Literature DB >> 28168348

Insights into cellular signalling by G protein coupled receptor transactivation of cell surface protein kinase receptors.

Rebecca Chaplin1, Lyna Thach1, Morley D Hollenberg2, Yingnan Cao3, Peter J Little1,3, Danielle Kamato4.   

Abstract

G protein coupled receptor (GPCR) signalling is mediated by transactivation independent and transactivation dependent pathways. GPCRs transactivate protein tyrosine kinase receptors (PTKRs) and protein serine/threonine kinase receptors (PS/TKR). Since the initial observations of transactivation dependent signalling, there has been an effort to understand the mechanisms behind this phenomena. GPCR signalling has evolved to include biased signalling. Biased signalling, whereby selected ligands can activate the same GPCR that can generate multiple signals, but drive only a unique response. To date, there has been no focus on the ability of biased agonists to activate the PTKR and PS/TKR transactivation pathways differentially. As such, this represents a novel direction for future research. This review will discuss the main mechanisms of GPCR mediated receptor transactivation and the pathways involved in intracellular responses.

Entities:  

Keywords:  Biased signalling; G-protein coupled receptors; Heterotrimeric G proteins; Serine/threonine kinase receptors; Transactivation signalling

Year:  2017        PMID: 28168348      PMCID: PMC5440347          DOI: 10.1007/s12079-017-0375-9

Source DB:  PubMed          Journal:  J Cell Commun Signal        ISSN: 1873-9601            Impact factor:   5.782


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