Department of Tissue Engineering, Institute of Basic Medical Sciences and Tissue Engineering Research Center, Academy of Military Medical Sciences, Beijing, China.
J Cell Mol Med. 2011 Sep;15(9):1878-86. doi: 10.1111/j.1582-4934.2010.01189.x.
This study attempted to use collagen-Matrigel as extracellular matrix (ECM) to supply cells with three-dimensional (3D) culture condition and employ alginate-poly-l-lysine-alginate (APA) microcapsules to control the formation of alveolus-like structure in vitro. We tested mice foetal pulmonary cells (FPCs) by immunohistochemistry after 2D culture. The alveolus-like structure was reconstructed by seeding FPCs in collagen-Matrigel mixed with APA microcapsules 1.5 ml. A self-made mould was used to keep the structure from contraction. Meanwhile, it provided static stretch to the structure. After 7, 14 and 21 days of culture, the alveolus-like structure was analysed histologically and immunohistochemically, or by scanning transmission electron microscopy (TEM). We also observed these structures under inverted phase contrast microscope. The expression of pro-surfactant protein C (SpC) was detected by reverse transcription-polymerase chain reaction (RT-PCR). We obtained fibroblasts, epithelial cells and alveolar type II (AE2) cells in FPCs. In the reconstructed structure, seeding cells surrounding the APA microcapsules constructed alveolus-like structures, the size of them ranges from 200 to 300 μm. In each reconstructed lung tissue sheet, microcapsules had integrity. Pan-cytokeratin, vimentin and SpC positive cells were observed in 7- and 14-day cultured structures. TEM showed lamellar bodies of AE2 cells in the reconstructed tissues whereas RT-PCR expressed SpC gene. Primary mice FPCs could form alveolus-like structures in collagen-Matrigel/APA microcapsules engineered scaffolds, which could maintain a differentiated state of AE2 cells.
本研究试图使用胶原-基质胶作为细胞外基质(ECM),为细胞提供三维(3D)培养条件,并采用藻酸盐-聚-L-赖氨酸-藻酸盐(APA)微胶囊控制体外肺泡样结构的形成。我们通过免疫组织化学方法对 2D 培养后的小鼠胎儿肺细胞(FPC)进行了检测。通过将 FPC 接种在含有 APA 微胶囊的胶原-基质胶混合物中,构建了 1.5ml 的肺泡样结构。使用自制模具保持结构不收缩,同时为结构提供静态拉伸。在培养 7、14 和 21 天后,对肺泡样结构进行组织学和免疫组织化学分析,或通过扫描传输电子显微镜(TEM)分析。我们还在倒置相差显微镜下观察了这些结构。通过逆转录-聚合酶链反应(RT-PCR)检测了前表面活性蛋白 C(SpC)的表达。我们从 FPC 中获得了成纤维细胞、上皮细胞和肺泡 II 型(AE2)细胞。在重建的结构中,接种细胞围绕 APA 微胶囊构建了肺泡样结构,其大小范围为 200 至 300μm。在每个重建的肺组织片中,微胶囊都保持完整。在培养 7 天和 14 天的结构中观察到泛细胞角蛋白、波形蛋白和 SpC 阳性细胞。TEM 显示重建组织中的 AE2 细胞有板层小体,而 RT-PCR 则表达 SpC 基因。原代小鼠 FPC 可在胶原-基质胶/APA 微胶囊工程支架中形成肺泡样结构,可维持 AE2 细胞的分化状态。