Yang Yi, Chen Xiao-hu, Li Fu-gui, Chen Yun-xian, Gu Li-qiang, Zhu Jia-kai, Li Ping
1 Department of Microsurgery and Orthopedic Trauma, The First Affiliated Hospital of Sun Yat-sen University , Guangzhou, 510080, China .
Cell Reprogram. 2015 Feb;17(1):69-76. doi: 10.1089/cell.2014.0043.
Human adipose-derived stem cells (hADSCs) may provide a suitable number of progenitors for the treatment of lymphatic edema; however, to date the protocols for inducing hADSCs into this tissue type have not been standardized. We wished to investigate the induction of hADSCs into lymphatic endothelial-like cells using vascular endothelial growth factor-C156S (VEGF-C156S) and other growth factors in vitro. hADSCs from healthy adult adipose tissue were purified using enzyme digestion. Differentiation was induced using medium containing VEGF-C156S and bovine fibroblast growth factor (bFGF). Differentiation was confirmed using immunostaining for lymphatic vessel endothelial hyaluronan receptor (LYVE-1) and fms-related tyrosine kinase 4 (FLT-4), two lymphatic endothelial cell markers. The expression levels of LYVE-1, prospero homeobox 1 (PROX-1), and FLT-4 throughout induction were assessed using reverse transcriptase quantitative polymerase chain reaction. hADSCs were successfully obtained by trypsin digest and purification. Flow cytometry showed these cells were similar to mesenchymal stem cells, with a high positive rate of CD13, CD29, CD44, and CD105, and a low positive rate of CD31, CD34, CD45, and HLA-DR. Induction to lymphatic endothelial-like cells was successful, with cells expressing high levels of LYVE-1, PROX-1, and FLT-4. Adipose-derived stem cells can be induced to differentiate into lymphatic endothelial-like cells using a medium containing VEGF-C156S, bFGF, and other growth factors. This population of lymphatic endothelial-like cells may be useful for lymphatic reconstruction in the future.
人脂肪来源干细胞(hADSCs)可能为淋巴水肿的治疗提供合适数量的祖细胞;然而,迄今为止,将hADSCs诱导分化为这种组织类型的方案尚未标准化。我们希望研究在体外使用血管内皮生长因子C156S(VEGF-C156S)和其他生长因子将hADSCs诱导分化为淋巴管内皮样细胞。采用酶消化法从健康成人脂肪组织中纯化hADSCs。使用含有VEGF-C156S和牛碱性成纤维细胞生长因子(bFGF)的培养基诱导分化。通过对淋巴管内皮透明质酸受体(LYVE-1)和fms相关酪氨酸激酶4(FLT-4)这两种淋巴管内皮细胞标志物进行免疫染色来确认分化。使用逆转录定量聚合酶链反应评估诱导过程中LYVE-1、prospero同源框蛋白1(PROX-1)和FLT-4的表达水平。通过胰蛋白酶消化和纯化成功获得了hADSCs。流式细胞术显示这些细胞与间充质干细胞相似,CD13、CD29、CD-4 和 CD105 的阳性率较高,而 CD31、CD34、CD45 和 HLA-DR 的阳性率较低。成功诱导分化为淋巴管内皮样细胞,细胞表达高水平的LYVE-1、PROX-1和FLT-4。使用含有VEGF-C156S、bFGF和其他生长因子的培养基可诱导脂肪来源干细胞分化为淋巴管内皮样细胞。这群淋巴管内皮样细胞未来可能对淋巴重建有用。