Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden; Universidad de Málaga, Instituto de Investigación Biomédica de Málaga, Facultad de Medicina, Campus de Teatinos s/n, 29071, Málaga, Spain.
Department of Neurobiology, Care Sciences and Society, Center for Alzheimer Research, Neuronal Oscillations Lab, Karolinska Institutet, 171 77, Stockholm, Sweden.
Neuropharmacology. 2020 Jun 15;170:108070. doi: 10.1016/j.neuropharm.2020.108070. Epub 2020 Mar 27.
The majority of the fibroblast growth factor receptor 1-serotonin 1 A receptor (FGFR1-5-HT1AR) heterocomplexes in the hippocampus appeared to be located mainly in the neuronal networks and a relevant target for antidepressant drugs. Through a neurochemical and electrophysiological analysis it was therefore tested in the current study if astrocytic FGFR1-5-HT1AR heterocomplexes also exist in hippocampus. They may modulate the structure and function of astroglia in the hippocampus leading to possible changes in the gamma oscillations. Localization of hippocampal FGFR1-5-HT1AR heterocomplexes in astrocytes was found using in situ proximity ligation assay combined with immunohistochemistry using glial fibrillary acidic protein (GFAP) immunoreactivity as a marker for astroglia. Acute i.c.v. treatment with 8-OH-DPAT alone or together with basic fibroblast growth factor (FGF2) significantly increased FGFR1-5-HT1AR heterocomplexes in the GFAP positive cells, especially in the polymorphic layer of the dentate gyrus (PoDG) but also in the CA3 area upon combined treatment. No other hippocampal regions were studied. Also, structural plasticity changes were observed in the astrocytes, especially in the PoDG region, upon these pharmacological treatments. They may also be of relevance for enhancing the astroglial volume transmission with increased modulation of the neuronal networks in the regions studied. The effects of combined FGF2 and 5-HT agonist treatments on gamma oscillations point to a significant antagonistic interaction in astroglial FGFR1-5-HT1AR heterocomplexes that may contribute to counteraction of the 5-HT1AR-mediated decrease of gamma oscillations. This article is part of the special issue entitled 'Serotonin Research: Crossing Scales and Boundaries'.
大多数海马中的成纤维细胞生长因子受体 1-5-羟色胺 1A 受体 (FGFR1-5-HT1AR) 异源复合物似乎主要位于神经元网络中,是抗抑郁药物的相关靶点。因此,在当前研究中通过神经化学和电生理学分析来测试,海马中是否也存在星形胶质细胞 FGFR1-5-HT1AR 异源复合物。它们可能调节海马星形胶质细胞的结构和功能,导致γ 振荡可能发生变化。通过原位接近连接测定法结合使用胶质纤维酸性蛋白 (GFAP) 免疫反应性作为星形胶质细胞标志物的免疫组织化学,发现海马 FGFR1-5-HT1AR 异源复合物在星形胶质细胞中的定位。单独或与碱性成纤维细胞生长因子 (FGF2) 一起急性脑室内处理 8-OH-DPAT 显著增加了 GFAP 阳性细胞中的 FGFR1-5-HT1AR 异源复合物,尤其是在齿状回的多形层 (PoDG) ,但在联合处理时在 CA3 区也有增加。未研究其他海马区域。在这些药物处理后,还观察到星形胶质细胞的结构可塑性变化,尤其是在 PoDG 区域。它们对于增强具有神经元网络增加调制的星形胶质细胞容积传递也可能是相关的。联合 FGF2 和 5-HT 激动剂处理对γ 振荡的影响表明在星形胶质细胞 FGFR1-5-HT1AR 异源复合物中存在显著的拮抗相互作用,这可能有助于对抗 5-HT1AR 介导的 γ 振荡减少。本文是题为“血清素研究:跨越尺度和边界”的特刊的一部分。