TY - JOUR
T1 - Identification of novel target genes in human lung tissue involved in chronic obstructive pulmonary disease
AU - Heinbockel, Lena
AU - Marwitz, Sebastian
AU - Schromm, Andra B.
AU - Watz, Henrik
AU - Kugler, Christian
AU - Ammerpohl, Ole
AU - Schnepf, Karoline
AU - Rabe, Klaus F.
AU - Droemann, Daniel
AU - Goldmann, Torsten
N1 - Funding Information:
The study was funded by the German Center for Lung Research (DZL), disease area COPD, Gen.2. Patient tissues were provided by the BioMaterialBank North, which is funded in part by the Airway Research Center North (ARCN),
Funding Information:
a member of the German Center for Lung Research (DZL), and is a member of popgen 2.0 network (P2N), which is supported by a grant from the German Ministry for Education and Research (01EY1103). The authors thank Bettina Baron-Lühr, Patricia Prilla, Stefanie Fox, Jasmin Tiebach, Kristin Wiczkowski, and Maria Lammers for their excellent technical assistance as well as Dr Klaas F. Franzen for providing the CSE.
Funding Information:
The author Lena Heinbockel is supported by the Deutsche Forschungsgemeinschaft (DFG, project DR797/3-1 611672). The authors report no other conflicts of interest in this work.
Publisher Copyright:
© 2018 Heinbockel et al.
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2018
Y1 - 2018
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85058437457&partnerID=8YFLogxK
U2 - 10.2147/COPD.S161958
DO - 10.2147/COPD.S161958
M3 - Journal articles
C2 - 30100715
AN - SCOPUS:85058437457
SN - 1176-9106
VL - 13
SP - 2255
EP - 2259
JO - International Journal of COPD
JF - International Journal of COPD
ER -