Literature DB >> 25937570

Crosstalk between Hippo and TGFβ: Subcellular Localization of YAP/TAZ/Smad Complexes.

Karin Grannas1, Linda Arngården1, Peter Lönn1, Magdalena Mazurkiewicz2, Andries Blokzijl1, Agata Zieba1, Ola Söderberg3.   

Abstract

The Hippo pathway plays a crucial role in growth control, proliferation and tumor suppression. Activity of the signaling pathway is associated with cell density sensing and tissue organization. Furthermore, the Hippo pathway helps to coordinate cellular processes through crosstalk with growth-factor-mediated signaling pathways such as TGFβ. Here we have examined the localization of interactions between proteins of the Hippo pathway (YAP/TAZ) and TGFβ (Smad2/3) signaling pathway by using in situ proximity ligation assays. We investigated the formation of protein complexes between YAP/TAZ and Smad2/3 and examined how these interactions were affected by TGFβ stimulation and cell density in HaCaT keratinocytes and in Smad4-deficient HT29 colon cancer cells. We demonstrate that TGFβ induces formation of YAP/TAZ-Smad2/3 complexes in HaCaT cells. Under sparse cell conditions, the complexes were detected to a higher degree and were predominantly located in the nucleus, while under dense culture conditions, the complexes were fewer and mainly located in the cytoplasm. Surprisingly, we could not detect any YAP/TAZ-Smad2/3 complexes in HT29 cells. To examine if Smad4 deficiency was responsible for the absence of interactions, we treated HaCaT cells with siRNA targeting Smad4. However, we could still observe complex formation in the siRNA-treated cells, suggesting that Smad4 is not essential for the YAP-Smad2/3 interaction. In conclusion, this study shows localized, density-dependent formation of YAP/TAZ-Smad2/3 complexes in HaCaT cells and provides evidence supporting a crosstalk between the Hippo and the TGFβ signaling pathways.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Hippo; Smad; TGFβ; in situ PLA; interaction

Mesh:

Substances:

Year:  2015        PMID: 25937570     DOI: 10.1016/j.jmb.2015.04.015

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  45 in total

1.  YAP and TAZ are distinct effectors of corneal myofibroblast transformation.

Authors:  Santoshi Muppala; Vijay Krishna Raghunathan; Iman Jalilian; Sara Thomasy; Christopher J Murphy
Journal:  Exp Eye Res       Date:  2018-12-19       Impact factor: 3.467

2.  Downregulation of WW domain-containing oxidoreductase leads to tamoxifen-resistance by the inactivation of Hippo signaling.

Authors:  Juan Li; Xuefei Feng; Canyu Li; Jie Liu; Pingping Li; Ruiqi Wang; He Chen; Peijun Liu
Journal:  Exp Biol Med (Maywood)       Date:  2019-06-02

3.  Functional characterization and circulating expression profile of dysregulated microRNAs in BAV-associated aortopathy.

Authors:  Silvia Pulignani; Andrea Borghini; Ilenia Foffa; Cecilia Vecoli; Lamia Ait-Alì; Maria Grazia Andreassi
Journal:  Heart Vessels       Date:  2019-09-27       Impact factor: 2.037

Review 4.  An overview of signaling pathways regulating YAP/TAZ activity.

Authors:  Boon Chin Heng; Xuehui Zhang; Dominique Aubel; Yunyang Bai; Xiaochan Li; Yan Wei; Martin Fussenegger; Xuliang Deng
Journal:  Cell Mol Life Sci       Date:  2020-08-03       Impact factor: 9.261

5.  In situ protein detection with enhanced specificity using DNA-conjugated antibodies and proximity ligation.

Authors:  Agata Zieba; Fredrik Ponten; Mathias Uhlén; Ulf Landegren
Journal:  Mod Pathol       Date:  2017-09-22       Impact factor: 7.842

Review 6.  Human ovarian tissue in-vitro culture: primordial follicle activation as a new strategy for female fertility preservation.

Authors:  Zeinab Ghezelayagh; Niloofar Khoshdel-Rad; Bita Ebrahimi
Journal:  Cytotechnology       Date:  2022-01-04       Impact factor: 2.058

7.  Targeted Disruption of Lats1 and Lats2 in Mice Impairs Adrenal Cortex Development and Alters Adrenocortical Cell Fate.

Authors:  Amélie Ménard; Nour Abou Nader; Adrien Levasseur; Guillaume St-Jean; Marie Le Gad- Le Roy; Derek Boerboom; Marie-Odile Benoit-Biancamano; Alexandre Boyer
Journal:  Endocrinology       Date:  2020-05-01       Impact factor: 4.736

8.  Pathogenesis of non-alcoholic fatty liver disease mediated by YAP.

Authors:  Ping Chen; Qihui Luo; Chao Huang; Qi Gao; Like Li; Jingfei Chen; Bing Chen; Wentao Liu; Wen Zeng; Zhengli Chen
Journal:  Hepatol Int       Date:  2018-01-12       Impact factor: 6.047

9.  Increased Cthrc1 Activates Normal Fibroblasts and Suppresses Keloid Fibroblasts by Inhibiting TGF-β/Smad Signal Pathway and Modulating YAP Subcellular Location.

Authors:  Meng-Jie Zhao; Si-Yuan Chen; Xiao-Ying Qu; Bilal Abdul-Fattah; Ting Lai; Meng Xie; Shi-di Wu; You-Wen Zhou; Chang-Zheng Huang
Journal:  Curr Med Sci       Date:  2018-10-20

10.  LEM domain-containing protein 3 antagonizes TGFβ-SMAD2/3 signaling in a stiffness-dependent manner in both the nucleus and cytosol.

Authors:  Dwight M Chambers; Leandro Moretti; Jennifer J Zhang; Spencer W Cooper; Davis M Chambers; Philip J Santangelo; Thomas H Barker
Journal:  J Biol Chem       Date:  2018-08-14       Impact factor: 5.157

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