Journal article
The local molecular signature of human peripheral neuropathic pain
- Abstract:
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Focal nerve injuries are often associated with neuropathic pain. Preclinical research suggests altered neuroimmune signalling underlies such neuropathic pain; however, its cause remains poorly understood in humans. In this multicentre cohort study, we describe the local cellular and molecular signature of neuropathic pain at the lesion site, using Morton's neuroma as a human model system of neuropathic pain (n = 22; 18 women) compared with nerves from participants without nerve injury (n = 11; 4 women). Immunofluorescent staining revealed demyelination and chronic infiltration of immune cells in Morton's neuroma. RNA bulk sequencing identified 3349 differentially expressed genes between Morton's neuroma and controls. Gene ontology enrichment analysis and weighted gene co-expression network analyses revealed modules specific for host defence and neurogenesis. Deconvolution analysis confirmed higher densities of macrophages and B cells in Morton's neuroma than control samples. Modules associated with defence response, neurogenesis, and muscle system development as well as macrophage cell populations identified by deconvolution correlated with patients' paroxysmal or evoked pain. Of note, we identified a consistently differentially expressed gene signature (MARCO, CD163, STAB1), indicating the presence of a specific M(GC) subset of macrophages. MARCO gene expression correlated with paroxysmal pain. Targeted immunofluorescent analyses confirmed higher densities of intraneural CD163+MARCO+ macrophage subsets in Morton's neuroma. Our findings provide detailed insight into the local molecular signature in the context of human focal nerve injury. There is clear evidence for an ongoing role of the immune system in chronic peripheral neuropathic pain in humans, with macrophages and specifically the M(GC) MARCO+ subset implicated.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 2.0MB, Terms of use)
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- Publisher copy:
- 10.1097/j.pain.0000000000003472
Authors
- Funder identifier:
- https://ror.org/001aqnf71
- Grant:
- MR/W002388/1
- Publisher:
- Lippincott, Williams & Wilkins
- Journal:
- Pain More from this journal
- Volume:
- 166
- Issue:
- 5
- Pages:
- 1143-1156
- Publication date:
- 2024-11-25
- Acceptance date:
- 2024-09-10
- DOI:
- EISSN:
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1872-6623
- ISSN:
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0304-3959
- Language:
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English
- Keywords:
- Pubs id:
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2067153
- Local pid:
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pubs:2067153
- Deposit date:
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2024-11-27
Terms of use
- Copyright holder:
- Sandy-Hindmarch et al.
- Copyright date:
- 2024
- Rights statement:
- Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the International Association for the Study of Pain. This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
- Notes:
- This research was funded in whole, or in part, by the Wellcome Trust [222101/Z/20/ Z]. For the purpose of Open Access, the author has applied a CC BY public copyright license to any author accepted manuscript version arising from this submission.
- Licence:
- CC Attribution (CC BY)
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