The local molecular signature of human peripheral neuropathic pain

<p>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 molecul...

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Main Authors: Sandy-Hindmarch, OP, Chang, P-S, Scheuren, PS, De Schoenmacker, I, Hubli, M, Loizou, C, Wirth, S, Mahadevan, D, Wiberg, A, Furniss, D, Calvo, M, Bennett, DLH, Denk, F, Baskozos, G, Schmid, AB
Format: Journal article
Language:English
Published: Lippincott, Williams & Wilkins 2024
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author Sandy-Hindmarch, OP
Chang, P-S
Scheuren, PS
De Schoenmacker, I
Hubli, M
Loizou, C
Wirth, S
Mahadevan, D
Wiberg, A
Furniss, D
Calvo, M
Bennett, DLH
Denk, F
Baskozos, G
Schmid, AB
author_facet Sandy-Hindmarch, OP
Chang, P-S
Scheuren, PS
De Schoenmacker, I
Hubli, M
Loizou, C
Wirth, S
Mahadevan, D
Wiberg, A
Furniss, D
Calvo, M
Bennett, DLH
Denk, F
Baskozos, G
Schmid, AB
author_sort Sandy-Hindmarch, OP
collection OXFORD
description <p>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 (<em>MARCO, CD163, STAB1</em>)<em>,</em>&nbsp;indicating the presence of a specific M(GC) subset of macrophages.&nbsp;<em>MARCO</em>&nbsp;gene expression correlated with paroxysmal pain. Targeted immunofluorescent analyses confirmed higher densities of intraneural CD163<sup>+</sup>MARCO<sup>+</sup>&nbsp;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<sup>+</sup>&nbsp;subset implicated.</p>
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spelling oxford-uuid:e6eb8002-e512-4fb8-887a-d8b5a9160aff2024-11-27T11:09:29ZThe local molecular signature of human peripheral neuropathic painJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:e6eb8002-e512-4fb8-887a-d8b5a9160affEnglishSymplectic ElementsLippincott, Williams & Wilkins2024Sandy-Hindmarch, OPChang, P-SScheuren, PSDe Schoenmacker, IHubli, MLoizou, CWirth, SMahadevan, DWiberg, AFurniss, DCalvo, MBennett, DLHDenk, FBaskozos, GSchmid, AB<p>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 (<em>MARCO, CD163, STAB1</em>)<em>,</em>&nbsp;indicating the presence of a specific M(GC) subset of macrophages.&nbsp;<em>MARCO</em>&nbsp;gene expression correlated with paroxysmal pain. Targeted immunofluorescent analyses confirmed higher densities of intraneural CD163<sup>+</sup>MARCO<sup>+</sup>&nbsp;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<sup>+</sup>&nbsp;subset implicated.</p>
spellingShingle Sandy-Hindmarch, OP
Chang, P-S
Scheuren, PS
De Schoenmacker, I
Hubli, M
Loizou, C
Wirth, S
Mahadevan, D
Wiberg, A
Furniss, D
Calvo, M
Bennett, DLH
Denk, F
Baskozos, G
Schmid, AB
The local molecular signature of human peripheral neuropathic pain
title The local molecular signature of human peripheral neuropathic pain
title_full The local molecular signature of human peripheral neuropathic pain
title_fullStr The local molecular signature of human peripheral neuropathic pain
title_full_unstemmed The local molecular signature of human peripheral neuropathic pain
title_short The local molecular signature of human peripheral neuropathic pain
title_sort local molecular signature of human peripheral neuropathic pain
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