dc.contributor.author |
Tomasovic, Ana |
|
dc.contributor.author |
Kurrle, Nina |
|
dc.contributor.author |
Wempe, Frank |
|
dc.contributor.author |
De-Zolt, Siike |
|
dc.contributor.author |
Scheibe, Susan |
|
dc.contributor.author |
Koli, Katri |
|
dc.contributor.author |
Serchinger, Martin |
|
dc.contributor.author |
Schnuetgen, Frank |
|
dc.contributor.author |
Sueruen, Duran |
|
dc.contributor.author |
Sterner-Kock, Anja |
|
dc.contributor.author |
Weissmann, Norbert |
|
dc.contributor.author |
von Meichner, Harald |
|
dc.date.accessioned |
2017-06-28T12:06:01Z |
|
dc.date.available |
2017-06-28T12:06:01Z |
|
dc.date.issued |
2017-05 |
|
dc.identifier.citation |
Tomasovic , A , Kurrle , N , Wempe , F , De-Zolt , S , Scheibe , S , Koli , K , Serchinger , M , Schnuetgen , F , Sueruen , D , Sterner-Kock , A , Weissmann , N & von Meichner , H 2017 , ' Ltbp4 regulates Pdgfr beta expression via TGF beta-dependent modulation of Nrf2 transcription factor function ' , Matrix Biology , vol. 59 , pp. 109-120 . https://doi.org/10.1016/j.matbio.2016.09.006 |
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dc.identifier.other |
PURE: 86160540 |
|
dc.identifier.other |
PURE UUID: 22c4124e-110f-4e3c-b49a-d8fdbb576cd6 |
|
dc.identifier.other |
WOS: 000399510100008 |
|
dc.identifier.other |
Scopus: 84994491924 |
|
dc.identifier.uri |
http://hdl.handle.net/10138/195373 |
|
dc.description.abstract |
Latent transforming growth factor beta binding protein 4 (LTBP4) belongs to the fibrillin/LTBP family of proteins and plays an important role as a structural component of extracellular matrix (ECM) and local regulator of TGF beta signaling. We have previously reported that Ltbp4S knock out mice (Ltbp4S-/-) develop centrilobular emphysema reminiscent of late stage COPD, which could be partially rescued by inactivating the antioxidant protein Sestrin 2 (Sesn2). More recent studies showed that Sesn2 knock out mice upregulate Pdgfr beta-controlled alveolar maintenance programs that protect against cigarette smoke induced pulmonary emphysema. Based on this, we hypothesized that the emphysema of Ltbp4S-/- mice is primarily caused by defective Pdgfr beta signaling. Here we show that LTBP4 induces Pdgfr beta signaling by inhibiting the antioxidant Nr12/Keap1 pathway in a TGF beta-dependent manner. Overall, our data identified Ltbp4 as a major player in lung remodeling and injury repair. (C) 2016 The Authors. Published by Elsevier B.V. |
en |
dc.format.extent |
12 |
|
dc.language.iso |
eng |
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dc.relation.ispartof |
Matrix Biology |
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dc.rights |
cc_by |
|
dc.rights.uri |
info:eu-repo/semantics/openAccess |
|
dc.subject |
Ltbp4 |
|
dc.subject |
Tgf beta |
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dc.subject |
Pdgfr beta |
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dc.subject |
Nrf2 |
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dc.subject |
ROS |
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dc.subject |
Emphysema |
|
dc.subject |
GROWTH-FACTOR-BETA |
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dc.subject |
OBSTRUCTIVE PULMONARY-DISEASE |
|
dc.subject |
SMOOTH-MUSCLE-CELLS |
|
dc.subject |
C-MYC |
|
dc.subject |
ACTIVATION |
|
dc.subject |
BINDING |
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dc.subject |
FIBROBLASTS |
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dc.subject |
RECEPTOR |
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dc.subject |
LUNG |
|
dc.subject |
TRANSFORMING-GROWTH-FACTOR-BETA-1 |
|
dc.subject |
3111 Biomedicine |
|
dc.title |
Ltbp4 regulates Pdgfr beta expression via TGF beta-dependent modulation of Nrf2 transcription factor function |
en |
dc.type |
Article |
|
dc.contributor.organization |
Research Programs Unit |
|
dc.contributor.organization |
Translational Cancer Biology (TCB) Research Programme |
|
dc.contributor.organization |
Katri Koli / Principal Investigator |
|
dc.contributor.organization |
University of Helsinki |
|
dc.contributor.organization |
Medicum |
|
dc.contributor.organization |
Transplantation Laboratory |
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dc.description.reviewstatus |
Peer reviewed |
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dc.relation.doi |
https://doi.org/10.1016/j.matbio.2016.09.006 |
|
dc.relation.issn |
0945-053X |
|
dc.rights.accesslevel |
openAccess |
|
dc.type.version |
publishedVersion |
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