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在人肺移植后闭塞性细支气管炎综合征中发生上皮细胞 Clar 细胞损伤。

Epithelial clara cell injury occurs in bronchiolitis obliterans syndrome after human lung transplantation.

机构信息

Division of Pulmonary and Critical Care Medicine-Duke University Medical Center, Durham, North Carolina, USA.

出版信息

Am J Transplant. 2012 Nov;12(11):3076-84. doi: 10.1111/j.1600-6143.2012.04201.x. Epub 2012 Aug 6.

Abstract

Bronchiolitis obliterans syndrome (BOS) is a condition of progressive airflow obstruction that affects a majority of lung transplant recipients and limits long-term posttransplant survival. Although epithelial injury appears central to the development of BOS, little is known regarding the specific epithelial cell types that are affected in this condition. We hypothesized that BOS would involve preferential injury to the secretory Clara cells that function in innate defense and epithelial repair. To test this hypothesis, we assessed tissue transcript, tissue protein and lung fluid protein expression of Clara cell secretory protein (CCSP), a marker for Clara cells, in lung transplant recipients with BOS, BOS-free patients and in donor controls. Our results demonstrate that CCSP tissue transcript and protein expression are significantly reduced in lung transplant recipients with BOS compared to BOS-free or donor controls. In addition, we demonstrate that CCSP protein levels are significantly reduced in the lung fluid of patients with BOS compared to BOS-free controls, in cross-sectional and longitudinal analysis. Collectively, these complementary results illustrate that BOS involves a selective alteration in the distribution and function of bronchiolar Clara cells.

摘要

闭塞性细支气管炎综合征(BOS)是一种进行性气流阻塞的疾病,影响大多数肺移植受者,并限制移植后的长期生存。尽管上皮损伤似乎是 BOS 发展的核心,但对于在这种情况下受影响的特定上皮细胞类型知之甚少。我们假设 BOS 会涉及到分泌性 Clara 细胞的优先损伤,Clara 细胞在先天防御和上皮修复中起作用。为了验证这一假设,我们评估了 BOS 患者、BOS 无患者和供体对照者的组织转录本、组织蛋白和肺液蛋白中 Clara 细胞分泌蛋白(CCSP)的表达,CCSP 是 Clara 细胞的标志物。我们的结果表明,与 BOS 无患者或供体对照者相比,BOS 患者的 CCSP 组织转录本和蛋白表达显著降低。此外,我们还证明,与 BOS 无患者对照者相比,BOS 患者的肺液中 CCSP 蛋白水平在横断面和纵向分析中均显著降低。综上所述,这些互补的结果表明 BOS 涉及到细支气管 Clara 细胞的分布和功能的选择性改变。

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