Lykhmus Olena, Voytenko Larysa P, Lips Katrin S, Bergen Ivonne, Krasteva-Christ Gabriela, Vetter Douglas E, Kummer Wolfgang, Skok Maryna
Laboratory of Cell Receptors Immunology, Palladin Institute of Biochemistry (NAS Ukraine)Kiev, Ukraine.
Laboratory of Experimental Trauma Surgery, Justus-Liebig University GiessenGiessen, Germany.
Front Cell Neurosci. 2017 Sep 12;11:282. doi: 10.3389/fncel.2017.00282. eCollection 2017.
The α9 and α10 nicotinic acetylcholine receptor (nAChR) subunits are likely to be the evolutionary precursors to the entire cys-loop superfamily of ligand-gated ion channels, which includes acetylcholine, GABA, glycine and serotonin ionotropic receptors. nAChRs containing α9 and α10 subunits are found in the inner ear, dorsal root ganglia and many non-excitable tissues, but their expression in the central nervous system has not been definitely demonstrated. Here we show the presence of both α9 and α10 nAChR subunits in the mouse brain by RT-PCR and immunochemical approaches with a range of nAChR subunit-selective antibodies, which selectivity was demonstrated in the brain preparations of α7-/-, α9-/- and α10-/- mice. The α9 and α10 RNA transcripts were found in medulla oblongata (MO), cerebellum, midbrain (MB), thalamus and putamen (TP), somatosensory cortex (SC), frontal cortex (FC) and hippocampus. High α9-selective signal in ELISA was observed in the FC, SC, MO, TP and hippocampus and α10-selective signal was the highest in MO and FC. The α9 and α10 proteins were found in the brain mitochondria, while their presence on the plasma membrane has not been definitely confirmed The α7-, α9- and α10-selective antibodies stained mainly neurons and hypertrophied astrocytes, but not microglia. The α9- and α10-positive cells formed ordered structures or zones in cerebellum and superior olive (SO) and were randomly distributed among α7-positive cells in the FC; they were found in CA1, CA3 and CA4, but not in CA2 region of the hippocampus. The α9 and α10 subunits were up-regulated in α7-/- mice and both α7 and α9 subunits were down-regulated in α10-/- mice. We conclude that α9 and α10 nAChR subunits are expressed in distinct neurons of the mouse brain and in the brain mitochondria and are compensatory up-regulated in the absence of α7 subunits.
α9和α10烟碱型乙酰胆碱受体(nAChR)亚基可能是配体门控离子通道整个半胱氨酸环超家族的进化前体,该超家族包括乙酰胆碱、GABA、甘氨酸和5-羟色胺离子型受体。含有α9和α10亚基的nAChR存在于内耳、背根神经节和许多非兴奋性组织中,但它们在中枢神经系统中的表达尚未得到明确证实。在此,我们通过逆转录聚合酶链反应(RT-PCR)和免疫化学方法,使用一系列nAChR亚基选择性抗体,证明了小鼠大脑中同时存在α9和α10 nAChR亚基,这些抗体的选择性在α7 - / -、α9 - / -和α10 - / -小鼠的脑标本中得到了证实。在延髓(MO)、小脑、中脑(MB)、丘脑和壳核(TP)、体感皮层(SC)、额叶皮层(FC)和海马体中发现了α9和α10 RNA转录本。在ELISA中,在FC、SC、MO、TP和海马体中观察到高α9选择性信号,而α10选择性信号在MO和FC中最高。在脑线粒体中发现了α9和α10蛋白,但其在质膜上的存在尚未得到明确证实。α7、α9和α10选择性抗体主要标记神经元和肥大的星形胶质细胞,而不标记小胶质细胞。α9和α10阳性细胞在小脑中形成有序结构或区域,在上橄榄核(SO)中也有,并且在FC中随机分布于α7阳性细胞之间;在海马体的CA1、CA3和CA4区域中发现了它们,但在CA2区域中未发现。α9和α10亚基在α7 - / -小鼠中上调,而α7和α9亚基在α10 - / -小鼠中均下调。我们得出结论,α9和α10 nAChR亚基在小鼠大脑的不同神经元以及脑线粒体中表达,并且在没有α7亚基的情况下会进行代偿性上调。