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肺泡毛细血管发育不良/肺静脉排列异常时肺中血管生成和血管发生相关蛋白的表达:一项免疫组织化学研究

Expression of angiogenic and vasculogenic proteins in the lung in alveolar capillary dysplasia/misalignment of pulmonary veins: an immunohistochemical study.

作者信息

Sen Partha, Choudhury Tiyashi, Smith E O'Brian, Langston Claire

机构信息

Department of Pediatrics and Pathology, Baylor College of Medicine, Texas Children's Hospital, Houston, TX, USA.

出版信息

Pediatr Dev Pathol. 2010 Sep-Oct;13(5):354-61. doi: 10.2350/09-04-0640-OA.1. Epub 2010 Mar 23.

DOI:10.2350/09-04-0640-OA.1
PMID:20331367
Abstract

Alveolar capillary dysplasia with misalignment of pulmonary veins (ACD/MPV) is a rare, universally fatal developmental disorder of the lung affecting both the parenchyma and the vasculature. Its cause remains incompletely understood; the occurrence of familial cases has suggested a genetic abnormality. While several candidate genes have been studied previously, the affected pathway(s) have not yet been fully defined. The expression patterns of 8 gene products (endothelial nitric oxide synthase-3, fetal liver kinase-1, hypoxia inducible factor 1α, Von Hippel Lindau protein, 3 vascular endothelial growth factors [VEGF147, VEGFC1, and VEGFA20], and activin receptor-like kinase 1), all known to have a role in vascular development in the lung, were studied in 13 ACD/MPV and 17 control lungs by immunohistochemistry to further address the underlying molecular abnormality. Expression was graded with regard to degree and extent for multiple components of the lung parenchyma and pulmonary vasculature for each antibody. Statistical analyses of the data using the Mann-Whitney test revealed only a few significant differences (P ≤ 0.05) in degree of expression between ACD/MPV and control lung samples and do not clearly implicate one of these genes in ACD/MPV.

摘要

肺泡毛细血管发育不良伴肺静脉异位引流(ACD/MPV)是一种罕见的、普遍致命的肺部发育障碍疾病,会影响肺实质和脉管系统。其病因仍未完全明确;家族性病例的出现提示存在基因异常。虽然此前已对多个候选基因进行了研究,但相关的致病途径尚未完全明确。本研究采用免疫组化方法,对13例ACD/MPV病例及17例对照肺组织中8种已知在肺血管发育中起作用的基因产物(内皮型一氧化氮合酶-3、胎儿肝激酶-1、缺氧诱导因子1α、冯希佩尔-林道蛋白、3种血管内皮生长因子[VEGF147、VEGFC1和VEGFA20]以及激活素受体样激酶1)的表达模式进行了研究,以进一步明确潜在的分子异常。针对每种抗体,对肺实质和肺血管多个组成部分的表达程度和范围进行评分。采用曼-惠特尼检验对数据进行统计分析,结果显示ACD/MPV病例与对照肺组织样本之间仅在表达程度上存在少数显著差异(P≤0.05),但并未明确表明这些基因中的某一个与ACD/MPV有关。

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引用本文的文献

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Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins (ACD/MPV): A Case Series.肺泡毛细血管发育不良伴肺静脉错位(ACD/MPV):病例系列
Case Rep Crit Care. 2013;2013:327250. doi: 10.1155/2013/327250. Epub 2013 Jan 8.
3
Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain.
散发的和家族性肺泡毛细血管发育不良伴肺静脉异位连接病例中的新型 FOXF1 突变提示其 DNA 结合域的作用。
Hum Mutat. 2013 Jun;34(6):801-11. doi: 10.1002/humu.22313. Epub 2013 Apr 12.
4
Interstitial lung disease in infants: new classification system, imaging technique, clinical presentation and imaging findings.婴儿间质性肺病:新的分类系统、影像学技术、临床表现和影像学表现。
Pediatr Radiol. 2013 Jan;43(1):3-13; quiz p.128-9. doi: 10.1007/s00247-012-2524-x. Epub 2012 Nov 15.