人尿路上皮细胞胶原载体在大鼠体内的生物相容性研究

L. Daum, S. Maurer, M. Vaegler, K. Sievert
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引用次数: 3

摘要

组织工程、基质稳定的自体尿路上皮是尿道重建的一种新选择,特别是对于无法获得其他自体移植物的患者。尿路上皮组织的体外工程需要生物材料作为细胞载体,以增加细胞基植入物的稳定性。本研究的目的是研究一种新的高度标准化的工业生产的牛胶原i型细胞载体(CCC),其适合作为人尿路上皮细胞(HUC)的载体基质。作为体内生物相容性测试,这些植入物的行为和降解将在裸鼠模型中得到证实。通过免疫细胞化学对组织活检扩增的HUC进行表型分析,并将其植入CCC。在体内应用时,将pkh26标记的HUC高密度植入CCC,并将构建物植入裸鼠腹直肌。在1周、2周和4周后研究尿路基质植入物的整合、细胞存活和降解。对AE1/AE3和p63(上皮表型)、CK20(分化)、E-Cadherin和ZO-1(连接形成)进行多层尿路基质构建的免疫组织学表征。免疫细胞化学染色显示分离细胞具有尿路上皮特征,未见成纤维细胞和肌细胞。在12只裸大鼠中,尿路上皮基质植入物与宿主组织融合良好,未观察到炎症。免疫荧光分析证实了上皮表型、粘附性和紧密连接形成、分层HUC培养物的均匀多层形成以及尿路上皮表型和体外分化,在裸鼠模型中研究的cc -基质还显示出有希望的生物相容性。因此,本研究证明了CCC作为尿路上皮细胞基质的极好适用性,并建议将其用于大型动物模型的临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In Vivo Biocompatibility Testing of a Collagen Cell Carrier Seeded withHuman Urothelial Cells in Rats
Tissue-engineered, matrix-stabilized autologous urothelium is a new option for urethral reconstruction, particularly for patients for whom other autologous grafts are not available. In vitro engineering of urothelial tissue requires biomaterials as cell carriers that increase the stability of cell-based implants. The aim of this study was to investigate a new highly standardized, industrially manufactured bovine collagen type I-based cell carrier (CCC) for its suitability as a carrier matrix for human urothelial cells (HUC). As an in vivo biocompatibility test the behaviour and degradation of these implants was to be proven in a nude rat model. Expanded HUC from tissue biopsies were phenotypically analysed by immuno¬cyto¬chemistry and seeded onto CCC. For in vivo application, CCC was seeded with PKH26-labelled HUC in high density and constructs were implanted onto the rectus abdominis muscle of nude rats. Integration, cell survival, and degradation of the urothelium-matrix-implants were studied after 1, 2, and 4 weeks. Immunohistological characterization of multilayered urothelium-matrix-constructs was performed for AE1/AE3 and p63 (epithelial phenotype), CK20 (differentiation), and E-Cadherin and ZO-1 (junction formation). Immunocytochemical staining showed urothelial character of the isolated cells and the absence of fibroblasts and muscle cells. In twelve nude rats, urothelium-matrix-implants integrated well into the host tissue where no inflammation was observed. Immuno¬fluorescence analysis confirmed epithelial phenotype, adherence and tight junction formation homogeneous multilayer formation of stratified HUC cultures as well as urothelial phenotype and differentiation in vitro the CCC-matrix additionally revealed promising biocompatibility investigated in a nude rat model. Thus, this study demonstrates excellent suitability of CCC as a matrix for urothelial cells and recommends its use in a large animal model with regard to clinical application.
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