Liu Yun-song, Lv Long-wei, Zhou Yong-sheng, Ma Gui-e, Zhang Xiao, Fan Cong, Shao Xiao
Department of Prosthodonties, Peking University School and Hospital of Stomatology, Beijing, China.
Beijing Da Xue Xue Bao Yi Xue Ban. 2012 Dec 18;44(6):916-20.
To explore the effect of human adipose-derived stromal cells (hASCs) on the osteogenesis during the process of bone formation in vivo, and to lay the foundation of further investigations on the mechanism of in vivo osteogenesis of hASCs.
hASCs were isolated from adipose tissue by the method of collagenase digestion, and were routinely proliferated and passaged. In the in vivo study 16 nude mice were used and 4 groups were set and implanted subcutaneously into the back of nude mice: (1) blank; (2) β-tricalcium phosphate (β-TCP) scaffold only (scaffold control group); (3) β-TCP scaffold with human fibroblasts (negative cell control group); (4) β-TCP scaffold with hASCs (test group). After 1 week, 2 weeks, 4 weeks and 6 weeks of implantation, samples from the 4 nude mice were collected at each time point. Scanning electron microscope (SEM) observation and histological staining were performed to evaluate the in vivo osteogenesis of hASCs.
SEM images showed that large amount of extracellular matrix (ECM) could be observed around hASCs in test group after 2 weeks of implantation. At the time point of 4 weeks, mineral deposit was found in ECM. At the time point of 6 weeks, the mineral deposit was observed to increase significantly. HE staining showed that the ECM with eosinophilic staining could be observed around hASCs after 2 weeks of implantation. At the time point of 4 weeks, newly-formed bone-like tissue could be found in ECM around the scaffold materials. At the time point of 6 weeks, more bone-like tissues were observed in ECM with typical structure of bone tissue. In comparison, no obvious mineralization and bone-like tissue were found in other groups.
hASCs play important roles in the process of osteogenesis in vivo, including secretion of large amount of ECM, acceleration of the mineralization of ECM and guidance for the formation of bone-like tissues.
探讨人脂肪来源的间充质干细胞(hASCs)在体内骨形成过程中对成骨的影响,为进一步研究hASCs体内成骨机制奠定基础。
采用胶原酶消化法从脂肪组织中分离hASCs,并进行常规增殖和传代。在体内研究中,选用16只裸鼠,分为4组,皮下植入裸鼠背部:(1)空白组;(2)仅β-磷酸三钙(β-TCP)支架(支架对照组);(3)含人成纤维细胞的β-TCP支架(阴性细胞对照组);(4)含hASCs的β-TCP支架(试验组)。植入后1周、2周、4周和6周,每个时间点收集4只裸鼠的样本。进行扫描电子显微镜(SEM)观察和组织学染色,以评估hASCs的体内成骨情况。
SEM图像显示,植入2周后试验组hASCs周围可观察到大量细胞外基质(ECM)。4周时,ECM中发现矿物质沉积。6周时,矿物质沉积明显增加。HE染色显示,植入2周后hASCs周围可观察到嗜酸性染色的ECM。4周时,支架材料周围的ECM中可发现新形成的类骨组织。6周时,ECM中观察到更多具有典型骨组织结构的类骨组织。相比之下,其他组未发现明显的矿化和类骨组织。
hASCs在体内成骨过程中发挥重要作用,包括分泌大量ECM、加速ECM矿化以及引导类骨组织形成。