Department of Chemistry and Neuro Technology Center at Columbia University , New York , New York 10027 , United States.
Department of Psychiatry , Columbia University , New York , New York 10032 , United States.
ACS Chem Neurosci. 2018 May 16;9(5):925-934. doi: 10.1021/acschemneuro.7b00320. Epub 2018 Feb 2.
Ongoing efforts in our laboratories focus on design of optical reporters known as fluorescent false neurotransmitters (FFNs) that enable the visualization of uptake into, packaging within, and release from individual monoaminergic neurons and presynaptic sites in the brain. Here, we introduce the molecular probe FFN246 as an expansion of the FFN platform to the serotonergic system. Combining the acridone fluorophore with the ethylamine recognition element of serotonin, we identified FFN54 and FFN246 as substrates for both the serotonin transporter and the vesicular monoamine transporter 2 (VMAT2). A systematic structure-activity study revealed the basic structural chemotype of aminoalkyl acridones required for serotonin transporter (SERT) activity and enabled lowering the background labeling of these probes while maintaining SERT activity, which proved essential for obtaining sufficient signal in the brain tissue (FFN246). We demonstrate the utility of FFN246 for direct examination of SERT activity and SERT inhibitors in 96-well cell culture assays, as well as specific labeling of serotonergic neurons of the dorsal raphe nucleus in the living tissue of acute mouse brain slices. While we found only minor FFN246 accumulation in serotonergic axons in murine brain tissue, FFN246 effectively traces serotonin uptake and packaging in the soma of serotonergic neurons with improved photophysical properties and loading parameters compared to known serotonin-based fluorescent tracers.
我们实验室目前的研究重点是设计光学报告分子,即荧光假神经递质(FFN),使其能够可视化摄取、包装和释放单个单胺能神经元和大脑中的突触前部位。在这里,我们引入了分子探针 FFN246,这是对血清素能系统的 FFN 平台的扩展。我们将吖啶酮荧光团与血清素的乙胺识别元件结合,鉴定出 FFN54 和 FFN246 是血清素转运体和囊泡单胺转运体 2(VMAT2)的底物。系统的构效关系研究揭示了用于血清素转运体(SERT)活性的氨基烷基吖啶酮的基本结构化学类型,并降低了这些探针的背景标记,同时保持 SERT 活性,这对于在脑组织中获得足够的信号(FFN246)是必不可少的。我们展示了 FFN246 在 96 孔细胞培养测定中用于直接检测 SERT 活性和 SERT 抑制剂的用途,以及在急性小鼠脑切片的活体组织中对背侧中缝核的血清素能神经元进行特异性标记的用途。虽然我们只发现 FFN246 在小鼠脑组织中的血清素能轴突中有少量积累,但与已知的基于血清素的荧光示踪剂相比,FFN246 有效地追踪了血清素的摄取和包装到血清素能神经元的体部,具有改进的光物理性质和加载参数。