Distinct Patterns of Internalization of Different Calcitonin Gene-Related Peptide Receptors

Joseph J. Gingell, Tayla A. Rees, Erica R. Hendrikse, Andrew Siow, David Rennison, John Scotter, Paul W.R. Harris, Margaret A. Brimble, Christopher S. Walker*, Debbie L. Hay

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Calcitonin gene-related peptide (CGRP) is a neuropeptide that is involved in the transmission of pain. Drugs targeting CGRP or a CGRP receptor are efficacious in the treatment of migraine. The canonical CGRP receptor is a complex of a G protein-coupled receptor, the calcitonin-like receptor (CLR), with an accessory protein, receptor activity-modifying protein 1 (RAMP1). A second receptor, the AMY1 receptor, a complex of the calcitonin receptor with RAMP1, is a dual high-affinity receptor for CGRP and amylin. Receptor regulatory processes, such as internalization, are crucial for controlling peptide and drug responsiveness. Given the importance of CGRP receptor activity in migraine we compared the internalization profiles of both receptors for CGRP using novel fluorescent probes and a combination of live cell imaging, fixed cell imaging, and ELISA. This revealed stark differences in the regulation of each receptor with the AMY1 receptor unexpectedly showing little internalization.

Original languageEnglish
Pages (from-to)296-304
Number of pages9
JournalACS Pharmacology and Translational Science
Volume3
Issue number2
DOIs
Publication statusPublished - 10 Apr 2020

Bibliographical note

Publisher Copyright:
Copyright © 2020 American Chemical Society.

Keywords

  • amylin
  • CGRP
  • GPCR
  • internalization
  • migraine
  • receptor activity-modifying protein

ASJC Scopus subject areas

  • Pharmacology
  • Pharmacology (medical)

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