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组织工程皮肤种子细胞的同期快速分离
引用本文:杨斌,洪清琦,徐令,丘日升,张琳,董月桐. 组织工程皮肤种子细胞的同期快速分离[J]. 中国修复重建外科杂志, 2006, 20(7): 754-757
作者姓名:杨斌  洪清琦  徐令  丘日升  张琳  董月桐
作者单位:1. 中山大学附属第二医院(孙逸仙纪念医院)整形外科,广州,510120
2. 中山大学附属第二医院干细胞研究中心,广州,510120
基金项目:广东省科技计划;广东省自然科学基金
摘    要:目的 寻找一种快速可行的同期分离组织工程皮肤种子细胞——表皮细胞及成纤维细胞的方法。方法 取手术切除包皮,利用Ⅰ型胶原酶结合胰蛋白酶消化法,同期分离表皮细胞及成纤维细胞,观察细胞形态。对表皮细胞及表皮干细胞行PAN—FITC、K19-FITC荧光免疫染色及K19流式细胞仪鉴定;对成纤维细胞行波形蛋白FITC免疫荧光鉴定。并分别对两种细胞培养7d,观察其生长情况。结果 应用Ⅰ型胶原酶结合胰蛋白酶,在3h内快速分离得到表皮细胞及成纤维细胞,免疫荧光染色表皮细胞PAN—FITC染色均为阳性、K19-FITC染色部分阳性,流式细胞仪鉴定其K19阳性表达的细胞接近17%。表皮细胞培养48h开始呈克隆样增长,至7d生长停滞,向终末的角细胞分化。成纤维细胞体外培养7d可扩增100倍,波形蛋白FITC免疫荧光染色呈阳性。结论 利用胶原酶结合胰蛋白酶消化法可在3h内同期分离到用于构建复合型组织工程皮肤的种子细胞,为复合组织工程皮肤的快速构建提供了可能。

关 键 词:组织工程  皮肤  表皮干细胞  快速分离
收稿时间:2005-10-11
修稿时间:2006-04-29

FAST HARVEST OF SEED CELLS FOR COMPOSITE TISSUE ENGINEERED SKIN AT ONE TIME
YANG Bin, HONG Qingqi, XU Ling,et al.. FAST HARVEST OF SEED CELLS FOR COMPOSITE TISSUE ENGINEERED SKIN AT ONE TIME[J]. Chinese journal of reparative and reconstructive surgery, 2006, 20(7): 754-757
Authors:YANG Bin   HONG Qingqi   XU Ling  et al.
Affiliation:Department of Plastic Surgery, Second Affiliated Hospital, Sun Yat-Sen University, Guangzhou Guangdong, 510120, P. R. China
Abstract:OBJECTIVE: To find a feasible method that can fast isolate seed cells, keratinocyte stem cell and fibroblasts, for composite tissue engineered skin. METHODS: The foreskin could be attained from posthectomy, the subcutaneous tissue was removed completely, and the full-thick skin was cut into pieces, 2 mm x 2 mm in size, then the pieces were submerged into a centrifuge tube containing collagenase I in a oscillator. After 3-hour digestion at 37 degrees C, the dermis was dissolved completely with all the fibroblasts in the digestion solution and the epidermis could be separated easily. With more than 10-minute digestion in trypsin at 37 degrees C, the epidermal cells could be harvested. Then flowcytometry and FITC-immunofluorescence for cytokeratin 19 of epidermal cells and FITC-immunofluorescence of vimentin of fibroblast were conducted to identify keratinocyte stem cells in the epidermal cells and fibroblasts in the digestion solution. Moreover, epidermal cells and fibroblasts were cultured in vitro for 7 days to investigate their biological behavior. RESULTS: Using collagenase I combined with trypsin, epidermal cells and fibroblasts could be isolated at one time within 3 hours. Up to 17% cells demonstrated cytokeratin 19 positive in the epidermal cells, with fibroblast vimentin positive. The amount of fibroblast could be enlarged to more than 100 times within 6 days, but the putative keratinocyte stem cells were difficult for subculture. CONCLUSION: Seed cells for composite tissue engineered skin could be harvested fast at one time, that made it possible to reconstruct composite tissue-engineered skin in vitro.
Keywords:Tissue engineering Skin Keratinocyte stem cells Fast isolation
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