Zhao Liping, Sundaram Sumati, Le Andrew V, Huang Angela H, Zhang Jiasheng, Hatachi Go, Beloiartsev Arkadi, Caty Michael G, Yi Tai, Leiby Katherine, Gard Ashley, Kural Mehmet H, Gui Liqiong, Rocco Kevin A, Sivarapatna Amogh, Calle Elizabeth, Greaney Allison, Urbani Luca, Maghsoudlou Panagiotis, Burns Alan, DeCoppi Paolo, Niklason Laura E
2 Department of Anesthesiology, Yale University , New Haven, Connecticut.
1 Department of Biomedical Engineering, Yale University , New Haven, Connecticut.
Tissue Eng Part A. 2016 Sep;22(17-18):1086-97. doi: 10.1089/ten.TEA.2016.0132.
Here we report the creation of a novel tracheal construct in the form of an engineered, acellular tissue-stent biocomposite trachea (TSBT). Allogeneic or xenogeneic smooth muscle cells are cultured on polyglycolic acid polymer-metal stent scaffold leading to the formation of a tissue comprising cells, their deposited collagenous matrix, and the stent material. Thorough decellularization then produces a final acellular tubular construct. Engineered TSBTs were tested as end-to-end tracheal replacements in 11 rats and 3 nonhuman primates. Over a period of 8 weeks, no instances of airway perforation, infection, stent migration, or erosion were observed. Histological analyses reveal that the patent implants remodel adaptively with native host cells, including formation of connective tissue in the tracheal wall and formation of a confluent, columnar epithelium in the graft lumen, although some instances of airway stenosis were observed. Overall, TSBTs resisted collapse and compression that often limit the function of other decellularized tracheal replacements, and additionally do not require any cells from the intended recipient. Such engineered TSBTs represent a model for future efforts in tracheal regeneration.
在此,我们报告了一种新型气管构建体的创建,其形式为工程化的无细胞组织支架生物复合气管(TSBT)。将同种异体或异种平滑肌细胞培养在聚乙醇酸聚合物-金属支架上,从而形成一种由细胞、其沉积的胶原基质和支架材料组成的组织。然后进行彻底的脱细胞处理,产生最终的无细胞管状构建体。对工程化的TSBTs作为端到端气管替代物在11只大鼠和3只非人灵长类动物中进行了测试。在8周的时间里,未观察到气道穿孔、感染、支架迁移或侵蚀的情况。组织学分析表明,尽管观察到一些气道狭窄的情况,但植入的TSBTs能与天然宿主细胞进行适应性重塑,包括气管壁中结缔组织的形成以及移植管腔内汇合的柱状上皮的形成。总体而言,TSBTs能抵抗塌陷和压缩,而塌陷和压缩常常限制其他脱细胞气管替代物的功能,此外,TSBTs不需要来自预期受体的任何细胞。这种工程化的TSBTs代表了未来气管再生研究的一个模型。