Literature DB >> 23699745

Glucose transporter-1 distribution in fibrotic lung disease: association with [¹⁸F]-2-fluoro-2-deoxyglucose-PET scan uptake, inflammation, and neovascularization.

Souheil El-Chemaly1, Daniela Malide2, Jianhua Yao3, Steven D Nathan4, Ivan O Rosas5, William A Gahl6, Joel Moss7, Bernadette R Gochuico6.   

Abstract

BACKGROUND: [¹⁸F]-2-fluoro-2-deoxyglucose (FDG)-PET scan uptake is increased in areas of fibrosis and honeycombing in patients with idiopathic pulmonary fibrosis (IPF). Glucose transporter-1 (Glut-1) is known to be the main transporter for FDG. There is a paucity of data regarding the distribution of Glut-1 and the cells responsible for FDG binding in fibrotic lung diseases.
METHODS: We applied immunofluorescence to localize Glut-1 in normal, IPF, and Hermansky-Pudlak syndrome (HPS) pulmonary fibrosis lung tissue specimens as well as an array of 19 different lung neoplasms. In addition, we investigated Glut-1 expression in inflammatory cells from BAL fluid (BALF) from healthy volunteers, subjects with IPF, and subjects with HPS pulmonary fibrosis.
RESULTS: In normal lung tissue, Glut-1 immunoreactivity was seen on the surface of erythrocytes. In tissue sections from fibrotic lung diseases (IPF and HPS pulmonary fibrosis), Glut-1 immunoreactivity was present on the surface of erythrocytes and inflammatory cells. BALF inflammatory cells from healthy control subjects showed no immunoreactivity; BALF cells from subjects with IPF and HPS pulmonary fibrosis showed Glut-1 immunoreactivity associated with neutrophils and alveolar macrophages.
CONCLUSIONS: Glut-1 transporter expression in normal lung is limited to erythrocytes. In fibrotic lung, erythrocytes and inflammatory cells express Glut-1. Together, these data suggest that FDG-PET scan uptake in IPF could be explained by enhanced inflammatory and erythrocytes uptake due to neovascularization seen in IPF and not an upregulation of metabolic rate in pneumocytes. Thus, FDG-PET scan may detect inflammation and neovascularization in lung fibrosis.

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Year:  2013        PMID: 23699745      PMCID: PMC3673664          DOI: 10.1378/chest.12-1359

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  29 in total

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2.  PET imaging in patients with bronchioloalveolar cell carcinoma.

Authors:  Laura E Heyneman; Edward F Patz
Journal:  Lung Cancer       Date:  2002-12       Impact factor: 5.705

3.  Pulmonary function and high-resolution CT findings in patients with an inherited form of pulmonary fibrosis, Hermansky-Pudlak syndrome, due to mutations in HPS-1.

Authors:  M Brantly; N A Avila; V Shotelersuk; C Lucero; M Huizing; W A Gahl
Journal:  Chest       Date:  2000-01       Impact factor: 9.410

4.  Activation of Glut1 glucose transporter in human erythrocytes.

Authors:  J Z Zhang; F Ismail-Beigi
Journal:  Arch Biochem Biophys       Date:  1998-08-01       Impact factor: 4.013

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Authors:  K Higashi; Y Ueda; H Seki; K Yuasa; M Oguchi; T Noguchi; M Taniguchi; H Tonami; T Okimura; I Yamamoto
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7.  Pigment epithelium-derived factor in idiopathic pulmonary fibrosis: a role in aberrant angiogenesis.

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10.  FDG-PET imaging in lung cancer: how sensitive is it for bronchioloalveolar carcinoma?

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4.  Apoptotic PET Imaging of Rat Pulmonary Fibrosis with Small-Molecule Radiotracer.

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Review 5.  Hermansky-Pudlak Syndrome.

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9.  A YAP/TAZ-miR-130/301 molecular circuit exerts systems-level control of fibrosis in a network of human diseases and physiologic conditions.

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10.  Thoracic [18F]fluorodeoxyglucose uptake measured by positron emission tomography/computed tomography in pulmonary hypertension.

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