Kreber Lily, Liu Lumei, Dharmadhikari Sayali, Tan Zheng Hong, Chan Coreena, Huddle Joey, Hussein Zakarie, Shontz Kimberly, Breuer Christopher K, Johnson Jed, Chiang Tendy
College of Medicine, The Ohio State University, Columbus, Ohio, U.S.A.
Center for Regenerative Medicine, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, Ohio, U.S.A.
Laryngoscope. 2024 Mar;134(3):1155-1162. doi: 10.1002/lary.30955. Epub 2023 Aug 14.
Composite tracheal grafts (CTG) combining decellularized scaffolds with external biomaterial support have been shown to support host-derived neotissue formation. In this study, we examine the biocompatibility, graft epithelialization, vascularization, and patency of three prototype CTG using a mouse microsurgical model.
Tracheal replacement, regenerative medicine, biocompatible airway splints, animal model.
CTG electrospun splints made by combining partially decellularized tracheal grafts (PDTG) with polyglycolic acid (PGA), poly(lactide-co-ε-caprolactone) (PLCL), or PLCL/PGA were orthotopically implanted in mice (N = 10/group). Tracheas were explanted two weeks post-implantation. Micro-Computed Tomography was conducted to assess for graft patency, and histological analysis was used to assess for epithelialization and neovascularization.
Most animals (greater than 80%) survived until the planned endpoint and did not exhibit respiratory symptoms. MicroCT confirmed the preservation of graft patency. Grossly, the PDTG component of CTG remained intact. Examining the electrospun component of CTG, PGA degraded significantly, while PLCL+PDTG and PLCL/PGA + PDTG maintained their structure. Microvasculature was observed across the surface of CTG and infiltrating the pores. There were no signs of excessive cellular infiltration or encapsulation. Graft microvasculature and epithelium appear similar in all groups, suggesting that CTG did not hinder endothelialization and epithelialization.
We found that all electrospun nanofiber CTGs are biocompatible and did not affect graft patency, endothelialization and epithelialization. Future directions will explore methods to accelerate graft regeneration of CTG.
N/A Laryngoscope, 134:1155-1162, 2024.
已证明将脱细胞支架与外部生物材料支持相结合的复合气管移植物(CTG)可支持宿主来源的新组织形成。在本研究中,我们使用小鼠显微手术模型检查了三种原型CTG的生物相容性、移植物上皮化、血管化和通畅性。
气管置换、再生医学、生物相容性气道夹板、动物模型。
将通过将部分脱细胞气管移植物(PDTG)与聚乙醇酸(PGA)、聚(丙交酯-共-ε-己内酯)(PLCL)或PLCL/PGA相结合制成的CTG电纺夹板原位植入小鼠体内(每组N = 10只)。植入后两周取出气管。进行微型计算机断层扫描以评估移植物的通畅性,并使用组织学分析评估上皮化和新血管形成。
大多数动物(超过80%)存活至计划的终点,且未出现呼吸道症状。微型计算机断层扫描证实移植物通畅得以保留。大体上,CTG的PDTG成分保持完整。检查CTG的电纺成分,PGA显著降解,而PLCL+PDTG和PLCL/PGA+PDTG保持其结构。在CTG表面观察到微血管,并渗透到孔隙中。没有过度细胞浸润或包囊的迹象。所有组的移植物微血管和上皮看起来相似,表明CTG不阻碍内皮化和上皮化。
我们发现所有电纺纳米纤维CTG均具有生物相容性,且不影响移植物通畅性、内皮化和上皮化。未来的方向将探索加速CTG移植物再生的方法。
无。《喉镜》,2024年,第134卷,第1155 - 1162页