Department of Physiology and Pathophysiology, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg R3E 0J9, Canada.
Department of Physiology and Pathophysiology, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg R3E 0J9, Canada.
Neuroscience. 2023 Jul 15;523:31-46. doi: 10.1016/j.neuroscience.2023.05.009. Epub 2023 May 22.
Spinal sympathetic preganglionic neurons (SPNs) are among the many neuronal populations in the mammalian central nervous system (CNS) where there is evidence for electrical coupling between cell pairs linked by gap junctions composed of connexin36 (Cx36). Understanding the organization of this coupling in relation to autonomic functions of spinal sympathetic systems requires knowledge of how these junctions are deployed among SPNs. Here, we document the distribution of immunofluorescence detection of Cx36 among SPNs identified by immunolabelling of their various markers, including choline acetyltransferase, nitric oxide and peripherin in adult and developing mouse and rat. In adult animals, labelling of Cx36 was exclusively punctate and dense concentrations of Cx36-puncta were distributed along the entire length of the spinal thoracic intermediolateral cell column (IML). These puncta were also seen in association with SPN dendritic processes in the lateral funiculus, the intercalated and central autonomic areas and those within and extending medially from the IML. All labelling for Cx36 was absent in spinal cords of Cx36 knockout mice. High densities of Cx36-puncta were already evident among clusters of SPNs in the IML of mouse and rat at postnatal days 10-12. In Cx36::eGFP mice, eGFP reporter was absent in SPNs, thus representing false negative detection, but was localized to some glutamatergic and GABAergic synaptic terminals. Some eGFP terminals were found contacting SPN dendrites. These results indicate widespread Cx36 expression in SPNs, further supporting evidence of electrical coupling between these cells, and suggest that SPNs are innervated by neurons that themselves may be electrically coupled.
脊髓交感节前神经元 (SPN) 是哺乳动物中枢神经系统 (CNS) 中许多神经元群体之一,有证据表明这些神经元之间通过由连接蛋白 36 (Cx36) 组成的缝隙连接进行电耦联。了解这种偶联在脊髓交感神经系统自主功能中的组织方式,需要了解这些连接在 SPN 中的分布情况。在这里,我们记录了通过免疫标记 Cx36 的各种标记物(包括胆碱乙酰转移酶、一氧化氮和外周蛋白)鉴定的 SPN 中 Cx36 免疫荧光检测的分布情况,包括成年和发育中的小鼠和大鼠。在成年动物中,Cx36 的标记是点状的,Cx36 点状密集区沿整个脊髓胸段中间外侧细胞柱 (IML) 分布。这些点状结构也与外侧束中的 SPN 树突过程、中间和自主区域以及 IML 内和从内侧延伸的区域中的 SPN 树突过程相关。在 Cx36 敲除小鼠的脊髓中,Cx36 的所有标记均缺失。在出生后第 10-12 天的小鼠和大鼠的 IML 中,已经可以看到 Cx36 点状密集区存在于 SPN 簇中。在 Cx36::eGFP 小鼠中,eGFP 报告基因在 SPN 中缺失,因此代表假阴性检测,但定位在一些谷氨酸能和 GABA 能突触末端。一些 eGFP 末端被发现与 SPN 树突接触。这些结果表明 SPN 中广泛表达 Cx36,进一步支持这些细胞之间存在电偶联的证据,并表明 SPN 被自身可能存在电偶联的神经元支配。