Abstract
G protein-coupled receptors (GPCRs), critical for cellular communication and signaling, represent the largest cell surface protein family and play important roles in numerous pathophysiological processes. Consequently, GPCRs have become a primary focus in drug discovery efforts. Beyond their traditional G protein-dependent signaling pathways, GPCRs are also capable of activating alternative signaling mechanisms, including G protein-independent signaling, biased signaling, and signaling crosstalk. A particularly novel signaling mode employed by these receptors is GPCR transactivation, which enables cross-communication between GPCRs and other receptor types. Intriguingly, GPCR transactivation by distinct GPCRs has also been identified. In this review, I provide an overview of the known GPCR transactivation mechanisms and explore recently uncovered GPCR transactivation mediated by adhesion-class GPCRs (aGPCRs). These aGPCR-GPCR transactivation processes regulate unique cell type-specific functions, offering an exciting opportunity to develop therapies that precisely modulate specific GPCR-mediated biological effects.
Original language | English |
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Article number | 552 |
Journal | International Journal of Molecular Sciences |
Volume | 26 |
Issue number | 2 |
DOIs | |
State | Published - 10 01 2025 |
Bibliographical note
Publisher Copyright:© 2025 by the author.
Keywords
- adhesion GPCR
- GPCR transactivation
- protease
- receptor
- signaling
- Cell Adhesion/genetics
- Animals
- Signal Transduction
- Humans
- Transcriptional Activation
- Receptors, G-Protein-Coupled/metabolism