Literature DB >> 10890930

Expression of thyroid transcription factor-1 in congenital cystic adenomatoid malformation of the lung.

R A Morotti1, M C Gutierrez, F Askin, S A Profitt, S E Wert, J A Whitsett, M A Greco.   

Abstract

Congenital cystic adenomatoid malformation (CCAM) is an abnormality of branching morphogenesis of the lung. CCAM types 1, 2, and 3 exhibit a cellular composition that is different from that of CCAM type 4 when evaluated with bronchiolar and alveolar cell markers. Thyroid transcription factor 1 (TTF-1) regulates early lung development. To evaluate the potential role of TTF-1 in the development of CCAM, TTF-1 expression in CCAM was compared to that of fetal lungs at varying gestational ages. Twenty-three CCAM cases (17 type 1, two type 2, two type 3, and two type 4) and 11 fetal lungs (3 pseudoglandular, 4 canalicular, and 4 terminal sac stages) were analyzed using a rabbit polyclonal antiserum to rat TTF-1. Nuclear staining for TTF-1 was observed in ciliated and nonciliated cells of the bronchial and bronchiolar epithelia and in cells lining the distal air spaces by 12 weeks gestational age. By mid-gestation, proximal bronchial cells were TTF-1 negative, except for the basal cells, while TTF-1 staining was maintained in distal bronchiolar and alveolar cells. TTF-1 expression decreased in both bronchial, bronchiolar, and alveolar epithelia with advancing gestational age and cytodifferentiation. At term, TTF-1 expression persisted in a few bronchial and bronchiolar basal cells and in all alveolar type II cells, whereas type I cells were negative. In CCAM, TTF-1 was detected in the nuclei of epithelial cells lining the cysts. TTF-1 was expressed in a majority of the bronchiolar-like epithelial cells of the cysts in CCAM types 1, 2, and 3, where almost 100% of the cells were TTF-1 positive. In contrast, TTF-1 expression in the alveolar-like epithelium of CCAM type 4 cysts was restricted to type II cells and only 30%-60% of the lining cells were TTF-1 positive. These results support the hypothesis that CCAM types 1, 2, and 3 reflect abnormalities in lung morphogenesis and differentiation that are distinct from those for CCAM type 4. The role played by TTF-1 in the development of CCAM, if any, is not clear.

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Year:  2000        PMID: 10890930     DOI: 10.1007/s100240010092

Source DB:  PubMed          Journal:  Pediatr Dev Pathol        ISSN: 1093-5266


  11 in total

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Review 2.  Congenital pulmonary airway malformations: state-of-the-art review for pediatrician's use.

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3.  Cancer gene mutations in congenital pulmonary airway malformation patients.

Authors:  Jacob Shujui Hsu; Ruizhong Zhang; Fanny Yeung; Clara S M Tang; John K L Wong; Man-Ting So; Huimin Xia; Pak Sham; Paul K Tam; Miaoxin Li; Kenneth K Y Wong; Maria-Mercè Garcia-Barcelo
Journal:  ERJ Open Res       Date:  2019-02-04

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5.  Immortalization of human alveolar epithelial cells to investigate nanoparticle uptake.

Authors:  Sarah J Kemp; Andrew J Thorley; Julia Gorelik; Michael J Seckl; Michael J O'Hare; Alexandre Arcaro; Yuri Korchev; Peter Goldstraw; Teresa D Tetley
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6.  Aberrant cell adhesion molecule expression in human bronchopulmonary sequestration and congenital cystic adenomatoid malformation.

Authors:  Maryann V Volpe; Eunice Chung; Jason P Ulm; Brian F Gilchrist; Steven Ralston; Karen T Wang; Heber C Nielsen
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7.  FGF10 Signaling differences between type I pleuropulmonary blastoma and congenital cystic adenomatoid malformation.

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8.  Congenital Cystic Adenomatoid Malformation Diagnosed During First-Trimester Ultrasound Scan.

Authors:  Georges A Markou; Georgios Dafereras; Christophe Poncelet
Journal:  Am J Case Rep       Date:  2018-01-01

Review 9.  Narrative review of congenital lung lesions.

Authors:  Shaun M Kunisaki
Journal:  Transl Pediatr       Date:  2021-05

10.  Mechanism of lung development in the aetiology of adult congenital pulmonary airway malformations.

Authors:  Bethany Taylor; Alexandra Rice; Andrew G Nicholson; Matthew Hind; Charlotte H Dean
Journal:  Thorax       Date:  2020-07-30       Impact factor: 9.139

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