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首页> 外文期刊>Acta Histochemica: Zeitschrift fur Histologische Topochemie >Neurons and satellite glial cells in adult rat lumbar dorsal root ganglia express connexin 36
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Neurons and satellite glial cells in adult rat lumbar dorsal root ganglia express connexin 36

机译:成人大鼠腰椎背根神经节快递Connexin 36中的神经元和卫星胶质细胞

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Previous studies have shown that following peripheral nerve injury there was a downregulation of the gap junction protein connexin 36 (Cx36) in the spinal cord; however, it is not known whether Cx36 protein is expressed in the dorsal root ganglia (DRGs), nor if its levels are altered following peripheral nerve injuries. Here we address these aspects in the adult rat lumbar DRG. Cx36 mRNA was detected using qRT-PCR, and Cx36 protein was identified in DRG sections using immunohistochemistry (IHC) and immunofluorescence (IF). Double staining revealed that Cx36 co-localizes with both anti-beta-III tubulin, a neuronal marker, and anti-glutamine synthetase, a satellite glial cell (SGC) marker. In neurons, Cx36 staining was mostly uniform in somata and fibers of all sizes and its intensity increased at the cell membranes. This labeling pattern was in contrast with Cx36 IF dots mainly found at junctional membranes in islet beta cells used as a control tissue. Co-staining with anti-Cx43 and anti-Cx36 showed that whereas mostly uniform staining of Cx36 was found throughout neurons and SGCs, Cx43 IF puncta were localized to SGCs. Cx36 mRNA was expressed in normal lumbar DRG, and it was significantly down-regulated in L4 DRG of rats that underwent sciatic nerve injury resulting in persistent hypersensitivity. Collectively, these findings demonstrated that neurons and SGCs express Cx36 protein in normal DRG, and suggested that perturbation of Cx36 levels may contribute to chronic neuropathic pain resulting from a peripheral nerve injury.
机译:先前的研究表明,在外周神经损伤以下,脊髓中间隙结蛋白Cancexin 36(CX36)下调了下调;然而,尚不清楚CX36蛋白是否在背根神经节(DRG)中表达,也不是在周围神经损伤后其水平改变。在这里,我们在成人大鼠腰椎DRG中解决了这些方面。使用QRT-PCR检测CX36 mRNA,使用免疫组织化学(IHC)和免疫荧光(IF)在DRG部分中鉴定CX36蛋白。双染色显示CX36与抗β-III微管蛋白,神经元标记和抗谷氨酰胺合成酶,卫星胶质细胞(SGC)标记共定位。在神经元中,CX36染色在各种尺寸的躯体和纤维中大部分均匀,并且其强度在细胞膜增加。如果主要在用作对照组织的胰岛β细胞中的连接膜,则该标记模式与CX36相反。用抗CX43和抗CX36共染色表明,如果在整个神经元和SGCS中,发现CX36的均匀染色,如果PQUCTA定位于SGCs,则在CX43中发现CX36。 CX36 mRNA在正常的腰部DRG中表达,并且在L4 DRG的大鼠中显着下调,该大鼠接受了坐骨神经损伤,导致持续的超敏反应。总的来说,这些研究结果表明,神经元和SGCs表达正常DRG中的CX36蛋白,并表明CX36水平的扰动可能有助于慢性神经损伤导致的慢性神经性疼痛。

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