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Identification of novel target genes in human lung tissue involved in chronic obstructive pulmonary disease
INTRODUCTION: As part of a study aimed at illuminating at least some of the complex molecular events taking place in COPD, we screened tissues by means of transcriptome analyses. MATERIALS AND METHODS: Tissues were subjected to transcriptome analysis. Candidate genes were identified and validated by...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065552/ https://www.ncbi.nlm.nih.gov/pubmed/30100715 http://dx.doi.org/10.2147/COPD.S161958 |
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author | Heinbockel, Lena Marwitz, Sebastian Schromm, Andra B Watz, Henrik Kugler, Christian Ammerpohl, Ole Schnepf, Karoline Rabe, Klaus F Droemann, Daniel Goldmann, Torsten |
author_facet | Heinbockel, Lena Marwitz, Sebastian Schromm, Andra B Watz, Henrik Kugler, Christian Ammerpohl, Ole Schnepf, Karoline Rabe, Klaus F Droemann, Daniel Goldmann, Torsten |
author_sort | Heinbockel, Lena |
collection | PubMed |
description | INTRODUCTION: As part of a study aimed at illuminating at least some of the complex molecular events taking place in COPD, we screened tissues by means of transcriptome analyses. MATERIALS AND METHODS: Tissues were subjected to transcriptome analysis. Candidate genes were identified and validated by immunohistochemistry. Primary human lung cells were subjected to stimulation with cigarette smoke extract for further validation by real time PCR. RESULTS: Six candidate genes were selected for further investigations: Aquaporin 3 (AQP3), extracellular matrix protein 1 (ECM1), four and a half LIM domain 1 (FHL1), milk fat globule epidermal growth factor 8 (MFGE8, lactadherin), phosphodiesterase 4D-interacting protein (PDE4DIP), and creatine transporter SLC6A8. All six proteins were allocated to distinct cell types by immunohistochemistry. Upon stimulation with cigarette smoke extract, human type II pneumocytes showed a dose-dependent down-regulation of MFGE8, while ECM1 and FHL1 also tended to be down-regulated. Although present, none of the candidates was regulated by cigarette smoke extract in primary human macrophages. DISCUSSION: MFGE8 turned out to be an interesting new candidate gene in COPD deserving further studies. |
format | Online Article Text |
id | pubmed-6065552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60655522018-08-10 Identification of novel target genes in human lung tissue involved in chronic obstructive pulmonary disease Heinbockel, Lena Marwitz, Sebastian Schromm, Andra B Watz, Henrik Kugler, Christian Ammerpohl, Ole Schnepf, Karoline Rabe, Klaus F Droemann, Daniel Goldmann, Torsten Int J Chron Obstruct Pulmon Dis Original Research INTRODUCTION: As part of a study aimed at illuminating at least some of the complex molecular events taking place in COPD, we screened tissues by means of transcriptome analyses. MATERIALS AND METHODS: Tissues were subjected to transcriptome analysis. Candidate genes were identified and validated by immunohistochemistry. Primary human lung cells were subjected to stimulation with cigarette smoke extract for further validation by real time PCR. RESULTS: Six candidate genes were selected for further investigations: Aquaporin 3 (AQP3), extracellular matrix protein 1 (ECM1), four and a half LIM domain 1 (FHL1), milk fat globule epidermal growth factor 8 (MFGE8, lactadherin), phosphodiesterase 4D-interacting protein (PDE4DIP), and creatine transporter SLC6A8. All six proteins were allocated to distinct cell types by immunohistochemistry. Upon stimulation with cigarette smoke extract, human type II pneumocytes showed a dose-dependent down-regulation of MFGE8, while ECM1 and FHL1 also tended to be down-regulated. Although present, none of the candidates was regulated by cigarette smoke extract in primary human macrophages. DISCUSSION: MFGE8 turned out to be an interesting new candidate gene in COPD deserving further studies. Dove Medical Press 2018-07-26 /pmc/articles/PMC6065552/ /pubmed/30100715 http://dx.doi.org/10.2147/COPD.S161958 Text en © 2018 Heinbockel et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Heinbockel, Lena Marwitz, Sebastian Schromm, Andra B Watz, Henrik Kugler, Christian Ammerpohl, Ole Schnepf, Karoline Rabe, Klaus F Droemann, Daniel Goldmann, Torsten Identification of novel target genes in human lung tissue involved in chronic obstructive pulmonary disease |
title | Identification of novel target genes in human lung tissue involved in chronic obstructive pulmonary disease |
title_full | Identification of novel target genes in human lung tissue involved in chronic obstructive pulmonary disease |
title_fullStr | Identification of novel target genes in human lung tissue involved in chronic obstructive pulmonary disease |
title_full_unstemmed | Identification of novel target genes in human lung tissue involved in chronic obstructive pulmonary disease |
title_short | Identification of novel target genes in human lung tissue involved in chronic obstructive pulmonary disease |
title_sort | identification of novel target genes in human lung tissue involved in chronic obstructive pulmonary disease |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065552/ https://www.ncbi.nlm.nih.gov/pubmed/30100715 http://dx.doi.org/10.2147/COPD.S161958 |
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