Division of Pulmonary and Critical Care Medicine, Department of Medicine, Medical School, University of Wisconsin, Clinical Science Center, Madison, 53792-9988, USA.
BMC Pulm Med. 2012 Aug 17;12:44. doi: 10.1186/1471-2466-12-44.
Neutrophils sequestered in lower respiratory tract secretions in the inflamed lung may undergo apoptosis and/or necrosis and release toxic cellular contents that can injure airways or parenchyma. This study examined the viability of neutrophils retrieved from the proximal airways of lung transplant recipients with bacterial tracheobronchitis.
Integrity and stability of intracellular proteins in neutrophils from proximal airways and peripheral blood from lung transplant recipients with bacterial tracheobronchitis were analyzed via Western blot analysis and determination of neutrophil viability by morphologic appearance and flow cytometry.
Neutrophils in tracheobronchial secretions from lung transplant recipients with cystic fibrosis who had normal chest radiographic imaging but bronchoscopic evidence of purulent tracheobronchitis post-transplant were necrotic and associated with degradation of intracellular protein annexin 1. The neutrophil influx was compartmentalized to large airways and not detected in peripheral bronchoalveolar airspaces sampled via bronchoalveolar lavage. Peripheral blood neutrophils from healthy subjects cultured in vitro demonstrated that annexin 1 degradation, particularly to a 33 kDa annexin 1 breakdown product (A1-BP), was associated with neutrophil necrosis, but not apoptosis. Although annexin 1 degradation was not specific to neutrophil necrosis, it was a sensitive marker of intracellular protein degradation associated with neutrophil necrosis. Annexin 1 degradation to 33 kDa A1-BP was not observed in peripheral blood neutrophils from healthy subjects, but annexin 1 appeared to be degraded in peripheral blood neutrophils of lung transplant recipients despite a normal morphologic appearance of these cells.
Neutrophils were necrotic from the proximal airways of lung transplant recipients with bacterial tracheobronchitis, and this process may begin when neutrophils are still in the systemic circulation prior to sequestration in inflamed airways. Annexin 1 degradation to 33 kDa A1-BP may be useful as a sensitive marker to detect neutrophil necrosis.
在发炎的肺部中,被隔离在下呼吸道分泌物中的中性粒细胞可能会发生凋亡和/或坏死,并释放出可能损伤气道或实质的有毒细胞内容物。本研究检测了患有细菌性气管支气管炎的肺移植受者近端气道中回收的中性粒细胞的活力。
通过 Western blot 分析和形态学外观及流式细胞术测定中性粒细胞活力来分析来自患有细菌性气管支气管炎的肺移植受者近端气道和外周血的中性粒细胞的细胞内蛋白完整性和稳定性。
在有囊性纤维化的肺移植受者的气管支气管分泌物中的中性粒细胞发生了坏死,并伴有细胞内蛋白 annexin 1 的降解,尽管这些受者的胸部 X 线成像正常,但在移植后出现脓性气管支气管炎的支气管镜证据。中性粒细胞的涌入局限于大气道,而在外周支气管肺泡气空间中通过支气管肺泡灌洗并未检测到。体外培养的健康受试者的外周血中性粒细胞显示,annexin 1 降解,特别是到 33 kDa annexin 1 降解产物(A1-BP),与中性粒细胞坏死有关,但与凋亡无关。虽然 annexin 1 降解不是中性粒细胞坏死的特异性标志物,但它是与中性粒细胞坏死相关的细胞内蛋白降解的敏感标志物。在健康受试者的外周血中性粒细胞中未观察到 annexin 1 降解为 33 kDa A1-BP,但尽管这些细胞的形态正常,在肺移植受者的外周血中性粒细胞中似乎发生了 annexin 1 降解。
来自患有细菌性气管支气管炎的肺移植受者的近端气道中的中性粒细胞发生了坏死,并且这个过程可能在中性粒细胞在被隔离在发炎的气道之前仍在全身循环中时就开始了。annexin 1 降解为 33 kDa A1-BP 可能是一种有用的敏感标志物,可用于检测中性粒细胞坏死。