Department of Surgery, University of Virginia Health System, Charlottesville, Va.
Department of Surgery, University of Virginia Health System, Charlottesville, Va.
J Thorac Cardiovasc Surg. 2013 Apr;145(4):940-947.e1. doi: 10.1016/j.jtcvs.2012.07.098. Epub 2012 Aug 28.
Loss of epithelial cells is one of the key factors that lead to airway fibrosis. Loss of epithelial cells may decrease the barrier to host cell infiltration into the lumen, allowing deposition of extracellular matrix, with subsequent obliteration of the airway. The objective of this study was to determine whether injection of epithelial cells/progenitor cells from the recipient into the lumen of the donor trachea could prevent bronchiolitis obliterans (BO) in a mouse heterotopic tracheal transplantation (HTT) model.
A major histocompatibility complex class I and class II mismatch of mouse HTT model of BO was used. Epithelial cells from recipient mice were isolated and reinjected into the lumen of the allografts on day 3 after transplantation. Rag-1 knock-out and isografts were also performed as controls. The grafts were analyzed by immunohistochemistry and densitometric analysis.
The results demonstrated that tracheal epithelium was lost by day 3, regenerated between 3 to 7 days, and was lost again in all allografts, but not in the isografts or in Rag-1 knock-out groups by day 12. The reconstituted epithelium was donor originated on day 7 based on green fluorescent protein staining. Furthermore, with the injection of recipient cells into the tracheal lumen, loss of the epithelium was not observed and the luminal obliteration was significantly less in the allografts.
Injection of recipient epithelial cells prevents the second phase of epithelial loss and significantly decreases BO development in an HTT model. Clinically, the use of injected recipient epithelial cells could be a novel treatment for BO.
上皮细胞的丢失是导致气道纤维化的关键因素之一。上皮细胞的丢失可能会降低宿主细胞向管腔浸润的屏障,允许细胞外基质的沉积,随后气道被阻塞。本研究的目的是确定将受体的上皮细胞/祖细胞注射到供体气管的管腔中是否可以预防小鼠异位气管移植(HTT)模型中的细支气管闭塞(BO)。
使用 BO 的小鼠 HTT 模型的主要组织相容性复合体 I 类和 II 类错配。从受体小鼠中分离上皮细胞,并在移植后第 3 天将其重新注入同种异体移植物的管腔中。还进行了 Rag-1 敲除和同种异体移植作为对照。通过免疫组织化学和密度测定分析对移植物进行分析。
结果表明,气管上皮在第 3 天丢失,在第 3 至 7 天之间再生,并且在所有同种异体移植物中再次丢失,但在第 12 天的同种异体移植物或 Rag-1 敲除组中没有丢失。基于绿色荧光蛋白染色,第 7 天重建的上皮来源于供体。此外,通过将受体细胞注入气管腔中,观察到上皮细胞的丢失减少,同种异体移植物中的管腔闭塞明显减少。
将受体上皮细胞注射到气管腔内可防止第二阶段上皮细胞丢失,并显著减少 HTT 模型中的 BO 发生。临床上,注射受体上皮细胞可能是 BO 的一种新的治疗方法。