Role of endocytosis in signalling and regulation of G-protein-coupled receptors

2001 ◽  
Vol 29 (4) ◽  
pp. 500-504 ◽  
Author(s):  
M. von Zastrow

Many G-protein-coupled receptors (GPCRs) undergo agonist-induced endocytosis. Endocytosis contributes to distinct processes that regulate the number and functional activity of receptors present in the plasma membrane, contributing to the well described processes of receptor sequestration and down-regulation. Emerging evidence suggests additional functions of endocytosis in mediating GPCR signalling via certain effector pathways, such as mitogen-activated protein kinase modules. The diverse functions of endocytosis raise fundamental questions about the nature of the vesicular carriers and membrane pathways that mediate the endocytic trafficking of specific GPCRs. Insights into the biochemical and functional properties of endocytic vesicles containing internalized opioid and adrenergic receptors will be discussed. Progress towards understanding the mechanisms that control the specificity with which distinct GPCRs are sorted to specialized sub-populations of endocytic vesicles will be highlighted.

1997 ◽  
Vol 272 (31) ◽  
pp. 19125-19132 ◽  
Author(s):  
Gregory J. Della Rocca ◽  
Tim van Biesen ◽  
Yehia Daaka ◽  
Deirdre K. Luttrell ◽  
Louis M. Luttrell ◽  
...  

2000 ◽  
Vol 78 (4) ◽  
pp. 267-292 ◽  
Author(s):  
Daya R Varma ◽  
Xing-Fei Deng

α1-Adrenoceptors (α1AR) are G protein-coupled receptors and include α1A, α1B, and α1D subtypes corresponding to cloned α1a, α1b, and α1d, respectively. α1AR mediate several cardiovascular actions of sympathomimetic amines such as vasoconstriction and cardiac inotropy, hypertrophy, metabolism, and remodeling. α1AR subtypes are products of separate genes and differ in structure, G protein-coupling, tissue distribution, signaling, regulation, and functions. Both α1AAR and α1BAR mediate positive inotropic responses. On the other hand, cardiac hypertrophy is primarily mediated by α1AAR. The only demonstrated major function of α1DAR is vasoconstriction. α1AR are coupled to phospholipase C, phospholipase D, and phospholipase A2; they increase intracellular Ca2+ and myofibrillar sensitivity to Ca2+ and cause translocation of specific phosphokinase C isoforms to the particulate fraction. Cardiac hypertrophic responses to α1AR agonists might involve activation of phosphokinase C and mitogen-activated protein kinase via Gq. α1AR subtypes might interact with each other and with other receptors and signaling mechanisms.Key words: cardiac hypertrophy, inotropic responses, central α1-adrenoreceptors, arrythmias.


1999 ◽  
Vol 274 (20) ◽  
pp. 13978-13984 ◽  
Author(s):  
Gregory J. Della Rocca ◽  
Stuart Maudsley ◽  
Yehia Daaka ◽  
Robert J. Lefkowitz ◽  
Louis M. Luttrell

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