Insights into cellular signalling by G protein coupled receptor transactivation of cell surface protein kinase receptors View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2017-02-06

AUTHORS

Rebecca Chaplin, Lyna Thach, Morley D. Hollenberg, Yingnan Cao, Peter J. Little, Danielle Kamato

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. More... »

PAGES

117-125

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s12079-017-0375-9

DOI

http://dx.doi.org/10.1007/s12079-017-0375-9

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1083687919

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/28168348


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