Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Heinbockel, Lena, Marwitz, Sebastian, Schromm, Andra B, Watz, Henrik, Kugler, Christian, Ammerpohl, Ole, Schnepf, Karoline, Rabe, Klaus F, Droemann, Daniel, Goldmann, Torsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
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
_version_ 1783342883392192512
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
work_keys_str_mv AT heinbockellena identificationofnoveltargetgenesinhumanlungtissueinvolvedinchronicobstructivepulmonarydisease
AT marwitzsebastian identificationofnoveltargetgenesinhumanlungtissueinvolvedinchronicobstructivepulmonarydisease
AT schrommandrab identificationofnoveltargetgenesinhumanlungtissueinvolvedinchronicobstructivepulmonarydisease
AT watzhenrik identificationofnoveltargetgenesinhumanlungtissueinvolvedinchronicobstructivepulmonarydisease
AT kuglerchristian identificationofnoveltargetgenesinhumanlungtissueinvolvedinchronicobstructivepulmonarydisease
AT ammerpohlole identificationofnoveltargetgenesinhumanlungtissueinvolvedinchronicobstructivepulmonarydisease
AT schnepfkaroline identificationofnoveltargetgenesinhumanlungtissueinvolvedinchronicobstructivepulmonarydisease
AT rabeklausf identificationofnoveltargetgenesinhumanlungtissueinvolvedinchronicobstructivepulmonarydisease
AT droemanndaniel identificationofnoveltargetgenesinhumanlungtissueinvolvedinchronicobstructivepulmonarydisease
AT goldmanntorsten identificationofnoveltargetgenesinhumanlungtissueinvolvedinchronicobstructivepulmonarydisease