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Actin Cytoskeleton Regulates Hippo Signaling

Hippo pathway controls the organ size by modulating cell proliferation and apoptosis. However, the upstream regulation of hippo signaling by actin cytoskeleton is not clear. To elucidate the role of actin as an upstream regulator of Hippo signaling, the levels of F (filamentous)-actin in cells were...

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Detalles Bibliográficos
Autores principales: Reddy, Pradeep, Deguchi, Masashi, Cheng, Yuan, Hsueh, Aaron J. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770699/
https://www.ncbi.nlm.nih.gov/pubmed/24040060
http://dx.doi.org/10.1371/journal.pone.0073763
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author Reddy, Pradeep
Deguchi, Masashi
Cheng, Yuan
Hsueh, Aaron J. W.
author_facet Reddy, Pradeep
Deguchi, Masashi
Cheng, Yuan
Hsueh, Aaron J. W.
author_sort Reddy, Pradeep
collection PubMed
description Hippo pathway controls the organ size by modulating cell proliferation and apoptosis. However, the upstream regulation of hippo signaling by actin cytoskeleton is not clear. To elucidate the role of actin as an upstream regulator of Hippo signaling, the levels of F (filamentous)-actin in cells were elevated using jasplakinolide, an actin-stabilizing drug. Induction of F-actin formation in HeLa cells resulted in decreased phosphorylation of YAP, a key effector molecule for Hippo signaling. The activated YAP is localized to the cell nucleus and YAP increase was associated with increased expression of downstream CCN growth factors CCN1/CYR61 and CCN2/CTGF. The effect of the actin-stabilizing drug was blocked when YAP levels were suppressed in YAP “knock-down” cells. In summary, using an actin-stabilizing drug we show that actin cytoskeleton is one of the upstream regulators of Hippo signaling capable of activating YAP and increasing its downstream CCN growth factors.
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spelling pubmed-37706992013-09-13 Actin Cytoskeleton Regulates Hippo Signaling Reddy, Pradeep Deguchi, Masashi Cheng, Yuan Hsueh, Aaron J. W. PLoS One Research Article Hippo pathway controls the organ size by modulating cell proliferation and apoptosis. However, the upstream regulation of hippo signaling by actin cytoskeleton is not clear. To elucidate the role of actin as an upstream regulator of Hippo signaling, the levels of F (filamentous)-actin in cells were elevated using jasplakinolide, an actin-stabilizing drug. Induction of F-actin formation in HeLa cells resulted in decreased phosphorylation of YAP, a key effector molecule for Hippo signaling. The activated YAP is localized to the cell nucleus and YAP increase was associated with increased expression of downstream CCN growth factors CCN1/CYR61 and CCN2/CTGF. The effect of the actin-stabilizing drug was blocked when YAP levels were suppressed in YAP “knock-down” cells. In summary, using an actin-stabilizing drug we show that actin cytoskeleton is one of the upstream regulators of Hippo signaling capable of activating YAP and increasing its downstream CCN growth factors. Public Library of Science 2013-09-11 /pmc/articles/PMC3770699/ /pubmed/24040060 http://dx.doi.org/10.1371/journal.pone.0073763 Text en © 2013 Reddy 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
Reddy, Pradeep
Deguchi, Masashi
Cheng, Yuan
Hsueh, Aaron J. W.
Actin Cytoskeleton Regulates Hippo Signaling
title Actin Cytoskeleton Regulates Hippo Signaling
title_full Actin Cytoskeleton Regulates Hippo Signaling
title_fullStr Actin Cytoskeleton Regulates Hippo Signaling
title_full_unstemmed Actin Cytoskeleton Regulates Hippo Signaling
title_short Actin Cytoskeleton Regulates Hippo Signaling
title_sort actin cytoskeleton regulates hippo signaling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770699/
https://www.ncbi.nlm.nih.gov/pubmed/24040060
http://dx.doi.org/10.1371/journal.pone.0073763
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