Okazaki M, Krupnick A S, Kornfeld C G, Lai J M, Ritter J H, Richardson S B, Huang H J, Das N A, Patterson G A, Gelman A E, Kreisel D
Division of Cardiothoracic Surgery, Department of Surgery, Washington University in St. Louis, St. Louis, MO, USA.
Am J Transplant. 2007 Jun;7(6):1672-9. doi: 10.1111/j.1600-6143.2007.01819.x.
Outcomes after lung transplantation are markedly inferior to those after other solid organ transplants. A better understanding of cellular and molecular mechanisms contributing to lung graft injury will be critical to improve outcomes. Advances in this field have been hampered by the lack of a mouse model of lung transplantation. Here, we report a mouse model of vascularized aerated single lung transplantation utilizing cuff techniques. We show that syngeneic grafts have normal histological appearance with minimal infiltration of T lymphocytes. Allogeneic grafts show acute cellular rejection with infiltration of T lymphocytes and recipient-type antigen presenting cells. Our data show that we have developed a physiological model of lung transplantation in the mouse, which provides ample opportunity for the study of nonimmune and immune mechanisms that contribute to lung allograft injury.
肺移植后的结果明显不如其他实体器官移植。更好地理解导致肺移植损伤的细胞和分子机制对于改善结果至关重要。该领域的进展因缺乏肺移植小鼠模型而受阻。在此,我们报告一种利用套管技术的血管化充气单肺移植小鼠模型。我们发现同基因移植具有正常的组织学外观,T淋巴细胞浸润极少。异基因移植表现为急性细胞排斥,伴有T淋巴细胞和受体型抗原呈递细胞浸润。我们的数据表明,我们已在小鼠中建立了肺移植的生理模型,这为研究导致肺同种异体移植损伤的非免疫和免疫机制提供了充足的机会。