted cell concentration=5X10(6) /mL or higher). They produced neocartilage after 12 weeks in vivo culture; however, intact induced cell pellets implanted subcutaneously rapidly lost their differentiated phenotype.
Chondrogenesis of hASC in vitro can be induced by combining pellet culture and hTGF beta2 treatment. Predifferentiated hASC embedded in alginate gel have the ability of producing neocartilage in vivo.
研究人转化生长因子β2(hTGFβ2)体外诱导人脂肪来源干细胞(hASC)的成软骨潜能,并探讨预分化的hASC在体内能否产生新软骨。
从皮下脂肪组织分离hASC,添加hTGFβ2后进行团块培养。通过RT-PCR、蛋白质印迹法、甲苯胺蓝染色及II型胶原免疫组织化学染色检测成软骨分化情况。在体内研究中,将完整的诱导细胞团块或包埋于不同浓度藻酸盐凝胶中的释放细胞皮下植入裸鼠体内。在不同时间点取材,进行组织学和免疫组织化学检查以评估软骨形成情况。
RT-PCR分析显示,诱导7 d后hASC开始产生聚集蛋白聚糖和II型胶原,并在整个培养期持续表达。蛋白质印迹分析、甲苯胺蓝阳性染色及II型胶原免疫组织化学也证实了这一点。从团块中分离的细胞重新接种于单层培养后,与原代的纺锤形相比呈现多边形形态。当包埋于藻酸盐凝胶中时(植入细胞浓度=5×10⁶/mL或更高),hASC从诱导细胞团块中释放出来。体内培养12周后它们产生了新软骨;然而,皮下植入的完整诱导细胞团块迅速丧失其分化表型。
通过团块培养联合hTGFβ2处理可诱导hASC在体外发生软骨形成。包埋于藻酸盐凝胶中的预分化hASC在体内具有产生新软骨的能力。