Bensussen Seth, Shankar Sneha, Ching Kimberley H, Zemel Dana, Ta Tina L, Mount Rebecca A, Shroff Sanaya N, Gritton Howard J, Fabris Pierre, Vanbenschoten Hannah, Beck Connor, Man Heng-Ye, Han Xue
Department of Biomedical Engineering, Boston University, Boston, MA 02215, USA.
Department of Biology, Boston University, Boston, MA 02215, USA.
iScience. 2020 Jul 24;23(7):101330. doi: 10.1016/j.isci.2020.101330. Epub 2020 Jun 30.
Fibronectin intrabodies generated with mRNA display (FingRs) are a recently developed tool for labeling excitatory or inhibitory synapses, with the benefit of not altering endogenous synaptic protein expression levels or synaptic transmission. Here, we generated a viral vector FingR toolbox that allows for multi-color, neuron-type-specific labeling of excitatory or inhibitory synapses in multiple brain regions. We screened various fluorophores, FingR fusion configurations, and transcriptional control regulations in adeno-associated virus (AAV) and retrovirus vector designs. We report the development of a red FingR variant and demonstrated dual labeling of excitatory and inhibitory synapses in the same cells. Furthermore, we developed cre-inducible FingR AAV variants and demonstrated their utility, finding that the density of inhibitory synapses in aspiny striatal cholinergic interneurons remained unchanged in response to dopamine depletion. Finally, we generated FingR retroviral vectors, which enabled us to track the development of excitatory and inhibitory synapses in hippocampal adult-born granule cells.
通过mRNA展示技术产生的纤连蛋白胞内抗体(FingRs)是一种最近开发的用于标记兴奋性或抑制性突触的工具,其优点是不会改变内源性突触蛋白表达水平或突触传递。在这里,我们构建了一个病毒载体FingR工具箱,可对多个脑区的兴奋性或抑制性突触进行多色、神经元类型特异性标记。我们在腺相关病毒(AAV)和逆转录病毒载体设计中筛选了各种荧光团、FingR融合构型和转录调控规则。我们报告了一种红色FingR变体的开发,并展示了在同一细胞中对兴奋性和抑制性突触的双重标记。此外,我们开发了cre诱导型FingR AAV变体并证明了其效用,发现无棘纹状体胆碱能中间神经元中抑制性突触的密度在多巴胺耗竭后保持不变。最后,我们构建了FingR逆转录病毒载体,这使我们能够追踪海马成年新生颗粒细胞中兴奋性和抑制性突触的发育。