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Dissecting the signaling features of the multi-protein complex GPCR/β-arrestin/ERK1/2. | LitMetric

Dissecting the signaling features of the multi-protein complex GPCR/β-arrestin/ERK1/2.

Eur J Cell Biol

Instituto de Fisiología Celular (UNAM), México City, 04510, Mexico. Electronic address:

Published: June 2018

AI Article Synopsis

  • GPCRs are crucial for regulating various physiological processes and are linked to many diseases, making them important drug targets for about 25% of marketed medications.
  • Upon binding to an agonist, GPCRs trigger multiple signaling pathways that lead to significant cellular activities such as gene transcription, survival, and differentiation.
  • This review focuses on the GPCR-β-arrestin-ERK1/2 signaling module, examining its unique role and the attention it has garnered in research due to its molecular and physiological implications.

Article Abstract

G protein-coupled receptors (GPCRs) have emerged as key biological entities that regulate a plethora of physiological processes and participate in the onset and development of many diseases. Moreover, these receptors are important targets of almost 25% of the current therapeutic drugs in the market. Upon agonist binding, GPCRs activate a great number of signaling pathways, resulting in important cellular events like gene transcription, survival, proliferation and differentiation. In order to activate such events, GPCRs interact with a variety of scaffold and molecular entities, particularly with G proteins, but also with β-arrestins and the extracellular signal-regulated kinases 1 and 2 (ERK1/2) pathway, forming unique signaling modules. The aim of this review is to analyze the signaling features of the multi-protein complex GPCR-β-arrestin-ERK1/2, a unique signaling module that has received considerable attention from different research groups due to its molecular and physiological roles in diverse cellular contexts.

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Source
http://dx.doi.org/10.1016/j.ejcb.2018.04.001DOI Listing

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