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Cell type–specific super-resolution imaging reveals an increase in calcium-permeable AMPA receptors at spinal peptidergic terminals as an anatomical correlate of inflammatory pain

Woodhams, Stephen G.; Markus, Robert; Gowler, Peter R.W.; Self, Timothy J.; Chapman, Victoria

Cell type–specific super-resolution imaging reveals an increase in calcium-permeable AMPA receptors at spinal peptidergic terminals as an anatomical correlate of inflammatory pain Thumbnail


Authors

STEPHEN WOODHAMS STEPHEN.WOODHAMS@NOTTINGHAM.AC.UK
Teaching Associate Neuroscience (Fixed T

Robert Markus

Peter R.W. Gowler

Timothy J. Self



Abstract

Spinal hyperexcitability is a key event in the development of persistent pain, and arises partly from alterations in the number and localization of α-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA)-type glutamate receptors. However, determining precisely where these changes occur is challenging due to the requirement for multiplex labelling and nanoscale resolution. The recent development of super-resolution light microscopy provides new tools to address these challenges. Here, we apply combined confocal/direct STochastic Optical Reconstruction Microscopy (dSTORM) to reveal changes in calcium-permeable subunits of AMPA-type glutamate receptors (GluA1) at identified spinal cord dorsal horn (SCDH) peptidergic axon terminals in a model of inflammatory pain. L4/5 lumbar spinal cord was collected from adult male C57BL/6J mice 24 hours after unilateral hind paw injection of saline or 1% carrageenan (n = 6/group). Tissue was immunolabelled for markers of peptidergic axon terminals (substance P; SP), presynaptic active zones (Bassoon), and GluA1. Direct stochastic optical reconstruction microscopy revealed a 59% increase in total GluA1 immunolabelling in the SCDH in the carrageenan group, which was not detected by confocal microscopy. Cell type–specific analyses identified a 10-fold increase in GluA1 localized to SP+ structures, and identified GluA1 nanodomains that scaled with behavioural hypersensitivity, and were associated with synaptic release sites. These findings demonstrate that dSTORM has the sensitivity and power to detect nanoscale anatomical changes in the SCDH, and provides new evidence for synaptic insertion of GluA1+-AMPA-Rs at spinal peptidergic nociceptive terminals in a model of inflammatory pain.

Citation

Woodhams, S. G., Markus, R., Gowler, P. R., Self, T. J., & Chapman, V. (2019). Cell type–specific super-resolution imaging reveals an increase in calcium-permeable AMPA receptors at spinal peptidergic terminals as an anatomical correlate of inflammatory pain. PAIN, 160(11), 2641-2650. https://doi.org/10.1097/j.pain.0000000000001672

Journal Article Type Article
Acceptance Date Jul 30, 2019
Publication Date 2019-11
Deposit Date Oct 25, 2019
Publicly Available Date Oct 25, 2019
Journal PAIN
Print ISSN 0304-3959
Electronic ISSN 1872-6623
Publisher Lippincott, Williams & Wilkins
Peer Reviewed Peer Reviewed
Volume 160
Issue 11
Pages 2641-2650
DOI https://doi.org/10.1097/j.pain.0000000000001672
Keywords Anesthesiology and Pain Medicine; Neurology; Clinical Neurology
Public URL https://nottingham-repository.worktribe.com/output/2965556
Publisher URL https://journals.lww.com/pain/Abstract/2019/11000/Cell_type_specific_super_resolution_imaging.23.aspx

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