Format

Send to

Choose Destination
Eur J Pain. 2018 Oct;22(9):1685-1690. doi: 10.1002/ejp.1251. Epub 2018 Jun 11.

Parathyroid hormone-related peptide activates and modulates TRPV1 channel in human DRG neurons.

Author information

1
Department of Anesthesiology, Washington University Pain Center, Washington University in St. Louis School of Medicine, USA.
2
Center for the Investigation of Membrane Excitable Diseases, Washington University in St. Louis School of Medicine, USA.

Abstract

Parathyroid hormone-related peptide (PTHrP) is associated with advanced tumor growth and metastasis, especially in breast, prostate and myeloma cancers that metastasize to bones, resulting in debilitating chronic pain conditions. Our recent studies revealed that the receptor for PTHrP, PTH1R, is expressed in mouse DRG sensory neurons, and its activation leads to flow-activation and modulation of TRPV1 channel function, resulting in peripheral heat and mechanical hypersensitivity. In order to verify the translatability of our findings in rodents to humans, we explored whether this signalling axis operates in primary human DRG sensory neurons. Analysis of gene expression data from recently reported RNA deep sequencing experiments performed on mouse and human DRGs reveals that PTH1R is expressed in DRG and tibial nerve. Furthermore, exposure of cultured human DRG neurons to PTHrP leads to slow-sustained activation of TRPV1 and modulation of capsaicin-induced channel activation. Both activation and modulation of TRPV1 by PTHrP were dependent on PKC activity. Our findings suggest that functional PTHrP/PTH1R-TRPV1 signalling exists in human DRG neurons, which could contribute to local nociceptor excitation in the vicinity of metastatic bone tumor microenvironment.

PMID:
29797679
DOI:
10.1002/ejp.1251

Supplemental Content

Full text links

Icon for Wiley
Loading ...
Support Center