Wirtshafter Hannah S, Disterhoft John F
Department of Neuroscience, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611
Department of Neuroscience, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611.
J Neurosci. 2022 Jun 1;42(22):4538-4554. doi: 10.1523/JNEUROSCI.1750-21.2022.
Calcium imaging using GCaMP indicators and miniature microscopes has been used to image cellular populations during long timescales and in different task phases, as well as to determine neuronal circuit topology and organization. Because the hippocampus (HPC) is essential for tasks of memory, spatial navigation, and learning, calcium imaging of large populations of HPC neurons can provide new insight on cell changes over time during these tasks. All reported HPC calcium imaging experiments have been done in mouse. However, rats have many behavioral and physiological experimental advantages over mice. In this paper, we present the first (to our knowledge) calcium imaging from CA1 HPC in freely moving male rats. Using the UCLA Miniscope, we demonstrate that, in rat, hundreds of cells can be visualized and held across weeks. We show that calcium events in these cells are highly correlated with periods of movement, with few calcium events occurring during periods without movement. We additionally show that an extremely large percent of cells recorded during a navigational task are place cells (77.3 ± 5.0%, surpassing the percent seen during mouse calcium imaging), and that these cells enable accurate decoding of animal position and can be held over days with consistent place fields in a consistent spatial map. A detailed protocol is included, and implications of these advancements on imaging and place field literature are discussed. calcium imaging in freely moving animals allows the visualization of cellular activity across days. In this paper, we present the first Ca2+ recording from CA1 hippocampus (HPC) in freely moving rats. We demonstrate that hundreds of cells can be visualized and held across weeks, and that calcium activity corresponds to periods of movement. We show that a high percentage (77.3 ± 5.0%) of imaged cells are place cells, and that these place cells enable accurate decoding and can be held stably over days with little change in field location. Because the HPC is essential for many tasks involving memory, navigation, and learning, imaging of large populations of HPC neurons can shed new insight on cellular activity changes and organization.
使用GCaMP指示剂和微型显微镜进行的钙成像已被用于在长时间尺度和不同任务阶段对细胞群体进行成像,以及确定神经元回路的拓扑结构和组织。由于海马体(HPC)对于记忆、空间导航和学习任务至关重要,对大量HPC神经元进行钙成像可以为这些任务期间细胞随时间的变化提供新的见解。所有已报道的HPC钙成像实验均在小鼠身上进行。然而,大鼠在行为和生理实验方面比小鼠具有许多优势。在本文中,我们展示了(据我们所知)首次在自由活动的雄性大鼠的CA1 HPC中进行的钙成像。使用加州大学洛杉矶分校微型显微镜,我们证明,在大鼠中,数百个细胞可以在数周内被可视化并持续监测。我们表明,这些细胞中的钙事件与运动周期高度相关,在无运动期间几乎没有钙事件发生。我们还表明,在导航任务期间记录的细胞中,极大部分是位置细胞(77.3±5.0%,超过了在小鼠钙成像中看到的比例),并且这些细胞能够准确解码动物位置,并且可以在数天内保持一致的位置场,在一致的空间地图中保持稳定。本文包含了详细的实验方案,并讨论了这些进展对成像和位置场文献的影响。在自由活动的动物中进行钙成像可以在数天内可视化细胞活动。在本文中,我们展示了首次在自由活动的大鼠的CA1海马体(HPC)中进行的Ca2+记录。我们证明,数百个细胞可以在数周内被可视化并持续监测,并且钙活动与运动周期相对应。我们表明,高比例(77.3±5.0%)的成像细胞是位置细胞,并且这些位置细胞能够进行准确解码,并且可以在数天内稳定保持,场位置变化很小。由于HPC对于许多涉及记忆、导航和学习的任务至关重要,对大量HPC神经元进行成像可以为细胞活动变化和组织提供新的见解。