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Pro-neurotrophins, sortilin, and nociception

Nerve growth factor (NGF) signaling is important in the development and functional maintenance of nociceptors, but it also plays a central role in initiating and sustaining heat and mechanical hyperalgesia following inflammation. NGF signaling in pain has traditionally been thought of as primarily e...

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Autores principales: Lewin, Gary R, Nykjaer, Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232910/
https://www.ncbi.nlm.nih.gov/pubmed/24494677
http://dx.doi.org/10.1111/ejn.12466
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author Lewin, Gary R
Nykjaer, Anders
author_facet Lewin, Gary R
Nykjaer, Anders
author_sort Lewin, Gary R
collection PubMed
description Nerve growth factor (NGF) signaling is important in the development and functional maintenance of nociceptors, but it also plays a central role in initiating and sustaining heat and mechanical hyperalgesia following inflammation. NGF signaling in pain has traditionally been thought of as primarily engaging the classic high-affinity receptor tyrosine kinase receptor TrkA to initiate sensitization events. However, the discovery that secreted proforms of nerve NGF have biological functions distinct from the processed mature factors raised the possibility that these proneurotrophins (proNTs) may have distinct function in painful conditions. ProNTs engage a novel receptor system that is distinct from that of mature neurotrophins, consisting of sortilin, a type I membrane protein belonging to the VPS10p family, and its co-receptor, the classic low-affinity neurotrophin receptor p75NTR. Here, we review how this new receptor system may itself function with or independently of the classic TrkA system in regulating inflammatory or neuropathic pain.
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spelling pubmed-42329102014-12-19 Pro-neurotrophins, sortilin, and nociception Lewin, Gary R Nykjaer, Anders Eur J Neurosci Special Issue: Neurobiology of Pain Nerve growth factor (NGF) signaling is important in the development and functional maintenance of nociceptors, but it also plays a central role in initiating and sustaining heat and mechanical hyperalgesia following inflammation. NGF signaling in pain has traditionally been thought of as primarily engaging the classic high-affinity receptor tyrosine kinase receptor TrkA to initiate sensitization events. However, the discovery that secreted proforms of nerve NGF have biological functions distinct from the processed mature factors raised the possibility that these proneurotrophins (proNTs) may have distinct function in painful conditions. ProNTs engage a novel receptor system that is distinct from that of mature neurotrophins, consisting of sortilin, a type I membrane protein belonging to the VPS10p family, and its co-receptor, the classic low-affinity neurotrophin receptor p75NTR. Here, we review how this new receptor system may itself function with or independently of the classic TrkA system in regulating inflammatory or neuropathic pain. BlackWell Publishing Ltd 2014-02 2014-02-04 /pmc/articles/PMC4232910/ /pubmed/24494677 http://dx.doi.org/10.1111/ejn.12466 Text en Copyright © 2014 Federation of European Neuroscience Societies and John Wiley & Sons Ltd http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Special Issue: Neurobiology of Pain
Lewin, Gary R
Nykjaer, Anders
Pro-neurotrophins, sortilin, and nociception
title Pro-neurotrophins, sortilin, and nociception
title_full Pro-neurotrophins, sortilin, and nociception
title_fullStr Pro-neurotrophins, sortilin, and nociception
title_full_unstemmed Pro-neurotrophins, sortilin, and nociception
title_short Pro-neurotrophins, sortilin, and nociception
title_sort pro-neurotrophins, sortilin, and nociception
topic Special Issue: Neurobiology of Pain
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232910/
https://www.ncbi.nlm.nih.gov/pubmed/24494677
http://dx.doi.org/10.1111/ejn.12466
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