Dai Niann-Tzyy, Yeh Ming-Kung, Liu Demeral David, Adams E F, Chiang Chiao-Hsi, Yen Chung-Yang, Shih Chien-Ming, Sytwu Huey-Kang, Chen Tim-Mo, Wang Hsian-Jenn, Williamson M R, Coombes A G A
National Defense Medical Center (NDMC), Tri-service General Hospital, Taipei, Taiwan, ROC.
Biochem Biophys Res Commun. 2005 Apr 15;329(3):905-8. doi: 10.1016/j.bbrc.2005.02.059.
Tissue engineering of skin based on collagen:PCL biocomposites using a designed co-culture system is reported. The collagen:PCL biocomposites having collagen:PCL (w/w) ratios of 1:4, 1:8, and 1:20 have been proven to be biocompatible materials to support both adult normal human epidermal Keratinocyte (NHEK) and mouse 3T3 fibroblast growth in cell culture, respectively, by Dai, Coombes, et al. in 2004. Films of collagen:PCL biocomposites were prepared using non-crosslinking method by impregnation of lyophilized collagen mats with PCL/dichloromethane solutions followed by solvent evaporation. To mimic the dermal/epidermal structure of skin, the 1:20 collagen:PCL biocomposites were selected for a feasibility study of a designed co-culture technique that would subsequently be used for preparing fibroblast/biocomposite/keratinocyte skin models. A 55.3% increase in cell number was measured in the designed co-culture system when fibroblasts were seeded on both sides of a biocomposite film compared with cell culture on one surface of the biocomposite in the feasibility study. The co-culture of human keratinocytes and 3T3 fibroblasts on each side of the membrane was therefore studied using the same co-culture system by growing keratinocytes on the top surface of membrane for 3 days and 3T3 fibroblasts underneath the membrane for 6 days. Scanning electron microscopy (SEM) and immunohistochemistry assay revealed good cell attachment and proliferation of both human keratinocytes and 3T3 fibroblasts with these two types of cells isolated well on each side of the membrane. Using a modified co-culture technique, a co-cultured skin model presenting a confluent epidermal sheet on one side of the biocomposite film and fibroblasts populated on the other side of the film was developed successfully in co-culture system for 28 days under investigations by SEM and immunohistochemistry assay. Thus, the design of a co-culture system based on 1:20 (w/w) collagen:PCL biocomposite membranes for preparation of a bi-layered skin model with differentiated epidermal sheet was proven in principle. The approach to skin modeling reported here may find application in tissue engineering and screening of new pharmaceuticals.
聚己内酯(PCL)生物复合材料并使用设计的共培养系统进行皮肤组织工程的研究。戴、库姆斯等人在2004年已证明,胶原蛋白与PCL(重量/重量)比例为1:4、1:8和1:20的胶原蛋白:PCL生物复合材料是生物相容性材料,分别能在细胞培养中支持成人正常人类表皮角质形成细胞(NHEK)和小鼠3T3成纤维细胞生长。通过用PCL/二氯甲烷溶液浸渍冻干的胶原垫,然后蒸发溶剂,采用非交联方法制备了胶原蛋白:PCL生物复合材料薄膜。为模拟皮肤的真皮/表皮结构,选择1:20的胶原蛋白:PCL生物复合材料进行设计的共培养技术可行性研究,该技术随后将用于制备成纤维细胞/生物复合材料/角质形成细胞皮肤模型。在可行性研究中,当将成纤维细胞接种在生物复合材料膜的两侧时,与在生物复合材料一个表面上进行细胞培养相比,在设计的共培养系统中测得细胞数量增加了55.3%。因此,使用相同的共培养系统,通过在膜的顶表面培养角质形成细胞3天,在膜下方培养3T3成纤维细胞6天,研究了人角质形成细胞和3T3成纤维细胞在膜两侧的共培养情况。扫描电子显微镜(SEM)和免疫组织化学分析显示,人角质形成细胞和3T3成纤维细胞均有良好的细胞附着和增殖,且这两种细胞在膜的两侧分离良好。通过改良的共培养技术,在共培养系统中成功培养28天,开发出一种共培养皮肤模型,该模型在生物复合材料膜的一侧呈现汇合的表皮片,在膜的另一侧有聚集的成纤维细胞,经SEM和免疫组织化学分析研究。因此,原则上证明了基于1:20(重量/重量)胶原蛋白:PCL生物复合膜设计共培养系统以制备具有分化表皮片的双层皮肤模型的方法。本文报道的皮肤建模方法可能在组织工程和新药物筛选中找到应用。