Shi Jian-Guo, Fu Wei-Jun, Wang Xiao-Xiong, Xu Yong-De, Li Gang, Hong Bao-Fa, Hu Kun, Cui Fu-Zhai, Wang Yan, Zhang Xu
Department of Urology, Chinese People's Liberation Army General Hospital, Military Postgraduate Medical College, No.28 Fuxing Road, Hai dian District, Beijing, 100853, People's Republic of China.
Cell Tissue Res. 2012 Mar;347(3):737-746. doi: 10.1007/s00441-011-1317-0. Epub 2012 Jan 31.
Autologous urothelial cells (UCs) provide a cell source for urinary tissue engineering because they can be used safely due to their lack of immunogenicity. However, these cells cannot be harvested under the following circumstances: malignancy, infection and organ loss, etc. Human adipose-derived stem cells (HADSCs) possess the traits of high differentiation potential and ease of isolation, representing a promising resource for tissue engineering and regenerative medicine. Nevertheless, HADSCs have been poorly investigated in urology and the optimal approaches to induce HADSCs into urothelium are still under investigation. In this study, we hypothesized that the change of microenvironment by a conditioned medium was essential for the transdifferentiation of HADSCs into UCs. We then used a conditioned medium derived from urothelium to alternate the microenvironment of HADSCs. After 14 days of culture in a conditioned medium, about 25-50% HADSCs changed their morphology into polygonal epithelium-like shapes. In addition, these cells expressed up-regulating of urothelial lineage-specific markers (uroplakin 2and cytokeratin-18) and down-regulating of mesenchymal marker (vimentin) in RNA and protein level, respectively, which confirmed that HADSCs were induced into urothelial lineage cells. We also measured the growth factors in the conditioned medium in order to analyze the molecular mechanisms regulating transdifferentiation. We observed that the expression levels of PDGF-BB and VEGF were significantly higher than those of the control group after 14 days induction, suggesting they were abundantly secreted into the medium during the culturing period. In conclusion, HADSCs showed in vitro the upregulation of markers for differentiation towards urothelial cells by culturing in an urothelial-conditioned medium, which provides an alternative cell source for potential use in urinary tract tissue engineering.
自体尿路上皮细胞(UCs)为尿组织工程提供了一种细胞来源,因为它们缺乏免疫原性,可以安全使用。然而,在以下情况下无法获取这些细胞:恶性肿瘤、感染和器官缺失等。人脂肪来源干细胞(HADSCs)具有高分化潜能和易于分离的特性,是组织工程和再生医学的一种有前景的资源。然而,HADSCs在泌尿外科领域的研究较少,诱导HADSCs分化为尿路上皮细胞的最佳方法仍在研究中。在本研究中,我们假设条件培养基引起的微环境变化对于HADSCs向UCs的转分化至关重要。然后我们使用源自尿路上皮的条件培养基来改变HADSCs的微环境。在条件培养基中培养14天后,约25%-50%的HADSCs将形态转变为多边形上皮样形状。此外,这些细胞在RNA和蛋白质水平上分别上调了尿路上皮谱系特异性标志物(uroplakin 2和细胞角蛋白-18)的表达,并下调了间充质标志物(波形蛋白)的表达,这证实了HADSCs被诱导分化为尿路上皮谱系细胞。我们还测量了条件培养基中的生长因子,以分析调节转分化的分子机制。我们观察到,诱导14天后,PDGF-BB和VEGF的表达水平显著高于对照组,表明它们在培养期间大量分泌到培养基中。总之,通过在尿路上皮条件培养基中培养,HADSCs在体外显示出向尿路上皮细胞分化标志物的上调,这为尿路组织工程提供了一种潜在的替代细胞来源。