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PMID: 24532814 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

The Hippo-YAP signaling pathway and contact inhibition of growth.

Journal of cell science ·Vol. 127 ·No. Pt 4 ·2014-02-15 ·Pages 709-17

Gumbiner BM, Kim NG

Abstract

The Hippo-YAP pathway mediates the control of cell proliferation by contact inhibition as well as other attributes of the physical state of cells in tissues. Several mechanisms sense the spatial and physical organization of cells, and function through distinct upstream modules to stimulate Hippo-YAP signaling: adherens junction or cadherin-catenin complexes, epithelial polarity and tight junction complexes, the FAT-Dachsous morphogen pathway, as well as cell shape, actomyosin or mechanotransduction. Soluble extracellular factors also regulate Hippo pathway signaling, often inhibiting its activity. Indeed, the Hippo pathway mediates a reciprocal relationship between contact inhibition and mitogenic signaling. As a result, cells at the edges of a colony, a wound in a tissue or a tumor are more sensitive to ambient levels of growth factors and more likely to proliferate, migrate or differentiate through a YAP and/or TAZ-dependent process. Thus, the Hippo-YAP pathway senses and responds to the physical organization of cells in tissues and coordinates these physical cues with classic growth-factor-mediated signaling pathways. This Commentary is focused on the biological significance of Hippo-YAP signaling and how upstream regulatory modules of the pathway interact to produce biological outcomes.

Keywords
Cadherin Hippo Mechanotransduction Mitogenesis Polarity YAP
MeSH Terms
Animals Cell Adhesion Cell Communication Cell Cycle Proteins Cell Polarity Cell Proliferation Hippo Signaling Pathway Humans Intercellular Signaling Peptides and Proteins/physiology Nuclear Proteins/metabolism Protein Serine-Threonine Kinases/metabolism Signal Transduction Transcription Factors/metabolism
Chemicals
Cell Cycle Proteins Intercellular Signaling Peptides and Proteins Nuclear Proteins Transcription Factors YY1AP1 protein, human Protein Serine-Threonine Kinases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Gumbiner Barry M
Department of Cell Biology, University of Virginia School of Medicine, Charlottesville, VA 22908, USA.
Kim Nam-Gyun
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Article Info
Journal
Journal of cell science
Abbr.
J Cell Sci
ISSN
1477-9137
Published
2014-02-15
Pages
709-17
Language
English
Region
England
NLM ID
0052457
PMCID
PMC3924201
Subset
IM
Grants
NIGMS NIH HHS · R01 GM098615 · United States
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