Differential expression of GluN2 NMDA receptor subunits in the dorsal horn of male and female rats. Issue 1 (1st January 2021)

• Record Type: Journal Article
• Authors: Temi, Santa; Rudyk, Christopher; Armstrong, Jennifer; Landrigan, Jeffrey A.; Dedek, Chris; Salmaso, Natalina; Hildebrand, Michael E.
• Is Part Of: Channels. Volume 15:Issue 1(2021)
• Page Start: 179
• Page End: 192
• Publication Date: 2021-01-01
• Subjects: GluN2 -- GluN2A -- GluN2B -- GluN2D -- NMDA receptor -- CGRP -- dorsal horn -- sex -- spinal cord -- laminae; Ion channels -- Periodicals; 572.3
• DOI: 10.1080/19336950.2020.1871205
• Languages: English
• ISSNs: 1933-6950

Abstract

ABSTRACT: N-methyl-D-aspartate receptors (NMDARs) are excitatory ionotropic glutamate receptors expressed throughout the CNS, including in the spinal dorsal horn. The GluN2 subtypes of NMDAR subunit, which include GluN2A, GluN2B, and GluN2D in the dorsal horn, confer NMDARs with structural and functional variability, enabling heterogeneity in synaptic transmission and plasticity. Despite essential roles for NMDARs in physiological and pathological pain processing, the distribution and function of these specific GluN2 isoforms across dorsal horn laminae remain poorly understood. Surprisingly, there is a complete lack of knowledge of GluN2 expression in female rodents. We, therefore, investigated the relative expression of specific GluN2 variants in the dorsal horn of lumbar (L4/L5) spinal cord from both male and female rats. In order to detect synaptic GluN2 isoforms, we used pepsin antigen-retrieval to unmask these highly cross-linked protein complexes. We found that GluN2B and GluN2D are preferentially localized to the pain-processing superficial regions of the dorsal horn in males, while only GluN2B is predominantly localized to the superficial dorsal horn of female rats. The GluN2A subunit is diffusely localized to neuropil throughout the dorsal horn of both males and females, while GluN2B and GluN2D immunolabelling are found both in the neuropil and on the soma of dorsal horn neurons. Finally, we identified an unexpected enhanced expression of GluN2B in the medial division of the superficial dorsal horn, but in males only. These sex-specific localization patterns of GluN2-NMDAR subunits across dorsal horn laminae have significant implications for the understanding of divergent spinal mechanisms of pain processing.