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Updated: May 9, 2026

Culturing and Manipulation of O9-1 Neural Crest Cells
Published on: October 9, 2018
Hippo signaling goes long range
Veronica A Codelia1, Kenneth D Irvine
1Howard Hughes Medical Institute, Waksman Institute and Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ 08854, USA.
Abstract:
The Hippo-YAP pathway regulates organ size by modulating cell proliferation and apoptosis. Yu et al. now reveal that G-protein-coupled receptors act upstream of the transcriptional coactivators YAP/TAZ. This study reinforces the connection between the actin cytoskeleton and Hippo pathway activity and identifies a class of secreted extracellular regulators of YAP/TAZ activity.
Insights
G-protein-coupled receptors regulate organ size by controlling the Hippo-YAP pathway, influencing cell growth and death. This research links cell structure to pathway activity and uncovers new extracellular regulators of YAP/TAZ.
Area of Science:
- Cell Biology
- Molecular Biology
- Developmental Biology
Background:
- The Hippo-YAP pathway is a critical regulator of organ size, controlling cellular proliferation and apoptosis.
- Yeast and worm homologs of the Hippo pathway components are involved in cell shape and growth.
Discussion:
- This study demonstrates that G-protein-coupled receptors (GPCRs) function upstream of the YAP/TAZ transcriptional coactivators.
- The findings establish a link between the actin cytoskeleton, a key component of cell structure, and Hippo pathway signaling.
- A novel class of secreted extracellular regulators that modulate YAP/TAZ activity has been identified.
Key Insights:
- GPCRs act as upstream regulators of the Hippo-YAP pathway.
- The actin cytoskeleton plays a role in Hippo pathway activity.
- Secreted extracellular factors can control YAP/TAZ activity.
Outlook:
- Further investigation into GPCR signaling in organ size control.
- Exploring the therapeutic potential of targeting the Hippo-YAP pathway for regenerative medicine and cancer treatment.
- Characterizing the identified secreted extracellular regulators and their mechanisms of action.
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