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首页> 外文期刊>Urology >Differentiation of human adipose-derived stem cells Co-cultured with urothelium cell line toward a urothelium-like phenotype in a nude murine model
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Differentiation of human adipose-derived stem cells Co-cultured with urothelium cell line toward a urothelium-like phenotype in a nude murine model

机译:在裸鼠模型中,与尿路上皮细胞系共培养的人脂肪干细胞向尿路上皮样表型的分化

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Objective: To investigated the urothelium differentiation potential of adipose-derived stem cells (ASCs) that were coimplanted with the immortalized human bladder urothelium cell line (SV-HUC-1) into the subcutaneous tissue of athymic mice. Materials and Methods: The ASCs were isolated from the human adipose tissue of patients undergoing liposuction procedures and were expanded in vitro. After labeling with CM-DiI, the ASCs were mixed with SV-HUC-1 and implanted into the subcutaneous tissue of athymic mice for 2 and 4 weeks. The urothelium-specific markers uroplakin-Ia and uroplakin-II were detected by immunofluorescence. The transformation rate of ASCs into the urothelium phenotype was evaluated at each measurement point. Results: We found that 25.87% ?? 1.38% of ASCs expressed the urothelium-specific marker uroplakin-Ia and 23.60% ?? 2.57% of ASCs expressed uroplakin-II 2 weeks after coimplantation with SV-HUC-1 in vivo. After 4 weeks, 70.07% ?? 3.84% of ASCs expressed uroplakin-Ia and 65.56% ?? 2.94% expressed uroplakin-II. However, no obvious organizational multilayered urothelium structure, such as that of the native bladder mucosa, was found in the subcutaneous tissues of the athymic mice. Conclusion: The results of our study have demonstrated that ASCs could be differentiated toward the urothelium-like phenotype when they were coimplanted in direct contact with cells of a mature urothelium cell line, and the proportion of differentiated cells increased from 2 to 4 weeks. The differentiation potential of ASCs toward the urothelial cell type suggests that ASCs might have potential to be used in urinary tract repair with a tissue engineering approach in the future. ? 2013 Elsevier Inc.
机译:目的:研究与永生化人膀胱尿路上皮细胞系(SV-HUC-1)共植入到无胸腺小鼠皮下组织的脂​​肪干细胞(ASC)的尿路上皮分化潜能。材料与方法:ASCs是从接受抽脂手术的患者的人体脂肪组织中分离出来的,并在体外进行了扩增。用CM-DiI标记后,将ASC与SV-HUC-1混合并植入到无胸腺小鼠的皮下组织中2周和4周。通过免疫荧光检测尿路上皮特异性标志物uroplakin-Ia和uroplakin-II。在每个测量点评估ASCs向尿路上皮表型的转化率。结果:我们发现25.87% 1.38%的ASC表达尿路上皮特异性标记物uroplakin-Ia和23.60%??在体内与SV-HUC-1共植入后2周,2.57%的ASC表达了uroplakin-II。 4周后,70.07% 3.84%的ASC表达了uroplakin-Ia和65.56%?? 2.94%的人表达了uroplakin-II。然而,在无胸腺小鼠的皮下组织中未发现明显的组织化多层尿路上皮结构,例如天然膀胱粘膜的结构。结论:我们的研究结果表明,当ASC与成熟的尿路上皮细胞系细胞直接接触共植入时,它们可以分化为尿路上皮样表型,分化细胞的比例从2周增加到4周。 ASCs向尿路上皮细胞类型的分化潜力表明,ASCs将来可能会通过组织工程学方法用于尿路修复。 ? 2013爱思唯尔公司

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