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通过模拟皮肤微环境将脐带间充质干细胞转分化为表皮样细胞

Transdifferentiation of Umbilical Cord-Derived Mesenchymal Stem Cells Into Epidermal-Like Cells by the Mimicking Skin Microenvironment.

作者信息

Chen Deyun, Hao Haojie, Tong Chuan, Liu Jiejie, Dong Liang, Ti Dongdong, Hou Qian, Liu Huiling, Han Weidong, Fu Xiaobing

机构信息

Chinese PLA General Hospital, Beijing, China.

Chinese PLA General Hospital, Beijing, China

出版信息

Int J Low Extrem Wounds. 2015 Jun;14(2):136-45. doi: 10.1177/1534734615569913. Epub 2015 Feb 20.

DOI:10.1177/1534734615569913
PMID:25700709
Abstract

Human umbilical cord-derived mesenchymal stem cells (UC-MSCs) are multipotent, primitive, and have been widely used for skin tissue engineering. Their transdifferentiation is determined by the local microenvironment. In this study, we investigated the potential epidermal differentiation of UC-MSCs and the formation of epidermis substitutes in a 3-dimensional (3D) microenvironment, which was fabricated by UC-MSCs embedded into collagen-chitosan scaffolds (CCSs) combined with an air-liquid interface (ALI) culture system. Using fluorescence microscope, we observed that UC-MSCs were spindle-shaped and evenly distributed in the scaffold. Methyl thiazolyl blue tetrazolium bromide assay and Live/Dead assay indicated that the CCSs have good biocompatibility with UC-MSCs. Immunohistochemistry and western blotting assay showed that UC-MSCs on the surface of the CCSs were positive for the epidermal markers cytokeratin 19 and involucrin at 14 days. In addition, hematoxylin-eosin staining indicated that multilayered epidermis substitutes were established. The constructed epidermis substitutes were applied to treat full-thickness wounds in rats and proved to promote wound healing. In conclusion, manipulating the 3D microenvironment is a novel method for inducing the epidermal differentiation of MSCs to engineer epidermal substitutes, which provides an alternative strategy for skin tissue engineering.

摘要

人脐带间充质干细胞(UC-MSCs)具有多能性、原始性,已广泛应用于皮肤组织工程。它们的转分化由局部微环境决定。在本研究中,我们研究了UC-MSCs在三维(3D)微环境中的潜在表皮分化以及表皮替代物的形成,该微环境是通过将UC-MSCs嵌入胶原-壳聚糖支架(CCSs)并结合气液界面(ALI)培养系统构建而成。使用荧光显微镜,我们观察到UC-MSCs呈纺锤形且均匀分布在支架中。甲基噻唑基蓝四氮唑溴盐法和活/死细胞检测表明CCSs与UC-MSCs具有良好的生物相容性。免疫组织化学和蛋白质印迹分析表明,在第14天时,CCSs表面的UC-MSCs对表皮标志物细胞角蛋白19和外皮蛋白呈阳性。此外,苏木精-伊红染色表明建立了多层表皮替代物。构建的表皮替代物应用于治疗大鼠的全层伤口,并证明可促进伤口愈合。总之,操控3D微环境是诱导MSCs表皮分化以构建表皮替代物的一种新方法,为皮肤组织工程提供了一种替代策略。

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