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TAF4 Inactivation Reveals the 3 Dimensional Growth Promoting Activities of Collagen 6A3

Collagen 6A3 (Col6a3), a component of extracellular matrix, is often up-regulated in tumours and is believed to play a pro-oncogenic role. However the mechanisms of its tumorigenic activity are poorly understood. We show here that Col6a3 is highly expressed in densely growing mouse embryonic fibrobl...

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Autores principales: Martianov, Igor, Cler, Emilie, Duluc, Isabelle, Vicaire, Serge, Philipps, Muriel, Freund, Jean-Noel, Davidson, Irwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3911972/
https://www.ncbi.nlm.nih.gov/pubmed/24498316
http://dx.doi.org/10.1371/journal.pone.0087365
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author Martianov, Igor
Cler, Emilie
Duluc, Isabelle
Vicaire, Serge
Philipps, Muriel
Freund, Jean-Noel
Davidson, Irwin
author_facet Martianov, Igor
Cler, Emilie
Duluc, Isabelle
Vicaire, Serge
Philipps, Muriel
Freund, Jean-Noel
Davidson, Irwin
author_sort Martianov, Igor
collection PubMed
description Collagen 6A3 (Col6a3), a component of extracellular matrix, is often up-regulated in tumours and is believed to play a pro-oncogenic role. However the mechanisms of its tumorigenic activity are poorly understood. We show here that Col6a3 is highly expressed in densely growing mouse embryonic fibroblasts (MEFs). In MEFs where the TAF4 subunit of general transcription factor IID (TFIID) has been inactivated, elevated Col6a3 expression prevents contact inhibition promoting their 3 dimensional growth as foci and fibrospheres. Analyses of gene expression in densely growing Taf4(−/−) MEFs revealed repression of the Hippo pathway and activation of Wnt signalling. The Hippo activator Kibra/Wwc1 is repressed under dense conditions in Taf4(−/−) MEFs, leading to nuclear accumulation of the proliferation factor YAP1 in the cells forming 3D foci. At the same time, Wnt9a is activated and the Sfrp2 antagonist of Wnt signalling is repressed. Surprisingly, treatment of Taf4(−/−) MEFs with all-trans retinoic acid (ATRA) restores contact inhibition suppressing 3D growth. ATRA represses Col6a3 expression independently of TAF4 expression and Col6a3 silencing is sufficient to restore contact inhibition in Taf4(−/−) MEFs and to suppress 3D growth by reactivating Kibra expression to induce Hippo signalling and by inducing Sfrp2 expression to antagonize Wnt signalling. All together, these results reveal a critical role for Col6a3 in regulating both Hippo and Wnt signalling to promote 3D growth, and show that the TFIID subunit TAF4 is essential to restrain the growth promoting properties of Col6a3. Our data provide new insight into the role of extra cellular matrix components in regulating cell growth.
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spelling pubmed-39119722014-02-04 TAF4 Inactivation Reveals the 3 Dimensional Growth Promoting Activities of Collagen 6A3 Martianov, Igor Cler, Emilie Duluc, Isabelle Vicaire, Serge Philipps, Muriel Freund, Jean-Noel Davidson, Irwin PLoS One Research Article Collagen 6A3 (Col6a3), a component of extracellular matrix, is often up-regulated in tumours and is believed to play a pro-oncogenic role. However the mechanisms of its tumorigenic activity are poorly understood. We show here that Col6a3 is highly expressed in densely growing mouse embryonic fibroblasts (MEFs). In MEFs where the TAF4 subunit of general transcription factor IID (TFIID) has been inactivated, elevated Col6a3 expression prevents contact inhibition promoting their 3 dimensional growth as foci and fibrospheres. Analyses of gene expression in densely growing Taf4(−/−) MEFs revealed repression of the Hippo pathway and activation of Wnt signalling. The Hippo activator Kibra/Wwc1 is repressed under dense conditions in Taf4(−/−) MEFs, leading to nuclear accumulation of the proliferation factor YAP1 in the cells forming 3D foci. At the same time, Wnt9a is activated and the Sfrp2 antagonist of Wnt signalling is repressed. Surprisingly, treatment of Taf4(−/−) MEFs with all-trans retinoic acid (ATRA) restores contact inhibition suppressing 3D growth. ATRA represses Col6a3 expression independently of TAF4 expression and Col6a3 silencing is sufficient to restore contact inhibition in Taf4(−/−) MEFs and to suppress 3D growth by reactivating Kibra expression to induce Hippo signalling and by inducing Sfrp2 expression to antagonize Wnt signalling. All together, these results reveal a critical role for Col6a3 in regulating both Hippo and Wnt signalling to promote 3D growth, and show that the TFIID subunit TAF4 is essential to restrain the growth promoting properties of Col6a3. Our data provide new insight into the role of extra cellular matrix components in regulating cell growth. Public Library of Science 2014-02-03 /pmc/articles/PMC3911972/ /pubmed/24498316 http://dx.doi.org/10.1371/journal.pone.0087365 Text en © 2014 Martianov et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Martianov, Igor
Cler, Emilie
Duluc, Isabelle
Vicaire, Serge
Philipps, Muriel
Freund, Jean-Noel
Davidson, Irwin
TAF4 Inactivation Reveals the 3 Dimensional Growth Promoting Activities of Collagen 6A3
title TAF4 Inactivation Reveals the 3 Dimensional Growth Promoting Activities of Collagen 6A3
title_full TAF4 Inactivation Reveals the 3 Dimensional Growth Promoting Activities of Collagen 6A3
title_fullStr TAF4 Inactivation Reveals the 3 Dimensional Growth Promoting Activities of Collagen 6A3
title_full_unstemmed TAF4 Inactivation Reveals the 3 Dimensional Growth Promoting Activities of Collagen 6A3
title_short TAF4 Inactivation Reveals the 3 Dimensional Growth Promoting Activities of Collagen 6A3
title_sort taf4 inactivation reveals the 3 dimensional growth promoting activities of collagen 6a3
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3911972/
https://www.ncbi.nlm.nih.gov/pubmed/24498316
http://dx.doi.org/10.1371/journal.pone.0087365
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