University of Bonn, Faculty of Medicine, Institute for Experimental Epileptology and Cognition Research (IEECR), Bonn, Germany.
University Hospital Bonn, Bonn, Germany.
Elife. 2024 Jul 23;13:RP93804. doi: 10.7554/eLife.93804.
Genetically encoded calcium indicators (GECIs) such as GCaMP are invaluable tools in neuroscience to monitor neuronal activity using optical imaging. The viral transduction of GECIs is commonly used to target expression to specific brain regions, can be conveniently used with any mouse strain of interest without the need for prior crossing with a GECI mouse line, and avoids potential hazards due to the chronic expression of GECIs during development. A key requirement for monitoring neuronal activity with an indicator is that the indicator itself minimally affects activity. Here, using common adeno-associated viral (AAV) transduction procedures, we describe spatially confined aberrant Ca microwaves slowly travelling through the hippocampus following expression of GCaMP6, GCaMP7, or R-CaMP1.07 driven by the synapsin promoter with AAV-dependent gene transfer in a titre-dependent fashion. Ca microwaves developed in hippocampal CA1 and CA3, but not dentate gyrus nor neocortex, were typically first observed at 4 wk after viral transduction, and persisted up to at least 8 wk. The phenomenon was robust and observed across laboratories with various experimenters and setups. Our results indicate that aberrant hippocampal Ca microwaves depend on the promoter and viral titre of the GECI, density of expression, as well as the targeted brain region. We used an alternative viral transduction method of GCaMP which avoids this artefact. The results show that commonly used Ca-indicator AAV transduction procedures can produce artefactual Ca responses. Our aim is to raise awareness in the field of these artefactual transduction-induced Ca microwaves, and we provide a potential solution.
基因编码的钙指示剂(GECI),如 GCaMP,在神经科学中是监测神经元活动的宝贵工具,可通过光学成像实现。GECI 的病毒转导通常用于将表达靶向特定脑区,可以方便地与任何感兴趣的小鼠品系一起使用,而无需与 GECI 小鼠系预先杂交,并且避免了由于 GECI 在发育过程中的慢性表达而产生的潜在危险。使用指示剂监测神经元活动的一个关键要求是指示剂本身对活性的影响最小。在这里,我们使用常见的腺相关病毒(AAV)转导程序,描述了在突触素启动子驱动下表达 GCaMP6、GCaMP7 或 R-CaMP1.07 后,通过 AAV 依赖性基因转移以依赖滴度的方式在海马体中缓慢传播的空间受限的异常 Ca 微波。在病毒转导后 4 周左右,通常首先在海马体 CA1 和 CA3 中观察到 Ca 微波,而在至少 8 周内仍持续存在,但不在齿状回或新皮层中。该现象在具有各种实验者和设置的不同实验室中都是稳健且可观察到的。我们的结果表明,异常的海马体 Ca 微波取决于 GECI 的启动子和病毒滴度、表达密度以及靶向的脑区。我们使用了一种避免这种假象的替代 GCaMP 病毒转导方法。结果表明,常用的 Ca 指示剂 AAV 转导程序可能会产生人为的 Ca 反应。我们的目的是引起该领域对这些人为转导诱导的 Ca 微波的关注,并提供了一种潜在的解决方案。