Differential expression of GluN2 NMDA receptor subunits in the dorsal horn of male and female rats.

Santa Temi, Christopher Rudyk, Jennifer Armstrong, Jeffrey A Landrigan, Chris Dedek, Natalina Salmaso, Michael E Hildebrand
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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.

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GluN2 NMDA受体亚基在雌雄大鼠背角的差异表达。
n -甲基- d -天冬氨酸受体(NMDARs)是一种兴奋性的嗜离子性谷氨酸受体,表达于整个中枢神经系统,包括脊髓背角。NMDAR亚基的GluN2亚型,包括GluN2A、GluN2B和GluN2D,使NMDAR具有结构和功能的可变性,从而实现突触传递和可塑性的异质性。尽管NMDARs在生理和病理疼痛加工中发挥重要作用,但这些特异性GluN2亚型在背角椎板上的分布和功能仍然知之甚少。令人惊讶的是,对GluN2在雌性啮齿动物中的表达完全缺乏了解。因此,我们研究了雄性和雌性大鼠腰椎背角(L4/L5)脊髓特异性GluN2变异的相对表达。为了检测突触GluN2亚型,我们使用胃蛋白酶抗原检索来揭示这些高度交联的蛋白复合物。我们发现GluN2B和GluN2D优先定位于雄性大鼠的痛觉加工浅表区域,而只有GluN2B主要定位于雌性大鼠的浅表背角。GluN2A亚基广泛分布于雄性和雌性的整个背角神经节上,而GluN2B和GluN2D免疫标记在神经节和背角神经元的胞体上均有发现。最后,我们发现GluN2B在浅表背角内侧的表达出乎意料地增强,但仅在雄性中。GluN2-NMDAR亚基在背角椎板上的这些性别特异性定位模式对理解疼痛加工的不同脊柱机制具有重要意义。
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