Gregson Aric L, Hoji Aki, Injean Patil, Poynter Steven T, Briones Claudia, Palchevskiy Vyacheslav, Weigt S Sam, Shino Michael Y, Derhovanessian Ariss, Sayah David, Saggar Rajan, Ross David, Ardehali Abbas, Lynch Joseph P, Belperio John A
1 Division of Infectious Diseases, Department of Medicine.
2 Department of Transplantation, University of Pittsburgh, Pittsburgh, Pennsylvania.
Am J Respir Crit Care Med. 2015 Dec 15;192(12):1490-503. doi: 10.1164/rccm.201503-0558OC.
The mechanism by which acute allograft rejection leads to chronic rejection remains poorly understood despite its common occurrence. Exosomes, membrane vesicles released from cells within the lung allograft, contain a diverse array of biomolecules that closely reflect the biologic state of the cell and tissue from which they are released. Exosome transcriptomes may provide a better understanding of the rejection process. Furthermore, biomarkers originating from this transcriptome could provide timely and sensitive detection of acute cellular rejection (AR), reducing the incidence of severe AR and chronic lung allograft dysfunction and improving outcomes.
To provide an in-depth analysis of the bronchoalveolar lavage fluid exosomal shuttle RNA population after lung transplantation and evaluate for differential expression between acute AR and quiescence.
Serial bronchoalveolar lavage specimens were ultracentrifuged to obtain the exosomal pellet for RNA extraction, on which RNA-Seq was performed.
AR demonstrates an intense inflammatory environment, skewed toward both innate and adaptive immune responses. Novel, potential upstream regulators identified offer potential therapeutic targets.
Our findings validate bronchoalveolar lavage fluid exosomal shuttle RNA as a source for understanding the pathophysiology of AR and for biomarker discovery in lung transplantation.
尽管急性同种异体移植排斥反应很常见,但其导致慢性排斥反应的机制仍知之甚少。外泌体是肺同种异体移植内细胞释放的膜泡,含有多种生物分子,能密切反映其释放来源的细胞和组织的生物学状态。外泌体转录组可能有助于更好地理解排斥反应过程。此外,源自该转录组的生物标志物可及时、灵敏地检测急性细胞排斥反应(AR),降低严重AR和慢性肺同种异体移植功能障碍的发生率,改善治疗结果。
深入分析肺移植后支气管肺泡灌洗液体外泌体穿梭RNA群体,并评估急性AR与静止期之间的差异表达。
对系列支气管肺泡灌洗标本进行超速离心以获得用于RNA提取的外泌体沉淀,然后进行RNA测序。
AR表现出强烈的炎症环境,偏向先天性和适应性免疫反应。鉴定出的新型潜在上游调节因子提供了潜在的治疗靶点。
我们的研究结果证实支气管肺泡灌洗液体外泌体穿梭RNA是理解AR病理生理学和肺移植生物标志物发现的一个来源。