Hawes Jessica J, Brunzell Darlene H, Wynick David, Zachariou Venetia, Picciotto Marina R
Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut 06508, USA.
J Neurochem. 2005 Jun;93(5):1168-76. doi: 10.1111/j.1471-4159.2005.03105.x.
The galanin receptors GalR1, GalR2 and GalR3 are widely expressed throughout the mouse brain and are enriched in catecholaminergic nuclei. Here, we show that GalR1 protein levels are regulated by neuronal activity and changes in cAMP levels. GalR1, but not GalR2 or GalR3, is specifically up-regulated in the LC-like Cath.a cell line in a cAMP-dependent manner. GalR1 protein and mRNA levels are also up-regulated in the LC of galanin knockout mice, whereas GalR2 and GalR3 are not. Lack of galanin-maintained cAMP tone in the galanin knockout mouse appears to result in a loss of negative feedback resulting in increased levels of CREB phosphorylation and increased GalR1 expression. These findings suggest that changes in levels of GalR1 may play an important role in modulating signaling events and neuroplasticity underlying physiological functions of the LC.
甘丙肽受体GalR1、GalR2和GalR3在小鼠大脑中广泛表达,且在儿茶酚胺能核团中富集。在此,我们表明GalR1蛋白水平受神经元活动和cAMP水平变化的调节。GalR1,而非GalR2或GalR3,在LC样Cath.a细胞系中以cAMP依赖的方式特异性上调。在甘丙肽基因敲除小鼠的蓝斑中,GalR1蛋白和mRNA水平也上调,而GalR2和GalR3则不然。甘丙肽基因敲除小鼠中缺乏甘丙肽维持的cAMP张力似乎导致负反馈丧失,从而导致CREB磷酸化水平升高和GalR1表达增加。这些发现表明,GalR1水平的变化可能在调节蓝斑生理功能潜在的信号转导事件和神经可塑性中起重要作用。