Serum exosomal protein profiling for the non-invasive detection of cardiac allograft rejection

被引:77
作者
Kennel, Peter J. [1 ,2 ,9 ]
Saha, Amit [1 ]
Maldonado, Dawn A. [1 ]
Givens, Raymond [1 ]
Brunjes, Danielle L. [1 ]
Castillero, Estibaliz [3 ]
Zhang, Xiaokan [1 ]
Ji, Ruiping [1 ]
Yahi, Alexandre [4 ]
George, Isaac [3 ]
Mancini, Donna M. [1 ,5 ]
Koller, Antonius [6 ]
Fine, Barry [1 ]
Zorn, Emmanuel [7 ]
Colombo, Paolo C. [1 ]
Tatonetti, Nicholas [4 ]
Chen, Emily I. [7 ,8 ]
Schulze, P. Christian [1 ,9 ]
机构
[1] Columbia Univ, Dept Med, Med Ctr, Div Cardiol, New York, NY USA
[2] Weill Cornell Med Coll, Dept Med, New York, NY USA
[3] Columbia Univ, Dept Surg, Med Ctr, Div Cardiothorac Surg, New York, NY USA
[4] Columbia Univ, Dept Biomed Informat, New York, NY USA
[5] Mt Sinai Heart, New York, NY USA
[6] Columbia Univ, Herbert Irving Comprehens Canc Ctr, Med Ctr, New York, NY USA
[7] Columbia Univ, Columbia Ctr Translat Immunol, Med Ctr, New York, NY USA
[8] Columbia Univ, Dept Pharmacol, Med Ctr, New York, NY USA
[9] Friedrich Schiller Univ Jena, Univ Hosp Jena, Div Cardiol, Dept Internal Med 1, D-07747 Jena, Germany
关键词
heart transplantation; rejection monitoring; btomarker; exosome; AMERICAN-HEART-ASSOCIATION; LIPID-BINDING PROTEIN; AUTOPHAGIC CELL-DEATH; INTERNATIONAL SOCIETY; TRANSPLANT REJECTION; MASS-SPECTROMETRY; EXTRACELLULAR VESICLES; ENDOMYOCARDIAL BIOPSY; WORKING FORMULATION; PROSTATE-CANCER;
D O I
10.1016/j.healun.2017.07.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Exosomes are cell-derived circulating vesicles that play an important role in cell cell communication. Exosomes are actively assembled and carry messenger RNAs, microRNAs and proteins. The "gold standard" for cardiac allograft surveillance is endomyocardial biopsy (EMB), an invasive technique with a distinct complication profile. The development of novel, non-invasive methods for the early diagnosis of allograft rejection is warranted. We hypothesized that the exosomal proteome is altered in acute rejection, allowing for a distinction between non-rejection and rejection episodes. METHODS: Serum samples were collected from heart transplant (HTx) recipients with no rejection, acute cellular rejection (ACR) and antibody-mediated rejection (AMR). Liquid chromatography tandem mass spectrometry (LC-MS/MS) analysis of serum exosome was performed using a mass spectrometer (Orbitrap Fusion Tribrid). RESULTS: Principal component analysis (PCA) revealed a clustering of 3 groups: (1) control and heart failure (HF); (2) HTx without rejection; and (3) ACR and AMR. A total of 45 proteins were identified that could distinguish between groups (q < 0.05). Comparison of serum exosomal proteins from control, HF and non-rejection HTx revealed 17 differentially expressed proteins in at least 1 group (q < 0.05). Finally, comparisons of non-rejection HTx, ACR and AMR serum exosomes revealed 15 differentially expressed proteins in at least 1 group (q < 0.05). Of these 15 proteins, 8 proteins are known to play a role in the immune response. Of note, the majority of proteins identified were associated with complement activation, adaptive immunity such as immunoglobulin components and coagulation. CONCLUSIONS: Characterizing of circulating exosomal proteome in different cardiac disease states reveals unique protein expression patterns indicative of the respective pathologies. Our data suggest that HTx and allograft rejection alter the circulating exosomal protein content. Exosomal protein analysis could be a novel approach to detect and monitor acute transplant rejection and lead to the development of predictive and prognostic biomarkers. (C) 2018 International Society for Heart and Lung Transplantation. All rights reserved.
引用
收藏
页码:409 / 417
页数:9
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