猪肺移植原发性移植物功能障碍的蛋白质组分析揭示了肺泡-毛细血管屏障变化是呼出气体中粒子流速高的基础

A. Niroomand, G. Hirdman, N. Bèchet, H. Ghaidan, M. Stenlo, Sven Kjellström, Marc Isaksson, E. Broberg, Leif Pierre, S. Hyllén, F. Olm, Sandra Lindstedt
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引用次数: 0

摘要

原发性移植物功能障碍(PGD)仍然是肺移植(LTx)受者面临的一项挑战,是导致早期疗效不佳的主要原因。需要新的方法来更详细地监测和了解 PGD 的病理生理学。测量呼出气体中的颗粒流速(PFR)是在蛋白质组水平上监测和了解该疾病的一种新工具。共有22头受体猪接受了正位左侧LTx手术,并在术后第3天进行了PGD评估。通过质谱分析评估了呼出气体颗粒(EBPs),并将其蛋白质组与组织活检和支气管肺泡灌洗液(BALF)进行了比较。研究结果在 11 名人体移植受者的 EBPs 中得到了证实。与无 PGD 的受者[116.6 (79.7-307.4) ppm, p = 0.0005]相比,有 PGD 的受者的 PFR [686.4 (449.7-8,824.0) 颗粒/分钟 (ppm)]明显更高。猪和人的 EBP 蛋白再现了在 BAL 中发现的蛋白,这表明它可以替代更具侵入性的技术。此外,粘连蛋白和紧密连接蛋白在 PGD 组织中表达不足。组织学和蛋白质组分析发现,肺泡-毛细血管屏障发生了显著变化,这也是 PGD PFR 高的原因。建议将呼气测量作为床旁快速、无创的 PGD 测量方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proteomic Analysis of Primary Graft Dysfunction in Porcine Lung Transplantation Reveals Alveolar-Capillary Barrier Changes Underlying the High Particle Flow Rate in Exhaled Breath
Primary graft dysfunction (PGD) remains a challenge for lung transplantation (LTx) recipients as a leading cause of poor early outcomes. New methods are needed for more detailed monitoring and understanding of the pathophysiology of PGD. The measurement of particle flow rate (PFR) in exhaled breath is a novel tool to monitor and understand the disease at the proteomic level. In total, 22 recipient pigs underwent orthotopic left LTx and were evaluated for PGD on postoperative day 3. Exhaled breath particles (EBPs) were evaluated by mass spectrometry and the proteome was compared to tissue biopsies and bronchoalveolar lavage fluid (BALF). Findings were confirmed in EBPs from 11 human transplant recipients. Recipients with PGD had significantly higher PFR [686.4 (449.7–8,824.0) particles per minute (ppm)] compared to recipients without PGD [116.6 (79.7–307.4) ppm, p = 0.0005]. Porcine and human EBP proteins recapitulated proteins found in the BAL, demonstrating its utility instead of more invasive techniques. Furthermore, adherens and tight junction proteins were underexpressed in PGD tissue. Histological and proteomic analysis found significant changes to the alveolar-capillary barrier explaining the high PFR in PGD. Exhaled breath measurement is proposed as a rapid and non-invasive bedside measurement of PGD.
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